Difference between revisions of "Staging page"

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[[#top|Back to Top]]
 
[[#top|Back to Top]]
 
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{{#lst:Section editor transclusions|anhl}}
! colspan="2" align="center" style="color:white; font-size:125%; background-color:#4a1486" |'''Section editor'''
 
|-
 
| style="background-color:#F0F0F0" |[[File:Hilal.jpg|frameless|upright=0.3|center]]
 
|<big>Talal Hilal, MD<br>University of Mississippi<br>Jackson, MS</big><br>[[File:Social-twitter-icon.png|frameless|upright=0.1]] [https://twitter.com/THilalMD THilalMD]
 
|-
 
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<div style="background-color: #deebf6; border: 1px solid #808000; padding: 5px; {{border-radius|16px}}"><font size="4"><b>{{#ask: [[-Has subobject::{{FULLPAGENAME}}]] |?Variant |limit=10000|format=sum}} [[Tutorial#Variants|variants]] on this page</b></font></div>
 
<div style="background-color: #deebf6; border: 1px solid #808000; padding: 5px; {{border-radius|16px}}"><font size="4"><b>{{#ask: [[-Has subobject::{{FULLPAGENAME}}]] |?Variant |limit=10000|format=sum}} [[Tutorial#Variants|variants]] on this page</b></font></div>
 
|}
 
|}
<big>'''Note: most of these regimens include complex dose adjustments based on therapeutic troughs, concomitant medications, and other factors. Therefore, the focus on this page will be inclusion of drug names and references, but not necessarily drug dosages.'''</big>
+
'''''Note 1:''' Regimens specifically intended for HIV-related Burkitt lymphoma can be found on the [[HIV-associated_lymphoma|HIV-associated lymphoma]] page.''
 +
'''''Note 2:''' The regimens on this page are primarily intended for the sporadic form of Burkitt lymphoma and some other high-grade B-cell lymphomas. In the future we plan to add regimens for the endemic form of Burkitt lymphoma.
 +
For pediatric regimens, please visit the [[Non-Hodgkin lymphoma, pediatric|pediatric NHL page]].
 
{{TOC limit|limit=3}}
 
{{TOC limit|limit=3}}
 
=Guidelines=
 
=Guidelines=
==ASBMT==
+
==[https://www.nccn.org/ NCCN]==
*'''2012:''' Martin et al. [http://www.ncbi.nlm.nih.gov/pmc/articles/pmc3404151/ First- and second-line systemic treatment of acute graft-versus-host disease: recommendations of the American Society of Blood and Marrow Transplantation]
+
*[https://www.nccn.org/professionals/physician_gls/pdf/b-cell.pdf NCCN Guidelines - B-cell Lymphomas]
==EBMT/ELN==
+
*[https://www.nccn.org/professionals/physician_gls/pdf/ped_b-cell.pdf NCCN Guidelines - Pediatric Aggressive Mature B-Cell Lymphomas]
*'''2013:''' Ruutu et al. [https://doi.org/10.1038/bmt.2013.107 Prophylaxis and treatment of GVHD: EBMT-ELN working group recommendations for a standardized practice]
+
=Untreated, pre-phase=
==ESBMT==
+
==CVP {{#subobject:1a817a|Regimen=1}}==
*'''2020:''' Penack et al. [https://doi.org/10.1016/s2352-3026(19)30256-x Prophylaxis and management of graft versus host disease after stem-cell transplantation for haematological malignancies: updated consensus recommendations of the European Society for Blood and Marrow Transplantation]
+
CVP: '''<u>C</u>'''yclophosphamide, '''<u>V</u>'''incristine, '''<u>P</u>'''rednisone
=="How I Treat"==
+
<br>COP: '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>P</u>'''rednisone
*'''2020:''' Martin PJ. How I treat steroid-refractory acute graft-versus-host disease. Blood. 2020 May 7;135(19):1630-1638. [https://doi.org/10.1182/blood.2019000960 link to original article] [https://pubmed.ncbi.nlm.nih.gov/32202630 PubMed]
 
*'''2019:''' Sarantopoulos S, Cardones AR, Sullivan KM. How I treat refractory chronic graft-versus-host disease. Blood. 2019;133(11):1191-1200. [https://www.ncbi.nlm.nih.gov/pmc/articles/pmc6418480/ link to PMC article]
 
*'''2014:''' Flowers ME, Martin PJ. How we treat chronic graft-versus-host disease. Blood. 2015 Jan 22;125(4):606-15 [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4304105/ link to PMC article]
 
=Prevention=
 
''This is very basic for now, to expand in the future. Information can also be found under individual regimens on the [[Allogeneic_HSCT|allogeneic HSCT]] page.''
 
==Cyclophosphamide, Mycophenolate mofetil, Tacrolimus==
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:8ajb82|Variant=1}}===
+
===Regimen {{#subobject:865d9b|Variant=1}}===
{| class="wikitable" style="width: 40%; text-align:center;"  
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
! style="width: 50%" |Study
+
!style="width: 33%"|Study
! style="width: 50%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 33%"|Years of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633246/ Luznik et al. 2008]
+
|[https://doi.org/10.1093/annonc/mdi403 Diviné et al. 2005 (LMB95)]
| style="background-color:#91cf61" |Non-randomized
+
|1996-2001
 +
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
|[https://doi.org/10.1016/j.bbmt.2012.06.019 Solomon et al. 2012]
+
|[https://doi.org/10.1016/S0140-6736(15)01317-3 Ribrag et al. 2016 (LMBA-02)]
| style="background-color:#91cf61" |Phase 2
+
|2004-2010
 +
|style="background-color:#91cf61"|Non-randomized portion of phase 3 RCT
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#b3e2cd">
+
''This regimen is for group B (unresected stage I, non-abdominal stage II and any stage III or IV disease without CNS or bone marrow involvement) or group C (CNS and/or bone marrow involvement).''
====Immunosuppressive therapy====
+
====Chemotherapy====
*[[Cyclophosphamide (Cytoxan)]]
+
*[[Cyclophosphamide (Cytoxan)]] 300 mg/m<sup>2</sup> IV once on day 1
*[[Mycophenolate mofetil (CellCept)]]
+
*[[Vincristine (Oncovin)]] 1 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once on day 1
*[[Tacrolimus (Prograf)]]
+
====Glucocorticoid therapy====
 +
*[[Prednisone (Sterapred)]] 60 mg/m<sup>2</sup>/day IV or PO on days 1 to 7
 +
====CNS therapy, prophylaxis (group B)====
 +
*[[Methotrexate (MTX)]] 15 mg IT once on day 1
 +
*[[Hydrocortisone (Cortef)]] (dose not specified) IT once on day 1 (admixed with MTX)
 +
====CNS therapy, treatment (group C)====
 +
*[[Methotrexate (MTX)]] 15 mg IT once per day on days 1, 3, 5
 +
*[[Cytarabine (Ara-C)]] 40 mg IT once per day on days 1, 3, 5
 +
*[[Hydrocortisone (Cortef)]] (dose not specified) IT once per day on days 1, 3, 5 (admixed with MTX & Ara-C)
 +
'''One course'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 +
====Subsequent treatment====
 +
*LMB95: [[#COPADM|COPADM]]
 +
*LMBA-02: [[#COPADM|COPADM]] versus [[#R-COPADM|R-COPADM]]
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#Luznik L, O'Donnell PV, Symons HJ, Chen AR, Leffell MS, Zahurak M, Gooley TA, Piantadosi S, Kaup M, Ambinder RF, Huff CA, Matsui W, Bolaños-Meade J, Borrello I, Powell JD, Harrington E, Warnock S, Flowers M, Brodsky RA, Sandmaier BM, Storb RF, Jones RJ, Fuchs EJ. HLA-haploidentical bone marrow transplantation for hematologic malignancies using nonmyeloablative conditioning and high-dose, posttransplantation cyclophosphamide. Biol Blood Marrow Transplant. 2008 Jun;14(6):641-50. [https://doi.org/10.1016/j.bbmt.2008.03.005 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633246/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/18489989 PubMed]
+
# '''LMB95:''' Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. [https://doi.org/10.1093/annonc/mdi403 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/16284057 PubMed]
#Solomon SR, Sizemore CA, Sanacore M, Zhang X, Brown S, Holland HK, Morris LE, Bashey A. Haploidentical transplantation using T cell replete peripheral blood stem cells and myeloablative conditioning in patients with high-risk hematologic malignancies who lack conventional donors is well tolerated and produces excellent relapse-free survival: results of a prospective phase II trial. Biol Blood Marrow Transplant. 2012 Dec;18(12):1859-66. Epub 2012 Aug 1. [https://doi.org/10.1016/j.bbmt.2012.06.019 link to original article] [https://pubmed.ncbi.nlm.nih.gov/22863841 PubMed]
+
# '''LMBA-02:''' Ribrag V, Koscielny S, Bosq J, Leguay T, Casasnovas O, Fornecker LM, Recher C, Ghesquieres H, Morschhauser F, Girault S, Le Gouill S, Ojeda-Uribe M, Mariette C, Cornillon J, Cartron G, Verge V, Chassagne-Clément C, Dombret H, Coiffier B, Lamy T, Tilly H, Salles G. Rituximab and dose-dense chemotherapy for adults with Burkitt's lymphoma: a randomised, controlled, open-label, phase 3 trial. Lancet. 2016 Jun 11;387(10036):2402-11. Epub 2016 Apr 11. [https://doi.org/10.1016/S0140-6736(15)01317-3 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/27080498 PubMed] NCT00180882
==Cyclophosphamide & Cyclosporine==
+
==Cyclophosphamide & Prednisone {{#subobject:44cd80|Regimen=1}}==
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:9134yg|Variant=1}}===
+
===Regimen variant #1, 1000/300 {{#subobject:4f2b02|Variant=1}}===
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
+
{| class="wikitable" style="width: 40%; text-align:center;"  
!style="width: 20%"|Study
+
!style="width: 25%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
+
|-
!style="width: 20%"|Comparator
+
|[https://doi.org/10.1002/cncr.23522 Oriol et al. 2008]
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
+
|style="background-color:#91cf61"|Non-randomized
 
|-
 
|-
|[https://doi.org/10.1182/bloodadvances.2021005847 Broers et al. 2022 (HOVON-96)]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4271177/ Hoelzer et al. 2014 (GMALL-B-ALL/NHL 2002)]
|2013-2018
+
|style="background-color:#91cf61"|Non-randomized
| style="background-color:#1a9851" |Phase 3 (E-switch-ic)
 
|[[#Cyclosporine_.26_Mycophenolic_acid_88|CsA & MPA]]
 
| style="background-color:#1a9850" |Superior GRFS
 
 
|-
 
|-
 
|}
 
|}
 +
''Note: GMALL-B-ALL/NHL 2002 is fairly similar to the [[Burkitt_lymphoma#GMALL-R|GMALL-R regimen]], with some minor differences. See text for details.''
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Immunosuppressive therapy====
+
====Chemotherapy====
*[[Cyclophosphamide (Cytoxan)]]
+
*[[Cyclophosphamide (Cytoxan)]] 200 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
*[[Cyclosporine]]
+
====Glucocorticoid therapy====
</div></div>
+
*[[Prednisone (Sterapred)]] 60 mg/m<sup>2</sup>/day IV or PO on days 1 to 5
===References===
+
====CNS therapy, prophylaxis====
#'''HOVON-96:''' Broers AEC, de Jong CN, Bakunina K, Hazenberg MD, van Marwijk Kooy M, de Groot MR, van Gelder M, Kuball J, van der Holt B, Meijer E, Cornelissen JJ. Posttransplant cyclophosphamide for prevention of graft-versus-host disease: results of the prospective randomized HOVON-96 trial. Blood Adv. 2022 Jun 14;6(11):3378-3385. [https://doi.org/10.1182/bloodadvances.2021005847 link to original article] [https://pubmed.ncbi.nlm.nih.gov/35143644/ PubMed] NL2128
+
*[[Cytarabine (Ara-C)]] 40 mg IT once on day 1, admixed with methotrexate and dexamethasone
==Cyclosporine & Methotrexate==
+
*[[Methotrexate (MTX)]] 15 mg IT once on day 1, admixed with cytarabine and dexamethasone
 +
*[[Dexamethasone (Decadron)]] 20 mg IT once on day 1, admixed with cytarabine and methotrexate
 +
'''One course'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 +
====Subsequent treatment====
 +
*Oriol et al. 2008: PETHEMA induction; see text for details
 +
*GMALL-B-ALL/NHL 2002: Induction; see text for details
 +
</div></div><br>
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen===
+
===Regimen variant #2, 1000/420 {{#subobject:73d35c|Variant=1}}===
{| class="wikitable sortable" style="width: 100%; text-align:center;"
+
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 20%" |Study
+
!style="width: 25%"|Study
! style="width: 20%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
! style="width: 20%" |Comparator
 
! style="width: 20%" |[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
! style="width: 20%" |[[Levels_of_Evidence#Toxicity|Comparative Toxicity]]
 
 
|-
 
|-
|[http://www.bloodjournal.org/content/92/7/2303.long Ratanatharathorn et al. 1998]
+
|[https://doi.org/10.1200/JCO.2001.19.20.4014 Lee et al. 2001 (CALGB 9251)]
| style="background-color:#1a9851" |Phase 3 (C)
+
|style="background-color:#91cf61"|Non-randomized
|[[#Methotrexate_.26_Tacrolimus|Methotrexate & Tacrolimus]]
 
| style="background-color:#d73027" |Inferior aGVHD rate
 
|
 
 
|-
 
|-
|[https://doi.org/10.1016/S1470-2045(09)70225-6 Finke et al. 2009 (AP-AS-21-DE)]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996561/ Rizzieri et al. 2014 (CALGB 10-002)]
| style="background-color:#1a9851" |Phase 3 (C)
+
|style="background-color:#91cf61"|Phase 2
|[[#Cyclosporine.2C_Methotrexate.2C_ATG|Cyclosporine, MTX, ATG]]
 
| style="background-color:#ffffbf" |Seems not superior
 
| style="background-color:#eeee01" |Similar NRM
 
|-
 
|[https://doi.org/10.1182/blood.2020009050 Kennedy et al. 2021]
 
| style="background-color:#1a9851" |Phase 3 (C)
 
|[[#Cyclosporine.2C_MTX.2C_Tocilizumab_99|Cyclosporine, MTX, Tocilizumab]]
 
| style="background-color:#ffffbf" |Did not meet primary endpoint
 
|style="background-color:#ffffbf" |Similar NRM
 
 
|-
 
|-
 
|}
 
|}
''Note: while AP-AS-21-DE did not meet its primary endpoint, there was a clear finding of superior control of cGVHD in the experimental arm.''
+
''CALGB 9251 is an earlier version of CALGB 10-002 that demonstrated that cranial radiation can be omitted in the treatment of Burkitt lymphoma.''
<div class="toccolours" style="background-color:#b3e2cd">
+
====Chemotherapy====
====Immunosuppressive therapy====
+
*[[Cyclophosphamide (Cytoxan)]] 200 mg/m<sup>2</sup> IV once per day on days 1 to 5
*[[Cyclosporine]]
+
====Glucocorticoid therapy====
*[[Methotrexate (MTX)]]
+
*[[Prednisone (Sterapred)]] 60 mg/m<sup>2</sup>/day PO on days 1 to 7
 +
====Supportive therapy====
 +
*[[Allopurinol (Zyloprim)]] 300 mg PO once per day on days 1 to 14 (includes first week of cycle 2)
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 +
====Subsequent treatment====
 +
*CALGB 9251: See text for details
 +
*CALGB 10-002: [[#CALGB_10-002_regimen|CALGB 10-002 main regimen]]
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#Ratanatharathorn V, Nash RA, Przepiorka D, Devine SM, Klein JL, Weisdorf D, Fay JW, Nademanee A, Antin JH, Christiansen NP, van der Jagt R, Herzig RH, Litzow MR, Wolff SN, Longo WL, Petersen FB, Karanes C, Avalos B, Storb R, Buell DN, Maher RM, Fitzsimmons WE, Wingard JR. Phase III study comparing methotrexate and tacrolimus (prograf, FK506) with methotrexate and cyclosporine for graft-versus-host disease prophylaxis after HLA-identical sibling bone marrow transplantation. Blood. 1998 Oct 1;92(7):2303-14. [http://www.bloodjournal.org/content/92/7/2303.long link to original article] [https://pubmed.ncbi.nlm.nih.gov/9746768 PubMed]
+
# '''CALGB 9251:''' Lee EJ, Petroni GR, Schiffer CA, Freter CE, Johnson JL, Barcos M, Frizzera G, Bloomfield CD, Peterson BA. Brief-duration high-intensity chemotherapy for patients with small noncleaved-cell lymphoma or FAB L3 acute lymphocytic leukemia: results of Cancer and Leukemia Group B study 9251. J Clin Oncol. 2001 Oct 15;19(20):4014-22. [https://doi.org/10.1200/JCO.2001.19.20.4014 link to original article] [https://pubmed.ncbi.nlm.nih.gov/11600602 PubMed]
#'''AP-AS-21-DE:''' Finke J, Bethge WA, Schmoor C, Ottinger HD, Stelljes M, Zander AR, Volin L, Ruutu T, Heim DA, Schwerdtfeger R, Kolbe K, Mayer J, Maertens JA, Linkesch W, Holler E, Koza V, Bornhäuser M, Einsele H, Kolb HJ, Bertz H, Egger M, Grishina O, Socié G; ATG-Fresenius Trial Group. Standard graft-versus-host disease prophylaxis with or without anti-T-cell globulin in haematopoietic cell transplantation from matched unrelated donors: a randomised, open-label, multicentre phase 3 trial. Lancet Oncol. 2009 Sep;10(9):855-64. Epub 2009 Aug 18. [https://doi.org/10.1016/S1470-2045(09)70225-6 link to original article] [https://pubmed.ncbi.nlm.nih.gov/19695955 PubMed] NCT00655343
+
## '''Update:''' Rizzieri DA, Johnson JL, Niedzwiecki D, Lee EJ, Vardiman JW, Powell BL, Barcos M, Bloomfield CD, Schiffer CA, Peterson BA, Canellos GP, Larson RA. Intensive chemotherapy with and without cranial radiation for Burkitt leukemia and lymphoma: final results of Cancer and Leukemia Group B Study 9251. Cancer. 2004 Apr 1;100(7):1438-48. [https://doi.org/10.1002/cncr.20143 link to original article] [https://pubmed.ncbi.nlm.nih.gov/15042678 PubMed]
##'''Update:''' Socié G, Schmoor C, Bethge WA, Ottinger HD, Stelljes M, Zander AR, Volin L, Ruutu T, Heim DA, Schwerdtfeger R, Kolbe K, Mayer J, Maertens JA, Linkesch W, Holler E, Koza V, Bornhäuser M, Einsele H, Kolb HJ, Bertz H, Egger M, Grishina O, Finke J; ATG-Fresenius Trial Group. Chronic graft-versus-host disease: long-term results from a randomized trial on graft-versus-host disease prophylaxis with or without anti-T-cell globulin ATG-Fresenius. Blood. 2011 Jun 9;117(23):6375-82. Epub 2011 Apr 5. [http://www.bloodjournal.org/content/117/23/6375.long link to original article] [https://pubmed.ncbi.nlm.nih.gov/21467544 PubMed]
+
<!-- Results previously presented at the 49th ASH Annual Meeting, Atlanta, Georgia, December 8-11, 2007. -->
##'''Update:''' Finke J, Schmoor C, Bethge WA, Ottinger H, Stelljes M, Volin L, Heim D, Bertz H, Grishina O, Socie G. Long-term outcomes after standard graft-versus-host disease prophylaxis with or without anti-human-T-lymphocyte immunoglobulin in haemopoietic cell transplantation from matched unrelated donors: final results of a randomised controlled trial. Lancet Haematol. 2017 Jun;4(6):e293-e301. [https://doi.org/10.1016/s2352-3026(17)30081-9 link to original article] [https://pubmed.ncbi.nlm.nih.gov/28583289/ PubMed]
+
# Oriol A, Ribera JM, Bergua J, Giménez Mesa E, Grande C, Esteve J, Brunet S, Moreno MJ, Escoda L, Hernandez-Rivas JM, Hoelzer D; PETHEMA. High-dose chemotherapy and immunotherapy in adult Burkitt lymphoma: comparison of results in human immunodeficiency virus-infected and noninfected patients. Cancer. 2008 Jul 1;113(1):117-25. [https://doi.org/10.1002/cncr.23522 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/18457327 PubMed]
# Kennedy GA, Tey SK, Buizen L, Varelias A, Gartlan KH, Curley C, Olver SD, Chang K, Butler JP, Misra A, Subramoniapillai E, Morton AJ, Durrant S, Henden AS, Moore J, Ritchie D, Gottlieb D, Cooney J, Paul SK, Hill GR. A phase 3 double-blind study of the addition of tocilizumab vs placebo to cyclosporin/methotrexate GVHD prophylaxis. Blood. 2021 Apr 8;137(14):1970-1979. [https://doi.org/10.1182/blood.2020009050 link to original article] [https://pubmed.ncbi.nlm.nih.gov/33512442/ PubMed]
+
# '''CALGB 10-002:''' Rizzieri DA, Johnson JL, Byrd JC, Lozanski G, Blum KA, Powell BL, Shea TC, Nattam S, Hoke E, Cheson BD, Larson RA; Alliance for Clinical Trials In Oncology. Improved efficacy using rituximab and brief duration, high intensity chemotherapy with filgrastim support for Burkitt or aggressive lymphomas: Cancer and Leukemia Group B study 10 002. Br J Haematol. 2014 Apr;165(1):102-11. Epub 2014 Jan 15. [https://doi.org/10.1111/bjh.12736 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996561/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/24428673 PubMed]
==Cyclosporine, Methotrexate, ATG==
+
# '''GMALL-B-ALL/NHL 2002:''' Hoelzer D, Walewski J, Döhner H, Viardot A, Hiddemann W, Spiekermann K, Serve H, Dührsen U, Hüttmann A, Thiel E, Dengler J, Kneba M, Schaich M, Schmidt-Wolf IG, Beck J, Hertenstein B, Reichle A, Domanska-Czyz K, Fietkau R, Horst HA, Rieder H, Schwartz S, Burmeister T, Gökbuget N; German Multicenter Study Group for Adult Acute Lymphoblastic Leukemia. Improved outcome of adult Burkitt lymphoma/leukemia with rituximab and chemotherapy: report of a large prospective multicenter trial. Blood. 2014 Dec 18;124(26):3870-9. Epub 2014 Oct 30. [http://www.bloodjournal.org/content/124/26/3870 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4271177/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/25359988 PubMed]
 +
=Untreated=
 +
==BASIC {{#subobject:eb66c6|Regimen=1}}==
 +
BASIC: '''<u>B</u>'''rief, '''<u>A</u>'''nthracycline-'''<u>S</u>'''paring, '''<u>I</u>'''ntensive '''<u>C</u>'''yclophosphamide
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen===
+
===Regimen {{#subobject:301df4|Variant=1}}===
{| class="wikitable sortable" style="width: 100%; text-align:center;"
+
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 20%" |Study
+
!style="width: 25%"|Study
! style="width: 20%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
! style="width: 20%" |Comparator
 
! style="width: 20%" |[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
! style="width: 20%" |[[Levels_of_Evidence#Toxicity|Comparative Toxicity]]
 
|-
 
|[https://doi.org/10.1016/S1470-2045(09)70225-6 Finke et al. 2009 (AP-AS-21-DE)]
 
| style="background-color:#1a9851" |Phase 3 (E-esc)
 
|[[#Cyclosporine_.26_Methotrexate|Cyclosporine & MTX]]
 
| style="background-color:#ffffbf" |Seems not superior
 
| style="background-color:#eeee01" |Similar NRM
 
 
|-
 
|-
|[https://doi.org/10.1016/S2352-3026(19)30220-0 Walker et al. 2020 (CBMTG 0801)]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234101/ Kasamon et al. 2012 (J0409)]
| style="background-color:#1a9851" |Phase 3 (E-esc)
+
|style="background-color:#91cf61"|Non-randomized
|[[#Cyclosporine_.26_Methotrexate|Cyclosporine & MTX]]
 
| style="background-color:#91cf60" |Seems to have superior OS
 
| style="background-color:#ffffbf" |Similar NRM
 
 
|-
 
|-
 
|}
 
|}
''Note: while AP-AS-21-DE did not meet its primary endpoint, there was a clear finding of superior control of cGVHD in the experimental arm.''
 
