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异基因造血细胞移植后复发或进展的淋巴瘤患者的生存情况。

Survival of Lymphoma Patients Experiencing Relapse or Progression after an Allogeneic Hematopoietic Cell Transplantation.

机构信息

Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin; Division of Hematology, The Ohio State University, Columbus, Ohio.

Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin; Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.

出版信息

Biol Blood Marrow Transplant. 2018 May;24(5):983-988. doi: 10.1016/j.bbmt.2018.01.015. Epub 2018 Feb 2.

Abstract

Outcome and management of patients who relapse after allogeneic hematopoietic cell transplantation (allo-HCT) has evolved in the recent decade. Using a multi-institutional retrospective database we report the predictive factors and survival of lymphoma patients who relapse after allo-HCT. We evaluated 495 allo-HCT recipients transplanted between 2000 and 2015 at 3 academic US medical centers. Landmark analysis evaluating predictive factors was performed at 1 month after allo-HCT relapse with a primary endpoint of postrelapse overall survival (PR-OS). A total of 175 lymphoma patients (35%) experienced relapse after allo-HCT. Of these, 126 patients, median age 46 years (range, 19 to 71), were assessable. Most patients (86%) received subsequent therapy; 80 patients received targeted agents and 19 donor lymphocyte infusion. On univariate analysis median PR-OS for patients with Hodgkin lymphoma was 47.9 months compared with 11.3 months in patients with indolent and 10.1 months in aggressive non-Hodgkin lymphoma (P = .04). On multivariate analysis postrelapse therapy administration (no therapy versus targeted therapy: hazard ratio, .21 [95% confidence interval, .10 to .45]; no therapy versus nontargeted therapy: hazard ratio, .26 [95% confidence interval, .11 to .57]), late relapse 130 days after allo-HCT (relative to early relapse: hazard ratio, .25; P < .001), and Eastern Cooperative Oncology Group performance status of 0 to 1 (versus Eastern Cooperative Oncology Group performance status ≥ 2: hazard ratio, .49; P = .003) were associated with a significantly reduced risk of mortality. Patients relapsing ≥ 130 days from the time of allo-HCT yielded PR-OS of 48.8 months compared with 6.5 months in patients with early relapse (P < .001). Our data suggest that in the modern era, therapies used for patients experiencing lymphoma relapse after allo-HCT can extend survival.

摘要

在最近十年中,异基因造血细胞移植(allo-HCT)后复发患者的治疗结果和管理方法已经发生了变化。本研究使用多机构回顾性数据库,报告了 allo-HCT 后复发的淋巴瘤患者的预测因素和生存情况。我们评估了 3 家美国学术医疗中心在 2000 年至 2015 年间接受 allo-HCT 的 495 名患者。在 allo-HCT 复发后 1 个月进行了评估预测因素的里程碑分析,主要终点是复发后总生存期(PR-OS)。共有 175 例(35%)淋巴瘤患者在 allo-HCT 后复发。其中,126 例患者可评估,中位年龄为 46 岁(范围 19 岁至 71 岁)。大多数患者(86%)接受了后续治疗;80 例患者接受了靶向治疗,19 例患者接受了供者淋巴细胞输注。单因素分析显示,霍奇金淋巴瘤患者的中位 PR-OS 为 47.9 个月,而惰性和侵袭性非霍奇金淋巴瘤患者的中位 PR-OS 分别为 11.3 个月和 10.1 个月(P=0.04)。多因素分析显示,复发后接受治疗(无治疗与靶向治疗:风险比,0.21[95%置信区间,0.10 至 0.45];无治疗与非靶向治疗:风险比,0.26[95%置信区间,0.11 至 0.57])、allo-HCT 后 130 天以后复发(与早期复发相比:风险比,0.25;P<0.001)和东部肿瘤协作组体力状态 0 至 1(与东部肿瘤协作组体力状态≥2 相比:风险比,0.49;P=0.003)与死亡率降低显著相关。allo-HCT 后 130 天以后复发的患者的 PR-OS 为 48.8 个月,而早期复发的患者的 PR-OS 为 6.5 个月(P<0.001)。本研究数据表明,在现代,用于 allo-HCT 后淋巴瘤复发患者的治疗方法可以延长生存时间。

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