Difference between revisions of "Transplant conditioning regimens"

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==BEAC==
 
==BEAC==
 
BEAC: '''<u>B</u>'''iCNU, '''<u>E</u>'''toposide, '''<u>A</u>'''ra-C, '''<u>C</u>'''yclophosphamide
 
BEAC: '''<u>B</u>'''iCNU, '''<u>E</u>'''toposide, '''<u>A</u>'''ra-C, '''<u>C</u>'''yclophosphamide
 +
 
===Regimen ===
 
===Regimen ===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#00CD00;
 
style="background:#00CD00;
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BEAM: '''<u>B</u>'''iCNU, '''<u>E</u>'''toposide, '''<u>A</u>'''ra-C, '''<u>M</u>'''elphalan
 
BEAM: '''<u>B</u>'''iCNU, '''<u>E</u>'''toposide, '''<u>A</u>'''ra-C, '''<u>M</u>'''elphalan
 
===Regimen #1, Jo et al. 2008===
 
===Regimen #1, Jo et al. 2008===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#00CD00;
 
style="background:#00CD00;
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===Regimen #2, Stewart et al. 2006===
 
===Regimen #2, Stewart et al. 2006===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
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*Patients <70 kg: [[Filgrastim (Neupogen)]] 300 mcg SC once per day starting on day +7 after stem cell transplant
 
*Patients <70 kg: [[Filgrastim (Neupogen)]] 300 mcg SC once per day starting on day +7 after stem cell transplant
 
*Patients >70 kg (reference did not clarify which dosage to use for patients who are exactly 70 kg): [[Filgrastim (Neupogen)]] 480 mcg SC once per day starting on day +7 after stem cell transplant
 
*Patients >70 kg (reference did not clarify which dosage to use for patients who are exactly 70 kg): [[Filgrastim (Neupogen)]] 480 mcg SC once per day starting on day +7 after stem cell transplant
*Trimethoprim/Sulfamethoxazole (Bactrim DS) (160/800 mg) PO BID on Monday and Thursdays, until 6 months after BEAM
+
*[[Trimethoprim/Sulfamethoxazole (Bactrim DS)]] (160/800 mg) PO BID on Monday and Thursdays, until 6 months after BEAM
''While ANC <500''
+
''While ANC <500:''
*Ciprofloxacin (Cipro) 500 mg PO BID
+
*[[Ciprofloxacin (Cipro)]] 500 mg PO BID
*Fluconazole (Diflucan) 100 mg PO once per day or mycostatin 500,000 units swish & swallow QID
+
*[[Fluconazole (Diflucan)]] 100 mg PO once per day or mycostatin 500,000 units swish & swallow QID
 
*[[Acyclovir (Zovirax)]] 400 mg PO TID
 
*[[Acyclovir (Zovirax)]] 400 mg PO TID
  
 
===Regimen #3, Josting et al. 2005===
 
===Regimen #3, Josting et al. 2005===
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
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# Stewart DA, Bahlis N, Valentine K, Balogh A, Savoie L, Morris DG, Jones A, Brown C, Russell JA. Upfront double high-dose chemotherapy with DICEP followed by BEAM and autologous stem cell transplantation for poor-prognosis aggressive non-Hodgkin lymphoma. Blood. 2006 Jun 15;107(12):4623-7. Epub 2006 Feb 7. [http://bloodjournal.hematologylibrary.org/content/107/12/4623.long link to original article] '''contains protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/16467197 PubMed] content property of [http://hemonc.org HemOnc.org]
 
# Stewart DA, Bahlis N, Valentine K, Balogh A, Savoie L, Morris DG, Jones A, Brown C, Russell JA. Upfront double high-dose chemotherapy with DICEP followed by BEAM and autologous stem cell transplantation for poor-prognosis aggressive non-Hodgkin lymphoma. Blood. 2006 Jun 15;107(12):4623-7. Epub 2006 Feb 7. [http://bloodjournal.hematologylibrary.org/content/107/12/4623.long link to original article] '''contains protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/16467197 PubMed] content property of [http://hemonc.org HemOnc.org]
 
# Jo JC, Kang BW, Jang G, Sym SJ, Lee SS, Koo JE, Kim JW, Kim S, Huh J, Suh C. BEAC or BEAM high-dose chemotherapy followed by autologous stem cell transplantation in non-Hodgkin's lymphoma patients: comparative analysis of efficacy and toxicity. Ann Hematol. 2008 Jan;87(1):43-8. Epub 2007 Aug 21. [http://www.springerlink.com/content/r764139714772803/ link to original article] '''contains protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/17710401 PubMed]
 
# Jo JC, Kang BW, Jang G, Sym SJ, Lee SS, Koo JE, Kim JW, Kim S, Huh J, Suh C. BEAC or BEAM high-dose chemotherapy followed by autologous stem cell transplantation in non-Hodgkin's lymphoma patients: comparative analysis of efficacy and toxicity. Ann Hematol. 2008 Jan;87(1):43-8. Epub 2007 Aug 21. [http://www.springerlink.com/content/r764139714772803/ link to original article] '''contains protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/17710401 PubMed]
# Gisselbrecht C, Glass B, Mounier N, Singh Gill D, Linch DC, Trneny M, Bosly A, Ketterer N, Shpilberg O, Hagberg H, Ma D, Brière J, Moskowitz CH, Schmitz N. Salvage regimens with autologous transplantation for relapsed large B-cell lymphoma in the rituximab era. J Clin Oncol. 2010 Sep 20;28(27):4184-90. doi: 10.1200/JCO.2010.28.1618. Epub 2010 Jul 26. Erratum in: J Clin Oncol. 2012 May 20;30(15):1896. [http://jco.ascopubs.org/content/28/27/4184.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/20660832 PubMed]
+
# Gisselbrecht C, Glass B, Mounier N, Singh Gill D, Linch DC, Trneny M, Bosly A, Ketterer N, Shpilberg O, Hagberg H, Ma D, Brière J, Moskowitz CH, Schmitz N. Salvage regimens with autologous transplantation for relapsed large B-cell lymphoma in the rituximab era. J Clin Oncol. 2010 Sep 20;28(27):4184-90. Epub 2010 Jul 26. Erratum in: J Clin Oncol. 2012 May 20;30(15):1896. [http://jco.ascopubs.org/content/28/27/4184.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/20660832 PubMed]
# Shimoni A, Avivi I, Rowe JM, Yeshurun M, Levi I, Or R, Patachenko P, Avigdor A, Zwas T, Nagler A. A randomized study comparing yttrium-90 ibritumomab tiuxetan (Zevalin) and high-dose BEAM chemotherapy versus BEAM alone as the conditioning regimen before autologous stem cell transplantation in patients with aggressive lymphoma. Cancer. 2012 Oct 1;118(19):4706-14. doi: 10.1002/cncr.27418. Epub 2012 Jan 17. [http://onlinelibrary.wiley.com/doi/10.1002/cncr.27418/full link to original article] [http://www.ncbi.nlm.nih.gov/pubmed/22252613 PubMed]
+
# Shimoni A, Avivi I, Rowe JM, Yeshurun M, Levi I, Or R, Patachenko P, Avigdor A, Zwas T, Nagler A. A randomized study comparing yttrium-90 ibritumomab tiuxetan (Zevalin) and high-dose BEAM chemotherapy versus BEAM alone as the conditioning regimen before autologous stem cell transplantation in patients with aggressive lymphoma. Cancer. 2012 Oct 1;118(19):4706-14. Epub 2012 Jan 17. [http://onlinelibrary.wiley.com/doi/10.1002/cncr.27418/full link to original article] [http://www.ncbi.nlm.nih.gov/pubmed/22252613 PubMed]
  
