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节拍性口服长春瑞滨单药治疗非小细胞肺癌的疗效和毒性:一项荟萃分析。

The efficacy and toxicity of metronomic oral vinorelbine monotherapy in patients with non-small cell lung cancer: a meta-analysis.

机构信息

Department of Oncology, The First Affiliated Hospital of Chengdu Medical College, 278 Baoguang Street, Xindu District, Chengdu, 610500, Sichuan, People's Republic of China.

出版信息

Int J Clin Oncol. 2020 Sep;25(9):1624-1634. doi: 10.1007/s10147-020-01707-9. Epub 2020 May 29.

DOI:10.1007/s10147-020-01707-9
PMID:32472208
Abstract

PURPOSE

To evaluate the efficacy and toxicity of metronomic oral vinorelbine monotherapy in patients with stage IIIB/IV and advanced non-small cell lung cancer (NSCLC).

METHODS

The PubMed, Embase, Cochrane library, Wanfang, and CNKI databases were searched for relevant studies. The overall response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and incidence of severe adverse events (grade ≥ 3 adverse events; grade 3/4 AEs) were calculated using the methods of merging ratios and means. Merged ratios and means and their 95% confidence intervals (CIs) were used to descriptively analyze the efficacy and toxicity of metronomic oral vinorelbine monotherapy in patients with stage IIIB/IV and advanced NSCLC.

RESULTS

The ORR and DCR achieved with metronomic oral vinorelbine monotherapy were 12% (95% CI 5-20) and 48% (95% CI 38-59), respectively. Median PFS and OS were 3.46 months (95% CI 2.49-4.43) and 8.22 months (95% CI 7.21-9.24), respectively. The incidence of grade 3/4 AEs was 16% (95% CI 10-22). The more common grade 3/4 AEs were neutropenia 9% (95% CI 2-20) and leukopenia 8% (95% CI 1-19).

CONCLUSION

Metronomic oral vinorelbine monotherapy has a certain effect on patients with stage IIIB/IV and advanced NSCLC, especially for untreated elderly patients. It offers the advantages of convenience, lower cost and acceptable incidence of severe adverse events.

摘要

目的

评估节拍口服长春瑞滨治疗 IIIB/IV 期和晚期非小细胞肺癌(NSCLC)的疗效和毒性。

方法

检索 PubMed、Embase、Cochrane 图书馆、万方和中国知网数据库,以评估节拍口服长春瑞滨治疗 IIIB/IV 期和晚期 NSCLC 的疗效和毒性。使用合并比和均值的方法计算总缓解率(ORR)、疾病控制率(DCR)、无进展生存期(PFS)、总生存期(OS)和严重不良事件发生率(等级≥3 不良事件;等级 3/4 AE)。使用合并比和均值及其 95%置信区间(CI)来描述性分析节拍口服长春瑞滨治疗 IIIB/IV 期和晚期 NSCLC 的疗效和毒性。

结果

节拍口服长春瑞滨治疗的 ORR 和 DCR 分别为 12%(95%CI 5-20)和 48%(95%CI 38-59)。中位 PFS 和 OS 分别为 3.46 个月(95%CI 2.49-4.43)和 8.22 个月(95%CI 7.21-9.24)。3/4 级 AE 的发生率为 16%(95%CI 10-22)。更常见的 3/4 级 AE 是中性粒细胞减少症 9%(95%CI 2-20)和白细胞减少症 8%(95%CI 1-19)。

结论

节拍口服长春瑞滨治疗 IIIB/IV 期和晚期 NSCLC 具有一定疗效,特别是对未经治疗的老年患者。它具有方便、成本低和可接受的严重不良事件发生率的优点。

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