首页> 外文期刊>Journal of Clinical Oncology >Allogeneic bone marrow transplantation for therapy-related myelodysplastic syndrome and acute myeloid leukemia: a long-term study of 70 patients-report of the French society of bone marrow transplantation.
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Allogeneic bone marrow transplantation for therapy-related myelodysplastic syndrome and acute myeloid leukemia: a long-term study of 70 patients-report of the French society of bone marrow transplantation.

机译:同种异体骨髓移植治疗与治疗相关的骨髓增生异常综合症和急性髓性白血病:一项对70名患者的长期研究-法国骨髓移植学会的报告。

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摘要

PURPOSE: To identify predictive factors of survival, relapse, and transplantation-related mortality (TRM) among patients with therapy-related myelodysplastic syndrome (t-MDS) or acute leukemia (t-AML) who underwent allogeneic bone marrow transplantation (BMT). PATIENTS AND METHODS: From 1980 to 1998, 70 patients underwent allogeneic BMT for t-MDS (n = 31) or t-AML (n = 39) after prior cytotoxic exposure. Thirty-three patients had received induction-type chemotherapy before BMT. At the time of transplantation, there were 24 patients in complete remission (CR) and 46 with active disease. RESULTS: With a median follow-up of 7.9 years (range, 1.1 to 18.8 years) after BMT, 16 patients are alive, whereas 19 died of relapse, 34 of TRM, and one of relapse of the primary disease. The estimated 2-year overall survival, event-free survival, relapse, and TRM rates were 30% (95% confidence interval [CI], 19% to 40%), 28% (95% CI, 18% to 39%), 42% (95% CI, 26% to 57%), and 49% (95% CI, 36% to 62%), respectively. In multivariable analysis, age greater than 37 years, male sex, positive recipient cytomegalovirus (CMV) serology, absence of CR at BMT, and intensive schedules used for conditioning were associated with poor outcome. CONCLUSION: BMT is an effective treatment for patients with t-MDS or t-AML who have responsive disease and, in particular, who have no poor-risk cytogenetic features. The poor results of the other patients, especially those with active disease at BMT, emphasize the need to delineate indications and perform prospective protocols.
机译:目的:确定接受同种异体骨髓移植(BMT)的治疗相关性骨髓增生异常综合征(t-MDS)或急性白血病(t-AML)患者的生存,复发和移植相关死亡率(TRM)的预测因素。患者与方法:从1980年至1998年,有70例患者在接受过先前的细胞毒性暴露后接受了异基因BMT的t-MDS(n = 31)或t-AML(n = 39)治疗。 33例患者在BMT之前接受了诱导型化疗。移植时,有24例完全缓解(CR),有46例患有活动性疾病。结果:BMT后中位随访7.9年(范围1.1到18.8年),有16例患者活着,而19例死于复发,34例TRM死亡和1例原发性疾病复发。估计的2年总生存率,无事件生存率,复发率和TRM率分别为30%(95%置信区间[CI],19%至40%),28%(95%CI,18%至39%) ,42%(95%CI,26%至57%)和49%(95%CI,36%至62%)。在多变量分析中,年龄大于37岁,男性,阳性接受者巨细胞病毒(CMV)血清学,BMT缺乏CR以及进行强化调理的时间表与不良预后相关。结论:BMT是对t-MDS或t-AML患者有反应性疾病,特别是没有低细胞遗传学特征的患者的有效治疗。其他患者的不良结果,特别是那些在BMT患有活动性疾病的患者,则表现出需要划定适应症并执行前瞻性治疗方案。

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