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慢性粒细胞白血病异基因干细胞移植后复发患者对伊马替尼的反应。

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

作者信息

Olavarria E, Ottmann O G, Deininger M, Clark R E, Bandini G, Byrne J, Lipton J, Vitek A, Michallet M, Siegert W, Ullmann A, Wassmann B, Niederwieser D, Fischer T

机构信息

Hammersmith Hospital, London, UK.

出版信息

Leukemia. 2003 Sep;17(9):1707-12. doi: 10.1038/sj.leu.2403068.

Abstract

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 hemato-logical 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.

摘要

我们研究了128例异基因干细胞移植(SCT)后复发的慢性髓性白血病(CML)患者。接受伊马替尼治疗时,51例患者处于慢性期(CP),31例处于加速期(AP),46例处于急变期(BC)。在51例处于CP期的患者中,14例为细胞遗传学复发,2例为分子学复发。复发与伊马替尼治疗之间的中位间隔时间为5个月(0 - 65个月)。共有50例患者在接受伊马替尼治疗前供体淋巴细胞输注治疗失败。总体血液学缓解率为84%(CP期复发患者为98%)。CP期患者的完全细胞遗传学缓解(CCR)为58%,AP期为48%,BC期患者为22%。25例患者(26%)获得完全分子学缓解,其中21例处于CP期或AP期。中位随访9个月,CP期、AP期和BC期患者的估计2年生存率分别为100%、86%和12%。在79例可评估患者中,45例(57%)在接受伊马替尼治疗后实现了完全供体嵌合,11例(14%)实现了混合嵌合。我们得出结论,伊马替尼对异基因SCT后复发的CML具有显著活性。CP期患者可获得持久的细胞遗传学和分子学缓解。

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