 
==Bor-HDM==
 
==Bor-HDM==
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===Regimen===
 
===Regimen===
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
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Supportive medications:
 
Supportive medications:
* "All patients received standard supportive care measures"
+
*"All patients received standard supportive care measures"
  
 
===References===
 
===References===
# Roussel M, Moreau P, Huynh A, Mary JY, Danho C, Caillot D, Hulin C, Fruchart C, Marit G, Pégourié B, Lenain P, Araujo C, Kolb B, Randriamalala E, Royer B, Stoppa AM, Dib M, Dorvaux V, Garderet L, Mathiot C, Avet-Loiseau H, Harousseau JL, Attal M; Intergroupe Francophone du Myélome (IFM). Bortezomib and high-dose melphalan as conditioning regimen before autologous stem cell transplantation in patients with de novo multiple myeloma: a phase 2 study of the Intergroupe Francophone du Myelome (IFM). Blood. 2010 Jan 7;115(1):32-7. doi:10.1182/blood-2009-06-229658. Epub 2009 Nov 2. [http://bloodjournal.hematologylibrary.org/content/115/1/32.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/19884643 PubMed]  
+
# Roussel M, Moreau P, Huynh A, Mary JY, Danho C, Caillot D, Hulin C, Fruchart C, Marit G, Pégourié B, Lenain P, Araujo C, Kolb B, Randriamalala E, Royer B, Stoppa AM, Dib M, Dorvaux V, Garderet L, Mathiot C, Avet-Loiseau H, Harousseau JL, Attal M; Intergroupe Francophone du Myélome (IFM). Bortezomib and high-dose melphalan as conditioning regimen before autologous stem cell transplantation in patients with de novo multiple myeloma: a phase 2 study of the Intergroupe Francophone du Myelome (IFM). Blood. 2010 Jan 7;115(1):32-7. Epub 2009 Nov 2. [http://bloodjournal.hematologylibrary.org/content/115/1/32.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/19884643 PubMed]  
  
 
==Busulfan & Melphalan==
 
==Busulfan & Melphalan==
  
 
===Regimen===
 
===Regimen===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
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===References===
 
===References===
# Yanada M, Tsuzuki M, Fujita H, Fujimaki K, Fujisawa S, Sunami K, Taniwaki M, Ohwada A, Tsuboi K, Maeda A, Takeshita A, Ohtake S, Miyazaki Y, Atsuta Y, Kobayashi Y, Naoe T, Emi N; Japan Adult Leukemia Study Group. Phase 2 study of arsenic trioxide followed by autologous hematopoietic cell transplantation for relapsed acute promyelocytic leukemia. Blood. 2013 Apr 18;121(16):3095-102. doi: 10.1182/blood-2012-11-466862. Epub 2013 Feb 14. [http://bloodjournal.hematologylibrary.org/content/121/16/3095.long link to original article] '''Contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/23412094 PubMed]
+
# Yanada M, Tsuzuki M, Fujita H, Fujimaki K, Fujisawa S, Sunami K, Taniwaki M, Ohwada A, Tsuboi K, Maeda A, Takeshita A, Ohtake S, Miyazaki Y, Atsuta Y, Kobayashi Y, Naoe T, Emi N; Japan Adult Leukemia Study Group. Phase 2 study of arsenic trioxide followed by autologous hematopoietic cell transplantation for relapsed acute promyelocytic leukemia. Blood. 2013 Apr 18;121(16):3095-102. Epub 2013 Feb 14. [http://bloodjournal.hematologylibrary.org/content/121/16/3095.long link to original article] '''Contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/23412094 PubMed]
  
 
==C-VAMP -> high-dose Melphalan (Alkeran)==
 
==C-VAMP -> high-dose Melphalan (Alkeran)==
 
C-VAMP: '''<u>C</u>'''yclophosphamide, '''<u>V</u>'''incristine, '''<u>A</u>'''driamycin, '''<u>M</u>'''ethyl'''<u>P</u>'''rednisolone
 
C-VAMP: '''<u>C</u>'''yclophosphamide, '''<u>V</u>'''incristine, '''<u>A</u>'''driamycin, '''<u>M</u>'''ethyl'''<u>P</u>'''rednisolone
 
===Regimen - multiple myeloma high-dose therapy===
 
===Regimen - multiple myeloma high-dose therapy===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#00CD00;
 
style="background:#00CD00;
Line 156: Line 155:
  
 
====Induction therapy====
 
====Induction therapy====
 +
*[[Cyclophosphamide (Cytoxan)]] 500 mg IV once per day on days 1, 8, 15
 +
**Cyclophosphamide was omitted in patients with a serum creatinine >3.4 mg/dL
 +
*[[Vincristine (Oncovin)]] 0.4 mg IV once per day on days 1 to 4 (total dose per cycle: 1.6 mg)
 
*[[Doxorubicin (Adriamycin)]] 9 mg/m2/day IV continuous infusion over 4 days (total dose per cycle: 36 mg/m2) on days 1 to 4
 
*[[Doxorubicin (Adriamycin)]] 9 mg/m2/day IV continuous infusion over 4 days (total dose per cycle: 36 mg/m2) on days 1 to 4
*[[Vincristine (Oncovin)]] 0.4 mg IV once per day on days 1 to 4 (total dose per cycle: 1.6 mg)
 
 
*[[Methylprednisolone (Solumedrol)]] 1000 mg/m2 (maximum dose per cycle of 1500 mg) PO/IV once per day on days 1 to 5
 
*[[Methylprednisolone (Solumedrol)]] 1000 mg/m2 (maximum dose per cycle of 1500 mg) PO/IV once per day on days 1 to 5
*[[Cyclophosphamide (Cytoxan)]] 500 mg IV once per day on days 1, 8, 15
 
**Cyclophosphamide was omitted in patients with a serum creatinine >3.4 mg/dL
 
 
   
 
   
 
'''21-day cycles, given until maximal response was achieved. A minimum of 3 cycles given before stem cell harvest.'''
 
'''21-day cycles, given until maximal response was achieved. A minimum of 3 cycles given before stem cell harvest.'''
  