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Immunosuppressive therapy====
+
====Chemotherapy====
*[[Cyclosporine|Cyclosporine]]
+
*[[Cyclophosphamide (Cytoxan)]] 1500 mg/m<sup>2</sup> IV over 60 minutes once on day 1
*[[Methotrexate (MTX)]]
+
*[[Vincristine (Oncovin)]] 1.4 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once on day 1
*[[Antithymocyte globulin, rabbit ATG (Grafalon)|Antithymocyte globulin, rabbit ATG (ATG-Fresenius)]]
+
*[[Methotrexate (MTX)]] 3000 mg/m<sup>2</sup> IV over 2 hours once on day 8
 +
====Glucocorticoid therapy====
 +
*[[Prednisone (Sterapred)]] 100 mg PO once per day on days 1 to 5
 +
====Targeted therapy====
 +
*[[Rituximab (Rituxan)]] 375 mg/m<sup>2</sup> IV once per day on days 1 & 8
 +
====Supportive therapy====
 +
*[[Mesna (Mesnex)]] 900 mg/m<sup>2</sup> IV in divided doses on day 1
 +
*[[Folinic acid (Leucovorin)]] 25 mg/m<sup>2</sup> IV Q6H, starting 24 hours after start of IV [[Methotrexate (MTX)]], until clearance
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 3 and continuing until post-nadir ANC greater than 500/uL
 +
====CNS therapy, prophylaxis====
 +
*[[Cytarabine (Ara-C)]] 100 mg IT once per day on days 1, 4, 11 (also day 8 if no IV MTX given)
 +
*[[Hydrocortisone (Cortef)]] 50 mg IT is optional (no parameters given)
 +
'''14-day cycle for 2 cycles'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 +
====Subsequent treatment====
 +
*[[#BASIC_2|BASIC intensification]]
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''AP-AS-21-DE:''' Finke J, Bethge WA, Schmoor C, Ottinger HD, Stelljes M, Zander AR, Volin L, Ruutu T, Heim DA, Schwerdtfeger R, Kolbe K, Mayer J, Maertens JA, Linkesch W, Holler E, Koza V, Bornhäuser M, Einsele H, Kolb HJ, Bertz H, Egger M, Grishina O, Socié G; ATG-Fresenius Trial Group. Standard graft-versus-host disease prophylaxis with or without anti-T-cell globulin in haematopoietic cell transplantation from matched unrelated donors: a randomised, open-label, multicentre phase 3 trial. Lancet Oncol. 2009 Sep;10(9):855-64. Epub 2009 Aug 18. [https://doi.org/10.1016/S1470-2045(09)70225-6 link to original article] [https://pubmed.ncbi.nlm.nih.gov/19695955 PubMed] NCT00655343
+
<!-- Presented in part at the 2009 American Society of Hematology annual meeting -->
##'''Update:''' Socié G, Schmoor C, Bethge WA, Ottinger HD, Stelljes M, Zander AR, Volin L, Ruutu T, Heim DA, Schwerdtfeger R, Kolbe K, Mayer J, Maertens JA, Linkesch W, Holler E, Koza V, Bornhäuser M, Einsele H, Kolb HJ, Bertz H, Egger M, Grishina O, Finke J; ATG-Fresenius Trial Group. Chronic graft-versus-host disease: long-term results from a randomized trial on graft-versus-host disease prophylaxis with or without anti-T-cell globulin ATG-Fresenius. Blood. 2011 Jun 9;117(23):6375-82. Epub 2011 Apr 5. [http://www.bloodjournal.org/content/117/23/6375.long link to original article] [https://pubmed.ncbi.nlm.nih.gov/21467544 PubMed]
+
# '''J0409:''' Kasamon YL, Brodsky RA, Borowitz MJ, Ambinder RF, Crilley PA, Cho SY, Tsai HL, Smith BD, Gladstone DE, Carraway HE, Huff CA, Matsui WH, Bolaños-Meade J, Jones RJ, Swinnen LJ. Brief intensive therapy for older adults with newly diagnosed Burkitt or atypical Burkitt lymphoma/leukemia. Leuk Lymphoma. 2013 Mar;54(3):483-90. Epub 2012 Aug 17. [https://doi.org/10.3109/10428194.2012.715346 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234101/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/22835045 PubMed]
##'''Update:''' Finke J, Schmoor C, Bethge WA, Ottinger H, Stelljes M, Volin L, Heim D, Bertz H, Grishina O, Socie G. Long-term outcomes after standard graft-versus-host disease prophylaxis with or without anti-human-T-lymphocyte immunoglobulin in haemopoietic cell transplantation from matched unrelated donors: final results of a randomised controlled trial. Lancet Haematol. 2017 Jun;4(6):e293-e301. [https://doi.org/10.1016/s2352-3026(17)30081-9 link to original article] [https://pubmed.ncbi.nlm.nih.gov/28583289/ PubMed]
+
==CALGB 10-002 regimen {{#subobject:12cddc|Regimen=1}}==
#'''CBMTG 0801:''' Walker I, Panzarella T, Couban S, Couture F, Devins G, Elemary M, Gallagher G, Kerr H, Kuruvilla J, Lee SJ, Moore J, Nevill T, Popradi G, Roy J, Schultz KR, Szwajcer D, Toze C, Foley R; Cell Therapy Transplant Canada. Addition of anti-thymocyte globulin to standard graft-versus-host disease prophylaxis versus standard treatment alone in patients with haematological malignancies undergoing transplantation from unrelated donors: final analysis of a randomised, open-label, multicentre, phase 3 trial. Lancet Haematol. 2020 Feb;7(2):e100-e111. Epub 2020 Jan 17. [https://doi.org/10.1016/S2352-3026(19)30220-0 link to original article] [https://pubmed.ncbi.nlm.nih.gov/31958417 PubMed] NCT01217723
 
==Cyclosporine, Methotrexate, Methylprednisolone==
 
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:9126b2|Variant=1}}===
+
===Protocol {{#subobject:36626c|Variant=1}}===
{| class="wikitable sortable" style="width: 100%; text-align:center;"
+
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 25%" |Study
+
!style="width: 25%"|Study
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
! style="width: 25%" |Comparator
 
! style="width: 25%" |[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
 
|-
 
|-
|[http://www.bloodjournal.org/content/96/7/2391.long Ruutu et al. 2000]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996561/ Rizzieri et al. 2014 (CALGB 10-002)]
| style="background-color:#1a9851" |Phase 3 (E-esc)
+
|style="background-color:#91cf61"|Phase 2
|[[#Cyclosporine_.26_Methotrexate|Cyclosporine & MTX]]
 
| style="background-color:#1a9850" |Lower rate of aGVHD
 
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#cbd5e8">
 +
====Preceding treatment====
 +
*[[#Cyclophosphamide_.26_Prednisone|Cyclophosphamide & Prednisone pre-phase]]
 +
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Immunosuppressive therapy====
+
====Chemotherapy, A cycles====
*[[Cyclosporine]]
+
*[[Ifosfamide (Ifex)]] as follows:
*[[Methotrexate (MTX)]]
+
**Cycles 2, 4, 6: 800 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
*[[Methylprednisolone (Solumedrol)]]
+
*[[Methotrexate (MTX)]] as follows:
 +
**Cycles 2, 4, 6: 150 mg/m<sup>2</sup> IV bolus once on day 1, then 1350 mg/m<sup>2</sup> IV continuous infusion over 23.5 hours (total dose per cycle: 1500 mg/m<sup>2</sup>)
 +
*[[Vincristine (Oncovin)]] as follows:
 +
**Cycles 2, 4, 6: 2 mg IV push once on day 1
 +
*[[Cytarabine (Ara-C)]] as follows:
 +
**Cycles 2, 4, 6: 1000 mg/m<sup>2</sup> IV over 2 hours once per day on days 4 & 5
 +
*[[Etoposide (Vepesid)]] as follows:
 +
**Cycles 2, 4, 6: 80 mg/m<sup>2</sup> IV over 60 minutes once per day on days 4 & 5
 +
====Glucocorticoid therapy, A cycles====
 +
*[[Dexamethasone (Decadron)]] as follows:
 +
**Cycles 2, 4, 6: 10 mg/m<sup>2</sup> (route not specified) once per day on days 1 to 5
 +
====Targeted therapy, A cycles====
 +
*[[Rituximab (Rituxan)]] as follows:
 +
**Cycle 2: 50 mg/m<sup>2</sup> IV once on day 8, then 375 mg/m<sup>2</sup> IV once per day on days 10 & 12
 +
**Cycles 4 & 6: 375 mg/m<sup>2</sup> IV once on day 8
 +
====CNS therapy, prophylaxis, A cycles====
 +
*[[Cytarabine (Ara-C)]] as follows:
 +
**Cycles 2, 4, 6: 40 mg IT on day 1
 +
*[[Methotrexate (MTX)]] as follows:
 +
**Cycles 2, 4, 6: 15 mg IT on day 1
 +
*[[Hydrocortisone (Cortef)]] as follows:
 +
**Cycles 2, 4, 6: 50 mg IT on day 1
 +
====Supportive therapy, A cycles====
 +
*[[Mesna (Mesnex)]] as follows:
 +
**Cycles 2, 4, 6: (dose not specified but presumably equal to ifosfamide dose) mixed with [[Ifosfamide (Ifex)]]
 +
*[[Folinic acid (Leucovorin)]] as follows:
 +
**Cycles 2, 4, 6: 25 mg/m<sup>2</sup> IV or PO once 36 hours after start of IV methotrexate, then 10 mg/m<sup>2</sup> every 6 hours until methotrexate level less than 50 nmol/L
 +
*[[Filgrastim (Neupogen)]] as follows:
 +
**Cycles 2, 4, 6: 5 mcg/kg SC once per day, starting on day 7 and continuing until ANC greater than 500/uL
 +
====Chemotherapy, B cycles====
 +
*[[Cyclophosphamide (Cytoxan)]] as follows:
 +
**Cycles 3, 5, 7: 200 mg/m<sup>2</sup> IV once per day on days 1 to 5
 +
*[[Methotrexate (MTX)]] as follows:
 +
**Cycles 3, 5, 7: 150 mg/m<sup>2</sup> IV bolus once on day 1, then 1350 mg/m<sup>2</sup> IV continuous infusion over 23.5 hours (total dose per cycle: 1500 mg/m<sup>2</sup>)
 +
*[[Vincristine (Oncovin)]] as follows:
 +
**Cycles 3, 5, 7: 2 mg IV push once on day 1
 +
*[[Doxorubicin (Adriamycin)]] as follows:
 +
**Cycles 3, 5, 7: 25 mg/m<sup>2</sup> IV once per day on days 4 & 5
 +
====Glucocorticoid therapy, B cycles====
 +
*[[Dexamethasone (Decadron)]] as follows:
 +
**Cycles 3, 5, 7: 10 mg/m<sup>2</sup> IV or PO once per day on days 1 to 5
 +
====Targeted therapy, B cycles====
 +
*[[Rituximab (Rituxan)]] as follows:
 +
**Cycles 3, 5, 7: 375 mg/m<sup>2</sup> IV once on day 8
 +
====CNS therapy, prophylaxis, B cycles====
 +
*[[Cytarabine (Ara-C)]] as follows:
 +
**Cycles 3, 5, 7: 40 mg IT on day 1
 +
*[[Methotrexate (MTX)]] as follows:
 +
**Cycles 3, 5, 7: 15 mg IT on day 1
 +
*[[Hydrocortisone (Cortef)]] as follows:
 +
**Cycles 3, 5, 7: 50 mg IT on day 1
 +
====Supportive therapy, B cycles====
 +
*[[Folinic acid (Leucovorin)]] as follows:
 +
**Cycles 3, 5, 7: 50 mg/m<sup>2</sup> IV or PO once 36 hours after start of IV methotrexate, then 10 mg/m<sup>2</sup> every 6 hours until methotrexate level less than 50 nmol/L
 +
*[[Filgrastim (Neupogen)]] as follows:
 +
**Cycles 3, 5, 7: 5 mcg/kg SC once per day, starting on day 7 and continuing until ANC greater than 500/uL
 +
'''21-day cycle for 6 cycles'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#Ruutu T, Volin L, Parkkali T, Juvonen E, Elonen E. Cyclosporine, methotrexate, and methylprednisolone compared with cyclosporine and methotrexate for the prevention of graft-versus-host disease in bone marrow transplantation from HLA-identical sibling donor: a prospective randomized study. Blood. 2000 Oct 1;96(7):2391-8. [http://www.bloodjournal.org/content/96/7/2391.long link to original article] [https://pubmed.ncbi.nlm.nih.gov/11001889 PubMed]
+
# '''CALGB 10-002:''' Rizzieri DA, Johnson JL, Byrd JC, Lozanski G, Blum KA, Powell BL, Shea TC, Nattam S, Hoke E, Cheson BD, Larson RA; Alliance for Clinical Trials In Oncology (ACTION). Improved efficacy using rituximab and brief duration, high intensity chemotherapy with filgrastim support for Burkitt or aggressive lymphomas: Cancer and Leukemia Group B study 10 002. Br J Haematol. 2014 Apr;165(1):102-11. Epub 2014 Jan 15. [https://doi.org/10.1111/bjh.12736 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996561/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/24428673 PubMed]
##'''Update:''' Ruutu T, Nihtinen A, Niittyvuopio R, Juvonen E, Volin L. A randomized study of cyclosporine and methotrexate with or without methylprednisolone for the prevention of graft-versus-host disease: Improved long-term survival with triple prophylaxis. Cancer. 2018 Feb 15;124(4):727-733. Epub 2017 Nov 7. [https://doi.org/10.1002/cncr.31100 link to original article] [https://pubmed.ncbi.nlm.nih.gov/29112242 PubMed]
+
==CODOX-M {{#subobject:383ac6|Regimen=1}}==
==Cyclosporine, Methotrexate, Prednisone==
+
CODOX-M: '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>DOX</u>'''orubicin, '''<u>M</u>'''ethotrexate
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:81a6b2|Variant=1}}===
+
===Regimen variant #1, "Original Magrath" {{#subobject:41cf47|Variant=1}}===
{| class="wikitable sortable" style="width: 100%; text-align:center;"
+
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 25%" |Study
+
!style="width: 25%"|Study
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
! style="width: 25%" |Comparator
 
! style="width: 25%" |[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
 
|-
 
|-
|[https://doi.org/10.1056/NEJM199310213291703 Chao et al. 1993]
+
|[https://doi.org/10.1200/jco.1996.14.3.925 Magrath et al. 1996 (NCI 89-C-41)]
| style="background-color:#1a9851" |Phase 3 (E-esc)
+
|style="background-color:#91cf61"|Phase 2
|[[#Cyclosporine_.26_Prednisone_88|Cyclosporine & Prednisone]]
 
| style="background-color:#91cf60" |Seems to have lower rate of grade II to IV aGVHD
 
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#b3e2cd">
+
''This is intended for low-risk patients.''
====Immunosuppressive therapy====
+
====Chemotherapy====
*[[Cyclosporine]]
+
*[[Cyclophosphamide (Cytoxan)]] 800 mg/m<sup>2</sup> IV once on day 1, then 200 mg/m<sup>2</sup> IV once per day on days 2 to 5
*[[Methotrexate (MTX)]]
+
*[[Vincristine (Oncovin)]] 1.5 mg/m<sup>2</sup> IV once per day on days 1 & 8
*[[Prednisone (Sterapred)]]
+
*[[Doxorubicin (Adriamycin)]] 40 mg/m<sup>2</sup> IV once on day 1
</div></div>
+
*[[Methotrexate (MTX)]] by the following age-based criteria:
===References===
+
**65 years or younger: 300 mg/m<sup>2</sup> IV over 60 minutes once on day 10, then 2700 mg/m<sup>2</sup> IV continuous infusion over 23 hours (total dose per cycle: 3000 mg/m<sup>2</sup>)
#Chao NJ, Schmidt GM, Niland JC, Amylon MD, Dagis AC, Long GD, Nademanee AP, Negrin RS, O'Donnell MR, Parker PM, Smith EP, Snyder DS, Stein AS, Wong RM, Blume KG, Forman SJ. Cyclosporine, methotrexate, and prednisone compared with cyclosporine and prednisone for prophylaxis of acute graft-versus-host disease. N Engl J Med. 1993 Oct 21;329(17):1225-30. [https://doi.org/10.1056/NEJM199310213291703 link to original article] [https://pubmed.ncbi.nlm.nih.gov/8413388 PubMed]
+
**Older than 65 years: 100 mg/m<sup>2</sup> IV over 60 minutes once on day 10, then 900 mg/m<sup>2</sup> IV continuous infusion over 23 hours (total dose per cycle: 1000 mg/m<sup>2</sup>)
==Cyclosporine & Mycophenolate mofetil==
+
====Supportive therapy====
 +
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> IV Q3H, starting 36 hours after start of IV [[Methotrexate (MTX)]] until 48 hours, then every 6 hours until methotrexate level undetectable
 +
*[[Folinic acid (Leucovorin)]] 15 mg PO once 24 hours after intrathecal [[Methotrexate (MTX)]]
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 13 and continuing until ANC greater than 1000/uL
 +
====CNS therapy, prophylaxis====
 +
*[[Cytarabine (Ara-C)]] 70 mg IT once per day on days 1 & 3
 +
*[[Methotrexate (MTX)]] 12 mg IT once on day 15
 +
'''3 cycles'''
 +
</div></div><br>
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:81a8h4|Variant=1}}===
+
===Regimen variant #2, "Modified Magrath" {{#subobject:d69e9b|Variant=1}}===
{| class="wikitable sortable" style="width: 100%; text-align:center;"
+
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 25%" |Study
+
!style="width: 25%"|Study
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
! style="width: 25%" |Comparator
 
! style="width: 25%" |[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
 
|-
 
|-
|[https://doi.org/10.1016/S2352-3026(19)30088-2 Sandmaier et al. 2019 (FH 2448.00)]
+
|[https://doi.org/10.1080/1042819031000141301 LaCasce et al. 2004]
| style="background-color:#1a9851" |Phase 3 (C)
+
|style="background-color:#ffffbe"|Phase 2, <20 pts
|[[#Cyclosporine.2C_Mycophenolate_mofetil.2C_Sirolimus|Cyclosporine, MMF, Sirolimus]]
 
| style="background-color:#d73027" |Higher rate of grade II to IV aGVHD
 
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#b3e2cd">
+
''Note that dose reductions for age greater than 65 years were not described in this publication. This is intended for low-risk patients (i.e., single site of disease less than 10 cm with normal LDH).''
====Immunosuppressive therapy====
+
====Chemotherapy====
*[[Cyclosporine]] 5 mg/kg PO twice per day from day -3 to day +96, then tapered off by day +150 in the absence of GVHD
+
*[[Cyclophosphamide (Cytoxan)]] 800 mg/m<sup>2</sup> IV once per day on days 1 & 2
*[[Mycophenolate mofetil (CellCept)]] 15 mg/kg PO three times per day from day 0 to day +30, then 15 mg/kg PO twice per day from day +31 to day +150, then tapered off by day +180 in the absence of GVHD
+
*[[Vincristine (Oncovin)]] 1.4 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once per day on days 1 & 10
 +
*[[Doxorubicin (Adriamycin)]] 50 mg/m<sup>2</sup> IV once on day 1
 +
*[[Methotrexate (MTX)]] 3000 mg/m<sup>2</sup> IV once on day 10
 +
====CNS therapy, prophylaxis====
 +
*[[Cytarabine (Ara-C)]] 50 mg IT on day 1
 +
*[[Methotrexate (MTX)]] 12 mg IT on day 1
 +
*[[Hydrocortisone (Cortef)]] 50 mg IT admixed with all chemotherapy
 +
====Supportive therapy====
 +
*[[Folinic acid (Leucovorin)]] 200 mg/m<sup>2</sup> IV once 24 hours after start of IV methotrexate, then 15 mg/m<sup>2</sup> every 6 hours until methotrexate level undetectable
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day on days 3 to 8, held for MTX, and restarted after clearance continuing until ANC greater than 1000/uL
 +
'''3 cycles'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''FH 2448.00:''' Sandmaier BM, Kornblit B, Storer BE, Olesen G, Maris MB, Langston AA, Gutman JA, Petersen SL, Chauncey TR, Bethge WA, Pulsipher MA, Woolfrey AE, Mielcarek M, Martin PJ, Appelbaum FR, Flowers MED, Maloney DG, Storb R. Addition of sirolimus to standard cyclosporine plus mycophenolate mofetil-based graft-versus-host disease prophylaxis for patients after unrelated non-myeloablative haemopoietic stem cell transplantation: a multicentre, randomised, phase 3 trial. Lancet Haematol. 2019 Aug;6(8):e409-e418. Epub 2019 Jun 24. [https://doi.org/10.1016/S2352-3026(19)30088-2 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/31248843 PubMed] NCT01231412
+
# '''NCI 89-C-41:''' Magrath I, Adde M, Shad A, Venzon D, Seibel N, Gootenberg J, Neely J, Arndt C, Nieder M, Jaffe E, Wittes RA, Horak ID. Adults and children with small non-cleaved-cell lymphoma have a similar excellent outcome when treated with the same chemotherapy regimen. J Clin Oncol. 1996 Mar;14(3):925-34. [https://doi.org/10.1200/jco.1996.14.3.925 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/8622041 PubMed]
==Cyclosporine, Mycophenolate mofetil, Sirolimus==
+
# '''UKLG LY06:''' Mead GM, Sydes MR, Walewski J, Grigg A, Hatton CS, Pescosta N, Guarnaccia C, Lewis MS, McKendrick J, Stenning SP, Wright D; UKLG. An international evaluation of CODOX-M and CODOX-M alternating with IVAC in adult Burkitt's lymphoma: results of United Kingdom Lymphoma Group LY06 study. Ann Oncol. 2002 Aug;13(8):1264-74. Erratum in: Ann Oncol. 2002 Dec;13(12):1961. Norbert, P [corrected to Pescosta, N]. [https://doi.org/10.1093/annonc/mdf253 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/12181251 PubMed]
 +
# Lacasce A, Howard O, Lib S, Fisher D, Weng A, Neuberg D, Shipp M. Modified Magrath regimens for adults with Burkitt and Burkitt-like lymphomas: preserved efficacy with decreased toxicity. Leuk Lymphoma. 2004 Apr;45(4):761-7. [https://doi.org/10.1080/1042819031000141301 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/15160953 PubMed]
 +
# '''MRC/NCRI LY10:''' Mead GM, Barrans SL, Qian W, Walewski J, Radford JA, Wolf M, Clawson SM, Stenning SP, Yule CL, Jack AS; UK National Cancer Research Institute Lymphoma Clinical Studies Group; Australasian Leukaemia and Lymphoma Group. A prospective clinicopathologic study of dose-modified CODOX-M/IVAC in patients with sporadic Burkitt lymphoma defined using cytogenetic and immunophenotypic criteria (MRC/NCRI LY10 trial). Blood. 2008 Sep 15;112(6):2248-60. Epub 2008 Jul 8. [http://www.bloodjournal.org/content/112/6/2248.long link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2532802/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/18612102 PubMed]
 +
# Maruyama D, Watanabe T, Maeshima AM, Nomoto J, Taniguchi H, Azuma T, Mori M, Munakata W, Kim SW, Kobayashi Y, Matsuno Y, Tobinai K. Modified cyclophosphamide, vincristine, doxorubicin, and methotrexate (CODOX-M)/ifosfamide, etoposide, and cytarabine (IVAC) therapy with or without rituximab in Japanese adult patients with Burkitt lymphoma (BL) and B cell lymphoma, unclassifiable, with features intermediate between diffuse large B cell lymphoma and BL. Int J Hematol. 2010 Dec;92(5):732-43. Epub 2010 Dec 1. [http://link.springer.com/article/10.1007/s12185-010-0728-0 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/21120644 PubMed]
 +
==CODOX-M/IVAC {{#subobject:ef0953|Regimen=1}}==
 +
CODOX-M/IVAC: '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>DOX</u>'''orubicin, '''<u>M</u>'''ethotrexate alternating with '''<u>I</u>'''fosfamide, '''<u>V</u>'''epesid (Etoposide), '''<u>A</u>'''ra-'''<u>C</u>''' (Cytarabine)
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:8ajb82|Variant=1}}===
+
===Protocol variant #1, "Original Magrath" {{#subobject:17967a|Variant=1}}===
{| class="wikitable sortable" style="width: 100%; text-align:center;"
+
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 25%" |Study
+
!style="width: 25%"|Study
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
! style="width: 25%" |Comparator
 
