TY - JOUR
T1 - Outcome of older patients with acute myeloid leukemia in first relapse
AU - Sarkozy, Clémentine
AU - Gardin, Claude
AU - Gachard, Nathalie
AU - Merabet, Fathia
AU - Turlure, Pascal
AU - Malfuson, Jean Valère
AU - Pautas, Cécile
AU - Micol, Jean Baptiste
AU - Thomas, Xavier
AU - Quesnel, Bruno
AU - Celli-Lebras, Karine
AU - Preudhomme, Claude
AU - Terré, Christine
AU - Fenaux, Pierre
AU - Chevret, Sylvie
AU - Castaigne, Sylvie
AU - Dombret, Hervé
PY - 2013/9/1
Y1 - 2013/9/1
N2 - To provide data for future drug evaluation, we analyzed the outcome of 393 patients aged 50 years or older (median, 64 years) with AML in first relapse after treatment in recent ALFA trials. Salvage options were retrospectively classified as follows: best supportive care (BSC), low-dose cytarabine (LDAC), gemtuzumab ozogamicin (GO), intensive chemotherapy (ICT), or ICT combined with GO. Second complete remission (CR2) rate was 31% and median post-relapse survival was 6.8 months (0, 17, 42.5, 53, and 80% and 3.2, 5.6, 8.9, 9, and 19.8 months in BSC, LDAC, GO, ICT, and ICT+GO subsets, respectively). Age, performance status, WBC, CR1 duration, and favorable AML karyotype, but not other cytogenetic or molecular features, influenced post-relapse outcome. Multivariate adjustment and propensity score matching showed that intensive salvage (ICT/ICT+GO/GO versus LDAC/BSC) was associated with longer post-relapse survival, at least in patients with CR1 duration ≥12 months (P=0.001 and 0.0005, respectively). Of interest, GO appeared to be as effective as standard ICT, and ICT+GO combination more effective than standard ICT. In conclusion, older patients with CR1 duration ≥12 months appeared to benefit from intensive salvage and results observed with GO-containing salvage suggest that GO combination studies should be actively pursued in this setting.
AB - To provide data for future drug evaluation, we analyzed the outcome of 393 patients aged 50 years or older (median, 64 years) with AML in first relapse after treatment in recent ALFA trials. Salvage options were retrospectively classified as follows: best supportive care (BSC), low-dose cytarabine (LDAC), gemtuzumab ozogamicin (GO), intensive chemotherapy (ICT), or ICT combined with GO. Second complete remission (CR2) rate was 31% and median post-relapse survival was 6.8 months (0, 17, 42.5, 53, and 80% and 3.2, 5.6, 8.9, 9, and 19.8 months in BSC, LDAC, GO, ICT, and ICT+GO subsets, respectively). Age, performance status, WBC, CR1 duration, and favorable AML karyotype, but not other cytogenetic or molecular features, influenced post-relapse outcome. Multivariate adjustment and propensity score matching showed that intensive salvage (ICT/ICT+GO/GO versus LDAC/BSC) was associated with longer post-relapse survival, at least in patients with CR1 duration ≥12 months (P=0.001 and 0.0005, respectively). Of interest, GO appeared to be as effective as standard ICT, and ICT+GO combination more effective than standard ICT. In conclusion, older patients with CR1 duration ≥12 months appeared to benefit from intensive salvage and results observed with GO-containing salvage suggest that GO combination studies should be actively pursued in this setting.
UR - http://www.scopus.com/inward/record.url?scp=84882601957&partnerID=8YFLogxK
U2 - 10.1002/ajh.23498
DO - 10.1002/ajh.23498
M3 - Article
C2 - 23749683
AN - SCOPUS:84882601957
SN - 0361-8609
VL - 88
SP - 758
EP - 764
JO - American Journal of Hematology
JF - American Journal of Hematology
IS - 9
ER -