In adults with standard-risk acute lymphoblastic leukemia, the greatest benefit is achieved from a matched sibling allogeneic transplantation in first.

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Presentation transcript:

In adults with standard-risk acute lymphoblastic leukemia, the greatest benefit is achieved from a matched sibling allogeneic transplantation in first complete remission, and an autologous transplantation is less effective than conventional consolidation/maintenance chemotherapy in all patients: final results of the International ALL Trial (MRC UKALL XII/ECOG E2993)‏ by Anthony H. Goldstone, Susan M. Richards, Hillard M. Lazarus, Martin S. Tallman, Georgina Buck, Adele K. Fielding, Alan K. Burnett, Raj Chopra, Peter H. Wiernik, Letizia Foroni, Elisabeth Paietta, Mark R. Litzow, David I. Marks, Jill Durrant, Andrew McMillan, Ian M. Franklin, Selina Luger, Niculae Ciobanu, and Jacob M. Rowe Blood Volume 111(4):1827-1833 February 15, 2008 ©2008 by American Society of Hematology

Outline of study and treatment demographics. Outline of study and treatment demographics. (A) Simplified overall schema of the study. MUD indicates matched unrelated donor transplantation; HD MTX, high-dose methotrexate. (B) Patient flow diagram. All randomized patients with the exception of 2 misdiagnoses were included in the comparison of autologous transplantation and chemotherapy. A large number of patients were lost, as in all transplantation studies, in the period from initial accrual to randomization. Only Ph-negative patients were eligible for the intent-to-treat donor versus no-donor analysis as Ph-positive patients without a donor were to have unrelated donor transplantation if possible. Anthony H. Goldstone et al. Blood 2008;111:1827-1833 ©2008 by American Society of Hematology

Survival of patients and donor versus no-donor analysis. Survival of patients and donor versus no-donor analysis. Overall survival from diagnosis for (A) all patients entered on the study, including Ph-positive; (B) Ph-negative and Ph-positive patients; (C) patients entered via MRC or ECOG; (D) donor versus no-donor for all Ph-negative patients; (E) donor versus no-donor for Ph-negative patients with high risk; and (F) donor versus no-donor for Ph-negative patients with standard risk. Anthony H. Goldstone et al. Blood 2008;111:1827-1833 ©2008 by American Society of Hematology

Relapse on study and mortality not associated with relapse. Relapse on study and mortality not associated with relapse. Relapse rate for (A) Ph-negative patients at standard risk; (B) Ph-negative patients at high risk; and (C) nonrelapse mortality for high-risk and standard-risk patients. Note the underlying mortality at 1 and 2 years among the no-donor group. Anthony H. Goldstone et al. Blood 2008;111:1827-1833 ©2008 by American Society of Hematology

Randomized chemotherapy versus autologous transplantation, measured from time of randomization. Randomized chemotherapy versus autologous transplantation, measured from time of randomization. (A) Event-free survival for all patients. (B) Overall survival for all (C) high-risk patients and (D) standard-risk patients. (E) Nonrelapse mortality for all patients undergoing chemotherapy or autologous transplantation. Anthony H. Goldstone et al. Blood 2008;111:1827-1833 ©2008 by American Society of Hematology

Overall survival from diagnosis for donor versus no-donor for Ph-negative patients censoring at first remission autologous transplantation. Overall survival from diagnosis for donor versus no-donor for Ph-negative patients censoring at first remission autologous transplantation. Estimation of the effect of sibling donor transplant versus chemotherapy in (A) all patients; (B) high-risk patients; and (C) standard-risk patients. Anthony H. Goldstone et al. Blood 2008;111:1827-1833 ©2008 by American Society of Hematology