! style="width: 25%" |[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
 
|-
 
|-
|[https://doi.org/10.1016/S2352-3026(19)30088-2 Sandmaier et al. 2019 (FH 2448.00)]
+
|[https://doi.org/10.1200/jco.1996.14.3.925 Magrath et al. 1996 (NCI 89-C-41)]
| style="background-color:#1a9851" |Phase 3 (E-esc)
+
|style="background-color:#91cf61"|Phase 2
|[[#Cyclosporine_.26_Mycophenolate_mofetil|Cyclosporine & MMF]]
 
| style="background-color:#1a9850" |Lower rate of grade II to IV aGVHD
 
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#b3e2cd">
+
''This is intended for high-risk patients.''
====Immunosuppressive therapy====
+
====Chemotherapy, Part 1: CODOX-M====
*[[Cyclosporine]] 5 mg/kg PO twice per day from day -3 to day +96, then tapered off by day +150 in the absence of GVHD
+
*[[Cyclophosphamide (Cytoxan)]] 800 mg/m<sup>2</sup> IV once on day 1, then 200 mg/m<sup>2</sup> IV once per day on days 2 to 5
*[[Mycophenolate mofetil (CellCept)]] 15 mg/kg PO three times per day from day 0 to day +30, then 15 mg/kg PO twice per day from day +31 to day +150, then tapered off by day +180 in the absence of GVHD
+
*[[Vincristine (Oncovin)]] 1.5 mg/m<sup>2</sup> IV once per day on days 1 & 8
*[[Sirolimus (Rapamune)]] 2 mg PO once per day from day -3 to day +150 (adjusted to maintain trough level of 3 to 12 ng/mL), then tapered off by day +180 in the absence of GVHD
+
*[[Doxorubicin (Adriamycin)]] 40 mg/m<sup>2</sup> IV once on day 1
</div></div>
+
*[[Methotrexate (MTX)]] by the following age-based criteria:
===References===
+
**65 years or younger: 300 mg/m<sup>2</sup> IV over 60 minutes once on day 10, then 2700 mg/m<sup>2</sup> IV continuous infusion over 23 hours (total dose per cycle: 3000 mg/m<sup>2</sup>)
#'''FH 2448.00:''' Sandmaier BM, Kornblit B, Storer BE, Olesen G, Maris MB, Langston AA, Gutman JA, Petersen SL, Chauncey TR, Bethge WA, Pulsipher MA, Woolfrey AE, Mielcarek M, Martin PJ, Appelbaum FR, Flowers MED, Maloney DG, Storb R. Addition of sirolimus to standard cyclosporine plus mycophenolate mofetil-based graft-versus-host disease prophylaxis for patients after unrelated non-myeloablative haemopoietic stem cell transplantation: a multicentre, randomised, phase 3 trial. Lancet Haematol. 2019 Aug;6(8):e409-e418. Epub 2019 Jun 24. [https://doi.org/10.1016/S2352-3026(19)30088-2 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/31248843 PubMed] NCT01231412
+
**Older than 65 years: 100 mg/m<sup>2</sup> IV over 60 minutes once on day 10, then 900 mg/m<sup>2</sup> IV continuous infusion over 23 hours (total dose per cycle: 1000 mg/m<sup>2</sup>)
==Methotrexate & Tacrolimus==
+
====Supportive therapy====
 +
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> IV Q3H, starting 36 hours after start of IV [[Methotrexate (MTX)]] until 48 hours, then every 6 hours until methotrexate level undetectable
 +
*[[Folinic acid (Leucovorin)]] 15 mg PO once 24 hours after intrathecal [[Methotrexate (MTX)]]
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 13 and continuing until ANC greater than 1000/uL
 +
====CNS therapy, prophylaxis====
 +
*[[Cytarabine (Ara-C)]] 70 mg IT once per day on days 1 & 3
 +
*[[Methotrexate (MTX)]] 12 mg IT once on day 15
 +
====Chemotherapy, Part 2: IVAC====
 +
*[[Ifosfamide (Ifex)]] by the following age-based criteria:
 +
**65 years or younger: 1500 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
 +
**Older than 65 years: 1000 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
 +
*[[Etoposide (Vepesid)]] 60 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
 +
*[[Cytarabine (Ara-C)]] by the following age-based criteria:
 +
**65 years or younger: 2000 mg/m<sup>2</sup> IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 8000 mg/m<sup>2</sup>)
 +
**Older than 65 years: 1000 mg/m<sup>2</sup> IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 4000 mg/m<sup>2</sup>)
 +
====Supportive therapy====
 +
*[[Mesna (Mesnex)]] by the following age-based criteria:
 +
**65 or younger: 300 mg/m<sup>2</sup> over 1 hour once per day on days 1 to 5 mixed with [[Ifosfamide (Ifex)]], then 300 mg/m<sup>2</sup> IV every four hours twice per day on days 1 to 5
 +
**Older than 65: 200 mg/m<sup>2</sup> over 1 hour once per day on days 1 to 5 mixed with [[Ifosfamide (Ifex)]], then 200 mg/m<sup>2</sup> IV every four hours twice per day on days 1 to 5
 +
*[[Folinic acid (Leucovorin)]] 15 mg PO once 24 hours after intrathecal methotrexate
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 7 and continuing until ANC greater than 1000/uL
 +
====CNS therapy, prophylaxis====
 +
*[[Methotrexate (MTX)]] 12 mg IT once on day 5
 +
'''2 cycles each of CODOX-M and IVAC (alternating)'''
 +
</div></div><br>
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen===
+
===Protocol variant #2 {{#subobject:3df4a3|Variant=1}}===
{| class="wikitable sortable" style="width: 100%; text-align:center;"
+
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 25%" |Study
+
!style="width: 25%"|Study
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
! style="width: 25%" |Comparator
 
! style="width: 25%" |[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
 
|-
 
|-
|[http://www.bloodjournal.org/content/92/7/2303.long Ratanatharathorn et al. 1998]
+
|[https://doi.org/10.1093/annonc/mdf253 Mead et al. 2002 (UKLG LY06)]
| style="background-color:#1a9851" |Phase 3 (C)
+
|style="background-color:#91cf61"|Phase 2
|[[#Cyclosporine_.26_Methotrexate|Cyclosporine & Methotrexate]]
 
| style="background-color:#1a9850" |Superior aGVHD rate
 
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#b3e2cd">
+
''This is intended for high-risk patients; modifications to the original NCI 89-C-41 are only in the CODOX-M portion.''
====Immunosuppressive therapy====
+
====Chemotherapy, Part 1: CODOX-M====
*[[Methotrexate (MTX)]]
+
*[[Cyclophosphamide (Cytoxan)]] 800 mg/m<sup>2</sup> IV once on day 1, then 200 mg/m<sup>2</sup> IV once per day on days 2 to 5
*[[Tacrolimus (Prograf)]]
+
*[[Vincristine (Oncovin)]] 1.5 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once per day on days 1 & 8
</div></div>
+
*[[Doxorubicin (Adriamycin)]] 40 mg/m<sup>2</sup> IV once on day 1
===References===
+
*[[Methotrexate (MTX)]] 1200 mg/m<sup>2</sup> IV over 60 minutes once on day 10, then 5520 mg/m<sup>2</sup> IV continuous infusion over 23 hours (total dose per cycle: 6720 mg/m<sup>2</sup>)
#Ratanatharathorn V, Nash RA, Przepiorka D, Devine SM, Klein JL, Weisdorf D, Fay JW, Nademanee A, Antin JH, Christiansen NP, van der Jagt R, Herzig RH, Litzow MR, Wolff SN, Longo WL, Petersen FB, Karanes C, Avalos B, Storb R, Buell DN, Maher RM, Fitzsimmons WE, Wingard JR. Phase III study comparing methotrexate and tacrolimus (prograf, FK506) with methotrexate and cyclosporine for graft-versus-host disease prophylaxis after HLA-identical sibling bone marrow transplantation. Blood. 1998 Oct 1;92(7):2303-14. [http://www.bloodjournal.org/content/92/7/2303.long link to original article] [https://pubmed.ncbi.nlm.nih.gov/9746768 PubMed]
+
====Supportive therapy====
==Methotrexate, Tacrolimus, Tocilizumab {{#subobject:fe1c2e|Regimen=1}}==
+
*[[Folinic acid (Leucovorin)]] 192 mg/m<sup>2</sup> IV once at 36 hours after start of IV methotrexate, then 12 mg/m<sup>2</sup> IV every 6 hours until MTX level less than 0.05
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 13 and continuing until ANC greater than 1000/uL
 +
====CNS therapy, prophylaxis====
 +
*[[Cytarabine (Ara-C)]] 70 mg IT once per day on days 1 & 3
 +
*[[Methotrexate (MTX)]] 12 mg IT once on day 15
 +
====Chemotherapy, Part 2: IVAC====
 +
*[[Ifosfamide (Ifex)]] by the following age-based criteria:
 +
**Age 65 years or younger: 1500 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
 +
**Age older than 65 years: 1000 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
 +
*[[Etoposide (Vepesid)]] 60 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
 +
*[[Cytarabine (Ara-C)]] by the following age-based criteria:
 +
**65 or younger: 2000 mg/m<sup>2</sup> IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 8000 mg/m<sup>2</sup>)
 +
**Older than 65: 1000 mg/m<sup>2</sup> IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 4000 mg/m<sup>2</sup>)
 +
====Supportive therapy====
 +
*[[Mesna (Mesnex)]] by the following age-based criteria:
 +
**65 years or younger: 300 mg/m<sup>2</sup> over 1 hour once per day on days 1 to 5 mixed with [[Ifosfamide (Ifex)]], then 300 mg/m<sup>2</sup> IV every four hours twice per day on days 1 to 5
 +
**Older than 65 years: 200 mg/m<sup>2</sup> over 1 hour once per day on days 1 to 5 mixed with [[Ifosfamide (Ifex)]], then 200 mg/m<sup>2</sup> IV every four hours twice per day on days 1 to 5
 +
*[[Folinic acid (Leucovorin)]] 15 mg PO once 24 hours after intrathecal methotrexate
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 7 and continuing until ANC greater than 1000/uL
 +
====CNS therapy, prophylaxis====
 +
*[[Methotrexate (MTX)]] 12 mg IT once on day 5
 +
'''2 cycles each of CODOX-M and IVAC (alternating)'''
 +
</div></div><br>
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:2d492b|Variant=1}}===
+
===Protocol variant #3, "Modified Magrath" {{#subobject:5382df|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 25%" |Study
+
!style="width: 25%"|Study
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865423/ Drobyski et al. 2018]
+
|[https://doi.org/10.1080/1042819031000141301 LaCasce et al. 2004]
| style="background-color:#91cf61" |Phase 2
+
|style="background-color:#ffffbe"|Phase 2, <20 pts
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#b3e2cd">
+
''All modifications are in Part 1: CODOX-M. Also note that dose reductions for age greater than 65 years were not described in this publication. This is intended for high-risk patients.''
====Immunosuppressive therapy====
+
====Chemotherapy, Part 1: CODOX-M====
*[[Methotrexate (MTX)]]
+
*[[Cyclophosphamide (Cytoxan)]] 800 mg/m<sup>2</sup> IV once per day on days 1 & 2
*[[Tacrolimus (Prograf)]]
+
*[[Vincristine (Oncovin)]] 1.4 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once per day on days 1 & 10
*[[Tocilizumab (Actemra)]]
+
*[[Doxorubicin (Adriamycin)]] 50 mg/m<sup>2</sup> IV once on day 1
</div></div>
+
*[[Methotrexate (MTX)]] 3000 mg/m<sup>2</sup> IV once on day 10
===References===
+
====CNS therapy, prophylaxis====
#Drobyski WR, Szabo A, Zhu F, Keever-Taylor C, Hebert KM, Dunn R, Yim S, Johnson B, D'Souza A, Eapen M, Fenske TS, Hari P, Hamadani M, Horowitz MM, Rizzo JD, Saber W, Shah N, Shaw B, Pasquini M. Tocilizumab, tacrolimus and methotrexate for the prevention of acute graft-versus-host disease: low incidence of lower gastrointestinal tract disease. Haematologica. 2018 Apr;103(4):717-727. Epub 2018 Jan 19. [http://www.haematologica.org/content/103/4/717 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865423/ linkt o PMC article] [https://pubmed.ncbi.nlm.nih.gov/29351985 PubMed]
+
*[[Cytarabine (Ara-C)]] 50 mg IT once per day on days 1 & 3
==Methotrexate, Tacrolimus, Vorinostat {{#subobject:ca16a7|Regimen=1}}==
+
*[[Methotrexate (MTX)]] 12 mg IT on day 1
 +
*[[Hydrocortisone (Cortef)]] 50 mg IT admixed with all chemotherapy
 +
====Supportive therapy====
 +
*[[Folinic acid (Leucovorin)]] 200 mg/m<sup>2</sup> IV once 24 hours after start of IV methotrexate, then 15 mg/m<sup>2</sup> every 6 hours until methotrexate level undetectable
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day on days 3 to 8, held for MTX, and restarted after clearance continuing until ANC greater than 1000/uL
 +
====Chemotherapy, Part 2: IVAC====
 +
*[[Ifosfamide (Ifex)]] 1500 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
 +
*[[Etoposide (Vepesid)]] 60 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
 +
*[[Cytarabine (Ara-C)]] 2000 mg/m<sup>2</sup> IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 8000 mg/m<sup>2</sup>)
 +
====CNS therapy, prophylaxis====
 +
*[[Methotrexate (MTX)]] 12 mg IT on day 5, admixed with [[Hydrocortisone (Cortef)]]
 +
*[[Hydrocortisone (Cortef)]] 50 mg IT on day 5, admixed with [[Methotrexate (MTX)]]
 +
====Supportive therapy====
 +
*[[Mesna (Mesnex)]] 300 mg/m<sup>2</sup> over 1 hour once per day on days 1 to 5 mixed with [[Ifosfamide (Ifex)]], then 300 mg/m<sup>2</sup> IV every four hours twice per day on days 1 to 5
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 6 and continuing until ANC greater than 1000/uL
 +
'''2 cycles each of CODOX-M and IVAC (alternating)'''
 +
</div></div><br>
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:191ac5|Variant=1}}===
+
===Protocol variant #4 {{#subobject:d0f19a|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 25%" |Study
+
!style="width: 25%"|Study
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[http://www.bloodjournal.org/content/130/15/1760.long Choi et al. 2017]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2532802/ Mead et al. 2008 (MRC/NCRI LY10)]
| style="background-color:#91cf61" |Phase 2
+
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#b3e2cd">
+
''This is intended for high-risk patients; modifications to the UKLG LY06 protocol are only in the CODOX-M portion.''
====Immunosuppressive therapy====
+
====Chemotherapy, Part 1: CODOX-M====
*[[Methotrexate (MTX)]] 5 mg/m<sup>2</sup> IV once per day on days +1, +3, +6, +11
+
*[[Cyclophosphamide (Cytoxan)]] 800 mg/m<sup>2</sup> IV once on day 1, then 200 mg/m<sup>2</sup> IV once per day on days 2 to 5
*[[Tacrolimus (Prograf)]] by one of the following routes, starting on day -3:
+
*[[Vincristine (Oncovin)]] 1.5 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once per day on days 1 & 8
**IV: 0.03 mg/kg/day
+
*[[Doxorubicin (Adriamycin)]] 40 mg/m<sup>2</sup> IV once on day 1
**PO: 0.045 mg/kg/day
+
*[[Methotrexate (MTX)]] 300 mg/m<sup>2</sup> IV over 60 minutes once on day 10, then 2700 mg/m<sup>2</sup> IV continuous infusion over 23 hours (total dose per cycle: 3000 mg/m<sup>2</sup>)
**Goal trough level of 8 to 12 ng/mL
+
====Supportive therapy====
**In absence of GVHD, tapering begins on day +100 and completes on day +180
+
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> IV once at 36 hours after start of IV methotrexate, then 15 mg/m<sup>2</sup> IV every 3 hours between hours 36 and 48, then 15 mg/m<sup>2</sup> IV every 6 hours until MTX level less than 0.05
*[[Vorinostat (Zolinza)]] 100 mg PO twice per day on days -10 to +100
+
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 13 and continuing until ANC greater than 1000/uL
</div></div>
+
====CNS therapy, prophylaxis====
===References===
+
*[[Cytarabine (Ara-C)]] 70 mg IT once per day on days 1 & 3
#Choi SW, Braun T, Henig I, Gatza E, Magenau J, Parkin B, Pawarode A, Riwes M, Yanik G, Dinarello CA, Reddy P. Vorinostat plus tacrolimus/methotrexate to prevent GVHD after myeloablative conditioning, unrelated donor HCT. Blood. 2017 Oct 12;130(15):1760-1767. Epub 2017 Aug 7. [http://www.bloodjournal.org/content/130/15/1760.long link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/28784598 PubMed]
+
*[[Methotrexate (MTX)]] 12 mg IT once on day 15
==Rabbit ATG==
+
====Chemotherapy, Part 2: IVAC====
====Immunosuppressive therapy====
+
*[[Ifosfamide (Ifex)]] by the following age-based criteria:
*[[Antithymocyte globulin, rabbit ATG (Thymoglobulin)]]
+
**65 years or younger: 1500 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
 +
**Older than 65 years: 1000 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
 +
*[[Etoposide (Vepesid)]] 60 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
 +
*[[Cytarabine (Ara-C)]] by the following age-based criteria:
 +
**65 or younger: 2000 mg/m<sup>2</sup> IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 8000 mg/m<sup>2</sup>)
 +
**Older than 65: 1000 mg/m<sup>2</sup> IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 4000 mg/m<sup>2</sup>)
 +
====Supportive therapy====
 +
*[[Mesna (Mesnex)]] by the following age-based criteria:
 +
**65 years or younger: 300 mg/m<sup>2</sup> over 1 hour once per day on days 1 to 5 mixed with [[Ifosfamide (Ifex)]], then 300 mg/m<sup>2</sup> IV every four hours twice per day on days 1 to 5
 +
**Older than 65 years: 200 mg/m<sup>2</sup> over 1 hour once per day on days 1 to 5 mixed with [[Ifosfamide (Ifex)]], then 200 mg/m<sup>2</sup> IV every four hours twice per day on days 1 to 5
 +
*[[Folinic acid (Leucovorin)]] 15 mg PO once 24 hours after intrathecal methotrexate
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 7 and continuing until ANC greater than 1000/uL
 +
====CNS therapy, prophylaxis====
 +
*[[Methotrexate (MTX)]] 12 mg IT once on day 5
 +
'''2 cycles each of CODOX-M and IVAC (alternating)'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#Walker I, Panzarella T, Couban S, Couture F, Devins G, Elemary M, Gallagher G, Kerr H, Kuruvilla J, Lee SJ, Moore J, Nevill T, Popradi G, Roy J, Schultz KR, Szwajcer D, Toze C, Foley R; Canadian Blood and Marrow Transplant Group. Pretreatment with anti-thymocyte globulin versus no anti-thymocyte globulin in patients with haematological malignancies undergoing haemopoietic cell transplantation from unrelated donors: a randomised, controlled, open-label, phase 3, multicentre trial. Lancet Oncol. 2016 Feb;17(2):164-173. Epub 2015 Dec 24. [https://doi.org/10.1016/s1470-2045(15)00462-3 link to original article] [https://pubmed.ncbi.nlm.nih.gov/26723083 PubMed] ISRCTN29899028
+
# '''NCI 89-C-41:''' Magrath I, Adde M, Shad A, Venzon D, Seibel N, Gootenberg J, Neely J, Arndt C, Nieder M, Jaffe E, Wittes RA, Horak ID. Adults and children with small non-cleaved-cell lymphoma have a similar excellent outcome when treated with the same chemotherapy regimen. J Clin Oncol. 1996 Mar;14(3):925-34. [https://doi.org/10.1200/jco.1996.14.3.925 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/8622041 PubMed]
#'''ATGFamilyStudy:''' Kröger N, Solano C, Wolschke C, Bandini G, Patriarca F, Pini M, Nagler A, Selleri C, Risitano A, Messina G, Bethge W, Pérez de Oteiza J, Duarte R, Carella AM, Cimminiello M, Guidi S, Finke J, Mordini N, Ferra C, Sierra J, Russo D, Petrini M, Milone G, Benedetti F, Heinzelmann M, Pastore D, Jurado M, Terruzzi E, Narni F, Völp A, Ayuk F, Ruutu T, Bonifazi F. Antilymphocyte globulin for prevention of chronic graft-versus-host disease. N Engl J Med. 2016 Jan 7;374(1):43-53. [https://doi.org/10.1056/NEJMoa1506002 link to original article] [https://pubmed.ncbi.nlm.nih.gov/26735993 PubMed] NCT00678275
+
# '''UKLG LY06:''' Mead GM, Sydes MR, Walewski J, Grigg A, Hatton CS, Pescosta N, Guarnaccia C, Lewis MS, McKendrick J, Stenning SP, Wright D; UKLG LY06 collaborators. An international evaluation of CODOX-M and CODOX-M alternating with IVAC in adult Burkitt's lymphoma: results of United Kingdom Lymphoma Group LY06 study. Ann Oncol. 2002 Aug;13(8):1264-74. Erratum in: Ann Oncol. 2002 Dec;13(12):1961. Norbert, P [corrected to Pescosta, N]. [https://doi.org/10.1093/annonc/mdf253 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/12181251 PubMed]
#'''ProfGVHD1:''' Locatelli F, Bernardo ME, Bertaina A, Rognoni C, Comoli P, Rovelli A, Pession A, Fagioli F, Favre C, Lanino E, Giorgiani G, Merli P, Pagliara D, Prete A, Zecca M. Efficacy of two different doses of rabbit anti-T-lymphocyte globulin to prevent graft-versus-host disease in children with haematological malignancies transplanted from an unrelated donor: a multicentre, randomised, open-label, phase 3 trial. Lancet Oncol. 2017 Aug;18(8):1126-1136. Epub 2017 Jul 10. [https://doi.org/10.1016/s1470-2045(17)30417-5 link to original article] [https://pubmed.ncbi.nlm.nih.gov/28705454 PubMed] NCT00934557
+
# Lacasce A, Howard O, Lib S, Fisher D, Weng A, Neuberg D, Shipp M. Modified Magrath regimens for adults with Burkitt and Burkitt-like lymphomas: preserved efficacy with decreased toxicity. Leuk Lymphoma. 2004 Apr;45(4):761-7. [https://doi.org/10.1080/1042819031000141301 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/15160953 PubMed]
==Sitagliptin, Sirolimus, Tacrolimus==
+
# '''MRC/NCRI LY10:''' Mead GM, Barrans SL, Qian W, Walewski J, Radford JA, Wolf M, Clawson SM, Stenning SP, Yule CL, Jack AS; UK National Cancer Research Institute Lymphoma Clinical Studies Group; Australasian Leukaemia and Lymphoma Group. A prospective clinicopathologic study of dose-modified CODOX-M/IVAC in patients with sporadic Burkitt lymphoma defined using cytogenetic and immunophenotypic criteria (MRC/NCRI LY10 trial). Blood. 2008 Sep 15;112(6):2248-60. Epub 2008 Jul 8. [http://www.bloodjournal.org/content/112/6/2248.long link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2532802/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/18612102 PubMed]
 +
# Maruyama D, Watanabe T, Maeshima AM, Nomoto J, Taniguchi H, Azuma T, Mori M, Munakata W, Kim SW, Kobayashi Y, Matsuno Y, Tobinai K. Modified cyclophosphamide, vincristine, doxorubicin, and methotrexate (CODOX-M)/ifosfamide, etoposide, and cytarabine (IVAC) therapy with or without rituximab in Japanese adult patients with Burkitt lymphoma (BL) and B cell lymphoma, unclassifiable, with features intermediate between diffuse large B cell lymphoma and BL. Int J Hematol. 2010 Dec;92(5):732-43. Epub 2010 Dec 1. [http://link.springer.com/article/10.1007/s12185-010-0728-0 link to original article] [https://pubmed.ncbi.nlm.nih.gov/21120644 PubMed]
 +
==COPAD {{#subobject:cc6dc7|Regimen=1}}==
 +
COPAD: '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>P</u>'''rednisone, '''<u>AD</u>'''riamycin (Doxorubicin)
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:9134b2|Variant=1}}===
+
===Regimen {{#subobject:862ad5|Variant=1}}===
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
!style="width: 33%"|Study
 
!style="width: 33%"|Study
Line 325: Line 476:
 
