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利妥昔单抗联合化疗治疗儿童成熟B细胞非霍奇金淋巴瘤:一项系统评价和荟萃分析。

Rituximab plus chemotherapy for pediatric mature B-cell non-Hodgkin's lymphoma: a systematic review and meta-analysis.

作者信息

Zhu Xiuli, Diao Yuqiao, Chen Yan

机构信息

Department of Pediatrics, The Fourth Hospital of Hebei Medical University Shijiazhuang 050000, Hebei, China.

出版信息

Am J Transl Res. 2025 Jul 15;17(7):4867-4878. doi: 10.62347/GOXN1938. eCollection 2025.

Abstract

OBJECTIVE

To conduct a systematic review and meta-analysis evaluating the efficacy and safety of rituximab combined with chemotherapy for the treatment of mature B-cell non-Hodgkin's lymphoma (NHL) in children and adolescents.

METHODS

A comprehensive search of PubMed, Embase, the Cochrane Library, and Web of Science was performed to identify relevant studies published up to October 2024. Eligible studies included those involving patients aged 0-15 years diagnosed with mature B-cell NHL. Data were extracted on event-free survival (EFS), overall survival (OS), complete remission rate (CRR), adverse events, immune reconstitution (IgG levels), and recurrence rates. Meta-analyses were conducted using RevMan 5.0.

RESULTS

A total of 11 studies comprising 1,522 participants were included. The addition of rituximab to chemotherapy significantly improved EFS (hazard ratio [HR] = 0.40, 95% confidence interval [CI]: 0.36-0.45, < 0.05) and OS (HR = 0.38, 95% CI: 0.34-0.42, P < 0.05). CRR was also significantly higher in the rituximab group (odds ratio [OR] = 2.72, 95% CI: 1.76-4.21, < 0.05). However, a higher incidence of adverse effects was observed (OR = OR= 1.92, 95% CI: 1.25-2.94, P < 0.05). There were no significant differences in recurrence rate or IgG levels between groups.

CONCLUSION

The addition of rituximab to chemotherapy significantly improved EFS, OS, and CRR in children and adolescents with mature B-cell NHL. Despite an increased risk of toxicity, the survival and remission benefits support the use of rituximab in this population.

摘要

目的

进行一项系统评价和荟萃分析,评估利妥昔单抗联合化疗治疗儿童和青少年成熟B细胞非霍奇金淋巴瘤(NHL)的疗效和安全性。

方法

全面检索了PubMed、Embase、Cochrane图书馆和Web of Science,以识别截至2024年10月发表的相关研究。符合条件的研究包括那些涉及0至15岁被诊断为成熟B细胞NHL的患者的研究。提取了无事件生存期(EFS)、总生存期(OS)、完全缓解率(CRR)、不良事件、免疫重建(IgG水平)和复发率的数据。使用RevMan 5.0进行荟萃分析。

结果

共纳入11项研究,涉及1522名参与者。化疗中加入利妥昔单抗显著改善了EFS(风险比[HR]=0.40,95%置信区间[CI]:0.36-0.45,P<0.05)和OS(HR=0.38,95%CI:0.34-0.42,P<0.05)。利妥昔单抗组的CRR也显著更高(优势比[OR]=2.72,95%CI:1.76-4.21,P<0.05)。然而观察到不良反应发生率更高(OR=1.92,95%CI:1.25-2.94,P<0.05)。两组之间的复发率或IgG水平没有显著差异。

结论

化疗中加入利妥昔单抗显著改善了成熟B细胞NHL儿童和青少年的EFS、OS和CRR。尽管毒性风险增加,但生存和缓解益处支持在该人群中使用利妥昔单抗。

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