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Efficacy of vinorelbine-based neoadjuvant chemotherapy in breast cancer: A systematic review and meta-analysis of randomized controlled trials

机译:长春瑞滨新辅助化疗在乳腺癌中的疗效:随机对照试验的系统评价和荟萃分析

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摘要

The present study aimed to compare the effects of vinorelbine-based neoadjuvant chemotherapy and vinorelbine-free regimens. A meta-analysis of all the relevant randomized controlled trials was performed to investigate the improvement in pathological complete response (pCR), overall response rate (ORR) and breast-conserving surgery (BCS). The PubMed and Embase databases were searched for relevant studies reporting randomized controlled trials comparing vinorelbine-based neoadjuvant chemotherapy with vinorelbine-free regimens until July 2013. Risk ratios/odds ratio and 95% confidence intervals (CIs) were used to estimate the association between vinorelbine in neoadjuvant chemotherapy and various efficacy outcomes. Fixed- or random-effect models were adopted to pool the data. Five eligible studies with a total of 1,495 patients were included in the meta-analysis. Compared to vinorelbine-free chemotherapy, vinorelbine-based regimens demonstrated no significant improvement in clinical outcomes including: pCR [relative risk (RR)=1.016; 95% CI, 0.738–1.399; P=0.922], ORR (RR=1.048; 95% CI, 0.969–1.133; P=0.239) and BCS (RR=1.764; 95% CI, 0.734–4.239; P=0.205). However, vinorelbine-based regimens were associated with a lower incidence of grade 3–4 alopecia (OR, 0.617; 95% CI, 0.448–0.848; P=0.003). In a hierarchical analysis for patients who received neoadjuvant chemotherapy, the proportion of subjects achieving pCR was significantly increased when HER2-amplified (RR=2.31; 95% CI, 1.20–4.43; P=0.01) and hormone receptor negative (RR=0.488; 95% CI, 0.263–0.908; P=0.023). The present review confirms that neoadjuvant chemotherapy vinorelbine-based regimens are unlikely to emerge as superior to pCR, ORR and BCS. Hierarchical analysis indicated that the HER2-amplified and hormone receptor-negative patients were significantly associated with a pathological response rate.
机译:本研究旨在比较基于长春瑞滨的新辅助化疗和无长春瑞滨的治疗方案的效果。进行了所有相关随机对照试验的荟萃分析,以研究病理完全缓解(pCR),总体缓解率(ORR)和保乳手术(BCS)的改善。搜索PubMed和Embase数据库以寻找相关研究,报告比较在2013年7月之前基于长春瑞滨的新辅助化疗与无长春瑞滨方案的随机对照试验。使用风险比/优势比和95%置信区间(CI)评估长春瑞滨之间的相关性在新辅助化疗和各种疗效结果中。采用固定或随机效应模型来汇总数据。荟萃分析包括五项符合条件的研究,共计1,495例患者。与不含长春瑞滨的化疗相比,基于长春瑞滨的方案在临床结局方面无明显改善,包括:pCR [相对风险(RR)= 1.016; 95%CI,0.738–1.399; P = 0.922],ORR(RR = 1.048; 95%CI,0.969-1.133; P = 0.239)和BCS(RR = 1.764; 95%CI,0.734-4.239; P = 0.205)。然而,以长春瑞滨为基础的治疗方案与3-4级脱发的发生率较低相关(OR,0.617; 95%CI,0.448-0.848; P = 0.003)。在对接受新辅助化疗的患者进行的分层分析中,当HER2扩增(RR = 2.31; 95%CI,1.20-1.43; P = 0.01)和激素受体阴性(RR = 0.488; H2 +)时,达到pCR的受试者比例显着增加。 95%CI,0.263-0.908; P = 0.023)。本综述证实,基于长春瑞滨的新辅助化疗方案不可能优于pCR,ORR和BCS。分层分析表明,HER2扩增和激素受体阴性的患者与病理反应率显着相关。

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