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://www.ncbi.nlm.nih.gov/pmc/articles/pmc7845486/ Farag et al. 2021 (IUSCC-0522)]
+
|[https://doi.org/10.1093/annonc/mdi403 Diviné et al. 2005 (LMB95)]
|2016-2018
+
|1996-2001
| style="background-color:#91cf61" |Phase 2
+
|style="background-color:#ffffbe"|Phase 2, <20 pts in this subgroup
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#b3e2cd">
+
''This regimen is for group A (completely resected stage I or abdominal stage II disease).''
====Immunosuppressive therapy====
+
====Chemotherapy====
*[[Sitagliptin (Januvia)]]
+
*[[Cyclophosphamide (Cytoxan)]] 250 mg/m<sup>2</sup> IV twice per day on days 2 to 4 (total dose per cycle: 1500 mg/m<sup>2</sup>)
*[[Sirolimus (Rapamune)]]
+
*[[Vincristine (Oncovin)]] 1.4 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once per day on days 1 & 6
*[[Tacrolimus (Prograf)]]
+
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV once on day 2
 +
====Glucocorticoid therapy====
 +
*[[Prednisone (Sterapred)]] 60 mg/m<sup>2</sup>/day IV or PO on days 1 to 6
 +
'''3 cycles; intervals were as short as possible, as soon as the ANC was greater than 1500/uL and platelet count was greater than 100 × 10<sup>9</sup>/L'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''IUSCC-0522:''' Farag SS, Abu Zaid M, Schwartz JE, Thakrar TC, Blakley AJ, Abonour R, Robertson MJ, Broxmeyer HE, Zhang S. Dipeptidyl Peptidase 4 Inhibition for Prophylaxis of Acute Graft-versus-Host Disease. N Engl J Med. 2021 Jan 7;384(1):11-19. [https://doi.org/10.1056/nejmoa2027372 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/pmc7845486/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/33406328 PubMed] NCT02683525
+
# '''LMB95:''' Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. [https://doi.org/10.1093/annonc/mdi403 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/16284057 PubMed]
=Treatment, aGVHD, all lines of therapy=
+
==COPADM {{#subobject:841673|Regimen=1}}==
==Ruxolitinib monotherapy {{#subobject:05e2b6|Regimen=1}}==
+
COPADM: '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>P</u>'''rednisone, '''<u>AD</u>'''riamycin (Doxorubicin), '''<u>M</u>'''ethotrexate
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:bhy62c|Variant=1}}===
+
===Protocol {{#subobject:39dc15|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 349: Line 503:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://www.ncbi.nlm.nih.gov/pmc/articles/pmc7229262/ Jagasia et al. 2020 (REACH1)]
+
|[https://doi.org/10.1093/annonc/mdi403 Diviné et al. 2005 (LMB95)]
|2016-2018
+
|1996-2001
| style="background-color:#91cf61" |Phase 2 (RT)
+
|style="background-color:#91cf61"|Phase 2
| style="background-color:#d3d3d3" |
+
|style="background-color:#d3d3d3"|
| style="background-color:#d3d3d3" |
+
|style="background-color:#d3d3d3"|
 
|-
 
|-
|[https://doi.org/10.1056/nejmoa1917635 Zeiser et al. 2020 (REACH2)]
+
|[https://doi.org/10.1016/S0140-6736(15)01317-3 Ribrag et al. 2016 (LMBA-02)]
|2017-2019
+
|2004-2010
| style="background-color:#1a9851" |Phase 3 (E-switch-ooc)
+
|style="background-color:#1a9851"|Phase 3 (C)
|Investigator's choice
+
|[[#R-COPADM|R-COPADM]]
| style="background-color:#1a9850" |Superior ORR
+
|style="background-color:#fc8d59"|Seems to have inferior EFS
 
|-
 
|-
 
|}
 
|}
 +
''This protocol is for group B (unresected stage I, non-abdominal stage II and any stage III or IV disease without CNS or bone marrow involvement) or group C (CNS and/or bone marrow involvement). Diviné et al. 2005 list the dose of HD-MTX as 3 mg/m<sup>2</sup> but this is presumed to be a typo.''
 +
<div class="toccolours" style="background-color:#cbd5e8">
 +
====Preceding treatment====
 +
*[[#CVP|COP prephase]]
 +
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Immunosuppressive therapy====
+
====Chemotherapy, COPADM #1====
*[[Ruxolitinib (Jakafi)]] 10 mg PO twice per day
+
*[[Cyclophosphamide (Cytoxan)]] 250 mg/m<sup>2</sup> IV twice per day on days 2 to 4 (total dose: 1500 mg/m<sup>2</sup>)
'''Continued for at least 56 days, tapered thereafter'''
+
*[[Vincristine (Oncovin)]] 1.4 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once on day 1
 +
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV once on day 2
 +
*[[Methotrexate (MTX)]] 3000 mg/m<sup>2</sup> IV over 3 hours once on day 1
 +
====Glucocorticoid therapy====
 +
*[[Prednisone (Sterapred)]] 60 mg/m<sup>2</sup>/day IV or PO on days 1 to 6
 +
====Supportive therapy====
 +
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> (route not specified) every 6 hours on days 2 to 4
 +
====CNS therapy, prophylaxis (group B)====
 +
*[[Methotrexate (MTX)]] 15 mg IT once per day on days 2 & 6
 +
*[[Hydrocortisone (Cortef)]] (dose not specified) IT once per day on days 2 & 6 (admixed with MTX)
 +
====CNS therapy, treatment (group C)====
 +
*[[Methotrexate (MTX)]] 15 mg IT once per day on days 2, 4, 6
 +
*[[Cytarabine (Ara-C)]] 40 mg IT once per day on days 2, 4, 6
 +
*[[Hydrocortisone (Cortef)]] (dose not specified) IT once per day on days 2, 4, 6 (admixed with MTX & Ara-C)
 +
'''One course'''
 +
''As soon as the ANC was greater than 1500/uL and platelet count was greater than 100 × 10<sup>9</sup>/L, patients proceeded to:''
 +
====Chemotherapy, COPADM #2====
 +
*[[Cyclophosphamide (Cytoxan)]] 500 mg/m<sup>2</sup> IV twice per day on days 2 to 4 (total dose: 3000 mg/m<sup>2</sup>)
 +
*[[Vincristine (Oncovin)]] 1.4 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once per day on days 1 & 6
 +
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV once on day 2
 +
*[[Methotrexate (MTX)]] 3000 mg/m<sup>2</sup> IV over 3 hours once on day 1
 +
====Glucocorticoid therapy====
 +
*[[Prednisone (Sterapred)]] 60 mg/m<sup>2</sup>/day IV or PO on days 1 to 6
 +
====Supportive therapy====
 +
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> (route not specified) every 6 hours on days 2 to 4
 +
====CNS therapy, prophylaxis (group B)====
 +
*[[Methotrexate (MTX)]] 15 mg IT once per day on days 2 & 6
 +
*[[Hydrocortisone (Cortef)]] (dose not specified) IT once per day on days 2 & 6 (admixed with MTX)
 +
====CNS therapy, treatment (group C)====
 +
*[[Methotrexate (MTX)]] 15 mg IT once per day on days 2, 4, 6
 +
*[[Cytarabine (Ara-C)]] 40 mg IT once per day on days 2, 4, 6
 +
*[[Hydrocortisone (Cortef)]] (dose not specified) IT once per day on days 2, 4, 6 (admixed with MTX & Ara-C)
 +
'''One course'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 +
====Subsequent treatment====
 +
*As soon as the ANC was greater than 1500/uL and platelet count was greater than 100 × 10<sup>9</sup>/L:
 +
**Group B: [[#Cytarabine_.26_Methotrexate_.28CYM.29|CYM]] consolidation
 +
**Group C: [[#CYVE|CYVE]] consolidation
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''REACH2:''' Zeiser R, von Bubnoff N, Butler J, Mohty M, Niederwieser D, Or R, Szer J, Wagner EM, Zuckerman T, Mahuzier B, Xu J, Wilke C, Gandhi KK, Socié G; REACH2 Trial Group. Ruxolitinib for Glucocorticoid-Refractory Acute Graft-versus-Host Disease. N Engl J Med. 2020 May 7;382(19):1800-1810. Epub 2020 Apr 22. [https://doi.org/10.1056/nejmoa1917635 link to original article] [https://pubmed.ncbi.nlm.nih.gov/32320566 PubMed] NCT02913261
+
# '''LMB95:''' Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. [https://doi.org/10.1093/annonc/mdi403 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/16284057 PubMed]
#'''REACH1:''' Jagasia M, Perales MA, Schroeder MA, Ali H, Shah NN, Chen YB, Fazal S, Dawkins FW, Arbushites MC, Tian C, Connelly-Smith L, Howell MD, Khoury HJ. Ruxolitinib for the treatment of steroid-refractory acute GVHD (REACH1): a multicenter, open-label phase 2 trial. Blood. 2020 May 14;135(20):1739-1749. [https://doi.org/10.1182/blood.2020004823 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/pmc7229262/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/32160294/ PubMed] NCT02953678
+
# '''LMBA-02:''' Ribrag V, Koscielny S, Bosq J, Leguay T, Casasnovas O, Fornecker LM, Recher C, Ghesquieres H, Morschhauser F, Girault S, Le Gouill S, Ojeda-Uribe M, Mariette C, Cornillon J, Cartron G, Verge V, Chassagne-Clément C, Dombret H, Coiffier B, Lamy T, Tilly H, Salles G. Rituximab and dose-dense chemotherapy for adults with Burkitt's lymphoma: a randomised, controlled, open-label, phase 3 trial. Lancet. 2016 Jun 11;387(10036):2402-11. Epub 2016 Apr 11. [https://doi.org/10.1016/S0140-6736(15)01317-3 link to original article] [https://pubmed.ncbi.nlm.nih.gov/27080498 PubMed] NCT00180882
=Treatment, cGVHD, all lines of therapy=
+
==DA-R-EPOCH {{#subobject:3c495a|Regimen=1}}==
==Cyclosporine & Prednisone {{#subobject:7a7c79|Regimen=1}}==
+
DA-R-EPOCH: '''<u>D</u>'''ose '''<u>A</u>'''djusted '''<u>R</u>'''ituximab, '''<u>E</u>'''toposide, '''<u>P</u>'''rednisone, '''<u>O</u>'''ncovin (Vincristine), '''<u>C</u>'''yclophosphamide, '''<u>H</u>'''ydroxydaunorubicin (Doxorubicin)
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:c940ce|Variant=1}}===
+
===Regimen {{#subobject:de3391|Variant=1}}===
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
+
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 25%" |Study
+
!style="width: 25%"|Study
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
! style="width: 25%" |Comparator
 
! style="width: 25%" |[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
 
|-
 
|-
|[http://www.bbmt.org/article/S1083-8791(01)50043-9 Arora et al. 2001]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901044/ Dunleavy et al. 2013 (NCI 93-C-0133)]
| style="background-color:#1a9851" |Randomized (C)
+
|style="background-color:#ffffbe"|Phase 2, <20 pts in this subgroup
|[[#Cyclosporine.2C_Prednisone.2C_Thalidomide_99|Cyclosporine, Prednisone, Thalidomide]]
 
| style="background-color:#ffffbf" |Seems not superior
 
 
|-
 
|-
 
|}
 
|}
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Immunosuppressive therapy====
+
====Targeted therapy====
*[[Cyclosporine|Cyclosporine]]
+
*[[Rituximab (Rituxan)]] 375 mg/m<sup>2</sup> IV over 3 hours once on day 1
*[[Prednisone (Sterapred)]]
+
====Chemotherapy====
 +
*[[Etoposide (Vepesid)]] 50 mg/m<sup>2</sup>/day IV continuous infusion over 96 hours, started on day 1 (total dose per cycle: 200 mg/m<sup>2</sup>)
 +
*[[Vincristine (Oncovin)]] 0.4 mg/m<sup>2</sup>/day IV continuous infusion over 96 hours, started on day 1 (total dose per cycle: 1.6 mg/m<sup>2</sup>)
 +
*[[Cyclophosphamide (Cytoxan)]] 750 mg/m<sup>2</sup> IV over 2 hours once on day 5
 +
*[[Doxorubicin (Adriamycin)]] 10 mg/m<sup>2</sup>/day IV continuous infusion over 96 hours, started on day 1 (total dose per cycle: 40 mg/m<sup>2</sup>)
 +
====Glucocorticoid therapy====
 +
*[[Prednisone (Sterapred)]] 60 mg/m<sup>2</sup> PO twice per day on days 1 to 5
 +
====Supportive therapy====
 +
*[[Filgrastim (Neupogen)]] 300 mcg SC once per day, starting on day 6 and continuing until ANC greater than 5000/uL above the nadir level
 +
*[[Trimethoprim-Sulfamethoxazole (Bactrim DS)]] one tablet PO TIW
 +
*[[Omeprazole (Prilosec)]] 20 mg PO once per day or equivalent
 +
*[[Docusate (Colace)]] as needed for constipation
 +
*[[Sennosides (Senna)]] as needed for constipation
 +
*[[Lactulose]] as needed for constipation
 +
====CNS therapy, prophylaxis====
 +
*[[Methotrexate (MTX)]] as follows:
 +
**Cycles 3 to 6: 12 mg IT once per day on days 1 & 5
 +
'''21-day cycle for 6 cycles if ANC greater than 1000/uL and platelets greater than 100 × 10<sup>9</sup>/L'''
 +
''If counts are below those levels, check daily CBC and continue growth factor support until counts are adequate and next cycle can start.''
 +
====Dose modifications====
 +
''Note this is different than some other DA-EPOCH regimens!''
 +
*Start cycle 1 as described above.
 +
*Obtain CBCs twice per week for nadir measurements.
 +
*If nadir ANC greater than or equal to 500/uL, increase etoposide, doxorubicin, and cyclophosphamide by 20% compared to previous cycle.
 +
*If nadir ANC less than 500/uL, use same doses as last cycle.
 +
*If nadir platelet count less than 25 × 10<sup>9</sup>/L, decrease etoposide, doxorubicin, and cyclophosphamide by 20% compared to previous cycle.
 +
**''Decreases below the cycle 1 starting dose only apply to cyclophosphamide, i.e., the lowest etoposide and doxorubicin would be dosed is at the original cycle 1 dose.''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#Arora M, Wagner JE, Davies SM, Blazar BR, Defor T, Enright H, Miller WJ, Weisdorf DF. Randomized clinical trial of thalidomide, cyclosporine, and prednisone versus cyclosporine and prednisone as initial therapy for chronic graft-versus-host disease. Biol Blood Marrow Transplant. 2001;7(5):265-73. [http://www.bbmt.org/article/S1083-8791(01)50043-9 link to original article] [https://pubmed.ncbi.nlm.nih.gov/11400948 PubMed]
+
<!-- # Dunleavy K, Little RF, Pittaluga S, Grant N, Shovlin M, Steinberg S, Yarchoan R, Janik J, Jaffe ES, Wilson WH. A prospective study of dose-adjusted (DA) EPOCH with rituximab in adults with newly diagnosed Burkitt lymphoma: a regimen with high efficacy and low toxicity. Ann Oncol 19(suppl4):83-84, abstr.9. 2008 Jun. [http://annonc.oxfordjournals.org/content/19/suppl_4.toc link to original article] '''contains dosing details in abstract''' -->
==Cyclosporine, Corticosteroids, Rituximab {{#subobject:9fffb0|Regimen=1}}==
+
# '''NCI 93-C-0133:''' Dunleavy K, Pittaluga S, Shovlin M, Steinberg SM, Cole D, Grant C, Widemann B, Staudt LM, Jaffe ES, Little RF, Wilson WH. Low-intensity therapy in adults with Burkitt's lymphoma. N Engl J Med. 2013 Nov 14;369(20):1915-25. [https://doi.org/10.1056/NEJMoa1308392 link to original article] [https://www.nejm.org/doi/suppl/10.1056/NEJMoa1308392/suppl_file/nejmoa1308392_appendix.pdf link to supplement] '''contains dosing details in supplement''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901044/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/24224624 PubMed] NCT00001337
 +
==GMALL-R {{#subobject:630893|Regimen=1}}==
 +
GMALL-R: '''<u>G</u>'''erman '''<u>M</u>'''ulticenter Study Group for the Treatment of Adult '''<u>A</u>'''cute '''<u>L</u>'''ymphoblastic '''<u>L</u>'''eukemia, '''<u>R</u>'''ituximab
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:0de254|Variant=1}}===
+
===Protocol {{#subobject:724602|Variant=1}}===
{| class="wikitable" style="width: 60%; text-align:center;"  
+
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 33%" |Study
+
!style="width: 25%"|Study
! style="width: 33%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
! style="width: 33%" |[[Levels_of_Evidence#Efficacy|Efficacy]]
 
 
|-
 
|-
|[http://www.bloodjournal.org/content/130/20/2186.long Malard et al. 2017]
+
|[https://doi.org/10.1002/cncr.27918 Ribera et al. 2013 (Burkimab)]
| style="background-color:#91cf61" |Phase 2
+
|style="background-color:#91cf61"|Phase 2
| style="background-color:#d4d4d4" |ORR at 12 mo: 83%
 
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#b3e2cd">
+
''Numbering of days is based on prephase->A->B->C; however, certain patient populations received different ordering of regimen, see below.''
====Immunosuppressive therapy====
+
====Chemotherapy, prephase====
*[[Cyclosporine|Cyclosporine]] 6 mg/kg PO twice per day
+
*[[Cyclophosphamide (Cytoxan)]] 200 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
**Or, continued at the dose at time of study entry
+
====Glucocorticoid therapy, prephase====
**Goal level 200 to 400 ng/mL
+
*[[Prednisone (Sterapred)]] 60 mg/m<sup>2</sup> IV bolus once per day on days 1 to 5
*[[:Category:Steroids|Corticosteroids]] equivalent to 1 mg/kg/day of [[Prednisone (Sterapred)]]
+
====Targeted therapy, A cycle====
*[[Rituximab (Rituxan)]] 375 mg/m<sup>2</sup> IV once per day on days 1, 8, 15, 22
+
*[[Rituximab (Rituxan)]] 375 mg/m<sup>2</sup> IV over 4 hours once on day 7
''Rituximab given as a 4-week course, repeated one month later if PR or better. Corticosteroids and CsA tapered per standard of care.''
+
====Chemotherapy, A cycle====
 +
*[[Vincristine (Oncovin)]] 2 mg IV bolus once on day 8
 +
*[[Methotrexate (MTX)]] by the following age-based criteria:
 +
**55 or younger: 1500 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 8
 +
**Older than 55 years: 750 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 8
 +
*[[Ifosfamide (Ifex)]] 800 mg/m<sup>2</sup> IV over 60 minutes once per day on days 8 to 12
 +
*[[Teniposide (Vumon)]] 100 mg/m<sup>2</sup> IV over 60 minutes once per day on days 11 & 12
 +
*[[Cytarabine (Ara-C)]] by the following age-based criteria:
 +
**55 or younger: 150 mg/m<sup>2</sup> IV over 60 minutes twice per day on days 11 & 12
 +
**Older than 55 years: 75 mg/m<sup>2</sup> IV over 60 minutes twice per day on days 11 & 12
 +
====Glucocorticoid therapy, A cycle====
 +
*[[Dexamethasone (Decadron)]] 10 mg/m<sup>2</sup> IV bolus once per day on days 8 to 12
 +
====Supportive therapy, A cycle====
 +
*[[Folinic acid (Leucovorin)]] (dose/route/schedule not specified), starting 12 hours after [[Methotrexate (MTX)]] infusion
 +
====Targeted therapy, B cycle====
 +
*[[Rituximab (Rituxan)]] 375 mg/m<sup>2</sup> IV over 4 hours once on day 28
 +
====Chemotherapy, B cycle====
 +
*[[Vincristine (Oncovin)]] 2 mg IV bolus once on day 29
 +
*[[Methotrexate (MTX)]] by the following age-based criteria:
 +
**55 or younger: 1500 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 29
 +
**Older than 55 years: 750 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 29
 +
*[[Cyclophosphamide (Cytoxan)]] 200 mg/m<sup>2</sup> IV over 60 minutes once per day on days 29 to 33
 +
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV over 15 minutes once per day on days 32 & 33
 +
====Glucocorticoid therapy, B cycle====
 +
*[[Dexamethasone (Decadron)]] 10 mg/m<sup>2</sup> IV bolus once per day on days 29 to 33
 +
====Supportive therapy, B cycle====
 +
*[[Folinic acid (Leucovorin)]] (dose/route/schedule not specified), starting 12 hours after [[Methotrexate (MTX)]] infusion
 +
====Targeted therapy, C cycle====
 +
*[[Rituximab (Rituxan)]] 375 mg/m<sup>2</sup> IV over 4 hours once on day 49
 +
====Chemotherapy, C cycle====
 +
*[[Vindesine (Eldisine)]] 3 mg/m<sup>2</sup> (maximum dose of 5 mg) IV bolus once on day 50
 +
*[[Methotrexate (MTX)]] by the following age-based criteria, starting on day 50:
 +
**55 or younger: 1500 mg/m<sup>2</sup> IV continuous infusion over 24 hours
 +
**Older than 55 years: 750 mg/m<sup>2</sup> IV continuous infusion over 24 hours
 +
*[[Etoposide (Vepesid)]] 250 mg/m<sup>2</sup> IV over 60 minutes once per day on days 53 & 54
 +
*[[Cytarabine (Ara-C)]] by the following age-based criteria, on day 54:
 +
**55 or younger: 2000 mg/m<sup>2</sup> IV over 3 hours twice per day
 +
**Older than 55 years: 1000 mg/m<sup>2</sup> IV over 3 hours twice per day
 +
====Glucocorticoid therapy, C cycle====
 +
*[[Dexamethasone (Decadron)]] 10 mg/m<sup>2</sup> IV bolus once per day on days 50 to 54
 +
====Supportive therapy, C cycle====
 +
*[[Folinic acid (Leucovorin)]] (dose/route/schedule not specified), starting 12 hours after [[Methotrexate (MTX)]] infusion
 +
'''Give regimen by the following criteria:'''
 +
*'''Advanced stage and younger than 55 years: A->B->C for 2 courses (6 total cycles)'''
 +
*'''Older than 55 years: Alternate A & B for 3 courses (6 total cycles)'''
 +
*'''Localized stage: 4 total cycles (unclear from protocol if this means A alternating with B or A->B->C->A)'''
 +
====CNS therapy, prophylaxis====
 +
*[[Methotrexate (MTX)]] 15 mg IT once per day on days 1, 8, 12, 29, 33
 +
*[[Cytarabine (Ara-C)]] 40 mg IT once per day on days 1, 8, 12, 29, 33
 +
*[[Dexamethasone (Decadron)]] 20 mg IT once per day on days 1, 8, 12, 29, 33
 +
'''8 doses total'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#Malard F, Labopin M, Yakoub-Agha I, Chantepie S, Guillaume T, Blaise D, Tabrizi R, Magro L, Vanhove B, Blancho G, Moreau P, Gaugler B, Chevallier P, Mohty M. Rituximab-based first-line treatment of cGVHD after allogeneic SCT: results of a phase 2 study. Blood. 2017 Nov 16;130(20):2186-2195. Epub 2017 Sep 1. [http://www.bloodjournal.org/content/130/20/2186.long link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/28864814 PubMed]
+
# '''Burkimab:''' Ribera JM, García O, Grande C, Esteve J, Oriol A, Bergua J, González-Campos J, Vall-Llovera F, Tormo M, Hernández-Rivas JM, García D, Brunet S, Alonso N, Barba P, Miralles P, Llorente A, Montesinos P, Moreno MJ, Hernández-Rivas JÁ, Bernal T. Dose-intensive chemotherapy including rituximab in Burkitt's leukemia or lymphoma regardless of human immunodeficiency virus infection status: final results of a phase 2 study (Burkimab). Cancer. 2013 May 1;119(9):1660-8. Epub 2013 Jan 29. [https://doi.org/10.1002/cncr.27918 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/23361927 PubMed] NCT00388193
==Cyclosporine, Sirolimus, Prednisone {{#subobject:1ffc79|Regimen=1}}==
+
==R-CODOX-M {{#subobject:89ebce|Regimen=1}}==
 +
R-CODOX-M: '''<u>R</u>'''ituximab, '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>DOX</u>'''orubicin, '''<u>M</u>'''ethotrexate
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:cc1bce|Variant=1}}===
+
===Regimen {{#subobject:310936|Variant=1}}===
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
+
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 25%" |Study
+
!style="width: 25%"|Study
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
! style="width: 25%" |Comparator
+
|-
! style="width: 25%" |[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
+
|[http://link.springer.com/article/10.1007/s12185-010-0728-0 Maruyama et al. 2010]
 +
|style="background-color:#ffffbe"|Pilot, <20 pts
 
|-
 
|-
|[http://www.haematologica.org/content/103/11/1915 Carpenter et al. 2018 (BMT CTN 0801)]
+
|[http://www.bloodjournal.org/content/124/19/2913.long Jacobson et al. 2014]
| style="background-color:#1a9851" |Phase 2/3 (C)
+
|style="background-color:#ffffbe"|Expert Recommendation
|[[#Sirolimus_.26_Prednisone_99|Sirolimus & Prednisone]]
 