*Stem cell mobilization was performed with administration of [[Cyclophosphamide (Cytoxan)]] 2000-4000 mg/m2 IV with hydration and [[Filgrastim (Neupogen)|G-CSF]] on days 5-12
+
*Stem cell mobilization was performed with administration of [[Cyclophosphamide (Cytoxan)]] 2000 to 4000 mg/m2 IV with hydration and [[Filgrastim (Neupogen)|G-CSF]] on days 5 to 12
  
 
====Melphalan (Alkeran) & transplant====
 
====Melphalan (Alkeran) & transplant====
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===Regimen===
 
===Regimen===
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
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Supportive medications:
 
Supportive medications:
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day starting on day +4, to continue until ANC >5000 once or >1500 twice
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day starting on day +4, to continue until ANC >5000 once or >1500 twice
*Levofloxacin (Levaquin) 500 mg PO once per day, starting on day +2, to continue until ANC ≥500
+
*[[Levofloxacin (Levaquin)]] 500 mg PO once per day, starting on day +2, to continue until ANC ≥500
*Fluconazole (Diflucan) 200 mg PO once per day, starting on day +1, to continue until ANC ≥500
+
*[[Fluconazole (Diflucan)]] 200 mg PO once per day, starting on day +1, to continue until ANC ≥500
 
*[[Acyclovir (Zovirax)]] 200 mg PO TID, starting on day -2, to continue until 1 year after ASCT
 
*[[Acyclovir (Zovirax)]] 200 mg PO TID, starting on day -2, to continue until 1 year after ASCT
 
*[[Trimethoprim/Sulfamethoxazole (Bactrim DS)]] 160/800 mg PO BID on Saturday and Sunday, to continue until 3 months after ASCT
 
*[[Trimethoprim/Sulfamethoxazole (Bactrim DS)]] 160/800 mg PO BID on Saturday and Sunday, to continue until 3 months after ASCT
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==Cyclophosphamide (Cytoxan), Etoposide (Vepesid), TBI==
 
==Cyclophosphamide (Cytoxan), Etoposide (Vepesid), TBI==
 
===Regimen===
 
===Regimen===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
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Supportive medications:
 
Supportive medications:
*Diphenhydramine (Benadryl) 25 mg (route not specified) once 2 hours before etoposide to prevent allergic reaction
+
*[[Diphenhydramine (Benadryl)]] 25 mg (route not specified) once 2 hours before [[Etoposide (Vepesid)]] to prevent allergic reaction
*Hydrocortisone (Cortef) 100 mg (route not specified) once 2 hours before etoposide to prevent allergic reaction
+
*[[Hydrocortisone (Cortef)]] 100 mg (route not specified) once 2 hours before [[Etoposide (Vepesid)]] to prevent allergic reaction
 
*"Continuous bladder irrigation and vigorous hydration were used" to protect against hemorrhagic cystitis
 
*"Continuous bladder irrigation and vigorous hydration were used" to protect against hemorrhagic cystitis
  
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==High-dose Melphalan (Alkeran)==
 
==High-dose Melphalan (Alkeran)==
 
===Regimen - immunoglobulin light-chain (AL) amyloidosis===
 
===Regimen - immunoglobulin light-chain (AL) amyloidosis===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
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*Patients who fulfilled all of these criteria--≤65 years old, cardiac ejection fraction ≥45%, and ≥2.5 x 10<sup>6</sup> CD34+ cells/kg collected--received [[Melphalan (Alkeran)]] 200 mg/m2 total dose IV divided over two consecutive days
 
*Patients who fulfilled all of these criteria--≤65 years old, cardiac ejection fraction ≥45%, and ≥2.5 x 10<sup>6</sup> CD34+ cells/kg collected--received [[Melphalan (Alkeran)]] 200 mg/m2 total dose IV divided over two consecutive days
 
*Patients with at least one of these criteria-->65 years old, cardiac ejection fraction 40-44%, or with 2.0-2.5 x 10<sup>6</sup> CD34+ cells/kg collected received [[Melphalan (Alkeran)]] 140 mg/m2 total dose IV divided over two consecutive days
 
*Patients with at least one of these criteria-->65 years old, cardiac ejection fraction 40-44%, or with 2.0-2.5 x 10<sup>6</sup> CD34+ cells/kg collected received [[Melphalan (Alkeran)]] 140 mg/m2 total dose IV divided over two consecutive days
*Autologous stem cell infusion occurs 24-72 hours after the last dose of melphalan
+
*Autologous stem cell infusion occurs 24 to 72 hours after the last dose of melphalan
  
 
===References===
 
===References===
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==TAM6==
 
==TAM6==
 
===Regimen===
 
===Regimen===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
Line 281: Line 279:
  
 
===Regimen - multiple myeloma high-dose therapy===
 
===Regimen - multiple myeloma high-dose therapy===
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#00CD00;
 
style="background:#00CD00;
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'''21-day cycles x 2 to 3 cycles, given in an alternating fashion with VMCP'''
 
'''21-day cycles x 2 to 3 cycles, given in an alternating fashion with VMCP'''
  
'''VMCP and BVAP are given in an alternating fashion x a total of 4-6 cycles'''; patients with a [[performance status|WHO performance status]] <3, creatinine <1.7 mg/dL (150 μmol/L), and bone marrow (collected after cycle 4) with greater than 200 million nucleated cells/kg would proceed to melphalan, total body irradiation (TBI), and transplant:
+
'''VMCP and BVAP are given in an alternating fashion x a total of 4 to 6 cycles'''; patients with a [[performance status|WHO performance status]] <3, creatinine <1.7 mg/dL (150 μmol/L), and bone marrow (collected after cycle 4) with greater than 200 million nucleated cells/kg would proceed to melphalan, total body irradiation (TBI), and transplant:
  
 
====Melphalan (Alkeran), TBI, and transplant====
 
====Melphalan (Alkeran), TBI, and transplant====
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===Regimen===
 
===Regimen===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#00CD00;
 
style="background:#00CD00;
Line 331: Line 328:
  
 
===References===
 
===References===
# Shimoni A, Avivi I, Rowe JM, Yeshurun M, Levi I, Or R, Patachenko P, Avigdor A, Zwas T, Nagler A. A randomized study comparing yttrium-90 ibritumomab tiuxetan (Zevalin) and high-dose BEAM chemotherapy versus BEAM alone as the conditioning regimen before autologous stem cell transplantation in patients with aggressive lymphoma. Cancer. 2012 Oct 1;118(19):4706-14. doi: 10.1002/cncr.27418. Epub 2012 Jan 17. [http://onlinelibrary.wiley.com/doi/10.1002/cncr.27418/full link to original article] [http://www.ncbi.nlm.nih.gov/pubmed/22252613 PubMed]
+
# Shimoni A, Avivi I, Rowe JM, Yeshurun M, Levi I, Or R, Patachenko P, Avigdor A, Zwas T, Nagler A. A randomized study comparing yttrium-90 ibritumomab tiuxetan (Zevalin) and high-dose BEAM chemotherapy versus BEAM alone as the conditioning regimen before autologous stem cell transplantation in patients with aggressive lymphoma. Cancer. 2012 Oct 1;118(19):4706-14. Epub 2012 Jan 17. [http://onlinelibrary.wiley.com/doi/10.1002/cncr.27418/full link to original article] [http://www.ncbi.nlm.nih.gov/pubmed/22252613 PubMed]
  
 
=Allogeneic (allo) stem cell transplant=
 
=Allogeneic (allo) stem cell transplant=
 
==BEAM==
 
==BEAM==
 
BEAM: '''<u>B</u>'''iCNU, '''<u>E</u>'''toposide, '''<u>A</u>'''ra-C, '''<u>M</u>'''elphalan
 
