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首页> 外文期刊>Bone marrow transplantation >Management of chronic myeloid leukaemia in relapse following donor lymphocyte infusion induced remission: a retrospective study of the Clinical Trials Committee of the British Society of Blood & Marrow Transplantation (BSBMT).
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Management of chronic myeloid leukaemia in relapse following donor lymphocyte infusion induced remission: a retrospective study of the Clinical Trials Committee of the British Society of Blood & Marrow Transplantation (BSBMT).

机译:供体淋巴细胞输注诱导的缓解后复发性慢性粒细胞白血病的处理:英国血液和骨髓移植临床试验委员会(BSBMT)的回顾性研究。

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摘要

Donor lymphocyte infusion (DLI) can restore remission in a high percentage of patients with chronic myeloid leukaemia (CML) who relapse after allogeneic stem cell transplant (SCT). Subsequent relapses after a DLI-induced remission do occur and the optimal management of these patients is not defined. A retrospective study of the practice of UK transplant centres was conducted. In all, 13 patients from seven centres were identified: all were treated for relapse post allogeneic SCT with DLI and achieved either a complete cytogenetic (n=5) or molecular (n=8) remission. All patients subsequently had a second relapse, at molecular (n=7), cytogenetic (n=4) and haematological (n=2) levels. Further DLI was used in the treatment of 11 patients, imatinib mesylate in three and chemotherapy in two. The two patients with haematological relapse died of blastic disease. The remaining 11 patients achieved either a complete cytogenetic (n=2) or molecular (n=9) remission. Nine patients remain in molecular remission at a median follow-up of 29 months, seven of whom had received DLI alone as treatment for second relapse, one DLI plus imatinib and one imatinib alone. Toxicity following DLI for second relapse was low. Longer follow-up will be required to see if these second DLI-induced remissions will be durable.
机译:异体干细胞移植(SCT)后复发的慢性髓细胞性白血病(CML)患者中,高比例的供体淋巴细胞输注(DLI)可恢复缓解。确实发生了DLI诱导的缓解后的随后复发,并且尚未定义这些患者的最佳治疗方法。对英国移植中心的做法进行了回顾性研究。总共确定了来自七个中心的13位患者:所有患者均接受了DLI治疗异基因SCT后复发,并获得了完全的细胞遗传学(n = 5)或分子(n = 8)缓解。随后所有患者均在分子水平(n = 7),细胞遗传学(n = 4)和血液学(n = 2)水平上再次复发。进一步的DLI用于治疗11例患者,甲磺酸伊马替尼3例,化疗2例。两名血液学复发的患者死于母细胞性疾病。其余11例患者达到了完全的细胞遗传学缓解(n = 2)或分子缓解(n = 9)。 9名患者在中位随访29个月后仍处于分子缓解状态,其中7例仅接受DLI作为第二次复发的治疗,1例DLI加伊马替尼和1例伊马替尼。 DLI第二次复发后的毒性较低。将需要更长的随访时间,以查看第二次DLI诱导的缓解是否持久。

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