| style="background-color:#ffffbf" |Seems not superior
 
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#b3e2cd">
+
''In the Jacobson et al. 2014 review, the authors describe a "Modified Magrath regimen of R-CODOX/R-IVAC" based on the timing and dosage of [https://doi.org/10.1080/1042819031000141301 LaCasce et al. 2004]. However, [https://doi.org/10.1080/1042819031000141301 LaCasce et al. 2004] did not include rituximab in the schema. Others have published retrospective series of this regimen; doses here are based on the review article. This is for low-risk patients (i.e., single site of disease less than 10 cm with normal LDH).''
====Immunosuppressive therapy====
+
====Targeted therapy====
*[[Cyclosporine|Cyclosporine]]
+
*[[Rituximab (Rituxan)]] as follows:
*[[Sirolimus (Rapamune)]]
+
**Cycle 1: 375 mg/m<sup>2</sup> IV once no earlier than day 3
*[[Prednisone (Sterapred)]]
+
**Cycle 2 onwards: 375 mg/m<sup>2</sup> IV once on day 1
 +
====Chemotherapy====
 +
*[[Cyclophosphamide (Cytoxan)]] 800 mg/m<sup>2</sup> IV once per day on days 1 & 2
 +
*[[Vincristine (Oncovin)]] 1.4 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once per day on days 1 & 15
 +
*[[Doxorubicin (Adriamycin)]] 50 mg/m<sup>2</sup> IV once on day 1
 +
*[[Methotrexate (MTX)]] 3000 mg/m<sup>2</sup> IV over 2 to 4 hours once on day 15
 +
====CNS therapy, prophylaxis====
 +
*[[Cytarabine (Ara-C)]] 50 mg IT once on day 1
 +
*[[Methotrexate (MTX)]] 12 mg IT once on day 1
 +
====CNS therapy, treatment (for CSF positive)====
 +
*Treatment as per CNS prophylaxis PLUS in cycle 1 only:
 +
*[[Cytarabine (Ara-C)]] 50 mg IT once on day 5
 +
*[[Methotrexate (MTX)]] 12 mg IT once on day 15
 +
====Supportive therapy====
 +
*[[Folinic acid (Leucovorin)]] 200 mg/m<sup>2</sup> IV once 24 hours after start of IV methotrexate, then 15 mg/m<sup>2</sup> every 6 hours until methotrexate level undetectable
 +
*[[Pegfilgrastim (Neulasta)]] 6 mg SC once on day 3
 +
'''3 cycles'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''BMT CTN 0801:''' Carpenter PA, Logan BR, Lee SJ, Weisdorf DJ, Johnston L, Costa LJ, Kitko CL, Bolaños-Meade J, Sarantopoulos S, Alousi AM, Abhyankar S, Waller EK, Mendizabal A, Zhu J, O'Brien KA, Lazaryan A, Wu J, Nemecek ER, Pavletic SZ, Cutler CS, Horowitz MM, Arora M; BMT CTN. A phase II/III randomized, multicenter trial of prednisone/sirolimus versus prednisone/ sirolimus/calcineurin inhibitor for the treatment of chronic graft-versus-host disease: BMT CTN 0801. Haematologica. 2018 Nov;103(11):1915-1924. Epub 2018 Jun 28. [http://www.haematologica.org/content/103/11/1915 link to original article] [https://pubmed.ncbi.nlm.nih.gov/29954931 PubMed]
+
# Maruyama D, Watanabe T, Maeshima AM, Nomoto J, Taniguchi H, Azuma T, Mori M, Munakata W, Kim SW, Kobayashi Y, Matsuno Y, Tobinai K. Modified cyclophosphamide, vincristine, doxorubicin, and methotrexate (CODOX-M)/ifosfamide, etoposide, and cytarabine (IVAC) therapy with or without rituximab in Japanese adult patients with Burkitt lymphoma (BL) and B cell lymphoma, unclassifiable, with features intermediate between diffuse large B cell lymphoma and BL. Int J Hematol. 2010 Dec;92(5):732-43. Epub 2010 Dec 1. [http://link.springer.com/article/10.1007/s12185-010-0728-0 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/21120644 PubMed]
==Ibrutinib monotherapy {{#subobject:5d9394|Regimen=1}}==
+
# '''Retrospective:''' Barnes JA, Lacasce AS, Feng Y, Toomey CE, Neuberg D, Michaelson JS, Hochberg EP, Abramson JS. Evaluation of the addition of rituximab to CODOX-M/IVAC for Burkitt's lymphoma: a retrospective analysis. Ann Oncol. 2011 Aug;22(8):1859-64. Epub 2011 Feb 21. [https://doi.org/10.1093/annonc/mdq677 link to original article] [https://pubmed.ncbi.nlm.nih.gov/21339382 PubMed]
 +
# '''Review:''' Jacobson C, LaCasce A. How I treat Burkitt lymphoma in adults. Blood. 2014 Nov 6;124(19):2913-20. Epub 2014 Sep 25. [http://www.bloodjournal.org/content/124/19/2913.long link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/25258344 PubMed]
 +
==R-CODOX-M/R-IVAC {{#subobject:2a898f|Regimen=1}}==
 +
R-CODOX-M/R-IVAC: '''<u>R</u>'''ituximab, '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>DOX</u>'''orubicin, '''<u>M</u>'''ethotrexate alternating with '''<u>R</u>'''ituximab, '''<u>I</u>'''fosfamide, '''<u>V</u>'''epesid (etoposide), '''<u>A</u>'''ra-'''<u>C</u>''' (Cytarabine)
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:7f34b4|Variant=1}}===
+
===Protocol {{#subobject:9e99df|Variant=1}}===
{| class="wikitable" style="color:white; background-color:#404040"
+
{| class="wikitable" style="width: 40%; text-align:center;"
|<small>'''FDA-recommended dose'''</small>
+
!style="width: 25%"|Study
 +
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[http://www.bloodjournal.org/content/124/19/2913.long Jacobson et al. 2014]
 +
|style="background-color:#ffffbe"|Expert Recommendation
 
|-
 
|-
 
|}
 
|}
{| class="wikitable" style="width: 60%; text-align:center;"  
+
''Note: In the Jacobson et al. 2014 review, the authors describe a "Modified Magrath regimen of R-CODOX/R-IVAC" based on the timing and dosage of [https://doi.org/10.1080/1042819031000141301 LaCasce et al. 2004]. However, [https://doi.org/10.1080/1042819031000141301 LaCasce et al. 2004] did not include rituximab in the schema. Others have published retrospective series of this regimen; doses here are based on the review article. This is for high-risk patients.''
! style="width: 33%" |Study
+
<div class="toccolours" style="background-color:#b3e2cd">
! style="width: 33%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
====Targeted therapy, R-CODOX-M portion====
! style="width: 33%" |[[Levels_of_Evidence#Efficacy|Efficacy]]
+
*[[Rituximab (Rituxan)]] as follows:
 +
**Cycle 1: 375 mg/m<sup>2</sup> IV once no earlier than day 3
 +
**Cycle 2 onwards: 375 mg/m<sup>2</sup> IV once on day 1
 +
====Chemotherapy, R-CODOX-M portion====
 +
*[[Cyclophosphamide (Cytoxan)]] 800 mg/m<sup>2</sup> IV once per day on days 1 & 2
 +
*[[Vincristine (Oncovin)]] 1.4 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once per day on days 1 & 15
 +
*[[Doxorubicin (Adriamycin)]] 50 mg/m<sup>2</sup> IV once on day 1
 +
*[[Methotrexate (MTX)]] 3000 mg/m<sup>2</sup> IV over 2 to 4 hours once on day 15
 +
====CNS therapy, prophylaxis, R-CODOX-M portion====
 +
*[[Cytarabine (Ara-C)]] 50 mg IT once per day on days 1 & 3
 +
*[[Methotrexate (MTX)]] 12 mg IT once on day 1
 +
====CNS therapy, treatment (for CSF positive), R-CODOX-M portion====
 +
*Treatment as per CNS prophylaxis PLUS in cycle 1 only:
 +
*[[Cytarabine (Ara-C)]] 50 mg IT once on day 5
 +
*[[Methotrexate (MTX)]] 12 mg IT once on day 15
 +
====Supportive therapy, R-CODOX-M portion====
 +
*[[Folinic acid (Leucovorin)]] 200 mg/m<sup>2</sup> IV once 24 hours after start of IV methotrexate, then 15 mg/m<sup>2</sup> every 6 hours until methotrexate level undetectable
 +
*[[Pegfilgrastim (Neulasta)]] 6 mg SC once on day 3
 +
====Targeted therapy, R-IVAC portion====
 +
*[[Rituximab (Rituxan)]] 375 mg/m<sup>2</sup> IV once on day 1
 +
====Chemotherapy, R-IVAC portion====
 +
*[[Ifosfamide (Ifex)]] 1500 mg/m<sup>2</sup> IV over 2 hours once per day on days 1 to 5
 +
*[[Etoposide (Vepesid)]] 60 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
 +
*[[Cytarabine (Ara-C)]] 2000 mg/m<sup>2</sup> IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 8000 mg/m<sup>2</sup>)
 +
====CNS therapy, prophylaxis, R-IVAC portion====
 +
*[[Methotrexate (MTX)]] 12 mg IT once on day 5
 +
====CNS therapy, treatment (for CSF positive), R-IVAC portion====
 +
*Treatment as per CNS prophylaxis PLUS in cycle 1 only:
 +
*[[Cytarabine (Ara-C)]] 50 mg IT once on day 3
 +
====Supportive therapy, R-IVAC portion====
 +
*[[Mesna (Mesnex)]] 300 mg/m<sup>2</sup> over 1 hour once per day on days 1 to 5 mixed with [[Ifosfamide (Ifex)]], then 300 mg/m<sup>2</sup> IV every four hours twice per day on days 1 to 5
 +
*[[Pegfilgrastim (Neulasta)]] 6 mg SC once on day 6
 +
'''Patients receive 2 cycles each of R-CODOX-M and R-IVAC (alternating)'''
 +
</div></div>
 +
===References===
 +
# Maruyama D, Watanabe T, Maeshima AM, Nomoto J, Taniguchi H, Azuma T, Mori M, Munakata W, Kim SW, Kobayashi Y, Matsuno Y, Tobinai K. Modified cyclophosphamide, vincristine, doxorubicin, and methotrexate (CODOX-M)/ifosfamide, etoposide, and cytarabine (IVAC) therapy with or without rituximab in Japanese adult patients with Burkitt lymphoma (BL) and B cell lymphoma, unclassifiable, with features intermediate between diffuse large B cell lymphoma and BL. Int J Hematol. 2010 Dec;92(5):732-43. Epub 2010 Dec 1. [http://link.springer.com/article/10.1007/s12185-010-0728-0 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/21120644 PubMed]
 +
# '''Retrospective:''' Barnes JA, Lacasce AS, Feng Y, Toomey CE, Neuberg D, Michaelson JS, Hochberg EP, Abramson JS. Evaluation of the addition of rituximab to CODOX-M/IVAC for Burkitt's lymphoma: a retrospective analysis. Ann Oncol. 2011 Aug;22(8):1859-64. Epub 2011 Feb 21. [https://doi.org/10.1093/annonc/mdq677 link to original article] [https://pubmed.ncbi.nlm.nih.gov/21339382 PubMed]
 +
# '''Review:''' Jacobson C, LaCasce A. How I treat Burkitt lymphoma in adults. Blood. 2014 Nov 6;124(19):2913-20. Epub 2014 Sep 25. [http://www.bloodjournal.org/content/124/19/2913.long link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/25258344 PubMed]
 +
==R-CODOX-M (Pegylated liposomal doxorubicin substituted) {{#subobject:9a2bc1|Regimen=1}}==
 +
R-CODOX-M: '''<u>R</u>'''ituximab, '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>DOX</u>'''il (Pegylated liposomal doxorubicin), '''<u>M</u>'''ethotrexate
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen {{#subobject:de5687|Variant=1}}===
 +
{| class="wikitable" style="width: 40%; text-align:center;"  
 +
!style="width: 25%"|Study
 +
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[http://www.bloodjournal.org/content/130/21/2243.long Miklos et al. 2017 (PCYC-1129-CA)]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841019/ Evens et al. 2013 (NU 06H2)]
| style="background-color:#91cf61" |Phase 1b/2 (RT)
+
|style="background-color:#91cf61"|Phase 2
| style="background-color:#bfd3e6" |Best ORR: 67%
 
 
|-
 
|-
 
|}
 
|}
<div class="toccolours" style="background-color:#b3e2cd">
+
''This regimen is for low-risk patients.''
====Immunosuppressive therapy====
+
====Targeted therapy====
*[[Ibrutinib (Imbruvica)]] 420 mg PO once per day
+
*[[Rituximab (Rituxan)]] 500 mg/m<sup>2</sup> IV once per day on days 0 & 8
 +
====Chemotherapy====
 +
*[[Cyclophosphamide (Cytoxan)]] 800 mg/m<sup>2</sup> IV over 60 minutes once on day 1, then 200 mg/m<sup>2</sup> IV over 60 minutes once per day on days 2 to 5
 +
*[[Vincristine (Oncovin)]] 1.5 mg/m<sup>2</sup> (maximum dose of 2 mg) IV push once per day on days 1 & 8
 +
*[[Pegylated liposomal doxorubicin (Doxil)]] 40 mg/m<sup>2</sup> IV once on day 1
 +
*[[Methotrexate (MTX)]] 300 mg/m<sup>2</sup> IV over 60 minutes once on day 10, then 2700 mg/m<sup>2</sup> IV continuous infusion over 23 hours (total dose per cycle: 3000 mg/m<sup>2</sup>)
 +
====CNS therapy, prophylaxis====
 +
*[[Cytarabine (Ara-C)]] 70 mg IT once on day 1
 +
*[[Methotrexate (MTX)]] by the following criteria:
 +
**LP: 12 mg IT once on day 3
 +
**Ommaya reservoir: 6 mg IT once on day 3
 +
====Supportive therapy====
 +
*[[Folinic acid (Leucovorin)]] 200 mg/m<sup>2</sup> IV once 36 hours after start of IV methotrexate, then 15 mg/m<sup>2</sup> IV every 6 hours until methotrexate level is less than 50 nmol/L
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day on days 6 & 7, then on day 14 onwards until ANC greater than 1500/uL
 +
'''3 cycles (length not specified)'''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''PCYC-1129-CA:''' Miklos D, Cutler CS, Arora M, Waller EK, Jagasia M, Pusic I, Flowers ME, Logan AC, Nakamura R, Blazar BR, Li Y, Chang S, Lal I, Dubovsky J, James DF, Styles L, Jaglowski S. Ibrutinib for chronic graft-versus-host disease after failure of prior therapy. Blood. 2017 Nov 23;130(21):2243-2250. Epub 2017 Sep 18. [http://www.bloodjournal.org/content/130/21/2243.long link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/28924018 PubMed] NCT02195869
+
# '''NU 06H2:''' Evens AM, Carson KR, Kolesar J, Nabhan C, Helenowski I, Islam N, Jovanovic B, Barr PM, Caimi PF, Gregory SA, Gordon LI. A multicenter phase II study incorporating high-dose rituximab and liposomal doxorubicin into the CODOX-M/IVAC regimen for untreated Burkitt's lymphoma. Ann Oncol. 2013 Dec;24(12):3076-81. Epub 2013 Oct 20. [https://doi.org/10.1093/annonc/mdt414 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841019/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/24146219 PubMed]
==Ruxolitinib monotherapy {{#subobject:05e2b6|Regimen=1}}==
+
==R-CODOX-M/R-IVAC (Pegylated liposomal doxorubicin substituted) {{#subobject:4ba54c|Regimen=1}}==
 +
R-CODOX-M/R-IVAC: '''<u>R</u>'''ituximab, '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>DOX</u>'''il (Pegylated liposomal doxorubicin), '''<u>M</u>'''ethotrexate alternating with '''<u>R</u>'''ituximab, '''<u>I</u>'''fosfamide, '''<u>V</u>'''epesid (Etoposide), '''<u>A</u>'''ra-'''<u>C</u>''' (Cytarabine)
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:bhy62c|Variant=1}}===
+
===Protocol {{#subobject:92910b|Variant=1}}===
{| class="wikitable" style="color:white; background-color:#404040"
+
{| class="wikitable" style="width: 40%; text-align:center;"
|<small>'''FDA-recommended dose'''</small>
+
!style="width: 25%"|Study
 +
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841019/ Evens et al. 2013 (NU 06H2)]
 +
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 +
''This protocol is for high-risk patients.''
 +
====Targeted therapy, R-CODOX-M portion====
 +
*[[Rituximab (Rituxan)]] 500 mg/m<sup>2</sup> IV once per day on days 0 & 8
 +
====Chemotherapy, R-CODOX-M portion====
 +
*[[Cyclophosphamide (Cytoxan)]] 800 mg/m<sup>2</sup> IV over 60 minutes once on day 1, then 200 mg/m<sup>2</sup> IV over 60 minutes once per day on days 2 to 5
 +
*[[Vincristine (Oncovin)]] 1.5 mg/m<sup>2</sup> (maximum dose of 2 mg) IV push once per day on days 1 & 8
 +
*[[Pegylated liposomal doxorubicin (Doxil)]] 40 mg/m<sup>2</sup> IV once on day 1
 +
*[[Methotrexate (MTX)]] 300 mg/m<sup>2</sup> IV over 60 minutes once on day 10, then 2700 mg/m<sup>2</sup> IV continuous infusion over 23 hours (total dose per cycle: 3000 mg/m<sup>2</sup>)
 +
====CNS therapy, prophylaxis, R-CODOX-M portion====
 +
*[[Cytarabine (Ara-C)]] 70 mg IT once per day on days 1 & 3
 +
*[[Methotrexate (MTX)]] 12 mg IT (or 6 mg into Ommaya) once on day 15
 +
====Supportive therapy, R-CODOX-M portion====
 +
*[[Folinic acid (Leucovorin)]] 200 mg/m<sup>2</sup> IV once 36 hours after start of IV methotrexate, then 15 mg/m<sup>2</sup> IV every 6 hours until methotrexate level is less than 50 nmol/L
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day on days 6 & 7, then on day 14 onwards until ANC greater than 1500/uL
 +
====Targeted therapy, R-IVAC portion====
 +
*[[Rituximab (Rituxan)]] 375 mg/m<sup>2</sup> IV once per day on days 0 & either 6 or 7
 +
====Chemotherapy, R-IVAC portion====
 +
*[[Ifosfamide (Ifex)]] 1500 mg/m<sup>2</sup> IV over 3 hours once per day on days 1 to 5
 +
*[[Etoposide (Vepesid)]] 60 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 5
 +
*[[Cytarabine (Ara-C)]] 2000 mg/m<sup>2</sup> IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 8000 mg/m<sup>2</sup>)
 +
====CNS therapy, prophylaxis, R-IVAC portion====
 +
*[[Methotrexate (MTX)]] 15 mg IT once on day 5
 +
====Supportive therapy, R-IVAC portion====
 +
*[[Mesna (Mesnex)]] 500 mg/m<sup>2</sup> mixed with first [[Ifosfamide (Ifex)]], then 1000 mg/m<sup>2</sup>/day IV continuous infusion over 120 hours (total dose per cycle: 5500 mg/m<sup>2</sup>)
 +
*[[Folinic acid (Leucovorin)]] 15 mg PO every 6 hours on day 6, starting 24 hours after intrathecal [[Methotrexate (MTX)]] (total dose per cycle: 60 mg)
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on either day 6 or 7 and continuing until ANC greater than 1500/uL
 +
'''Four alternating cycles of R-CODOX-M & R-IVAC'''
 +
</div></div>
 +
===References===
 +
# '''NU 06H2:''' Evens AM, Carson KR, Kolesar J, Nabhan C, Helenowski I, Islam N, Jovanovic B, Barr PM, Caimi PF, Gregory SA, Gordon LI. A multicenter phase II study incorporating high-dose rituximab and liposomal doxorubicin into the CODOX-M/IVAC regimen for untreated Burkitt's lymphoma. Ann Oncol. 2013 Dec;24(12):3076-81. Epub 2013 Oct 20. [https://doi.org/10.1093/annonc/mdt414 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841019/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/24146219 PubMed]
 +
==R-COPADM {{#subobject:c6bb81|Regimen=1}}==
 +
R-COPADM: '''<u>R</u>'''ituximab, '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>P</u>'''rednisone, '''<u>AD</u>'''riamycin (Doxorubicin), '''<u>M</u>'''ethotrexate
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen {{#subobject:85f5b8|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
Line 477: Line 865:
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://doi.org/10.1056/nejmoa2033122 Zeiser et al. 2021 (REACH3)]
+
|[https://doi.org/10.1016/S0140-6736(15)01317-3 Ribrag et al. 2016 (LMBA-02)]
|2017-2019
+
|2004-2010
| style="background-color:#1a9851" |Phase 3 (E-RT-switch-ooc)
+
|style="background-color:#1a9851"|Phase 3 (E-esc)
|Best available therapy
+
|[[#COPADM|COPADM]]
| style="background-color:#1a9850" |Superior ORR at week 24
+
|style="background-color:#91cf60"|Seems to have superior EFS
 
|-
 
|-
 
|}
 
|}
 +
''This regimen is for group B (unresected stage I, non-abdominal stage II and any stage III or IV disease without CNS or bone marrow involvement); see manuscript for details about the regimen for group C.''
 +
<div class="toccolours" style="background-color:#cbd5e8">
 +
====Preceding treatment====
 +
*[[#CVP|COP prephase]]
 +
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Immunosuppressive therapy====
+
====Targeted therapy====
*[[Ruxolitinib (Jakafi)]] 10 mg PO twice per day
+
*[[Rituximab (Rituxan)]] 375 mg/m<sup>2</sup> IV once per day on days 0 & 6
'''28-day cycle for at least 6 cycles'''
+
====Chemotherapy====
 +
*[[Cyclophosphamide (Cytoxan)]] 500 mg/m<sup>2</sup>/day IV on days 2 to 4
 +
*[[Vincristine (Oncovin)]] 1.4 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once on day 1
 +
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV once on day 2
 +
*[[Methotrexate (MTX)]] 3000 mg/m<sup>2</sup> IV once on day 1
 +
====Glucocorticoid therapy====
 +
*[[Prednisolone (Millipred)]] 60 mg/m<sup>2</sup>/day IV or PO on days 1 to 5
 +
====Supportive therapy====
 +
*[[Folinic acid (Leucovorin)]] (dose/route not specified) on days 2 to 6
 +
====CNS therapy, prophylaxis====
 +
*[[Methotrexate (MTX)]] 15 mg IT once per day on days 2 & 6
 +
*[[Hydrocortisone (Cortef)]] (dose not specified) IT once per day on days 2 & 6 (admixed with MTX)
 +
'''2 cycles (length not specified)'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 +
====Subsequent treatment====
 +
*[[#Cytarabine_.26_Methotrexate_.28CYM.29|CYM]] consolidation
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''REACH3:''' Zeiser R, Polverelli N, Ram R, Hashmi SK, Chakraverty R, Middeke JM, Musso M, Giebel S, Uzay A, Langmuir P, Hollaender N, Gowda M, Stefanelli T, Lee SJ, Teshima T, Locatelli F; REACH3 Investigators. Ruxolitinib for Glucocorticoid-Refractory Chronic Graft-versus-Host Disease. N Engl J Med. 2021 Jul 15;385(3):228-238. [https://doi.org/10.1056/nejmoa2033122 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/34260836/ PubMed] NCT03112603
+
# '''LMBA-02:''' Ribrag V, Koscielny S, Bosq J, Leguay T, Casasnovas O, Fornecker LM, Recher C, Ghesquieres H, Morschhauser F, Girault S, Le Gouill S, Ojeda-Uribe M, Mariette C, Cornillon J, Cartron G, Verge V, Chassagne-Clément C, Dombret H, Coiffier B, Lamy T, Tilly H, Salles G. Rituximab and dose-dense chemotherapy for adults with Burkitt's lymphoma: a randomised, controlled, open-label, phase 3 trial. Lancet. 2016 Jun 11;387(10036):2402-11. Epub 2016 Apr 11. [https://doi.org/10.1016/S0140-6736(15)01317-3 link to original article] [https://pubmed.ncbi.nlm.nih.gov/27080498 PubMed] NCT00180882
==Sirolimus, Tacrolimus, Prednisone {{#subobject:05e07b|Regimen=1}}==
+
==R-Hyper-CVAD/R-MA {{#subobject:6b7f66|Regimen=1}}==
 +
R-Hyper-CVAD/R-MA: '''<u>R</u>'''ituximab, '''<u>Hyper</u>'''fractionated '''<u>C</u>'''yclophosphamide, '''<u>V</u>'''incristine, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>D</u>'''examethasone altenating with '''<u>R</u>'''ituximab, '''<u>M</u>'''ethotrexate, '''<u>A</u>'''ra-C (Cytarabine)
 
<div class="toccolours" style="background-color:#eeeeee">
 
<div class="toccolours" style="background-color:#eeeeee">
===Regimen {{#subobject:bc128c|Variant=1}}===
+
===Regimen {{#subobject:1ae302|Variant=1}}===
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
+
{| class="wikitable" style="width: 40%; text-align:center;"  
! style="width: 25%" |Study
+
!style="width: 25%"|Study
! style="width: 25%" |[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
! style="width: 25%" |Comparator
 
