par Buyse, Marc;Squifflet, Pierre;Michiels, Stefan
;Lucchesi, Kathryn J.;Hellstrand, Kristoffer;Brune, Mats;Castaigne, Sylvie;Rowe, Jacob J.M.
Référence Haematologica, 96, 8, page (1106-1112)
Publication Publié, 2011-08

Référence Haematologica, 96, 8, page (1106-1112)
Publication Publié, 2011-08
Article révisé par les pairs
Résumé : | Background In trials designed to evaluate new therapies for hematologic malignancies, end points such as leukemia-free survival are often used as surrogates for overall survival in acute leukemia. We aimed to assess whether leukemia-free survival is an acceptable statistical surrogate for overall survival when applied to remission maintenance therapy for acute myeloid leukemia. Design and Methods Data were analyzed from a randomized Phase III trial of remission maintenance immunotherapy with histamine dihydrochloride plus low-dose interleukin-2 versus no treatment in adults with acute myeloid leukemia. A two-stage surrogate validation model was applied in which correlations between Kaplan-Meier estimates of leukemia-free survival and overall survival, and between log hazard ratios reflecting treatment effects were analyzed. Country of patient enrollment was the unit of analysis. Results Kaplan-Meier estimates of overall survival at 36, 48, and 60 months and leukemia-free survival at 24 months were reasonably correlated (R 2 ranging from 0.44 to 0.84) both for the overall (n=320) and first complete remission (n=261) populations. The effects of histamine dihydrochloride/ interleukin-2 on log hazard ratios for leukemia-free survival and overall survival were well correlated (R 2=0.88-0.93). Conclusions The significant correlations between overall survival and the surrogate end point (leukemia-free survival) and between the effect of histamine dihydrochloride/interleukin-2 on leukemia-free survival and overall survival satisfy the two-stage surrogate validation model. © 2011 Ferrata Storti Foundation. |