BEAM: '''<u>B</u>'''iCNU, '''<u>E</u>'''toposide, '''<u>A</u>'''ra-C, '''<u>M</u>'''elphalan
 +
 
===Regimen===
 
===Regimen===
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
Line 353: Line 350:
 
Supportive medications:
 
Supportive medications:
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day +7 and continued until engraftment
 
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day +7 and continued until engraftment
*GVHD prophylaxis with tacrolimus and methotrexate
+
*GVHD prophylaxis with [[Tacrolimus (Prograf)]] and [[Methotrexate (MTX)]]
 
*"Prophylactic antibiotics"
 
*"Prophylactic antibiotics"
  
Line 361: Line 358:
 
==Busulfan & Cyclophosphamide (BuCy)==
 
==Busulfan & Cyclophosphamide (BuCy)==
 
===Regimen===
 
===Regimen===
Level of Evidence:
 
 
<span  
 
<span  
 
style="background:#00CD00;
 
style="background:#00CD00;
Line 378: Line 374:
  
 
===References===
 
===References===
# Lee JH, Joo YD, Kim H, Ryoo HM, Kim MK, Lee GW, Lee JH, Lee WS, Park JH, Bae SH, Hyun MS, Kim DY, Kim SD, Min YJ, Lee KH. Randomized trial of myeloablative conditioning regimens: busulfan plus cyclophosphamide versus busulfan plus fludarabine. J Clin Oncol. 2013 Feb 20;31(6):701-9. doi:10.1200/JCO.2011.40.2362. Epub 2012 Nov 5. [http://jco.ascopubs.org/content/31/6/701.full link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/23129746 PubMed]
+
# Lee JH, Joo YD, Kim H, Ryoo HM, Kim MK, Lee GW, Lee JH, Lee WS, Park JH, Bae SH, Hyun MS, Kim DY, Kim SD, Min YJ, Lee KH. Randomized trial of myeloablative conditioning regimens: busulfan plus cyclophosphamide versus busulfan plus fludarabine. J Clin Oncol. 2013 Feb 20;31(6):701-9. Epub 2012 Nov 5. [http://jco.ascopubs.org/content/31/6/701.full link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/23129746 PubMed]
  
 
==Busulfan & Fludarabine (Flu/Bu; BuFlu)==
 
==Busulfan & Fludarabine (Flu/Bu; BuFlu)==
 
===Regimen #1, Russell et al. 2002 (Flu/Bu)===
 
===Regimen #1, Russell et al. 2002 (Flu/Bu)===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
Line 395: Line 391:
  
 
Supportive medications:
 
Supportive medications:
*Phenytoin (Dilantin) "loading" PO/IV, dosed to maintain therapeutic levels of 40 to 80 umol/L on days -5 to -2
+
*[[Phenytoin (Dilantin)]] "loading" PO/IV, dosed to maintain therapeutic levels of 40 to 80 umol/L on days -5 to -2
*Ciprofloxacin (Cipro) 500 mg PO BID as prophylaxis
+
*[[Ciprofloxacin (Cipro)]] 500 mg PO BID as prophylaxis
 
*[[Trimethoprim/Sulfamethoxazole (Bactrim DS)]] (dose not specified in reference, but assume 160/800 mg dose) PO 2 times a week as PCP prophylaxis
 
*[[Trimethoprim/Sulfamethoxazole (Bactrim DS)]] (dose not specified in reference, but assume 160/800 mg dose) PO 2 times a week as PCP prophylaxis
 
*No routine fungal prophylaxis
 
*No routine fungal prophylaxis
Line 406: Line 402:
 
*[[Cyclosporine modified (Neoral)]] or [[Cyclosporine non-modified (Sandimmune)]] PO/IV BID, with doses adjusted to maintain cyclosporine levels of 150 to 400 umol/L
 
*[[Cyclosporine modified (Neoral)]] or [[Cyclosporine non-modified (Sandimmune)]] PO/IV BID, with doses adjusted to maintain cyclosporine levels of 150 to 400 umol/L
 
*[[Methotrexate (MTX)]] 15 mg/m2 once on day 1; 10 mg/m2 once per day on days 3, 6, 11
 
*[[Methotrexate (MTX)]] 15 mg/m2 once on day 1; 10 mg/m2 once per day on days 3, 6, 11
*[[Folinic acid (Leucovorin)]] 5 mg started 24 hours after each dose of methotrexate and continued Q6H until 12 hours before the next dose of methotrexate
+
*[[Folinic acid (Leucovorin)]] 5 mg started 24 hours after each dose of [[Methotrexate (MTX)]] and continued Q6H until 12 hours before the next dose of [[Methotrexate (MTX)]]
  
 
===Regimen #2, Lee et al. 2013 (BuFlu)===
 
===Regimen #2, Lee et al. 2013 (BuFlu)===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#00CD00;
 
style="background:#00CD00;
Line 422: Line 418:
  
 
Supportive medications:
 
Supportive medications:
*"[[Cyclosporine non-modified (Sandimmune)|Cyclosporine]] alone or cyclosporine plus [[Methotrexate (MTX)|methotrexate]] according to the discretion of the attending physician"
+
*"[[Cyclosporine non-modified (Sandimmune)|Cyclosporine]] alone or with [[Methotrexate (MTX)|methotrexate]] according to the discretion of the attending physician"
 
*[[Filgrastim (Neupogen)]] 450 mcg SC once per day, starting on day +5 and continued until ANC >3,000
 
*[[Filgrastim (Neupogen)]] 450 mcg SC once per day, starting on day +5 and continued until ANC >3,000
  
 
===References===
 
===References===
 
# Russell JA, Tran HT, Quinlan D, Chaudhry A, Duggan P, Brown C, Stewart D, Ruether JD, Morris D, Glick S, Gyonyor E, Andersson BS. Once-daily intravenous busulfan given with fludarabine as conditioning for allogeneic stem cell transplantation: study of pharmacokinetics and early clinical outcomes. Biol Blood Marrow Transplant. 2002;8(9):468-76. [http://www.bbmt.org/article/S1083-8791%2802%2950007-0/abstract link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/12374451 PubMed]
 
# Russell JA, Tran HT, Quinlan D, Chaudhry A, Duggan P, Brown C, Stewart D, Ruether JD, Morris D, Glick S, Gyonyor E, Andersson BS. Once-daily intravenous busulfan given with fludarabine as conditioning for allogeneic stem cell transplantation: study of pharmacokinetics and early clinical outcomes. Biol Blood Marrow Transplant. 2002;8(9):468-76. [http://www.bbmt.org/article/S1083-8791%2802%2950007-0/abstract link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/12374451 PubMed]
# Lee JH, Joo YD, Kim H, Ryoo HM, Kim MK, Lee GW, Lee JH, Lee WS, Park JH, Bae SH, Hyun MS, Kim DY, Kim SD, Min YJ, Lee KH. Randomized trial of myeloablative conditioning regimens: busulfan plus cyclophosphamide versus busulfan plus fludarabine. J Clin Oncol. 2013 Feb 20;31(6):701-9. doi:10.1200/JCO.2011.40.2362. Epub 2012 Nov 5. [http://jco.ascopubs.org/content/31/6/701.full link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/23129746 PubMed]
+
# Lee JH, Joo YD, Kim H, Ryoo HM, Kim MK, Lee GW, Lee JH, Lee WS, Park JH, Bae SH, Hyun MS, Kim DY, Kim SD, Min YJ, Lee KH. Randomized trial of myeloablative conditioning regimens: busulfan plus cyclophosphamide versus busulfan plus fludarabine. J Clin Oncol. 2013 Feb 20;31(6):701-9. Epub 2012 Nov 5. [http://jco.ascopubs.org/content/31/6/701.full link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/23129746 PubMed]
  
