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接受苯达莫司汀治疗的淋巴瘤患者的巨细胞病毒感染的风险和影响。

Risk and impact of cytomegalovirus infection in lymphoma patients treated with bendamustine.

机构信息

Department of Medicine, Taipei Veterans General Hospital, No. 201, Sec. 2, Shipai Rd., Beitou Dist, Taipei, 112201, Taiwan.

Division of Transfusion Medicine, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.

出版信息

Ann Hematol. 2024 Oct;103(10):4099-4109. doi: 10.1007/s00277-024-05839-0. Epub 2024 Aug 19.

Abstract

Bendamustine is used to treat lymphoma with excellent efficacy but is known for its immunosuppressive effect. Cytomegalovirus (CMV) reactivation after bendamustine use has been reported. We aim to address the impact of CMV infection in lymphoma patients treated with bendamustine-containing regimens. We retrospectively analyzed lymphoma patients at Taipei Veterans General Hospital in Taiwan between September 1, 2010, and April 30, 2022. Clinically significant CMV infection (CS-CMVi) was defined as the first CMV reactivation after bendamustine use necessitating CMV therapy. Patients' baseline characteristics and laboratory data were recorded. The primary endpoint of the study was CS-CMVi. A time-dependent covariate Cox regression model was used to estimate the risk factors of CS-CMVi and mortality. A total of 211 lymphoma patients treated with bendamustine were enrolled. Twenty-seven (12.8%) had CS-CMVi. The cumulative incidence was 10.1 per 100 person-years during the three-year follow-up period. In the multivariate analysis, lines of therapy before bendamustine ≥ 1 (95% CI 1.10-24.76), serum albumin < 3.5 g/dL (95% CI 2.63-52.93), and liver disease (95% CI 1.51-28.61) were risk factors for CS-CMVi. In conclusion, CS-CMVi (95% confidence interval [CI] 1.23-10.73) was one of the major independent risk factors of mortality. Lines of therapy before bendamustine ≥ 1, hypoalbuminemia, and liver disease were risk factors for CS-CMVi in lymphoma patients treated with bendamustine.

摘要

苯达莫司汀用于治疗淋巴瘤疗效极佳,但已知其具有免疫抑制作用。有报道称,苯达莫司汀使用后会导致巨细胞病毒(CMV)再激活。我们旨在探讨含苯达莫司汀方案治疗的淋巴瘤患者中 CMV 感染的影响。我们回顾性分析了台湾台北荣民总医院 2010 年 9 月 1 日至 2022 年 4 月 30 日期间的淋巴瘤患者。临床显著的 CMV 感染(CS-CMVi)定义为苯达莫司汀使用后首次 CMV 再激活,需要 CMV 治疗。记录患者的基线特征和实验室数据。本研究的主要终点是 CS-CMVi。采用时依协变量 Cox 回归模型估计 CS-CMVi 和死亡率的危险因素。共纳入 211 例接受苯达莫司汀治疗的淋巴瘤患者。27 例(12.8%)发生 CS-CMVi。在 3 年的随访期间,CS-CMVi 的累积发生率为 10.1/100 人年。多变量分析显示,苯达莫司汀治疗前的治疗线数≥1(95%CI 1.10-24.76)、血清白蛋白<3.5 g/dL(95%CI 2.63-52.93)和肝病(95%CI 1.51-28.61)是 CS-CMVi 的危险因素。总之,CS-CMVi(95%置信区间 [CI] 1.23-10.73)是死亡的主要独立危险因素之一。苯达莫司汀治疗前的治疗线数≥1、低白蛋白血症和肝病是淋巴瘤患者发生 CS-CMVi 的危险因素。

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