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利妥昔单抗联合化疗治疗弥漫性大B细胞淋巴瘤的疗效与安全性:一项荟萃分析。

Efficacy and safety of rituximab combined with chemotherapy in the treatment of diffuse large B-cell lymphoma: a meta-analysis.

作者信息

Meng Fanlu, Zhong Diansheng, Zhang Linlin, Shao Yi, Ma Qing

机构信息

Department of Oncology, General Hospital of Tianjin Medical University Tianjin 30002, PR China.

出版信息

Int J Clin Exp Med. 2015 Oct 15;8(10):17515-22. eCollection 2015.

Abstract

The aim of this study is to systematically evaluate the safety and efficacy of rituximab plus CHOP (R-CHOP combined regimen) in patients with previously untreated diffuse large B cell lymphoma (DLBCL). Electronic database were searched for randomized-controlled studies only comparing R-CHOP to CHOP standard alone in patients with untreated DLBCL were included. The risk ratios (RRs) with their 95% corresponding intervals (95% CI) were employed to estimate the efficacy of overall response (OR), complete response (CR), risk of dying and relapse rate in followed-up period. Total ten case-control studies containing 2941 patients met the inclusion criteria. The addition of R to standard CHOP were showed to increase the proportion of CR (RR=1.23, 95% CI=1.13-1.35, P<0.00001) and OR (RR=1.39, 95% CI=1.24-1.55, P<0.00001) in a fixed-effect model, indicating that rituximab combined with CHOP regimen is efficacy than CHOP alone. It did not increase the overall risk of dying as a consequence of infection (RR=0.79, 95% CI=0.55-1.13, P=0.20). Furthermore, the relapse rates is significantly lower in R-CHOP (RR=0.52, 95% CI=0.38-0.71, P<0.0001). The adverse effects were also not significant (P>0.05). In summary, R-CHOP regimen is superior to standard CHOP in terms of overall response and complete response. It does not increase the incidence of adverse effects. However, more studies concerning different age groups and special patients are needed to discuss the potential role of R in DLBCL.

摘要

本研究旨在系统评估利妥昔单抗联合CHOP(R-CHOP联合方案)用于既往未治疗的弥漫性大B细胞淋巴瘤(DLBCL)患者的安全性和疗效。检索电子数据库,仅纳入比较R-CHOP与单纯CHOP标准方案治疗未治疗的DLBCL患者的随机对照研究。采用风险比(RRs)及其95%相应区间(95%CI)来估计随访期内总缓解率(OR)、完全缓解率(CR)、死亡风险和复发率的疗效。共有10项包含2941例患者的病例对照研究符合纳入标准。在固定效应模型中,在标准CHOP方案中加用R显示可提高CR比例(RR = 1.23,95%CI = 1.13 - 1.35,P < 0.00001)和OR(RR = 1.39,95%CI = 1.24 - 1.55,P < 0.00001),表明利妥昔单抗联合CHOP方案比单纯CHOP方案更有效。它并未增加因感染导致的总体死亡风险(RR = 0.79,95%CI = 0.55 - 1.13,P = 0.20)。此外,R-CHOP方案的复发率显著更低(RR = 0.52,95%CI = 0.38 - 0.71,P < 0.0001)。不良反应也不显著(P > 0.05)。总之,R-CHOP方案在总缓解率和完全缓解率方面优于标准CHOP方案。它并未增加不良反应的发生率。然而,需要更多关于不同年龄组和特殊患者的研究来探讨R在DLBCL中的潜在作用。

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