TY - JOUR
T1 - Individual patient data meta-analysis of allogeneic peripheral blood stem cell transplant vs bone marrow transplant in the management of hematological malignancies
T2 - Indirect assessment of the effect of day 11 methotrexate administration
AU - Bensinger, William I.
AU - Al-Jurf, Mahmoud
AU - Annasetti, Claudio
AU - Apperley, Jane F.
AU - Baynes, Roy
AU - Blaise, Didier
AU - Clarke, Mike
AU - Colcol, Ed
AU - Cornelissen, Jan J.
AU - Couban, Stephen
AU - Cutler, Corey
AU - Djulbegovic, Benjamin
AU - Gratwohl, Alois
AU - Heldal, Dag
AU - Hills, Robert K.
AU - Hozo, Iztok
AU - Kuentz, Mathieu
AU - Kumar, Ambuj
AU - Lipton, Jeffrey H.
AU - Miranda, Eliana C.M.
AU - Mohty, Mohamad
AU - Matcham, James
AU - Morton, James
AU - Panzarella, Tony
AU - Powles, Ray
AU - Richards, Sue
AU - Sahovic, Entezam
AU - Schmitz, Norbert
AU - Simpson, David R.
AU - Sirohi, Bhawna
AU - Soares, Heloisa P.
AU - de Souza, Carmino A.
AU - Van der Holt, B.
AU - Vigorito, Afonso C.
AU - Wheatley, Keith
N1 - Funding Information:
Funding source: Main funding for this project was provided by the NHI/NHLBI Grant # 1R01HL71650–01 (Drs Djulbegovic and Bensinger) and in part by The Jose Carreras Foundation Against Leukemia, NCI CA18029, CA18221 (Dr Bensinger), the Swiss National Research Foundation, and the French Ministry of Health (Programme Hospitalier de Recherche Clinique 1996) (Dr Gratwohl) and a grant from the Ligue Nationale de Lutte Contre le Cancer (Dr Blaise).
PY - 2006/10
Y1 - 2006/10
N2 - The effects of immunosuppressive regimens on the outcomes of patients with hematological malignancies undergoing allogeneic stem cell transplantation remain uncertain. We conducted an individual patient data meta-analysis using data from nine randomized trials comparing allogeneic peripheral blood stem cell (PBSCT) transplants to bone marrow (BMT) transplants, focusing on the administration of three vs four doses of methotrexate (MTX) as part of a regimen for graft-versus-host-disease (GVHD) prophylaxis which included cyclosporine. Six trials containing 573 patients prescribed four doses of MTX while three trials containing 534 patients prescribed three doses of MTX. Four doses of MTX conferred a statistically significant survival advantage, resulting in death odds ratio (OR) 0.67 (CI 0.52-0.88) (P=0.0036) for recipients of PBSC compared to BM; with three doses, there was no statistically significant difference. In the four-dose studies relapse rates were 36.6% among recipients of BM compared to 19.2% among recipients of PBSC (P=0.0015). The rates of relapse in the three dose studies were 26% for both PBSC and BM. We hypothesize that the fourth dose of MTX provides extra immunosuppression among BM recipients resulting in a reduced anti-leukemic effect. This hypothesis can only be proved or disproved by a prospective, randomized trial.
AB - The effects of immunosuppressive regimens on the outcomes of patients with hematological malignancies undergoing allogeneic stem cell transplantation remain uncertain. We conducted an individual patient data meta-analysis using data from nine randomized trials comparing allogeneic peripheral blood stem cell (PBSCT) transplants to bone marrow (BMT) transplants, focusing on the administration of three vs four doses of methotrexate (MTX) as part of a regimen for graft-versus-host-disease (GVHD) prophylaxis which included cyclosporine. Six trials containing 573 patients prescribed four doses of MTX while three trials containing 534 patients prescribed three doses of MTX. Four doses of MTX conferred a statistically significant survival advantage, resulting in death odds ratio (OR) 0.67 (CI 0.52-0.88) (P=0.0036) for recipients of PBSC compared to BM; with three doses, there was no statistically significant difference. In the four-dose studies relapse rates were 36.6% among recipients of BM compared to 19.2% among recipients of PBSC (P=0.0015). The rates of relapse in the three dose studies were 26% for both PBSC and BM. We hypothesize that the fourth dose of MTX provides extra immunosuppression among BM recipients resulting in a reduced anti-leukemic effect. This hypothesis can only be proved or disproved by a prospective, randomized trial.
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U2 - 10.1038/sj.bmt.1705488
DO - 10.1038/sj.bmt.1705488
M3 - Article
C2 - 16953207
AN - SCOPUS:33749434836
SN - 0268-3369
VL - 38
SP - 539
EP - 546
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 8
ER -