 
==Fludarabine and Low-dose TBI==
 
==Fludarabine and Low-dose TBI==
 
===Regimen===
 
===Regimen===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#00CD00;
 
style="background:#00CD00;
Line 447: Line 443:
  
 
===References===
 
===References===
# Gyurkocza B, Storb R, Storer BE, Chauncey TR, Lange T, Shizuru JA, Langston AA, Pulsipher MA, Bredeson CN, Maziarz RT, Bruno B, Petersen FB, Maris MB, Agura E, Yeager A, Bethge W, Sahebi F, Appelbaum FR, Maloney DG, Sandmaier BM. Nonmyeloablative allogeneic hematopoietic cell transplantation in patients with acute myeloid leukemia. J Clin Oncol. 2010 Jun 10;28(17):2859-67. doi:10.1200/JCO.2009.27.1460. Epub 2010 May 3. [http://jco.ascopubs.org/content/28/17/2859.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/20439626 PubMed]
+
# Gyurkocza B, Storb R, Storer BE, Chauncey TR, Lange T, Shizuru JA, Langston AA, Pulsipher MA, Bredeson CN, Maziarz RT, Bruno B, Petersen FB, Maris MB, Agura E, Yeager A, Bethge W, Sahebi F, Appelbaum FR, Maloney DG, Sandmaier BM. Nonmyeloablative allogeneic hematopoietic cell transplantation in patients with acute myeloid leukemia. J Clin Oncol. 2010 Jun 10;28(17):2859-67. Epub 2010 May 3. [http://jco.ascopubs.org/content/28/17/2859.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/20439626 PubMed]
  
 
==Fludarabine, Cyclophosphamide, & TBI for dUCB or haploidentical transplant==
 
==Fludarabine, Cyclophosphamide, & TBI for dUCB or haploidentical transplant==
Line 453: Line 449:
  
 
===Regimen #1, Brunstein et al. 2011 - dUCB transplantation===
 
===Regimen #1, Brunstein et al. 2011 - dUCB transplantation===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
Line 468: Line 464:
 
Supportive medications:
 
Supportive medications:
 
*[[Mesna (Mesnex)]] (dose/route/schedule not specified) and "vigorous IV hydration for uroprotection."
 
*[[Mesna (Mesnex)]] (dose/route/schedule not specified) and "vigorous IV hydration for uroprotection."
 +
*[[Filgrastim (Neupogen)]] 5 μg/kg SC once per day, starting on day +1, continued until ANC ≥2000/μL for 3 consecutive days
  
 
====GVHD Prophylaxis====
 
====GVHD Prophylaxis====
Line 474: Line 471:
 
*[[Cyclosporine modified (Neoral)|Cyclosporine A]] ([[Cyclosporine modified (Neoral)|Neoral]] vs. [[Cyclosporine non-modified (Sandimmune)|Sandimmune]] not specified, route not specified) with a goal trough of 200 to 400 ng/mL (starting date not specified) until day +100.  Patients without GVHD had their dose tapered by 10% each week starting on day +101, with discontinuation of cyclosporine A around day +180 to +200.  
 
*[[Cyclosporine modified (Neoral)|Cyclosporine A]] ([[Cyclosporine modified (Neoral)|Neoral]] vs. [[Cyclosporine non-modified (Sandimmune)|Sandimmune]] not specified, route not specified) with a goal trough of 200 to 400 ng/mL (starting date not specified) until day +100.  Patients without GVHD had their dose tapered by 10% each week starting on day +101, with discontinuation of cyclosporine A around day +180 to +200.  
 
*[[Tacrolimus (Prograf)]] (route not specified) with a goal trough level of 5 to 10 ng/mL could be substituted for cyclosporine.
 
*[[Tacrolimus (Prograf)]] (route not specified) with a goal trough level of 5 to 10 ng/mL could be substituted for cyclosporine.
*[[Filgrastim (Neupogen)]] 5 μg/kg SC once per day, starting on day +1, continued until ANC ≥2000/μL for 3 consecutive days
 
  
 
===Regimen #2, Brunstein et al. 2011 - Haploidentical===
 
===Regimen #2, Brunstein et al. 2011 - Haploidentical===
Level of Evidence:
+
 
 
<span  
 
<span  
 
style="background:#EEEE00;
 
style="background:#EEEE00;
Line 492: Line 488:
 
Supportive medications:
 
Supportive medications:
 
*[[Mesna (Mesnex)]] (dose/route/schedule not specified) and "vigorous IV hydration for uroprotection."
 
*[[Mesna (Mesnex)]] (dose/route/schedule not specified) and "vigorous IV hydration for uroprotection."
 +
*[[Filgrastim (Neupogen)]] 5 μg/kg SC once per day, starting on day +5, continued until ANC ≥1000/μL for 3 consecutive days
  
 
====GVHD Prophylaxis====
 
====GVHD Prophylaxis====
Line 497: Line 494:
 
*[[Mycophenolate mofetil (CellCept)]] 15 mg/kg (maximum daily dose of 3000 mg; route not specified) Q8H, starting on day +5, continued until day +35 or longer at physician discretion if active GVHD was present
 
*[[Mycophenolate mofetil (CellCept)]] 15 mg/kg (maximum daily dose of 3000 mg; route not specified) Q8H, starting on day +5, continued until day +35 or longer at physician discretion if active GVHD was present
 
*[[Tacrolimus (Prograf)]] (route not specified) with a goal trough level of 5 to 10 ng/mL, starting on day +5, continued until day +180
 
*[[Tacrolimus (Prograf)]] (route not specified) with a goal trough level of 5 to 10 ng/mL, starting on day +5, continued until day +180
*[[Filgrastim (Neupogen)]] 5 μg/kg SC once per day, starting on day +5, continued until ANC ≥1000/μL for 3 consecutive days
 
  
 
===References===
 
===References===
 
# Brunstein CG, Fuchs EJ, Carter SL, Karanes C, Costa LJ, Wu J, Devine SM, Wingard JR, Aljitawi OS, Cutler CS, Jagasia MH, Ballen KK, Eapen M, O'Donnell PV;Blood and Marrow Transplant Clinical Trials Network. Alternative donor transplantation after reduced intensity conditioning: results of parallel phase 2 trials using partially HLA-mismatched related bone marrow or unrelated double umbilical cord blood grafts. Blood. 2011 Jul 14;118(2):282-8. [http://bloodjournal.hematologylibrary.org/content/118/2/282.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/21527516 PubMed]
 
# Brunstein CG, Fuchs EJ, Carter SL, Karanes C, Costa LJ, Wu J, Devine SM, Wingard JR, Aljitawi OS, Cutler CS, Jagasia MH, Ballen KK, Eapen M, O'Donnell PV;Blood and Marrow Transplant Clinical Trials Network. Alternative donor transplantation after reduced intensity conditioning: results of parallel phase 2 trials using partially HLA-mismatched related bone marrow or unrelated double umbilical cord blood grafts. Blood. 2011 Jul 14;118(2):282-8. [http://bloodjournal.hematologylibrary.org/content/118/2/282.long link to original article] '''contains verified protocol''' [http://www.ncbi.nlm.nih.gov/pubmed/21527516 PubMed]

Revision as of 05:07, 19 November 2013

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Autologous (auto) stem cell transplant

BEAC

BEAC: BiCNU, Etoposide, Ara-C, Cyclophosphamide

Regimen

Phase III

Autologous blood stem cells are infused on day 0.