! style="width: 25%" |[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
 
|-
 
|-
|[http://www.haematologica.org/content/103/11/1915 Carpenter et al. 2018 (BMT CTN 0801)]
+
|[https://doi.org/10.1002/cncr.21776 Thomas et al. 2006]
| style="background-color:#1a9851" |Phase 2/3 (C)
+
|style="background-color:#ffffbe"|Pilot, <20 pts
|[[#Sirolimus_.26_Prednisone_99|Sirolimus & Prednisone]]
 
| style="background-color:#ffffbf" |Seems not superior
 
 
|-
 
|-
 
|}
 
|}
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
====Immunosuppressive therapy====
+
====Targeted therapy, Part A====
*[[Sirolimus (Rapamune)]]
+
*[[Rituximab (Rituxan)]] as follows:
*[[Tacrolimus (Prograf)]]
+
**Cycles 1 & 3: 375 mg/m<sup>2</sup> IV over 2 to 6 hours once per day on days 1 & 11
*[[Prednisone (Sterapred)]]
+
====Chemotherapy, Part A====
 +
*[[Cyclophosphamide (Cytoxan)]] as follows:
 +
**Cycles 1, 3, 5, 7: 300 mg/m<sup>2</sup> IV over 2 hours every 12 hours on days 1 to 3 (total dose per cycle: 1800 mg/m<sup>2</sup>)
 +
*[[Vincristine (Oncovin)]] as follows:
 +
**Cycles 1, 3, 5, 7: 2 mg IV once per day on days 4 & 11
 +
*[[Doxorubicin (Adriamycin)]] as follows:
 +
**Cycles 1, 3, 5, 7: 50 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 4
 +
====Glucocorticoid therapy, Part A====
 +
*[[Dexamethasone (Decadron)]] as follows:
 +
**Cycles 1, 3, 5, 7: 40 mg IV or PO once per day on days 1 to 4, 11 to 14
 +
====Supportive therapy, Part A====
 +
*[[Mesna (Mesnex)]] as follows:
 +
**Cycles 1, 3, 5, 7: 600 mg/m<sup>2</sup>/day IV continuous infusion over 72 hours, started on day 1, starting 1 hour before [[Cyclophosphamide (Cytoxan)]] and completed 12 hours after the last dose of [[Cyclophosphamide (Cytoxan)]] (total dose per cycle: 1800 mg/m<sup>2</sup>)
 +
*[[Filgrastim (Neupogen)]] as follows:
 +
**Cycles 1, 3, 5, 7: 10 mcg/kg SC once per day, starting 24 hours after completion of chemotherapy, given until WBC greater than 3 x 10<sup>9</sup>/L or bone pain present
 +
*ONE of the following antibiotics:
 +
**[[:Category:Fluoroquinolone|Fluoroquinolone]]
 +
**[[Trimethoprim-Sulfamethoxazole (Bactrim DS)]] 160/800 mg dose/route not specified
 +
*[[Fluconazole (Diflucan)]] dose/route not specified
 +
*ONE of the following antivirals:
 +
**[[Acyclovir (Zovirax)]] dose/route not specified
 +
**[[Valacyclovir (Valtrex)]] dose/route not specified
 +
'''Next cycle to start no sooner than 14 days or as soon as "unmaintained" WBC count is greater than 3 x 10<sup>9</sup>/L and platelet count greater than 50 x 10<sup>9</sup>/L'''
 +
====Dose modifications, Part A====
 +
*[[Vincristine (Oncovin)]] reduced to 1 mg for bilirubin greater than 2 mg/dL or NCI common toxicity criteria Grade 2+ peripheral neuropathy, omitted for bilirubin greater than 3 mg/dL or for ileus
 +
*[[Doxorubicin (Adriamycin)]] reduced by 50% for bilirubin 2 to 3 mg/dL, by 75% for bilirubin 3 to 5 mg/dL (eliminated for bilirubin greater than 5 mg/dL or for gastric/small-bowel involvement with Course 1 to reduce duration of myelosuppression given risk of perforation)
 +
====Targeted therapy, Part B====
 +
*[[Rituximab (Rituxan)]] as follows:
 +
**Cycles 2 & 4: 375 mg/m<sup>2</sup> IV over 2 to 6 hours once per day on days 2 & 8
 +
====Chemotherapy, Part B====
 +
*[[Methotrexate (MTX)]] as follows:
 +
**Cycles 2, 4, 6, 8: 1000 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 +
*[[Cytarabine (Ara-C)]] as follows:
 +
**Cycles 2, 4, 6, 8: 3000 mg/m<sup>2</sup> IV over 2 hours every 12 hours on days 2 & 3 (total dose per cycle: 12,000 mg/m<sup>2</sup>)
 +
====Supportive therapy, Part B====
 +
*[[Folinic acid (Leucovorin)]] as follows:
 +
**Cycles 2, 4, 6, 8: 50 mg IV once 12 hours after [[Methotrexate (MTX)]] is complete, then 15 mg IV every 6 hours until serum methotrexate level less than 100 nmol/L
 +
*[[Filgrastim (Neupogen)]] as follows:
 +
**Cycles 2, 4, 6, 8: 10 mcg/kg SC once per day, starting 24 hours after completion of chemotherapy, given until WBC greater than 3 x 10<sup>9</sup>/L or bone pain present
 +
*ONE of the following antibiotics:
 +
**[[:Category:Fluoroquinolone|Fluoroquinolone]]
 +
**[[Trimethoprim-Sulfamethoxazole (Bactrim DS)]] 160/800 mg dose/route not specified
 +
*[[Fluconazole (Diflucan)]] dose/route not specified
 +
*ONE of the following antivirals:
 +
**[[Acyclovir (Zovirax)]] dose/route not specified
 +
**[[Valacyclovir (Valtrex)]] dose/route not specified
 +
'''Next cycle to start no sooner than 14 days or as soon as "unmaintained" WBC count is greater than 3 x 10<sup>9</sup>/L and platelet count greater than 50 x 10<sup>9</sup>/L'''
 +
====Dose modifications, Part B====
 +
*[[Cytarabine (Ara-C)]] reduced to 1000 mg/m<sup>2</sup> for patients greater than or equal to 60 years old, creatinine greater than or equal to 1.5 mg/dL or 0 hour MTX level greater than or equal to 20,000 nmol/L
 +
*[[Methotrexate (MTX)]] reduced by 50% for creatinine clearance 10 to 50 mL/min (eliminated for less than 10 mL/min), by 25% to 75% for delayed excretion and/or nephrotoxicity with prior course (dependent on severity) or by 50% for pleural effusions/ascites with drainage of fluid as feasible.
 +
====CNS therapy, prophylaxis====
 +
*[[Methotrexate (MTX)]] by the following route-based criteria:
 +
**LP: 12 mg IT once on day 2
 +
**Ommaya reservoir: 6 mg IT once on day 2
 +
*[[Cytarabine (Ara-C)]] 100 mg IT once on day 7
 +
'''Given each cycle for a total of 16 intrathecal treatments.'''
 +
''If CNS disease present, therapy augmented to twice-weekly alternating (MTX, ara-C) treatments until CSF cell count normalizes and cytology is negative, then continues for 4 more alternating weekly treatments; prophylaxis course then resumes.''
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#'''BMT CTN 0801:''' Carpenter PA, Logan BR, Lee SJ, Weisdorf DJ, Johnston L, Costa LJ, Kitko CL, Bolaños-Meade J, Sarantopoulos S, Alousi AM, Abhyankar S, Waller EK, Mendizabal A, Zhu J, O'Brien KA, Lazaryan A, Wu J, Nemecek ER, Pavletic SZ, Cutler CS, Horowitz MM, Arora M; BMT CTN. A phase II/III randomized, multicenter trial of prednisone/sirolimus versus prednisone/ sirolimus/calcineurin inhibitor for the treatment of chronic graft-versus-host disease: BMT CTN 0801. Haematologica. 2018 Nov;103(11):1915-1924. Epub 2018 Jun 28. [http://www.haematologica.org/content/103/11/1915 link to original article] [https://pubmed.ncbi.nlm.nih.gov/29954931 PubMed]
+
# Thomas DA, Faderl S, O'Brien S, Bueso-Ramos C, Cortes J, Garcia-Manero G, Giles FJ, Verstovsek S, Wierda WG, Pierce SA, Shan J, Brandt M, Hagemeister FB, Keating MJ, Cabanillas F, Kantarjian H. Chemoimmunotherapy with hyper-CVAD plus rituximab for the treatment of adult Burkitt and Burkitt-type lymphoma or acute lymphoblastic leukemia. Cancer. 2006 Apr 1;106(7):1569-80. [https://doi.org/10.1002/cncr.21776 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/16502413 PubMed]
=Response criteria=
+
=Consolidation/Intensification therapy=
==2005 NIH cGVHD Consensus Panel==
+
==BASIC {{#subobject:eb66c6|Regimen=1}}==
 +
BASIC: '''<u>B</u>'''rief, '''<u>A</u>'''nthracycline-'''<u>S</u>'''paring, '''<u>I</u>'''ntensive '''<u>C</u>'''yclophosphamide
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Protocol {{#subobject:301df4|Variant=1}}===
 +
{| class="wikitable" style="width: 40%; text-align:center;"
 +
!style="width: 25%"|Study
 +
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234101/ Kasamon et al. 2012 (J0409)]
 +
|style="background-color:#91cf61"|Non-randomized
 +
|-
 +
|}
 +
<div class="toccolours" style="background-color:#cbd5e8">
 +
====Preceding treatment====
 +
*[[#BASIC|BASIC]] induction
 +
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Targeted therapy, part 1====
 +
*[[Rituximab (Rituxan)]] 375 mg/m<sup>2</sup> IV once on day 1
 +
====Chemotherapy, part 1====
 +
*[[Cyclophosphamide (Cytoxan)]] 50 mg/kg IV over 1 to 2 hours once per day on days 2 to 5
 +
====Supportive therapy, part 1====
 +
*[[Mesna (Mesnex)]] 40 mg/kg/day IV in divided doses on days 2 to 5
 +
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 11 and continuing until post-nadir ANC greater than 1000/uL
 +
'''One course, followed once post-nadir ANC greater than 1000/uL by:'''
 +
====Targeted therapy, part 2====
 +
*[[Rituximab (Rituxan)]] 375 mg/m<sup>2</sup> IV once per day on days 1, 8, 15, 22
 +
'''4-week course'''
 +
====CNS therapy, treatment, part 2====
 +
*(only given if there was prior CNS involvement):
 +
*[[Cytarabine (Ara-C)]] 100 mg IT once per week for 4 doses, then once every other week for 4 doses
 +
*[[Hydrocortisone (Cortef)]] 50 mg IT is optional (no parameters given)
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#Pavletic SZ, Martin P, Lee SJ, Mitchell S, Jacobsohn D, Cowen EW, Turner ML, Akpek G, Gilman A, McDonald G, Schubert M, Berger A, Bross P, Chien JW, Couriel D, Dunn JP, Fall-Dickson J, Farrell A, Flowers ME, Greinix H, Hirschfeld S, Gerber L, Kim S, Knobler R, Lachenbruch PA, Miller FW, Mittleman B, Papadopoulos E, Parsons SK, Przepiorka D, Robinson M, Ward M, Reeve B, Rider LG, Shulman H, Schultz KR, Weisdorf D, Vogelsang GB; Response Criteria Working Group. Measuring therapeutic response in chronic graft-versus-host disease: National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: IV. Response Criteria Working Group report. Biol Blood Marrow Transplant. 2006 Mar;12(3):252-66. [http://www.bbmt.org/article/S1083-8791(06)00070-X link to original article] [https://pubmed.ncbi.nlm.nih.gov/16503494 PubMed]
+
<!-- Presented in part at the 2009 American Society of Hematology annual meeting -->
==2014 NIH Response Criteria==
+
# '''J0409:''' Kasamon YL, Brodsky RA, Borowitz MJ, Ambinder RF, Crilley PA, Cho SY, Tsai HL, Smith BD, Gladstone DE, Carraway HE, Huff CA, Matsui WH, Bolaños-Meade J, Jones RJ, Swinnen LJ. Brief intensive therapy for older adults with newly diagnosed Burkitt or atypical Burkitt lymphoma/leukemia. Leuk Lymphoma. 2013 Mar;54(3):483-90. Epub 2012 Aug 17. [https://doi.org/10.3109/10428194.2012.715346 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234101/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/22835045 PubMed]
 +
==Cytarabine & Methotrexate (CYM) {{#subobject:b24b28|Regimen=1}}==
 +
CYM: '''<u>CY</u>'''tarabine, '''<u>M</u>'''ethotrexate
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen {{#subobject:d51545|Variant=1}}===
 +
{| class="wikitable sortable" style="width: 60%; text-align:center;"
 +
!style="width: 33%"|Study
 +
!style="width: 33%"|Years of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[https://doi.org/10.1093/annonc/mdi403 Diviné et al. 2005 (LMB95)]
 +
|1996-2001
 +
|style="background-color:#91cf61"|Phase 2
 +
|-
 +
|}
 +
''This regimen is for group B (unresected stage I, non-abdominal stage II and any stage III or IV disease without CNS or bone marrow involvement).''
 +
<div class="toccolours" style="background-color:#cbd5e8">
 +
====Preceding treatment====
 +
*[[#COPADM|COPADM]]
 +
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Chemotherapy====
 +
*[[Cytarabine (Ara-C)]] 100 mg/m<sup>2</sup>/day IV continuous infusion over 120 hours, started on day 2 (total dose per cycle: 500 mg/m<sup>2</sup>)
 +
*[[Methotrexate (MTX)]] 3000 mg/m<sup>2</sup> IV over 3 hours once on day 1
 +
====Supportive therapy====
 +
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> (route not specified) every 6 hours on days 2 to 4
 +
====CNS therapy, prophylaxis====
 +
*[[Methotrexate (MTX)]] 15 mg IT once on day 2
 +
*[[Cytarabine (Ara-C)]] 30 mg IT once on day 6
 +
*[[Hydrocortisone (Cortef)]] 15 mg IT once per day on days 2 & 6 (admixed with chemo)
 +
'''2 cycles; intervals were as short as possible, as soon as the ANC was greater than 1500/uL and platelet count was greater than 100 × 10<sup>9</sup>/L'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 +
====Subsequent treatment====
 +
*[[#COPADM_2|COPADM]] maintenance
 
</div></div>
 
</div></div>
 
===References===
 
===References===
#Lee SJ, Wolff D, Kitko C, Koreth J, Inamoto Y, Jagasia M, Pidala J, Olivieri A, Martin PJ, Przepiorka D, Pusic I, Dignan F, Mitchell SA, Lawitschka A, Jacobsohn D, Hall AM, Flowers ME, Schultz KR, Vogelsang G, Pavletic S. Measuring therapeutic response in chronic graft-versus-host disease. National Institutes of Health consensus development project on criteria for clinical trials in chronic graft-versus-host disease: IV. The 2014 Response Criteria Working Group report. Biol Blood Marrow Transplant. 2015 Jun;21(6):984-99. Epub 2015 Mar 19. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744804/ link to PMC article]
+
# '''LMB95:''' Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. [https://doi.org/10.1093/annonc/mdi403 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/16284057 PubMed]
=Scoring=
+
==CYVE {{#subobject:8cd382|Regimen=1}}==
==Glucksberg acute graft versus host (GVHD) scores==
+
CYVE: '''<u>CY</u>'''tarabine, '''<u>VE</u>'''pesid (Etoposide)
===Skin===
+
<div class="toccolours" style="background-color:#eeeeee">
*Stage 0: No rash
+
===Regimen {{#subobject:ba1c35|Variant=1}}===
*Stage 1: Maculopapular rash <25% of body surface area
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
*Stage 2: Maculopapular rash on 25-50% of body surface area
+
!style="width: 33%"|Study
*Stage 3: Generalized erythroderma
+
!style="width: 33%"|Years of enrollment
*Stage 4: Generalized erythroderma with bullous formation and desquamation
+
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
===Liver===
 
*Stage 0: Bilirubin <2 mg/dL
 
*Stage 1: Bilirubin 2-3 mg/dL
 
*Stage 2: Bilirubin 3.01-6 mg/dL
 
*Stage 3: Bilirubin 6.01-15 mg/dL
 
*Stage 4: Bilirubin >15 mg/dL
 
===GI===
 
*Stage 0: No diarrhea, or diarrhea less than 500 mL/day
 
*Stage 1: Diarrhea 500-999 mL/day
 
*Stage 2: Diarrhea 1000-1499 mL/day
 
*Stage 3: Diarrhea >1500 mL/day
 
*Stage 4: Severe abdominal pain, with or without ileus
 
===Glucksberg grade===
 
{| class="wikitable" style="text-align:center;"
 
! align="left" |Overall grade
 
!I
 
!II
 
!III
 
!IV
 
 
|-
 
|-
| align="left" |Skin
+
|[https://doi.org/10.1093/annonc/mdi403 Diviné et al. 2005 (LMB95)]
|1-2
+
|1996-2001
|1-3
+
|style="background-color:#ffffbe"|Phase 2, <20 pts in this subgroup
|2-3
 
|2-4
 
 
|-
 
|-
| align="left" |GI
+
|}
|0
+
''This regimen is for group C (CNS and/or bone marrow involvement). Note the unusual schedule of cytarabine; presumably the low-dose and high-dose portions are given at separate times in the 24 hour period but this detail is not further specified in the manuscript.''
|1
+
<div class="toccolours" style="background-color:#cbd5e8">
|2-3
+
====Preceding treatment====
|2-4
+
*[[#COPADM|COPADM]]
|-
+
</div>
| align="left" |Liver
+
<div class="toccolours" style="background-color:#b3e2cd">
|0
+
====Chemotherapy====
|1
+
*[[Cytarabine (Ara-C)]] by the following split schedule:
|2-4
+
**50 mg/m<sup>2</sup> IV over 12 hours once per day on days 1 to 5
|2-4
+
**3000 mg/m<sup>2</sup> IV over 3 hours once per day on days 2 to 5
 +
*[[Etoposide (Vepesid)]] 200 mg/m<sup>2</sup> IV once per day on days 2 to 5
 +
'''2 cycles; intervals were as short as possible, as soon as the ANC was greater than 1500/uL and platelet count was greater than 100 × 10<sup>9</sup>/L'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 +
====Subsequent treatment====
 +
*[[#COPAD.2FCYVE|COPAD alternating with CYVE]] maintenance
 +
</div></div>
 +
===References===
 +
# '''LMB95:''' Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. [https://doi.org/10.1093/annonc/mdi403 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/16284057 PubMed]
 +
=Maintenance therapy=
 +
==COPAD/CYVE {{#subobject:8337e0|Regimen=1}}==
 +
COPAD/CYVE: '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>P</u>'''rednisone, '''<u>AD</u>'''riamycin (Doxorubicin) alternating with '''<u>CY</u>'''tarabine, '''<u>VE</u>'''pesid (Etoposide)
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Protocol {{#subobject:16435a|Variant=1}}===
 +
{| class="wikitable sortable" style="width: 60%; text-align:center;"
 +
!style="width: 33%"|Study
 +
!style="width: 33%"|Years of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|Karnofsky performance scale
+
|[https://doi.org/10.1093/annonc/mdi403 Diviné et al. 2005 (LMB95)]
|90-100%
+
|1996-2001
|70-80%
+
|style="background-color:#ffffbe"|Phase 2, <20 pts in this subgroup
|50-60%
 
|30-40%
 
 
|-
 
|-
 
|}
 
|}
===IBMTR severity index===
+
''This protocol is for group C (CNS and/or bone marrow involvement). Note that the days of administration for the CYVE cycles are counted from the start of the respective COPAD cycles.''
The severity is the highest level which the patient reaches based on separate skin, liver, and GI staging.
+
<div class="toccolours" style="background-color:#cbd5e8">
{| class="wikitable" style="text-align:center;"
+
====Preceding treatment====
! align="left" |Overall grade
+
*[[#CYVE|CYVE]] consolidation
!A
+
</div>
!B
+
<div class="toccolours" style="background-color:#b3e2cd">
!C
+
====Chemotherapy, COPAD cycles====
!D
+
*[[Cyclophosphamide (Cytoxan)]] 500 mg/m<sup>2</sup> IV once per day on days 1 & 2
|-
+
*[[Vincristine (Oncovin)]] 1.4 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once on day 1
| align="left" |Skin
+
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV once on day 2
|1
+
====Glucocorticoid therapy====
|2
+
*[[Prednisone (Sterapred)]] 60 mg/m<sup>2</sup>/day PO on days 1 to 5
|3
+
====CNS therapy, treatment====
|4
+
''Note: this is only given with the first cycle of maintenance; patients with positive CNS at diagnosis were to also undergo 24 Gy of cranial irradiation.''
 +
*[[Methotrexate (MTX)]] 15 mg IT once on day 2
 +
*[[Cytarabine (Ara-C)]] 40 mg IT once on day 2
 +
*[[Hydrocortisone (Cortef)]] 15 mg IT once on day 2 (admixed with MTX & Ara-C)
 +
====Chemotherapy, CYVE cycles====
 +
*[[Cytarabine (Ara-C)]] 50 mg/m<sup>2</sup> SC twice per day on days 28 to 32
 +
*[[Etoposide (Vepesid)]] 150 mg/m<sup>2</sup> IV once per day on days 28 to 30
 +
'''4 alternating cycles (COPAD, then CYVE, then COPAD, then CYVE)'''
 +
</div></div>
 +
===References===
 +
# '''LMB95:''' Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. [https://doi.org/10.1093/annonc/mdi403 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/16284057 PubMed]
 +
==COPADM {{#subobject:ffa661|Regimen=1}}==
 +
COPADM: '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>P</u>'''rednisone, '''<u>AD</u>'''riamycin (Doxorubicin), '''<u>M</u>'''ethotrexate
 +
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen {{#subobject:79dd6f|Variant=1}}===
 +
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 +
!style="width: 33%"|Study
 +
!style="width: 33%"|Years of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
| align="left" |GI
+
|[https://doi.org/10.1093/annonc/mdi403 Diviné et al. 2005 (LMB95)]
|0
+
|1996-2001
|1-2
+
|style="background-color:#91cf61"|Phase 2
|3
 
|4
 
|-
 
| align="left" |Liver
 
|0
 
|1-2
 
|3
 
|4
 
 
|-
 
|-
 
|}
 
|}
==Chronic GVHD==
+
''This regimen is for group B (unresected stage I, non-abdominal stage II and any stage III or IV disease without CNS or bone marrow involvement).
===Localized===
+
<div class="toccolours" style="background-color:#cbd5e8">
*Localized skin and/or liver dysfunction due to chronic GVHD
+
====Preceding treatment====
===Extensive===
+
*[[#Cytarabine_.26_Methotrexate_.28CYM.29|CYM]] consolidation
*Generalized skin involvement or localized skin and/or liver dysfunction due to chronic GVHD '''plus at least one of the following''':
+
</div>
**Liver biopsy showing cirrhosis, chronic aggressive hepatitis, bridging necrosis
+
<div class="toccolours" style="background-color:#b3e2cd">
**Eye involvement, defined as [http://en.wikipedia.org/wiki/Schirmer's_test Schirmer's test] with less than 5 mm wetting
+
====Chemotherapy====
**Involvement of oral mucosa on lip biopsy or minor salivary glands
+
*[[Cyclophosphamide (Cytoxan)]] 500 mg/m<sup>2</sup> IV once per day on days 1 & 2
**Other organ involvement
+
*[[Vincristine (Oncovin)]] 1.4 mg/m<sup>2</sup> (maximum dose of 2 mg) IV once on day 1
*Overall severity categories: mild/moderate/severe
+
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV once on day 2
==References==
+
*[[Methotrexate (MTX)]] 3000 mg/m<sup>2</sup> IV over 3 hours once on day 1
#Thomas E, Storb R, Clift RA, Fefer A, Johnson FL, Neiman PE, Lerner KG, Glucksberg H, Buckner CD. Bone-marrow transplantation (first of two parts). N Engl J Med. 1975 Apr 17;292(16):832-43 [https://doi.org/10.1056/NEJM197504172921605 link to original article] [https://pubmed.ncbi.nlm.nih.gov/234595 PubMed]
+
====Glucocorticoid therapy====
#Thomas ED, Storb R, Clift RA, Fefer A, Johnson L, Neiman PE, Lerner KG, Glucksberg H, Buckner CD. Bone-marrow transplantation (second of two parts). N Engl J Med. 1975 Apr 24;292(17):895-902 [https://doi.org/10.1056/NEJM197504242921706 link to original article] '''(contains staging scale)''' [https://pubmed.ncbi.nlm.nih.gov/235092 PubMed]
+
*[[Prednisone (Sterapred)]] 60 mg/m<sup>2</sup>/day PO on days 1 to 5
#Rowlings PA, Przepiorka D, Klein JP, Gale RP, Passweg JR, Henslee-Downey PJ, Cahn JY, Calderwood S, Gratwohl A, Socié G, Abecasis MM, Sobocinski KA, Zhang MJ, Horowitz MM. IBMTR Severity Index for grading acute graft-versus-host disease: retrospective comparison with Glucksberg grade. Br J Haematol. 1997 Jun;97(4):855-64. [https://doi.org/10.1046/j.1365-2141.1997.1112925.x/pdf link to original article] [https://pubmed.ncbi.nlm.nih.gov/9217189 PubMed]
+
====Supportive therapy====
[[Category:Graft versus host disease regimens]]
+
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> (route not specified) every 6 hours on days 2 to 4
 +
====CNS therapy, prophylaxis====
 +
*[[Methotrexate (MTX)]] 15 mg IT once on day 2
 +
*[[Hydrocortisone (Cortef)]] 15 mg IT once on day 2 (admixed with MTX)
 +
'''One course'''
 +
</div></div>
 +
===References===
 +
# '''LMB95:''' Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. [https://doi.org/10.1093/annonc/mdi403 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/16284057 PubMed]
 +
[[Category:Burkitt lymphoma regimens]]
 
[[Category:Disease-specific pages]]
 
[[Category:Disease-specific pages]]
[[Category:Alloimmune hematologic conditions]]
+
[[Category:Aggressive lymphomas]]
 +
[[Category:Non-Hodgkin lymphomas]]

Revision as of 13:02, 17 October 2022

Section editor transclusions

0 regimens on this page
0 variants on this page

Note 1: Regimens specifically intended for HIV-related Burkitt lymphoma can be found on the HIV-associated lymphoma page. Note 2: The regimens on this page are primarily intended for the sporadic form of Burkitt lymphoma and some other high-grade B-cell lymphomas. In the future we plan to add regimens for the endemic form of Burkitt lymphoma. For pediatric regimens, please visit the pediatric NHL page.


Guidelines

NCCN

Untreated, pre-phase

CVP

CVP: Cyclophosphamide, Vincristine, Prednisone
COP: Cyclophosphamide, Oncovin (Vincristine), Prednisone

Regimen

Study Years of enrollment Evidence
Diviné et al. 2005 (LMB95) 1996-2001 Phase 2
Ribrag et al. 2016 (LMBA-02) 2004-2010 Non-randomized portion of phase 3 RCT

This regimen is for group B (unresected stage I, non-abdominal stage II and any stage III or IV disease without CNS or bone marrow involvement) or group C (CNS and/or bone marrow involvement).

