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同步放化疗后巩固化疗与单纯放化疗治疗局部晚期不可切除的 III 期非小细胞肺癌的荟萃分析

Consolidation chwemotherapy after concurrent chemoradiotherapy vs. chemoradiotherapy alone for locally advanced unresectable stage III non-small-cell lung cancer: A meta-analysis.

作者信息

Chang Xiu-Jun, Wang Zi-Tong, Yang Lei

机构信息

Department of Thoracic Surgery, Beijing Chest Hospital, Capital Medical University, Beijing Tuberculosis and Tumor Research Institute, Beijing 101149, P.R. China.

出版信息

Mol Clin Oncol. 2016 Aug;5(2):271-278. doi: 10.3892/mco.2016.910. Epub 2016 May 23.

DOI:10.3892/mco.2016.910
PMID:27446563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4950681/
Abstract

Concurrent chemoradiotherapy (CCRT) has been considered to be the standard of care for locally advanced unresectable stage III non-small-cell lung cancer (LA-NSCLC). Whether consolidation chemotherapy (CCT) following CCRT is able to further improve the clinical outcome remains unclear. We therefore undertook a meta-analysis to compare the two regimens for LA-NSCLC. A literature search was performed through PubMed, Embase, Cochrane Library and Chinese Biology Medicine, from their inception to November, 2015. Irrelevant studies were excluded using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses standards. Our primary endpoint was overall survival (OS), which was defined as the time from randomisation until death from any cause; the secondary endpoint was progression-free survival (PFS). All analyses were by intention-to-treat. Five phase III randomized controlled trials with 958 patients were included in the present meta-analysis. The results were expressed as odds ratios (ORs) with 95% confidence intervals (CIs). Compared with CCRT, CCT after CCRT was not associated with statistically significant differences in OS (OR=1.24; 95% CI: 0.89-1.72; P=0.21) or PFS (OR=1.16; 95% CI: 0.74-1.83; P=0.53), but increased the risk of toxicity, including infection (P=0.02), pneumonitis (P=0.003) and treatment-related death (P=0.04). There were no significant differences in terms of benefit according to particular patient characteristics, such as age, gender, performance status, tumor histology or clinical stage. Thus, the present study failed to support the use of CCT after CCRT over CCRT alone, as there was no significant OS and PFS benefit for LA-NSCLC patients, but the use of CCT after CCRT resulted in increased toxicity.

摘要

同步放化疗(CCRT)一直被视为局部晚期不可切除的 III 期非小细胞肺癌(LA-NSCLC)的标准治疗方案。CCRT 后进行巩固化疗(CCT)是否能够进一步改善临床疗效仍不明确。因此,我们进行了一项荟萃分析,以比较这两种治疗 LA-NSCLC 的方案。通过 PubMed、Embase、Cochrane 图书馆和中国生物医学数据库进行文献检索,检索时间范围从各数据库建库至 2015 年 11 月。使用系统评价和荟萃分析的首选报告项目标准排除无关研究。我们的主要终点是总生存期(OS),定义为从随机分组至因任何原因死亡的时间;次要终点是无进展生存期(PFS)。所有分析均采用意向性分析。本荟萃分析纳入了 5 项 III 期随机对照试验,共 958 例患者。结果以比值比(OR)及 95%置信区间(CI)表示。与 CCRT 相比,CCRT 后进行 CCT 在 OS(OR = 1.24;95%CI:0.89 - 1.72;P = 0.21)或 PFS(OR = 1.16;95%CI:0.74 - 1.83;P = 0.53)方面无统计学显著差异,但增加了毒性风险,包括感染(P = 0.02)、肺炎(P = 0.003)和治疗相关死亡(P = 0.04)。根据特定患者特征,如年龄、性别、体能状态、肿瘤组织学类型或临床分期,在获益方面无显著差异。因此,本研究不支持在 CCRT 后使用 CCT 而非单纯使用 CCRT,因为对于 LA-NSCLC 患者,OS 和 PFS 并无显著获益,但 CCRT 后使用 CCT 会导致毒性增加。

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