Supportive medications:

  • Filgrastim (Neupogen) 5 mcg/kg SC once per day starting on day +1, continued until there are 3 consecutive days with ANC ≥1000
  • Prophylaxis against opportunistic infections and management of febrile neutropenia per "active protocols"

References

  1. Jo JC, Kang BW, Jang G, Sym SJ, Lee SS, Koo JE, Kim JW, Kim S, Huh J, Suh C. BEAC or BEAM high-dose chemotherapy followed by autologous stem cell transplantation in non-Hodgkin's lymphoma patients: comparative analysis of efficacy and toxicity. Ann Hematol. 2008 Jan;87(1):43-8. Epub 2007 Aug 21. link to original article contains protocol PubMed

BEAM

BEAM: BiCNU, Etoposide, Ara-C, Melphalan

Regimen #1, Jo et al. 2008

Phase III

Autologous blood stem cells are infused on day 0.

Supportive medications:

  • Filgrastim (Neupogen) 5 mcg/kg SC once per day starting on day +1, continued until there are 3 consecutive days with ANC ≥1000
  • Prophylaxis against opportunistic infections and management of febrile neutropenia per "active protocols"

Regimen #2, Stewart et al. 2006

Phase II

Autologous blood stem cells are infused on day 0.

Supportive medications:

While ANC <500:

Regimen #3, Josting et al. 2005

Phase II

Paper did not specify which day peripheral blood stem cells were administered.

Regimen #4, Gisselbrecht et al. 2010

Autologous blood stem cells are infused on day 0, at least 24 hours after completion of BEAM.

References

  1. Josting A, Sieniawski M, Glossmann JP, Staak O, Nogova L, Peters N, Mapara M, Dörken B, Ko Y, Metzner B, Kisro J, Diehl V, Engert A. High-dose sequential chemotherapy followed by autologous stem cell transplantation in relapsed and refractory aggressive non-Hodgkin's lymphoma: results of a multicenter phase II study. Ann Oncol. 2005 Aug;16(8):1359-65. Epub 2005 Jun 6. link to original article contains protocol PubMed
  2. Stewart DA, Bahlis N, Valentine K, Balogh A, Savoie L, Morris DG, Jones A, Brown C, Russell JA. Upfront double high-dose chemotherapy with DICEP followed by BEAM and autologous stem cell transplantation for poor-prognosis aggressive non-Hodgkin lymphoma. Blood. 2006 Jun 15;107(12):4623-7. Epub 2006 Feb 7. link to original article contains protocol PubMed content property of HemOnc.org
  3. Jo JC, Kang BW, Jang G, Sym SJ, Lee SS, Koo JE, Kim JW, Kim S, Huh J, Suh C. BEAC or BEAM high-dose chemotherapy followed by autologous stem cell transplantation in non-Hodgkin's lymphoma patients: comparative analysis of efficacy and toxicity. Ann Hematol. 2008 Jan;87(1):43-8. Epub 2007 Aug 21. link to original article contains protocol PubMed
  4. Gisselbrecht C, Glass B, Mounier N, Singh Gill D, Linch DC, Trneny M, Bosly A, Ketterer N, Shpilberg O, Hagberg H, Ma D, Brière J, Moskowitz CH, Schmitz N. Salvage regimens with autologous transplantation for relapsed large B-cell lymphoma in the rituximab era. J Clin Oncol. 2010 Sep 20;28(27):4184-90. Epub 2010 Jul 26. Erratum in: J Clin Oncol. 2012 May 20;30(15):1896. link to original article contains verified protocol PubMed
  5. Shimoni A, Avivi I, Rowe JM, Yeshurun M, Levi I, Or R, Patachenko P, Avigdor A, Zwas T, Nagler A. A randomized study comparing yttrium-90 ibritumomab tiuxetan (Zevalin) and high-dose BEAM chemotherapy versus BEAM alone as the conditioning regimen before autologous stem cell transplantation in patients with aggressive lymphoma. Cancer. 2012 Oct 1;118(19):4706-14. Epub 2012 Jan 17. link to original article PubMed

Bor-HDM

Bor-HDM: Bortezomib, High Dose Melphalan

Regimen

Phase II

Autologous hematopoetic stem cell transplant on day 0.

Supportive medications:

  • "All patients received standard supportive care measures"

References

  1. Roussel M, Moreau P, Huynh A, Mary JY, Danho C, Caillot D, Hulin C, Fruchart C, Marit G, Pégourié B, Lenain P, Araujo C, Kolb B, Randriamalala E, Royer B, Stoppa AM, Dib M, Dorvaux V, Garderet L, Mathiot C, Avet-Loiseau H, Harousseau JL, Attal M; Intergroupe Francophone du Myélome (IFM). Bortezomib and high-dose melphalan as conditioning regimen before autologous stem cell transplantation in patients with de novo multiple myeloma: a phase 2 study of the Intergroupe Francophone du Myelome (IFM). Blood. 2010 Jan 7;115(1):32-7. Epub 2009 Nov 2. link to original article contains verified protocol PubMed

Busulfan & Melphalan

Regimen

Phase II

Day 0 is the day of transplantation.

References

  1. Yanada M, Tsuzuki M, Fujita H, Fujimaki K, Fujisawa S, Sunami K, Taniwaki M, Ohwada A, Tsuboi K, Maeda A, Takeshita A, Ohtake S, Miyazaki Y, Atsuta Y, Kobayashi Y, Naoe T, Emi N; Japan Adult Leukemia Study Group. Phase 2 study of arsenic trioxide followed by autologous hematopoietic cell transplantation for relapsed acute promyelocytic leukemia. Blood. 2013 Apr 18;121(16):3095-102. Epub 2013 Feb 14. link to original article Contains verified protocol PubMed

C-VAMP -> high-dose Melphalan (Alkeran)

C-VAMP: Cyclophosphamide, Vincristine, Adriamycin, MethylPrednisolone

Regimen - multiple myeloma high-dose therapy

Phase III

Induction therapy

21-day cycles, given until maximal response was achieved. A minimum of 3 cycles given before stem cell harvest.

