Response to imatinib in patients who relapse after allogeneic stem cell transplantation for chronic myeloid leukemia

被引:83
作者
Olavarria, E
Ottmann, OG
Deininger, M
Clark, RE
Bandini, G
Byrne, J
Lipton, J
Vitek, A
Michallet, M
Siegert, W
Ullmann, A
Wassmann, B
Niederwieser, D
Fischer, T
机构
[1] Hammersmith Hosp, Dept Haematol, Catherine Lewis Ctr, ICSM, London W12 0NN, England
[2] Univ Frankfurt, D-6000 Frankfurt, Germany
[3] OHSU, Portland, OR USA
[4] Royal Liverpool Univ Hosp, Liverpool, Merseyside, England
[5] Hosp San Orsola, Bologna, Italy
[6] City Hosp Nottingham, Nottingham, England
[7] Princess Margaret Hosp, Toronto, ON M4X 1K9, Canada
[8] Inst Hematol & Blood Transfus, CR-12820 Prague, Czech Republic
[9] Hop Edouard Herriot, Lyon, France
[10] Free Univ Berlin, Klinikum Rudolf Virchow, D-1000 Berlin, Germany
[11] Univ Mainz, D-6500 Mainz, Germany
[12] Univ Leipzig, Leipzig, Germany
关键词
imatinib; stem cell transplantation; CML; relapse;
D O I
10.1038/sj.leu.2403068
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We studied 128 patients with chronic myeloid leukemia (CML) relapsing after allogeneic stem cell transplantation (SCT). Disease at the time of treatment with Imatinib was in chronic phase (CP) in 51 patients, accelerated phase (AP) in 31 and blastic crisis (BC) in 46. Of the 51 patients in CP, 14 were in cytogenetic and two in molecular relapses. The median interval between relapse and Imatinib therapy was 5 months (0-65). A total of 50 patients had failed treatment with donor lymphocyte infusions prior to Imatinib. The overall hematological response rate was 84% (98% for patients relapsing in CP). The complete cytogenetic response (CCR) was 58% for patients in CP, 48% for AP and 22% for patients in BC. Complete molecular responses were obtained in 25 patients (26%), of whom 21 were in CP or AP. With a median follow-up of 9 months, the estimated 2-year survival for CP, AP and BC patients was 100, 86 and 12%, respectively. Out of 79 evaluable patients, 45 (57%) achieved full donor and 11 (14%) mixed chimerism after Imatinib. We conclude that Imatinib has significant activity against CML in relapse after allogeneic SCT. Durable cytogenetic and molecular remissions are obtainable in patients in CP.
引用
收藏
页码:1707 / 1712
页数:6
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