Difference between revisions of "Aric's Test Page"

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'''Diseases Studied: [[Acute myeloid leukemia]], [[Myelodysplastic syndrome]], [[Chronic myelogenous leukemia]], [[Chronic lymphocytic leukemia (CLL/SLL)]], [[Non-Hodgkin lymphoma]], [[Hypereosinophilic syndrome]]'''
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'''Graft types studied''': Matched Related / Unrelated Donor Bone Marrow or Mobilized Peripheral Blood Stem Cells
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====Chemotherapy====
 
====Chemotherapy====
 
*[[Fludarabine (Fludara)]] 50 mg/m<sup>2</sup> IV once per day on days -6 to -2
 
*[[Fludarabine (Fludara)]] 50 mg/m<sup>2</sup> IV once per day on days -6 to -2
 
*[[Busulfan (Myleran)]] 3.2 mg/kg (ideal body weight) IV once per day over 3 hours on days -5 to -2
 
*[[Busulfan (Myleran)]] 3.2 mg/kg (ideal body weight) IV once per day over 3 hours on days -5 to -2
  
====Supportive medications====
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====Graft versus Host Disease prophylaxis and key supportive medications:====
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*[[Antithymocyte globulin (ATG)|Antithymocyte globulin (Thymoglobulin, rabbit ATG)]] 0.5 mg/kg IV once on day -2; 2 mg/kg/day IV once per day on days -1 & 0 (total dose of 4.5 mg/kg)
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*[[Cyclosporine modified (Neoral)]] or [[Cyclosporine non-modified (Sandimmune)]] PO/IV BID, with doses adjusted to maintain cyclosporine levels of 150 to 400 umol/L
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*[[Methotrexate (MTX)]] 15 mg/m<sup>2</sup> once on day 1; 10 mg/m<sup>2</sup> once per day on days 3, 6, 11
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**[[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)]]
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*[[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
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*No routine use of growth factors
 
*No routine use of growth factors
 
*CMV negative blood
 
*CMV negative blood
 
====GVHD prophylaxis====
 
*[[Antithymocyte globulin (ATG)|Antithymocyte globulin (Thymoglobulin, rabbit ATG)]] 0.5 mg/kg IV once on day -2; 2 mg/kg/day IV once per day on days -1 & 0 (total dose of 4.5 mg/kg)
 
*[[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/m<sup>2</sup> once on day 1; 10 mg/m<sup>2</sup> once per day on days 3, 6, 11
 
*[[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)]]
 
  
 
===References===
 
===References===

Revision as of 03:23, 6 November 2017

Busulfan & Fludarabine

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BuFlu: Busulfan & Fludarabine Flu/Bu: Fludarabine & Busulfan

Regimen #1

Study Evidence Comparator Efficacy
Rambaldi et al. 2015 Phase III Busulfan & Cyclophosphamide Seems to improve 1 & 2 year NRM, similar OS

Diseases Studied: Acute myeloid leukemia

Graft types studied: Bone Marrow, Mobilized Peripheral Blood Stem Cells

Chemotherapy

Graft Vs. Host Disease prophylaxis and key supportive medications

Regimen #2

Study Evidence Comparator Efficacy
Andersson et al. 2008 Retrospective Busulfan & Cyclophosphamide Suggested improved outcomes, but shorter follow up
Kanakry et al. 2014 Phase II

Diseases Studied: Acute myeloid leukemia, Myelodysplastic syndrome, Acute lymphocytic leukemia

Graft types studied: Matched Related / Unrelated Donor Bone Marrow, Mobilized Peripheral Blood Stem Cells

Chemotherapy

  • Fludarabine (Fludara) 40 mg/m2 IV once per day over one hour on days -6 to -3 followed by
  • Busulfan (Myleran) 130 mg/kg IV once per day over three hours on days -6 to -3 (busulfan dosing targeted for optimal pharmacokinetics but different parameters each institution, please consult the original publication for optimal levels)

Graft versus Host Disease prophylaxis and key supportive medications:

#1 Tacrolimus & methotrexate based (Andersson et al.)

#2 Post-Transplant Cy based (Kanakry et al.)

Regimen #3

Study Evidence Comparator Efficacy
Lee et al. 2013 Phase III Busulfan & Cyclophosphamide Seems to have inferior OS

Diseases Studied: Acute myeloid leukemia, Myelodysplastic syndrome, Acute lymphocytic leukemia, Chronic myelogenous leukemia, Myelofibrosis

Graft types studied: Matched Related / Unrelated Donor Bone Marrow, Mobilized Peripheral Blood Stem Cells

Chemotherapy

Graft versus Host Disease prophylaxis and key supportive medications:

Regimen #4

Study Evidence
Russell et al. 2002 Phase II

Diseases Studied: Acute myeloid leukemia, Myelodysplastic syndrome, Chronic myelogenous leukemia, Chronic lymphocytic leukemia (CLL/SLL), Non-Hodgkin lymphoma, Hypereosinophilic syndrome

Graft types studied: Matched Related / Unrelated Donor Bone Marrow or Mobilized Peripheral Blood Stem Cells

Chemotherapy

Graft versus Host Disease prophylaxis and key 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
  3. Rambaldi A, Grassi A, Masciulli A, Boschini C, Micò MC, Busca A, Bruno B, Cavattoni I, Santarone S, Raimondi R, Montanari M, Milone G, Chiusolo P, Pastore D, Guidi S, Patriarca F, Risitano AM, Saporiti G, Pini M, Terruzzi E, Arcese W, Marotta G, Carella AM, Nagler A, Russo D, Corradini P, Alessandrino EP, Torelli GF, Scimè R, Mordini N, Oldani E, Marfisi RM, Bacigalupo A, Bosi A. Busulfan plus cyclophosphamide versus busulfan plus fludarabine as a preparative regimen for allogeneic haemopoietic stem-cell transplantation in patients with acute myeloid leukaemia: an open-label, multicentre, randomised, phase 3 trial. Lancet Oncol. 2015 Nov;16(15):1525-36. Epub 2015 Sep 28. link to original article PubMed