Chemotherapy

Glucocorticoid therapy

CNS therapy, prophylaxis (group B)

CNS therapy, treatment (group C)

One course

Subsequent treatment

References

  1. LMB95: Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. link to original article contains dosing details in manuscript PubMed
  2. LMBA-02: Ribrag V, Koscielny S, Bosq J, Leguay T, Casasnovas O, Fornecker LM, Recher C, Ghesquieres H, Morschhauser F, Girault S, Le Gouill S, Ojeda-Uribe M, Mariette C, Cornillon J, Cartron G, Verge V, Chassagne-Clément C, Dombret H, Coiffier B, Lamy T, Tilly H, Salles G. Rituximab and dose-dense chemotherapy for adults with Burkitt's lymphoma: a randomised, controlled, open-label, phase 3 trial. Lancet. 2016 Jun 11;387(10036):2402-11. Epub 2016 Apr 11. link to original article contains dosing details in manuscript PubMed NCT00180882

Cyclophosphamide & Prednisone

Regimen variant #1, 1000/300

Study Evidence
Oriol et al. 2008 Non-randomized
Hoelzer et al. 2014 (GMALL-B-ALL/NHL 2002) Non-randomized

Note: GMALL-B-ALL/NHL 2002 is fairly similar to the GMALL-R regimen, with some minor differences. See text for details.

Chemotherapy

Glucocorticoid therapy

CNS therapy, prophylaxis

One course

Subsequent treatment

  • Oriol et al. 2008: PETHEMA induction; see text for details
  • GMALL-B-ALL/NHL 2002: Induction; see text for details


Regimen variant #2, 1000/420

Study Evidence
Lee et al. 2001 (CALGB 9251) Non-randomized
Rizzieri et al. 2014 (CALGB 10-002) Phase 2

CALGB 9251 is an earlier version of CALGB 10-002 that demonstrated that cranial radiation can be omitted in the treatment of Burkitt lymphoma.

Chemotherapy

Glucocorticoid therapy

Supportive therapy

Subsequent treatment

References

  1. CALGB 9251: Lee EJ, Petroni GR, Schiffer CA, Freter CE, Johnson JL, Barcos M, Frizzera G, Bloomfield CD, Peterson BA. Brief-duration high-intensity chemotherapy for patients with small noncleaved-cell lymphoma or FAB L3 acute lymphocytic leukemia: results of Cancer and Leukemia Group B study 9251. J Clin Oncol. 2001 Oct 15;19(20):4014-22. link to original article PubMed
    1. Update: Rizzieri DA, Johnson JL, Niedzwiecki D, Lee EJ, Vardiman JW, Powell BL, Barcos M, Bloomfield CD, Schiffer CA, Peterson BA, Canellos GP, Larson RA. Intensive chemotherapy with and without cranial radiation for Burkitt leukemia and lymphoma: final results of Cancer and Leukemia Group B Study 9251. Cancer. 2004 Apr 1;100(7):1438-48. link to original article PubMed
  2. Oriol A, Ribera JM, Bergua J, Giménez Mesa E, Grande C, Esteve J, Brunet S, Moreno MJ, Escoda L, Hernandez-Rivas JM, Hoelzer D; PETHEMA. High-dose chemotherapy and immunotherapy in adult Burkitt lymphoma: comparison of results in human immunodeficiency virus-infected and noninfected patients. Cancer. 2008 Jul 1;113(1):117-25. link to original article contains dosing details in manuscript PubMed
  3. CALGB 10-002: Rizzieri DA, Johnson JL, Byrd JC, Lozanski G, Blum KA, Powell BL, Shea TC, Nattam S, Hoke E, Cheson BD, Larson RA; Alliance for Clinical Trials In Oncology. Improved efficacy using rituximab and brief duration, high intensity chemotherapy with filgrastim support for Burkitt or aggressive lymphomas: Cancer and Leukemia Group B study 10 002. Br J Haematol. 2014 Apr;165(1):102-11. Epub 2014 Jan 15. link to original article contains dosing details in manuscript link to PMC article PubMed
  4. GMALL-B-ALL/NHL 2002: Hoelzer D, Walewski J, Döhner H, Viardot A, Hiddemann W, Spiekermann K, Serve H, Dührsen U, Hüttmann A, Thiel E, Dengler J, Kneba M, Schaich M, Schmidt-Wolf IG, Beck J, Hertenstein B, Reichle A, Domanska-Czyz K, Fietkau R, Horst HA, Rieder H, Schwartz S, Burmeister T, Gökbuget N; German Multicenter Study Group for Adult Acute Lymphoblastic Leukemia. Improved outcome of adult Burkitt lymphoma/leukemia with rituximab and chemotherapy: report of a large prospective multicenter trial. Blood. 2014 Dec 18;124(26):3870-9. Epub 2014 Oct 30. link to original article contains dosing details in manuscript link to PMC article PubMed

Untreated

BASIC

BASIC: Brief, Anthracycline-Sparing, Intensive Cyclophosphamide

Regimen

Study Evidence
Kasamon et al. 2012 (J0409) Non-randomized

Chemotherapy

Glucocorticoid therapy

Targeted therapy

Supportive therapy

CNS therapy, prophylaxis

14-day cycle for 2 cycles

Subsequent treatment

References

  1. J0409: Kasamon YL, Brodsky RA, Borowitz MJ, Ambinder RF, Crilley PA, Cho SY, Tsai HL, Smith BD, Gladstone DE, Carraway HE, Huff CA, Matsui WH, Bolaños-Meade J, Jones RJ, Swinnen LJ. Brief intensive therapy for older adults with newly diagnosed Burkitt or atypical Burkitt lymphoma/leukemia. Leuk Lymphoma. 2013 Mar;54(3):483-90. Epub 2012 Aug 17. link to original article contains dosing details in manuscript link to PMC article PubMed

CALGB 10-002 regimen

Protocol

Study Evidence
Rizzieri et al. 2014 (CALGB 10-002) Phase 2

Chemotherapy, A cycles

  • Ifosfamide (Ifex) as follows:
    • Cycles 2, 4, 6: 800 mg/m2 IV over 60 minutes once per day on days 1 to 5
  • Methotrexate (MTX) as follows:
    • Cycles 2, 4, 6: 150 mg/m2 IV bolus once on day 1, then 1350 mg/m2 IV continuous infusion over 23.5 hours (total dose per cycle: 1500 mg/m2)
  • Vincristine (Oncovin) as follows:
    • Cycles 2, 4, 6: 2 mg IV push once on day 1
  • Cytarabine (Ara-C) as follows:
    • Cycles 2, 4, 6: 1000 mg/m2 IV over 2 hours once per day on days 4 & 5
  • Etoposide (Vepesid) as follows:
    • Cycles 2, 4, 6: 80 mg/m2 IV over 60 minutes once per day on days 4 & 5

Glucocorticoid therapy, A cycles

Targeted therapy, A cycles

  • Rituximab (Rituxan) as follows:
    • Cycle 2: 50 mg/m2 IV once on day 8, then 375 mg/m2 IV once per day on days 10 & 12
    • Cycles 4 & 6: 375 mg/m2 IV once on day 8

CNS therapy, prophylaxis, A cycles

Supportive therapy, A cycles

  • Mesna (Mesnex) as follows:
    • Cycles 2, 4, 6: (dose not specified but presumably equal to ifosfamide dose) mixed with Ifosfamide (Ifex)
  • Folinic acid (Leucovorin) as follows:
    • Cycles 2, 4, 6: 25 mg/m2 IV or PO once 36 hours after start of IV methotrexate, then 10 mg/m2 every 6 hours until methotrexate level less than 50 nmol/L
  • Filgrastim (Neupogen) as follows:
    • Cycles 2, 4, 6: 5 mcg/kg SC once per day, starting on day 7 and continuing until ANC greater than 500/uL

Chemotherapy, B cycles

Glucocorticoid therapy, B cycles

Targeted therapy, B cycles

CNS therapy, prophylaxis, B cycles

Supportive therapy, B cycles

  • Folinic acid (Leucovorin) as follows:
    • Cycles 3, 5, 7: 50 mg/m2 IV or PO once 36 hours after start of IV methotrexate, then 10 mg/m2 every 6 hours until methotrexate level less than 50 nmol/L
  • Filgrastim (Neupogen) as follows:
    • Cycles 3, 5, 7: 5 mcg/kg SC once per day, starting on day 7 and continuing until ANC greater than 500/uL

21-day cycle for 6 cycles

References

  1. CALGB 10-002: Rizzieri DA, Johnson JL, Byrd JC, Lozanski G, Blum KA, Powell BL, Shea TC, Nattam S, Hoke E, Cheson BD, Larson RA; Alliance for Clinical Trials In Oncology (ACTION). Improved efficacy using rituximab and brief duration, high intensity chemotherapy with filgrastim support for Burkitt or aggressive lymphomas: Cancer and Leukemia Group B study 10 002. Br J Haematol. 2014 Apr;165(1):102-11. Epub 2014 Jan 15. link to original article contains dosing details in manuscript link to PMC article PubMed

CODOX-M

CODOX-M: Cyclophosphamide, Oncovin (Vincristine), DOXorubicin, Methotrexate

Regimen variant #1, "Original Magrath"

Study Evidence
Magrath et al. 1996 (NCI 89-C-41) Phase 2

This is intended for low-risk patients.

Chemotherapy

  • Cyclophosphamide (Cytoxan) 800 mg/m2 IV once on day 1, then 200 mg/m2 IV once per day on days 2 to 5
  • Vincristine (Oncovin) 1.5 mg/m2 IV once per day on days 1 & 8
  • Doxorubicin (Adriamycin) 40 mg/m2 IV once on day 1
  • Methotrexate (MTX) by the following age-based criteria:
    • 65 years or younger: 300 mg/m2 IV over 60 minutes once on day 10, then 2700 mg/m2 IV continuous infusion over 23 hours (total dose per cycle: 3000 mg/m2)
    • Older than 65 years: 100 mg/m2 IV over 60 minutes once on day 10, then 900 mg/m2 IV continuous infusion over 23 hours (total dose per cycle: 1000 mg/m2)

Supportive therapy

CNS therapy, prophylaxis

3 cycles


Regimen variant #2, "Modified Magrath"

Study Evidence
LaCasce et al. 2004 Phase 2, <20 pts

Note that dose reductions for age greater than 65 years were not described in this publication. This is intended for low-risk patients (i.e., single site of disease less than 10 cm with normal LDH).

Chemotherapy

CNS therapy, prophylaxis

Supportive therapy

  • Folinic acid (Leucovorin) 200 mg/m2 IV once 24 hours after start of IV methotrexate, then 15 mg/m2 every 6 hours until methotrexate level undetectable
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day on days 3 to 8, held for MTX, and restarted after clearance continuing until ANC greater than 1000/uL

3 cycles

References

  1. NCI 89-C-41: Magrath I, Adde M, Shad A, Venzon D, Seibel N, Gootenberg J, Neely J, Arndt C, Nieder M, Jaffe E, Wittes RA, Horak ID. Adults and children with small non-cleaved-cell lymphoma have a similar excellent outcome when treated with the same chemotherapy regimen. J Clin Oncol. 1996 Mar;14(3):925-34. link to original article contains dosing details in manuscript PubMed
  2. UKLG LY06: Mead GM, Sydes MR, Walewski J, Grigg A, Hatton CS, Pescosta N, Guarnaccia C, Lewis MS, McKendrick J, Stenning SP, Wright D; UKLG. An international evaluation of CODOX-M and CODOX-M alternating with IVAC in adult Burkitt's lymphoma: results of United Kingdom Lymphoma Group LY06 study. Ann Oncol. 2002 Aug;13(8):1264-74. Erratum in: Ann Oncol. 2002 Dec;13(12):1961. Norbert, P [corrected to Pescosta, N]. link to original article contains dosing details in manuscript PubMed
  3. Lacasce A, Howard O, Lib S, Fisher D, Weng A, Neuberg D, Shipp M. Modified Magrath regimens for adults with Burkitt and Burkitt-like lymphomas: preserved efficacy with decreased toxicity. Leuk Lymphoma. 2004 Apr;45(4):761-7. link to original article contains dosing details in manuscript PubMed
  4. MRC/NCRI LY10: Mead GM, Barrans SL, Qian W, Walewski J, Radford JA, Wolf M, Clawson SM, Stenning SP, Yule CL, Jack AS; UK National Cancer Research Institute Lymphoma Clinical Studies Group; Australasian Leukaemia and Lymphoma Group. A prospective clinicopathologic study of dose-modified CODOX-M/IVAC in patients with sporadic Burkitt lymphoma defined using cytogenetic and immunophenotypic criteria (MRC/NCRI LY10 trial). Blood. 2008 Sep 15;112(6):2248-60. Epub 2008 Jul 8. link to original article contains dosing details in manuscript link to PMC article PubMed
  5. Maruyama D, Watanabe T, Maeshima AM, Nomoto J, Taniguchi H, Azuma T, Mori M, Munakata W, Kim SW, Kobayashi Y, Matsuno Y, Tobinai K. Modified cyclophosphamide, vincristine, doxorubicin, and methotrexate (CODOX-M)/ifosfamide, etoposide, and cytarabine (IVAC) therapy with or without rituximab in Japanese adult patients with Burkitt lymphoma (BL) and B cell lymphoma, unclassifiable, with features intermediate between diffuse large B cell lymphoma and BL. Int J Hematol. 2010 Dec;92(5):732-43. Epub 2010 Dec 1. link to original article contains dosing details in manuscript PubMed

CODOX-M/IVAC

CODOX-M/IVAC: Cyclophosphamide, Oncovin (Vincristine), DOXorubicin, Methotrexate alternating with Ifosfamide, Vepesid (Etoposide), Ara-C (Cytarabine)

Protocol variant #1, "Original Magrath"

Study Evidence
Magrath et al. 1996 (NCI 89-C-41) Phase 2

This is intended for high-risk patients.

Chemotherapy, Part 1: CODOX-M

  • Cyclophosphamide (Cytoxan) 800 mg/m2 IV once on day 1, then 200 mg/m2 IV once per day on days 2 to 5
  • Vincristine (Oncovin) 1.5 mg/m2 IV once per day on days 1 & 8
  • Doxorubicin (Adriamycin) 40 mg/m2 IV once on day 1
  • Methotrexate (MTX) by the following age-based criteria:
    • 65 years or younger: 300 mg/m2 IV over 60 minutes once on day 10, then 2700 mg/m2 IV continuous infusion over 23 hours (total dose per cycle: 3000 mg/m2)
    • Older than 65 years: 100 mg/m2 IV over 60 minutes once on day 10, then 900 mg/m2 IV continuous infusion over 23 hours (total dose per cycle: 1000 mg/m2)

Supportive therapy

CNS therapy, prophylaxis

Chemotherapy, Part 2: IVAC

  • Ifosfamide (Ifex) by the following age-based criteria:
    • 65 years or younger: 1500 mg/m2 IV over 60 minutes once per day on days 1 to 5
    • Older than 65 years: 1000 mg/m2 IV over 60 minutes once per day on days 1 to 5
  • Etoposide (Vepesid) 60 mg/m2 IV over 60 minutes once per day on days 1 to 5
  • Cytarabine (Ara-C) by the following age-based criteria:
    • 65 years or younger: 2000 mg/m2 IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 8000 mg/m2)
    • Older than 65 years: 1000 mg/m2 IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 4000 mg/m2)

Supportive therapy

  • Mesna (Mesnex) by the following age-based criteria:
    • 65 or younger: 300 mg/m2 over 1 hour once per day on days 1 to 5 mixed with Ifosfamide (Ifex), then 300 mg/m2 IV every four hours twice per day on days 1 to 5
    • Older than 65: 200 mg/m2 over 1 hour once per day on days 1 to 5 mixed with Ifosfamide (Ifex), then 200 mg/m2 IV every four hours twice per day on days 1 to 5
  • Folinic acid (Leucovorin) 15 mg PO once 24 hours after intrathecal methotrexate
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day, starting on day 7 and continuing until ANC greater than 1000/uL

CNS therapy, prophylaxis

2 cycles each of CODOX-M and IVAC (alternating)


Protocol variant #2

Study Evidence
Mead et al. 2002 (UKLG LY06) Phase 2

This is intended for high-risk patients; modifications to the original NCI 89-C-41 are only in the CODOX-M portion.

Chemotherapy, Part 1: CODOX-M

Supportive therapy

  • Folinic acid (Leucovorin) 192 mg/m2 IV once at 36 hours after start of IV methotrexate, then 12 mg/m2 IV every 6 hours until MTX level less than 0.05
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day, starting on day 13 and continuing until ANC greater than 1000/uL

CNS therapy, prophylaxis

Chemotherapy, Part 2: IVAC

  • Ifosfamide (Ifex) by the following age-based criteria:
    • Age 65 years or younger: 1500 mg/m2 IV over 60 minutes once per day on days 1 to 5
    • Age older than 65 years: 1000 mg/m2 IV over 60 minutes once per day on days 1 to 5
  • Etoposide (Vepesid) 60 mg/m2 IV over 60 minutes once per day on days 1 to 5
  • Cytarabine (Ara-C) by the following age-based criteria:
    • 65 or younger: 2000 mg/m2 IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 8000 mg/m2)
    • Older than 65: 1000 mg/m2 IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 4000 mg/m2)

Supportive therapy

  • Mesna (Mesnex) by the following age-based criteria:
    • 65 years or younger: 300 mg/m2 over 1 hour once per day on days 1 to 5 mixed with Ifosfamide (Ifex), then 300 mg/m2 IV every four hours twice per day on days 1 to 5
    • Older than 65 years: 200 mg/m2 over 1 hour once per day on days 1 to 5 mixed with Ifosfamide (Ifex), then 200 mg/m2 IV every four hours twice per day on days 1 to 5
  • Folinic acid (Leucovorin) 15 mg PO once 24 hours after intrathecal methotrexate
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day, starting on day 7 and continuing until ANC greater than 1000/uL

CNS therapy, prophylaxis

2 cycles each of CODOX-M and IVAC (alternating)


Protocol variant #3, "Modified Magrath"

Study Evidence
LaCasce et al. 2004 Phase 2, <20 pts

All modifications are in Part 1: CODOX-M. Also note that dose reductions for age greater than 65 years were not described in this publication. This is intended for high-risk patients.

Chemotherapy, Part 1: CODOX-M

CNS therapy, prophylaxis

Supportive therapy

  • Folinic acid (Leucovorin) 200 mg/m2 IV once 24 hours after start of IV methotrexate, then 15 mg/m2 every 6 hours until methotrexate level undetectable
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day on days 3 to 8, held for MTX, and restarted after clearance continuing until ANC greater than 1000/uL

Chemotherapy, Part 2: IVAC

CNS therapy, prophylaxis

Supportive therapy

  • Mesna (Mesnex) 300 mg/m2 over 1 hour once per day on days 1 to 5 mixed with Ifosfamide (Ifex), then 300 mg/m2 IV every four hours twice per day on days 1 to 5
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day, starting on day 6 and continuing until ANC greater than 1000/uL

2 cycles each of CODOX-M and IVAC (alternating)


Protocol variant #4

Study Evidence
Mead et al. 2008 (MRC/NCRI LY10) Phase 2

This is intended for high-risk patients; modifications to the UKLG LY06 protocol are only in the CODOX-M portion.

Chemotherapy, Part 1: CODOX-M

Supportive therapy

  • Folinic acid (Leucovorin) 15 mg/m2 IV once at 36 hours after start of IV methotrexate, then 15 mg/m2 IV every 3 hours between hours 36 and 48, then 15 mg/m2 IV every 6 hours until MTX level less than 0.05
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day, starting on day 13 and continuing until ANC greater than 1000/uL

CNS therapy, prophylaxis

Chemotherapy, Part 2: IVAC

  • Ifosfamide (Ifex) by the following age-based criteria:
    • 65 years or younger: 1500 mg/m2 IV over 60 minutes once per day on days 1 to 5
    • Older than 65 years: 1000 mg/m2 IV over 60 minutes once per day on days 1 to 5
  • Etoposide (Vepesid) 60 mg/m2 IV over 60 minutes once per day on days 1 to 5
  • Cytarabine (Ara-C) by the following age-based criteria:
    • 65 or younger: 2000 mg/m2 IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 8000 mg/m2)
    • Older than 65: 1000 mg/m2 IV over 3 hours every 12 hours on days 1 & 2 (total dose per cycle: 4000 mg/m2)

Supportive therapy

  • Mesna (Mesnex) by the following age-based criteria:
    • 65 years or younger: 300 mg/m2 over 1 hour once per day on days 1 to 5 mixed with Ifosfamide (Ifex), then 300 mg/m2 IV every four hours twice per day on days 1 to 5
    • Older than 65 years: 200 mg/m2 over 1 hour once per day on days 1 to 5 mixed with Ifosfamide (Ifex), then 200 mg/m2 IV every four hours twice per day on days 1 to 5
  • Folinic acid (Leucovorin) 15 mg PO once 24 hours after intrathecal methotrexate
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day, starting on day 7 and continuing until ANC greater than 1000/uL

CNS therapy, prophylaxis

2 cycles each of CODOX-M and IVAC (alternating)

References

  1. NCI 89-C-41: Magrath I, Adde M, Shad A, Venzon D, Seibel N, Gootenberg J, Neely J, Arndt C, Nieder M, Jaffe E, Wittes RA, Horak ID. Adults and children with small non-cleaved-cell lymphoma have a similar excellent outcome when treated with the same chemotherapy regimen. J Clin Oncol. 1996 Mar;14(3):925-34. link to original article contains dosing details in manuscript PubMed
  2. UKLG LY06: Mead GM, Sydes MR, Walewski J, Grigg A, Hatton CS, Pescosta N, Guarnaccia C, Lewis MS, McKendrick J, Stenning SP, Wright D; UKLG LY06 collaborators. An international evaluation of CODOX-M and CODOX-M alternating with IVAC in adult Burkitt's lymphoma: results of United Kingdom Lymphoma Group LY06 study. Ann Oncol. 2002 Aug;13(8):1264-74. Erratum in: Ann Oncol. 2002 Dec;13(12):1961. Norbert, P [corrected to Pescosta, N]. link to original article contains dosing details in manuscript PubMed
  3. Lacasce A, Howard O, Lib S, Fisher D, Weng A, Neuberg D, Shipp M. Modified Magrath regimens for adults with Burkitt and Burkitt-like lymphomas: preserved efficacy with decreased toxicity. Leuk Lymphoma. 2004 Apr;45(4):761-7. link to original article contains dosing details in manuscript PubMed
  4. MRC/NCRI LY10: Mead GM, Barrans SL, Qian W, Walewski J, Radford JA, Wolf M, Clawson SM, Stenning SP, Yule CL, Jack AS; UK National Cancer Research Institute Lymphoma Clinical Studies Group; Australasian Leukaemia and Lymphoma Group. A prospective clinicopathologic study of dose-modified CODOX-M/IVAC in patients with sporadic Burkitt lymphoma defined using cytogenetic and immunophenotypic criteria (MRC/NCRI LY10 trial). Blood. 2008 Sep 15;112(6):2248-60. Epub 2008 Jul 8. link to original article contains dosing details in manuscript link to PMC article PubMed
  5. Maruyama D, Watanabe T, Maeshima AM, Nomoto J, Taniguchi H, Azuma T, Mori M, Munakata W, Kim SW, Kobayashi Y, Matsuno Y, Tobinai K. Modified cyclophosphamide, vincristine, doxorubicin, and methotrexate (CODOX-M)/ifosfamide, etoposide, and cytarabine (IVAC) therapy with or without rituximab in Japanese adult patients with Burkitt lymphoma (BL) and B cell lymphoma, unclassifiable, with features intermediate between diffuse large B cell lymphoma and BL. Int J Hematol. 2010 Dec;92(5):732-43. Epub 2010 Dec 1. link to original article PubMed

COPAD

COPAD: Cyclophosphamide, Oncovin (Vincristine), Prednisone, ADriamycin (Doxorubicin)

Regimen

Study Years of enrollment Evidence
Diviné et al. 2005 (LMB95) 1996-2001 Phase 2, <20 pts in this subgroup

This regimen is for group A (completely resected stage I or abdominal stage II disease).

Chemotherapy

Glucocorticoid therapy

3 cycles; intervals were as short as possible, as soon as the ANC was greater than 1500/uL and platelet count was greater than 100 × 109/L

References

  1. LMB95: Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. link to original article contains dosing details in manuscript PubMed

COPADM

COPADM: Cyclophosphamide, Oncovin (Vincristine), Prednisone, ADriamycin (Doxorubicin), Methotrexate

Protocol

Study Years of enrollment Evidence Comparator Comparative Efficacy
Diviné et al. 2005 (LMB95) 1996-2001 Phase 2
Ribrag et al. 2016 (LMBA-02) 2004-2010 Phase 3 (C) R-COPADM Seems to have inferior EFS

This protocol is for group B (unresected stage I, non-abdominal stage II and any stage III or IV disease without CNS or bone marrow involvement) or group C (CNS and/or bone marrow involvement). Diviné et al. 2005 list the dose of HD-MTX as 3 mg/m2 but this is presumed to be a typo.