Melphalan (Alkeran) & transplant

An alternative to the above melphalan option was:

Interferon alfa maintenance therapy

References

  1. Child JA, Morgan GJ, Davies FE, Owen RG, Bell SE, Hawkins K, Brown J, Drayson MT, Selby PJ; Medical Research Council Adult Leukaemia Working Party. High-dose chemotherapy with hematopoietic stem-cell rescue for multiple myeloma. N Engl J Med. 2003 May 8;348(19):1875-83. link to original article contains verified protocol PubMed

CBV

CBV: Cyclophosphamide, BiCNU, VP-16

Regimen

Phase II

Supportive medications:

References

  1. Stiff PJ, Dahlberg S, Forman SJ, McCall AR, Horning SJ, Nademanee AP, Blume KG, LeBlanc M, Fisher RI. Autologous bone marrow transplantation for patients with relapsed or refractory diffuse aggressive non-Hodgkin's lymphoma: value of augmented preparative regimens--a Southwest Oncology Group trial. J Clin Oncol. 1998 Jan;16(1):48-55. link to original article contains verified protocol PubMed
  2. Damon LE, Johnson JL, Niedzwiecki D, Cheson BD, Hurd DD, Bartlett NL, Lacasce AS, Blum KA, Byrd JC, Kelly M, Stock W, Linker CA, Canellos GP. Immunochemotherapy and autologous stem-cell transplantation for untreated patients with mantle-cell lymphoma: CALGB 59909. J Clin Oncol. 2009 Dec 20;27(36):6101-8. Epub 2009 Nov 16. link to original article contains protocol PubMed

Cyclophosphamide (Cytoxan), Etoposide (Vepesid), TBI

Regimen

Phase II

Autologous hematopoetic stem cell transplant on day 0.

  • Cyclophosphamide (Cytoxan) 100 mg/kg IV over 1 to 2 hours once on day -2
  • Etoposide (Vepesid) 60 mg/kg IV over 4 hours once on day -4
  • Total body irradiation (TBI) with 150 cGy fractions given twice per day (fractions are at least 5 hours apart) x 8 fractions (total dose: 1200 cGy) over 4 days on days -8 to -5, with lung shielding for the final 600 Gy
    • Note: Table 1 of Stiff et al. 1998 lists the dosage of each fraction as being 120 cGy, in contrast to the body text under "treatment regimen" saying each fraction is 150 cGy. It is believed that the 150 cGy dose is correct since 8 fractions of this results in the correct total dose of 1200 cGy.

Supportive medications:

References

  1. Stiff PJ, Dahlberg S, Forman SJ, McCall AR, Horning SJ, Nademanee AP, Blume KG, LeBlanc M, Fisher RI. Autologous bone marrow transplantation for patients with relapsed or refractory diffuse aggressive non-Hodgkin's lymphoma: value of augmented preparative regimens--a Southwest Oncology Group trial. J Clin Oncol. 1998 Jan;16(1):48-55. link to original article contains verified protocol PubMed

High-dose Melphalan (Alkeran)

Regimen - immunoglobulin light-chain (AL) amyloidosis

Phase II

Eligibility criteria: Biopsy-proven amyloid disease and ≥1 major organ involved, evidence of plasma cell dyscrasia, no heart failure or arrhythmia that cannot be medically managed, cardiac ejection fraction ≥40%, no pleural effusions, supine systolic blood pressure ≥90 mmHg, O2 saturation ≥95% on room air, lung diffusing capacity ≥50% predicted, SWOG performance status ≤2 unless due to neuropathy.

  • Patients who fulfilled all of these criteria--≤65 years old, cardiac ejection fraction ≥45%, and ≥2.5 x 106 CD34+ cells/kg collected--received Melphalan (Alkeran) 200 mg/m2 total dose IV divided over two consecutive days
  • Patients with at least one of these criteria-->65 years old, cardiac ejection fraction 40-44%, or with 2.0-2.5 x 106 CD34+ cells/kg collected received Melphalan (Alkeran) 140 mg/m2 total dose IV divided over two consecutive days
  • Autologous stem cell infusion occurs 24 to 72 hours after the last dose of melphalan

References

  1. Skinner M, Sanchorawala V, Seldin DC, Dember LM, Falk RH, Berk JL, Anderson JJ, O'Hara C, Finn KT, Libbey CA, Wiesman J, Quillen K, Swan N, Wright DG. High-dose melphalan and autologous stem-cell transplantation in patients with AL amyloidosis: an 8-year study. Ann Intern Med. 2004 Jan 20;140(2):85-93. link to original article contains verified protocol PubMed

TAM6

Regimen

Phase II

  • Total body irradiation (TBI) with a total dose of 10 Gy over 3 days using twice per day fractions
  • Cytarabine (Cytosar) 1500 mg/m2 IV Q12H x 2 days (total of 4 total doses)
  • Melphalan (Alkeran) 140 mg/m2 IV

Peripheral stem cells are infused on day 0

Supportive medications: "Antimicrobial prophylaxis and use of G-CSF or erythropoietin were permitted according to physician decision."

References

  1. Delarue R, Haioun C, Ribrag V, Brice P, Delmer A, Tilly H, Salles G, Van Hoof A, Casasnovas O, Brousse N, Lefrere F, Hermine O; for the Groupe d'Etude des Lymphomes de l'Adulte (GELA). CHOP and DHAP plus rituximab followed by autologous stem cell transplantation in mantle cell lymphoma: a phase 2 study from the Groupe d'Etude des Lymphomes de l'Adulte. Blood. 2013 Jan 3;121(1):48-53. Epub 2012 Jun 20. link to original article contains verified protocol PubMed

VMCP & BVAP -> high-dose Melphalan (Alkeran)

VMCP: Vincristine, Melphalan, Cyclophosphamide, Prednisone
BVAP: BiCNU, Vincristine, Adriamycin, Prednisone

Regimen - multiple myeloma high-dose therapy

Phase III

VMCP induction therapy

21-day cycles x 2 to 3 cycles, given in an alternating fashion with BVAP

BVAP induction therapy

21-day cycles x 2 to 3 cycles, given in an alternating fashion with VMCP

VMCP and BVAP are given in an alternating fashion x a total of 4 to 6 cycles; patients with a WHO performance status <3, creatinine <1.7 mg/dL (150 μmol/L), and bone marrow (collected after cycle 4) with greater than 200 million nucleated cells/kg would proceed to melphalan, total body irradiation (TBI), and transplant:

Melphalan (Alkeran), TBI, and transplant

  • Melphalan (Alkeran) 140 mg/m2 IV (no other details given about its administration)
  • Total body irradiation (TBI) with a total dose of 8 Gy given over 4 days in 4 fractions, without lung shielding
  • Autologous hematopoietic stem cell transplant after melphalan and TBI
  • Interferon alfa treatment started after transplant when ANC >1500/mm3 and platelets >75,000/mm3

References

  1. Attal M, Harousseau JL, Stoppa AM, Sotto JJ, Fuzibet JG, Rossi JF, Casassus P, Maisonneuve H, Facon T, Ifrah N, Payen C, Bataille R. A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma. Intergroupe Français du Myélome. N Engl J Med. 1996 Jul 11;335(2):91-7. link to original article contains verified protocol PubMed

Z-BEAM

Z-BEAM: Zevalin, BiCNU, Etoposide, Ara-C, Melphalan

Regimen

Phase III

To be completed

References

  1. Shimoni A, Avivi I, Rowe JM, Yeshurun M, Levi I, Or R, Patachenko P, Avigdor A, Zwas T, Nagler A. A randomized study comparing yttrium-90 ibritumomab tiuxetan (Zevalin) and high-dose BEAM chemotherapy versus BEAM alone as the conditioning regimen before autologous stem cell transplantation in patients with aggressive lymphoma. Cancer. 2012 Oct 1;118(19):4706-14. Epub 2012 Jan 17. link to original article PubMed

Allogeneic (allo) stem cell transplant

BEAM

BEAM: BiCNU, Etoposide, Ara-C, Melphalan

Regimen

Phase II

Day 0 is the day of transplantation.

