[含苯达莫司汀方案治疗滤泡性淋巴瘤后 CD4+ T 淋巴细胞的减少可预测感染的发生和疗效】。]

Jin-Lian Li, Wan-Chuan Zhuang, Xing-Xing Chai
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引用次数: 0

摘要

目的研究含苯达莫司汀方案治疗滤泡性淋巴瘤(FL)的有效性、安全性及相关预后因素:收集2020年1月1日至2022年10月30日在连云港市第二人民医院和江苏省人民医院血液科接受含苯达莫司汀方案治疗的129例滤泡性淋巴瘤患者的临床资料。患者被分为三组:苄达莫司汀+利妥昔单抗组(BR)、苄达莫司汀+奥比妥珠单抗组(GB)、利妥昔单抗+环磷酰胺+表柔比星/多柔比星+文迪新+泼尼松组(R-CHOP)。回顾性分析了以本达莫司汀为基础的方案治疗FL的疗效、安全性和相关预后因素:结果:BR组的ORR为98%,GB组为94%,R-CHOP组为72.3%,CR率分别为61.2%、70%和40.4%。R-CHOP组的ORR和CR率与BR组和GB组相比有统计学差异(P<0.05)。BR组、GB组和R-CHOP组的3年PFS率分别为89.6%、90.9%和48.9%。R-CHOP组、BR组和GB组的3年PFS差异有统计学意义(P<0.05),而3年OS差异无统计学意义(P>0.05)。血液学不良反应主要是骨髓抑制。淋巴细胞和CD4+T淋巴细胞在治疗后6个月左右降至最低水平,BR组和GB组淋巴细胞减少发生率高于R-CHOP组,差异有统计学意义(P<0.05)。非血液学不良反应中发生率较高的是肺部感染、EB病毒感染、乙肝病毒再激活和胃肠道反应,3组间无统计学差异(P>0.05),且均可控制。CD4+T淋巴细胞计数的Receiver操作特征显示,BR组的AUC为0.802,临界值为258/uL;GB组的AUC为0.754,临界值为322/uL:结论:含苯达莫司汀方案治疗FL疗效较好,不良反应可控,但治疗后淋巴细胞明显减少,与各种CD20单克隆抗体联合治疗疗效不同。最低 CD4+T 淋巴细胞计数可作为 FL 感染发生和含本达莫司汀方案疗效的预测因素。
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[The Reduction of CD4+ T Lymphocytes after the Treatment of Follicular Lymphoma with the Bendamustine Containing Regimen May Predict the Occurrence of Infection and Efficacy].

Objective: To investigate the effectiveness, safety, and related prognostic factors of the treatment of follicular lymphoma (FL) with a regimen containing Bendamustine.

Methods: The clinical data of 129 FL patients who were treated with Bendamustine containing regimen were collected from January 1,2020 to October 30,2022 in the Hematology Department of Lianyungang Second People's Hospital and Jiangsu Provincial People's Hospital. The patients were divided into three groups: Bendamustine plus Rituximab (BR), Bendamustine plus Obinutuzumab (GB), Rituximab + Cyclophosphamide + Epirubicin / Doxorubicin + Vindesine + Prednisone (R-CHOP). The efficacy, safety and related prognostic factors of the treatment of FL with a regimen based on Bendamustine were retrospectively analyzed.

Results: The ORR was 98% for the BR group, 94% for the GB group, and 72.3% for the R-CHOP group, while the CR rate was 61.2%,70% and 40.4%, respectively. The ORR and CR rates of the R-CHOP group were statistically different from those of the BR group and GB group (P < 0.05). The 3-year PFS rate of the BR group, GB group, and R-CHOP group was 89.6%, 90.9%, 48.9%, respectively. There was a statistically significant difference in 3-year PFS between the R-CHOP group, BR group, and GB group (P < 0.05), while there was no statistically significant difference in 3-year OS(P >0.05). Hematological adverse reactions were mainly bone marrow suppression. Lymphocytes and CD4+T lymphocytes decreased to the lowest level about 6 months after treatment, and the incidence of lymphopenia in BR group and GB group was higher than that in R-CHOP group, with a statistical difference (P < 0.05). The higher incidence of non-Hematological adverse reactions were pulmonary infection, EB virus infection, hepatitis B virus reactivation, and gastrointestinal reactions without statistical difference in 3 groups (P >0.05), and were all controllable. The Receiver operating characteristic of CD4+T lymphocyte count showed that AUC of BR group was 0.802, and the critical value was 258/uL; AUC of GB group was 0.754 with a critical value of 322/uL.

Conclusion: The treatment of FL with the Bendamustine containing regimen has good efficacy and controllable adverse reactions, but lymphocytopenia was significant after treatment, and the curative efficacy in combination with various CD20 monoclonal antibodies was different. The lowest CD4+T lymphocyte count can be used as a predictive factor for the occurrence of infection and efficacy of the Bendamustine containing regimen for FL.

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中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
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