Preceding treatment

Chemotherapy, COPADM #1

Glucocorticoid therapy

Supportive therapy

CNS therapy, prophylaxis (group B)

CNS therapy, treatment (group C)

One course As soon as the ANC was greater than 1500/uL and platelet count was greater than 100 × 109/L, patients proceeded to:

Chemotherapy, COPADM #2

Glucocorticoid therapy

Supportive therapy

CNS therapy, prophylaxis (group B)

CNS therapy, treatment (group C)

One course

Subsequent treatment

  • As soon as the ANC was greater than 1500/uL and platelet count was greater than 100 × 109/L:
    • Group B: CYM consolidation
    • Group C: CYVE consolidation

References

  1. LMB95: Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. link to original article contains dosing details in manuscript PubMed
  2. LMBA-02: Ribrag V, Koscielny S, Bosq J, Leguay T, Casasnovas O, Fornecker LM, Recher C, Ghesquieres H, Morschhauser F, Girault S, Le Gouill S, Ojeda-Uribe M, Mariette C, Cornillon J, Cartron G, Verge V, Chassagne-Clément C, Dombret H, Coiffier B, Lamy T, Tilly H, Salles G. Rituximab and dose-dense chemotherapy for adults with Burkitt's lymphoma: a randomised, controlled, open-label, phase 3 trial. Lancet. 2016 Jun 11;387(10036):2402-11. Epub 2016 Apr 11. link to original article PubMed NCT00180882

DA-R-EPOCH

DA-R-EPOCH: Dose Adjusted Rituximab, Etoposide, Prednisone, Oncovin (Vincristine), Cyclophosphamide, Hydroxydaunorubicin (Doxorubicin)

Regimen

Study Evidence
Dunleavy et al. 2013 (NCI 93-C-0133) Phase 2, <20 pts in this subgroup

Targeted therapy

Chemotherapy

Glucocorticoid therapy

Supportive therapy

CNS therapy, prophylaxis

21-day cycle for 6 cycles if ANC greater than 1000/uL and platelets greater than 100 × 109/L If counts are below those levels, check daily CBC and continue growth factor support until counts are adequate and next cycle can start.

Dose modifications

Note this is different than some other DA-EPOCH regimens!

  • Start cycle 1 as described above.
  • Obtain CBCs twice per week for nadir measurements.
  • If nadir ANC greater than or equal to 500/uL, increase etoposide, doxorubicin, and cyclophosphamide by 20% compared to previous cycle.
  • If nadir ANC less than 500/uL, use same doses as last cycle.
  • If nadir platelet count less than 25 × 109/L, decrease etoposide, doxorubicin, and cyclophosphamide by 20% compared to previous cycle.
    • Decreases below the cycle 1 starting dose only apply to cyclophosphamide, i.e., the lowest etoposide and doxorubicin would be dosed is at the original cycle 1 dose.

References

  1. NCI 93-C-0133: Dunleavy K, Pittaluga S, Shovlin M, Steinberg SM, Cole D, Grant C, Widemann B, Staudt LM, Jaffe ES, Little RF, Wilson WH. Low-intensity therapy in adults with Burkitt's lymphoma. N Engl J Med. 2013 Nov 14;369(20):1915-25. link to original article link to supplement contains dosing details in supplement link to PMC article PubMed NCT00001337

GMALL-R

GMALL-R: German Multicenter Study Group for the Treatment of Adult Acute Lymphoblastic Leukemia, Rituximab

Protocol

Study Evidence
Ribera et al. 2013 (Burkimab) Phase 2

Numbering of days is based on prephase->A->B->C; however, certain patient populations received different ordering of regimen, see below.

Chemotherapy, prephase

Glucocorticoid therapy, prephase

Targeted therapy, A cycle

Chemotherapy, A cycle

  • Vincristine (Oncovin) 2 mg IV bolus once on day 8
  • Methotrexate (MTX) by the following age-based criteria:
    • 55 or younger: 1500 mg/m2 IV continuous infusion over 24 hours, started on day 8
    • Older than 55 years: 750 mg/m2 IV continuous infusion over 24 hours, started on day 8
  • Ifosfamide (Ifex) 800 mg/m2 IV over 60 minutes once per day on days 8 to 12
  • Teniposide (Vumon) 100 mg/m2 IV over 60 minutes once per day on days 11 & 12
  • Cytarabine (Ara-C) by the following age-based criteria:
    • 55 or younger: 150 mg/m2 IV over 60 minutes twice per day on days 11 & 12
    • Older than 55 years: 75 mg/m2 IV over 60 minutes twice per day on days 11 & 12

Glucocorticoid therapy, A cycle

Supportive therapy, A cycle

Targeted therapy, B cycle

Chemotherapy, B cycle

Glucocorticoid therapy, B cycle

Supportive therapy, B cycle

Targeted therapy, C cycle

Chemotherapy, C cycle

  • Vindesine (Eldisine) 3 mg/m2 (maximum dose of 5 mg) IV bolus once on day 50
  • Methotrexate (MTX) by the following age-based criteria, starting on day 50:
    • 55 or younger: 1500 mg/m2 IV continuous infusion over 24 hours
    • Older than 55 years: 750 mg/m2 IV continuous infusion over 24 hours
  • Etoposide (Vepesid) 250 mg/m2 IV over 60 minutes once per day on days 53 & 54
  • Cytarabine (Ara-C) by the following age-based criteria, on day 54:
    • 55 or younger: 2000 mg/m2 IV over 3 hours twice per day
    • Older than 55 years: 1000 mg/m2 IV over 3 hours twice per day

Glucocorticoid therapy, C cycle

Supportive therapy, C cycle

Give regimen by the following criteria:

  • Advanced stage and younger than 55 years: A->B->C for 2 courses (6 total cycles)
  • Older than 55 years: Alternate A & B for 3 courses (6 total cycles)
  • Localized stage: 4 total cycles (unclear from protocol if this means A alternating with B or A->B->C->A)

CNS therapy, prophylaxis

8 doses total

References

  1. Burkimab: Ribera JM, García O, Grande C, Esteve J, Oriol A, Bergua J, González-Campos J, Vall-Llovera F, Tormo M, Hernández-Rivas JM, García D, Brunet S, Alonso N, Barba P, Miralles P, Llorente A, Montesinos P, Moreno MJ, Hernández-Rivas JÁ, Bernal T. Dose-intensive chemotherapy including rituximab in Burkitt's leukemia or lymphoma regardless of human immunodeficiency virus infection status: final results of a phase 2 study (Burkimab). Cancer. 2013 May 1;119(9):1660-8. Epub 2013 Jan 29. link to original article contains dosing details in manuscript PubMed NCT00388193

R-CODOX-M

R-CODOX-M: Rituximab, Cyclophosphamide, Oncovin (Vincristine), DOXorubicin, Methotrexate

Regimen

Study Evidence
Maruyama et al. 2010 Pilot, <20 pts
Jacobson et al. 2014 Expert Recommendation

In the Jacobson et al. 2014 review, the authors describe a "Modified Magrath regimen of R-CODOX/R-IVAC" based on the timing and dosage of LaCasce et al. 2004. However, LaCasce et al. 2004 did not include rituximab in the schema. Others have published retrospective series of this regimen; doses here are based on the review article. This is for low-risk patients (i.e., single site of disease less than 10 cm with normal LDH).

Targeted therapy

  • Rituximab (Rituxan) as follows:
    • Cycle 1: 375 mg/m2 IV once no earlier than day 3
    • Cycle 2 onwards: 375 mg/m2 IV once on day 1

Chemotherapy

CNS therapy, prophylaxis

CNS therapy, treatment (for CSF positive)

Supportive therapy

3 cycles

References

  1. Maruyama D, Watanabe T, Maeshima AM, Nomoto J, Taniguchi H, Azuma T, Mori M, Munakata W, Kim SW, Kobayashi Y, Matsuno Y, Tobinai K. Modified cyclophosphamide, vincristine, doxorubicin, and methotrexate (CODOX-M)/ifosfamide, etoposide, and cytarabine (IVAC) therapy with or without rituximab in Japanese adult patients with Burkitt lymphoma (BL) and B cell lymphoma, unclassifiable, with features intermediate between diffuse large B cell lymphoma and BL. Int J Hematol. 2010 Dec;92(5):732-43. Epub 2010 Dec 1. link to original article contains dosing details in manuscript PubMed
  2. Retrospective: Barnes JA, Lacasce AS, Feng Y, Toomey CE, Neuberg D, Michaelson JS, Hochberg EP, Abramson JS. Evaluation of the addition of rituximab to CODOX-M/IVAC for Burkitt's lymphoma: a retrospective analysis. Ann Oncol. 2011 Aug;22(8):1859-64. Epub 2011 Feb 21. link to original article PubMed
  3. Review: Jacobson C, LaCasce A. How I treat Burkitt lymphoma in adults. Blood. 2014 Nov 6;124(19):2913-20. Epub 2014 Sep 25. link to original article contains dosing details in manuscript PubMed

R-CODOX-M/R-IVAC

R-CODOX-M/R-IVAC: Rituximab, Cyclophosphamide, Oncovin (Vincristine), DOXorubicin, Methotrexate alternating with Rituximab, Ifosfamide, Vepesid (etoposide), Ara-C (Cytarabine)

Protocol

Study Evidence
Jacobson et al. 2014 Expert Recommendation

Note: In the Jacobson et al. 2014 review, the authors describe a "Modified Magrath regimen of R-CODOX/R-IVAC" based on the timing and dosage of LaCasce et al. 2004. However, LaCasce et al. 2004 did not include rituximab in the schema. Others have published retrospective series of this regimen; doses here are based on the review article. This is for high-risk patients.

Targeted therapy, R-CODOX-M portion

  • Rituximab (Rituxan) as follows:
    • Cycle 1: 375 mg/m2 IV once no earlier than day 3
    • Cycle 2 onwards: 375 mg/m2 IV once on day 1

Chemotherapy, R-CODOX-M portion

CNS therapy, prophylaxis, R-CODOX-M portion

CNS therapy, treatment (for CSF positive), R-CODOX-M portion

Supportive therapy, R-CODOX-M portion

Targeted therapy, R-IVAC portion

Chemotherapy, R-IVAC portion

CNS therapy, prophylaxis, R-IVAC portion

CNS therapy, treatment (for CSF positive), R-IVAC portion

  • Treatment as per CNS prophylaxis PLUS in cycle 1 only:
  • Cytarabine (Ara-C) 50 mg IT once on day 3

Supportive therapy, R-IVAC portion

Patients receive 2 cycles each of R-CODOX-M and R-IVAC (alternating)

References

  1. Maruyama D, Watanabe T, Maeshima AM, Nomoto J, Taniguchi H, Azuma T, Mori M, Munakata W, Kim SW, Kobayashi Y, Matsuno Y, Tobinai K. Modified cyclophosphamide, vincristine, doxorubicin, and methotrexate (CODOX-M)/ifosfamide, etoposide, and cytarabine (IVAC) therapy with or without rituximab in Japanese adult patients with Burkitt lymphoma (BL) and B cell lymphoma, unclassifiable, with features intermediate between diffuse large B cell lymphoma and BL. Int J Hematol. 2010 Dec;92(5):732-43. Epub 2010 Dec 1. link to original article contains dosing details in manuscript PubMed
  2. Retrospective: Barnes JA, Lacasce AS, Feng Y, Toomey CE, Neuberg D, Michaelson JS, Hochberg EP, Abramson JS. Evaluation of the addition of rituximab to CODOX-M/IVAC for Burkitt's lymphoma: a retrospective analysis. Ann Oncol. 2011 Aug;22(8):1859-64. Epub 2011 Feb 21. link to original article PubMed
  3. Review: Jacobson C, LaCasce A. How I treat Burkitt lymphoma in adults. Blood. 2014 Nov 6;124(19):2913-20. Epub 2014 Sep 25. link to original article contains dosing details in manuscript PubMed

R-CODOX-M (Pegylated liposomal doxorubicin substituted)

R-CODOX-M: Rituximab, Cyclophosphamide, Oncovin (Vincristine), DOXil (Pegylated liposomal doxorubicin), Methotrexate

Regimen

Study Evidence
Evens et al. 2013 (NU 06H2) Phase 2

This regimen is for low-risk patients.

Targeted therapy

Chemotherapy

CNS therapy, prophylaxis

Supportive therapy

  • Folinic acid (Leucovorin) 200 mg/m2 IV once 36 hours after start of IV methotrexate, then 15 mg/m2 IV every 6 hours until methotrexate level is less than 50 nmol/L
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day on days 6 & 7, then on day 14 onwards until ANC greater than 1500/uL

3 cycles (length not specified)

References

  1. NU 06H2: Evens AM, Carson KR, Kolesar J, Nabhan C, Helenowski I, Islam N, Jovanovic B, Barr PM, Caimi PF, Gregory SA, Gordon LI. A multicenter phase II study incorporating high-dose rituximab and liposomal doxorubicin into the CODOX-M/IVAC regimen for untreated Burkitt's lymphoma. Ann Oncol. 2013 Dec;24(12):3076-81. Epub 2013 Oct 20. link to original article contains dosing details in manuscript link to PMC article PubMed

R-CODOX-M/R-IVAC (Pegylated liposomal doxorubicin substituted)

R-CODOX-M/R-IVAC: Rituximab, Cyclophosphamide, Oncovin (Vincristine), DOXil (Pegylated liposomal doxorubicin), Methotrexate alternating with Rituximab, Ifosfamide, Vepesid (Etoposide), Ara-C (Cytarabine)

Protocol

Study Evidence
Evens et al. 2013 (NU 06H2) Phase 2

This protocol is for high-risk patients.

Targeted therapy, R-CODOX-M portion

Chemotherapy, R-CODOX-M portion

CNS therapy, prophylaxis, R-CODOX-M portion

Supportive therapy, R-CODOX-M portion

  • Folinic acid (Leucovorin) 200 mg/m2 IV once 36 hours after start of IV methotrexate, then 15 mg/m2 IV every 6 hours until methotrexate level is less than 50 nmol/L
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day on days 6 & 7, then on day 14 onwards until ANC greater than 1500/uL

Targeted therapy, R-IVAC portion

Chemotherapy, R-IVAC portion

CNS therapy, prophylaxis, R-IVAC portion

Supportive therapy, R-IVAC portion

Four alternating cycles of R-CODOX-M & R-IVAC

References

  1. NU 06H2: Evens AM, Carson KR, Kolesar J, Nabhan C, Helenowski I, Islam N, Jovanovic B, Barr PM, Caimi PF, Gregory SA, Gordon LI. A multicenter phase II study incorporating high-dose rituximab and liposomal doxorubicin into the CODOX-M/IVAC regimen for untreated Burkitt's lymphoma. Ann Oncol. 2013 Dec;24(12):3076-81. Epub 2013 Oct 20. link to original article contains dosing details in manuscript link to PMC article PubMed

R-COPADM

R-COPADM: Rituximab, Cyclophosphamide, Oncovin (Vincristine), Prednisone, ADriamycin (Doxorubicin), Methotrexate

Regimen

Study Years of enrollment Evidence Comparator Comparative Efficacy
Ribrag et al. 2016 (LMBA-02) 2004-2010 Phase 3 (E-esc) COPADM Seems to have superior EFS

This regimen is for group B (unresected stage I, non-abdominal stage II and any stage III or IV disease without CNS or bone marrow involvement); see manuscript for details about the regimen for group C.

Preceding treatment

Targeted therapy

Chemotherapy

Glucocorticoid therapy

Supportive therapy

CNS therapy, prophylaxis

2 cycles (length not specified)

Subsequent treatment

  • CYM consolidation

References

  1. LMBA-02: Ribrag V, Koscielny S, Bosq J, Leguay T, Casasnovas O, Fornecker LM, Recher C, Ghesquieres H, Morschhauser F, Girault S, Le Gouill S, Ojeda-Uribe M, Mariette C, Cornillon J, Cartron G, Verge V, Chassagne-Clément C, Dombret H, Coiffier B, Lamy T, Tilly H, Salles G. Rituximab and dose-dense chemotherapy for adults with Burkitt's lymphoma: a randomised, controlled, open-label, phase 3 trial. Lancet. 2016 Jun 11;387(10036):2402-11. Epub 2016 Apr 11. link to original article PubMed NCT00180882

R-Hyper-CVAD/R-MA

R-Hyper-CVAD/R-MA: Rituximab, Hyperfractionated Cyclophosphamide, Vincristine, Adriamycin (Doxorubicin), Dexamethasone altenating with Rituximab, Methotrexate, Ara-C (Cytarabine)

Regimen

Study Evidence
Thomas et al. 2006 Pilot, <20 pts

Targeted therapy, Part A

  • Rituximab (Rituxan) as follows:
    • Cycles 1 & 3: 375 mg/m2 IV over 2 to 6 hours once per day on days 1 & 11

Chemotherapy, Part A

  • Cyclophosphamide (Cytoxan) as follows:
    • Cycles 1, 3, 5, 7: 300 mg/m2 IV over 2 hours every 12 hours on days 1 to 3 (total dose per cycle: 1800 mg/m2)
  • Vincristine (Oncovin) as follows:
    • Cycles 1, 3, 5, 7: 2 mg IV once per day on days 4 & 11
  • Doxorubicin (Adriamycin) as follows:
    • Cycles 1, 3, 5, 7: 50 mg/m2 IV continuous infusion over 24 hours, started on day 4

Glucocorticoid therapy, Part A

Supportive therapy, Part A

Next cycle to start no sooner than 14 days or as soon as "unmaintained" WBC count is greater than 3 x 109/L and platelet count greater than 50 x 109/L

Dose modifications, Part A

  • Vincristine (Oncovin) reduced to 1 mg for bilirubin greater than 2 mg/dL or NCI common toxicity criteria Grade 2+ peripheral neuropathy, omitted for bilirubin greater than 3 mg/dL or for ileus
  • Doxorubicin (Adriamycin) reduced by 50% for bilirubin 2 to 3 mg/dL, by 75% for bilirubin 3 to 5 mg/dL (eliminated for bilirubin greater than 5 mg/dL or for gastric/small-bowel involvement with Course 1 to reduce duration of myelosuppression given risk of perforation)

Targeted therapy, Part B

  • Rituximab (Rituxan) as follows:
    • Cycles 2 & 4: 375 mg/m2 IV over 2 to 6 hours once per day on days 2 & 8

Chemotherapy, Part B

  • Methotrexate (MTX) as follows:
    • Cycles 2, 4, 6, 8: 1000 mg/m2 IV continuous infusion over 24 hours, started on day 1
  • Cytarabine (Ara-C) as follows:
    • Cycles 2, 4, 6, 8: 3000 mg/m2 IV over 2 hours every 12 hours on days 2 & 3 (total dose per cycle: 12,000 mg/m2)

Supportive therapy, Part B

Next cycle to start no sooner than 14 days or as soon as "unmaintained" WBC count is greater than 3 x 109/L and platelet count greater than 50 x 109/L

Dose modifications, Part B

  • Cytarabine (Ara-C) reduced to 1000 mg/m2 for patients greater than or equal to 60 years old, creatinine greater than or equal to 1.5 mg/dL or 0 hour MTX level greater than or equal to 20,000 nmol/L
  • Methotrexate (MTX) reduced by 50% for creatinine clearance 10 to 50 mL/min (eliminated for less than 10 mL/min), by 25% to 75% for delayed excretion and/or nephrotoxicity with prior course (dependent on severity) or by 50% for pleural effusions/ascites with drainage of fluid as feasible.

CNS therapy, prophylaxis

Given each cycle for a total of 16 intrathecal treatments. If CNS disease present, therapy augmented to twice-weekly alternating (MTX, ara-C) treatments until CSF cell count normalizes and cytology is negative, then continues for 4 more alternating weekly treatments; prophylaxis course then resumes.

References

  1. Thomas DA, Faderl S, O'Brien S, Bueso-Ramos C, Cortes J, Garcia-Manero G, Giles FJ, Verstovsek S, Wierda WG, Pierce SA, Shan J, Brandt M, Hagemeister FB, Keating MJ, Cabanillas F, Kantarjian H. Chemoimmunotherapy with hyper-CVAD plus rituximab for the treatment of adult Burkitt and Burkitt-type lymphoma or acute lymphoblastic leukemia. Cancer. 2006 Apr 1;106(7):1569-80. link to original article contains dosing details in manuscript PubMed

Consolidation/Intensification therapy

BASIC

BASIC: Brief, Anthracycline-Sparing, Intensive Cyclophosphamide

Protocol

Study Evidence
Kasamon et al. 2012 (J0409) Non-randomized

Preceding treatment

Targeted therapy, part 1

Chemotherapy, part 1

Supportive therapy, part 1

  • Mesna (Mesnex) 40 mg/kg/day IV in divided doses on days 2 to 5
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day, starting on day 11 and continuing until post-nadir ANC greater than 1000/uL

One course, followed once post-nadir ANC greater than 1000/uL by:

Targeted therapy, part 2

4-week course

CNS therapy, treatment, part 2

  • (only given if there was prior CNS involvement):
  • Cytarabine (Ara-C) 100 mg IT once per week for 4 doses, then once every other week for 4 doses
  • Hydrocortisone (Cortef) 50 mg IT is optional (no parameters given)

References

  1. J0409: Kasamon YL, Brodsky RA, Borowitz MJ, Ambinder RF, Crilley PA, Cho SY, Tsai HL, Smith BD, Gladstone DE, Carraway HE, Huff CA, Matsui WH, Bolaños-Meade J, Jones RJ, Swinnen LJ. Brief intensive therapy for older adults with newly diagnosed Burkitt or atypical Burkitt lymphoma/leukemia. Leuk Lymphoma. 2013 Mar;54(3):483-90. Epub 2012 Aug 17. link to original article contains dosing details in manuscript link to PMC article PubMed

Cytarabine & Methotrexate (CYM)

CYM: CYtarabine, Methotrexate

Regimen

Study Years of enrollment Evidence
Diviné et al. 2005 (LMB95) 1996-2001 Phase 2

This regimen is for group B (unresected stage I, non-abdominal stage II and any stage III or IV disease without CNS or bone marrow involvement).

Preceding treatment

Chemotherapy

  • Cytarabine (Ara-C) 100 mg/m2/day IV continuous infusion over 120 hours, started on day 2 (total dose per cycle: 500 mg/m2)
  • Methotrexate (MTX) 3000 mg/m2 IV over 3 hours once on day 1

Supportive therapy

CNS therapy, prophylaxis

2 cycles; intervals were as short as possible, as soon as the ANC was greater than 1500/uL and platelet count was greater than 100 × 109/L

Subsequent treatment

References

  1. LMB95: Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. link to original article contains dosing details in manuscript PubMed

CYVE

CYVE: CYtarabine, VEpesid (Etoposide)

Regimen

Study Years of enrollment Evidence
Diviné et al. 2005 (LMB95) 1996-2001 Phase 2, <20 pts in this subgroup

This regimen is for group C (CNS and/or bone marrow involvement). Note the unusual schedule of cytarabine; presumably the low-dose and high-dose portions are given at separate times in the 24 hour period but this detail is not further specified in the manuscript.

Preceding treatment

Chemotherapy

  • Cytarabine (Ara-C) by the following split schedule:
    • 50 mg/m2 IV over 12 hours once per day on days 1 to 5
    • 3000 mg/m2 IV over 3 hours once per day on days 2 to 5
  • Etoposide (Vepesid) 200 mg/m2 IV once per day on days 2 to 5

2 cycles; intervals were as short as possible, as soon as the ANC was greater than 1500/uL and platelet count was greater than 100 × 109/L

Subsequent treatment

References

  1. LMB95: Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. link to original article contains dosing details in manuscript PubMed

Maintenance therapy

COPAD/CYVE

COPAD/CYVE: Cyclophosphamide, Oncovin (Vincristine), Prednisone, ADriamycin (Doxorubicin) alternating with CYtarabine, VEpesid (Etoposide)

Protocol

Study Years of enrollment Evidence
Diviné et al. 2005 (LMB95) 1996-2001 Phase 2, <20 pts in this subgroup

This protocol is for group C (CNS and/or bone marrow involvement). Note that the days of administration for the CYVE cycles are counted from the start of the respective COPAD cycles.

Preceding treatment

Chemotherapy, COPAD cycles

Glucocorticoid therapy

CNS therapy, treatment

Note: this is only given with the first cycle of maintenance; patients with positive CNS at diagnosis were to also undergo 24 Gy of cranial irradiation.

Chemotherapy, CYVE cycles

4 alternating cycles (COPAD, then CYVE, then COPAD, then CYVE)

References

  1. LMB95: Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. link to original article contains dosing details in manuscript PubMed

COPADM

COPADM: Cyclophosphamide, Oncovin (Vincristine), Prednisone, ADriamycin (Doxorubicin), Methotrexate

Regimen

Study Years of enrollment Evidence
Diviné et al. 2005 (LMB95) 1996-2001 Phase 2

This regimen is for group B (unresected stage I, non-abdominal stage II and any stage III or IV disease without CNS or bone marrow involvement).

Preceding treatment

  • CYM consolidation

Chemotherapy

Glucocorticoid therapy

Supportive therapy

CNS therapy, prophylaxis

One course

References

  1. LMB95: Diviné M, Casassus P, Koscielny S, Bosq J, Sebban C, Le Maignan C, Stamattoulas A, Dupriez B, Raphaël M, Pico JL, Ribrag V; GELA; GOELAMS. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol. 2005 Dec;16(12):1928-35. Epub 2005 Nov 10. link to original article contains dosing details in manuscript PubMed