Supportive medications:

References

  1. Przepiorka D, van Besien K, Khouri I, Hagemeister F, Samuels B, Folloder J, Ueno NT, Molldrem J, Mehra R, Körbling M, Giralt S, Gajewski J, Donato M, Cleary K, Claxton D, Braunschweig I, Andersson B, Anderlini P, Champlin R. Carmustine, etoposide, cytarabine and melphalan as a preparative regimen for allogeneic transplantation for high-risk malignant lymphoma. Ann Oncol. 1999 May;10(5):527-32. link to original article contains protocol PubMed

Busulfan & Cyclophosphamide (BuCy)

Regimen

Phase III

Day 0 is the day of transplantation.

Supportive medications:

References

  1. Lee JH, Joo YD, Kim H, Ryoo HM, Kim MK, Lee GW, Lee JH, Lee WS, Park JH, Bae SH, Hyun MS, Kim DY, Kim SD, Min YJ, Lee KH. Randomized trial of myeloablative conditioning regimens: busulfan plus cyclophosphamide versus busulfan plus fludarabine. J Clin Oncol. 2013 Feb 20;31(6):701-9. Epub 2012 Nov 5. link to original article contains verified protocol PubMed

Busulfan & Fludarabine (Flu/Bu; BuFlu)

Regimen #1, Russell et al. 2002 (Flu/Bu)

Phase II

Day 0 is the day of transplantation.

Supportive medications:

Acute GVHD prophylaxis:

Regimen #2, Lee et al. 2013 (BuFlu)

Phase III

Day 0 is the day of transplantation.

Supportive medications:

References

  1. Russell JA, Tran HT, Quinlan D, Chaudhry A, Duggan P, Brown C, Stewart D, Ruether JD, Morris D, Glick S, Gyonyor E, Andersson BS. Once-daily intravenous busulfan given with fludarabine as conditioning for allogeneic stem cell transplantation: study of pharmacokinetics and early clinical outcomes. Biol Blood Marrow Transplant. 2002;8(9):468-76. link to original article contains verified protocol PubMed
  2. Lee JH, Joo YD, Kim H, Ryoo HM, Kim MK, Lee GW, Lee JH, Lee WS, Park JH, Bae SH, Hyun MS, Kim DY, Kim SD, Min YJ, Lee KH. Randomized trial of myeloablative conditioning regimens: busulfan plus cyclophosphamide versus busulfan plus fludarabine. J Clin Oncol. 2013 Feb 20;31(6):701-9. Epub 2012 Nov 5. link to original article contains verified protocol PubMed

Fludarabine and Low-dose TBI

Regimen

Phase III

Day 0 is the day of transplantation.

  • Fludarabine (Fludara) 30 mg/m2 IV once per day on days -4 to -2
  • Total body irradiation (TBI) 2 Gy at a rate of 0.07-0.20 Gy/min on day 0

Supportive medications for GVHD prophylaxis:

References

  1. Gyurkocza B, Storb R, Storer BE, Chauncey TR, Lange T, Shizuru JA, Langston AA, Pulsipher MA, Bredeson CN, Maziarz RT, Bruno B, Petersen FB, Maris MB, Agura E, Yeager A, Bethge W, Sahebi F, Appelbaum FR, Maloney DG, Sandmaier BM. Nonmyeloablative allogeneic hematopoietic cell transplantation in patients with acute myeloid leukemia. J Clin Oncol. 2010 Jun 10;28(17):2859-67. Epub 2010 May 3. link to original article contains verified protocol PubMed

Fludarabine, Cyclophosphamide, & TBI for dUCB or haploidentical transplant

dUCB: double Umbilical Cord Blood

Regimen #1, Brunstein et al. 2011 - dUCB transplantation

Phase II

Day 0 is the day of transplantation.

Supportive medications:

  • Mesna (Mesnex) (dose/route/schedule not specified) and "vigorous IV hydration for uroprotection."
  • Filgrastim (Neupogen) 5 μg/kg SC once per day, starting on day +1, continued until ANC ≥2000/μL for 3 consecutive days

GVHD Prophylaxis

  • Mycophenolate mofetil (CellCept) 1000 mg (route not specified) Q8H for patients >50 kg, starting on day -3 "and continuing until day +30 or 7 days after engraftment, whichever was later"
    • Patients <50 kg received Mycophenolate mofetil (CellCept) 15 mg/kg (route not specified) Q8H, starting on day -3 "and continuing until day +30 or 7 days after engraftment, whichever was later"
  • Cyclosporine A (Neoral vs. Sandimmune not specified, route not specified) with a goal trough of 200 to 400 ng/mL (starting date not specified) until day +100. Patients without GVHD had their dose tapered by 10% each week starting on day +101, with discontinuation of cyclosporine A around day +180 to +200.
  • Tacrolimus (Prograf) (route not specified) with a goal trough level of 5 to 10 ng/mL could be substituted for cyclosporine.

Regimen #2, Brunstein et al. 2011 - Haploidentical

Phase II

Day 0 is the day of transplantation.

Supportive medications:

  • Mesna (Mesnex) (dose/route/schedule not specified) and "vigorous IV hydration for uroprotection."
  • Filgrastim (Neupogen) 5 μg/kg SC once per day, starting on day +5, continued until ANC ≥1000/μL for 3 consecutive days

GVHD Prophylaxis

  • Cyclophosphamide (Cytoxan) 50 mg/kg IBW IV over 1 to 2 hours once per day on days +3 (60 to 72 hours after marrow infusion) and +4
  • Mycophenolate mofetil (CellCept) 15 mg/kg (maximum daily dose of 3000 mg; route not specified) Q8H, starting on day +5, continued until day +35 or longer at physician discretion if active GVHD was present
  • Tacrolimus (Prograf) (route not specified) with a goal trough level of 5 to 10 ng/mL, starting on day +5, continued until day +180

References

  1. Brunstein CG, Fuchs EJ, Carter SL, Karanes C, Costa LJ, Wu J, Devine SM, Wingard JR, Aljitawi OS, Cutler CS, Jagasia MH, Ballen KK, Eapen M, O'Donnell PV;Blood and Marrow Transplant Clinical Trials Network. Alternative donor transplantation after reduced intensity conditioning: results of parallel phase 2 trials using partially HLA-mismatched related bone marrow or unrelated double umbilical cord blood grafts. Blood. 2011 Jul 14;118(2):282-8. link to original article contains verified protocol PubMed