成人急性淋巴细胞白血病的预后,单中心经验

IF 0.1 Q4 HEMATOLOGY Iraqi Journal of Hematology Pub Date : 2022-07-01 DOI:10.4103/ijh.ijh_41_22
H. Khudhur, Kawa M. Hasan, R. Polus, Ahmed K. Yassin, N. Mohammad, S. Najmaldeen
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引用次数: 0

摘要

背景:成人急性淋巴细胞白血病(ALL)在最佳情况下预后惨淡,5年总生存率(OS)未达到40%。目的:本研究的目的是评估伊拉克埃尔比勒成人ALL的预后,并观察预测他们更好生存的因素。患者和方法:我们分析了71例成人ALL患者的资料,年龄14-81岁(平均年龄:28.6岁)。诊断基于外周血膜、骨髓检查和流式细胞术。结果:中位OS为21个月,中位无复发生存期(RFS)为13个月。3年OS和3年RFS分别为49.3%和40.8%,5年OS和5年RFS分别为37.5%和32.5%。结论:预测生存率提高的因素包括在研究中;诊断年龄,首次诱导时的缓解效果,风险评估和同种异体干细胞移植的最佳反应。
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Outcome of adult acute lymphoblastic leukemia, a single-center experience
BACKGROUND: Adult acute lymphoblastic leukemia (ALL) has a dismal outcome within the optimal situations as the 5-year overall survival (OS) is not reaching 40%. OBJECTIVE: The objective of this study was to evaluate the outcome of adult ALL in Erbil, Iraq, and to see the factors predicting better survival among them. PATIENTS AND METHODS: We analyzed data from 71 adult ALL patients aged 14–81 years (mean age: 28.6 years). Diagnosis is based on the peripheral blood film, bone marrow examination, and flow cytometry. RESULTS: The median OS was 21 months and the median relapse-free survival (RFS) was 13 months. The 3-year OS and the 3-year RFS were 49.3% and 40.8%, respectively, while the 5-year OS and the 5-year RFS were 37.5% and 32.5%, respectively. CONCLUSION: Factors predicting better survival included in the study; age at diagnosis, remission achievement at first induction, risk assessment, and allogeneic stem cell transplantation optimal response.
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