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铂类药物为基础的化疗方案治疗初治的不可治愈的非小细胞肺癌的最佳方案:网状 Meta 分析。

The best platinum regimens for chemo-naive incurable non-small cell lung cancer: network meta-analysis.

机构信息

Department of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

Respiratory Center, Matsusaka Municipal Hospital, Mie, Japan.

出版信息

Sci Rep. 2017 Oct 13;7(1):13185. doi: 10.1038/s41598-017-13724-2.

DOI:10.1038/s41598-017-13724-2
PMID:29030633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5640659/
Abstract

Platinum regimens still play a key role in chemotherapy for incurable non-small cell lung cancer (NSCLC). Although guidelines list many platina regimens, the best regimens have not yet clarified. Electronic searches were carried out during November 26th-28th, 2016. We included individually randomized trials comparing two or more platinum regimes for incurable chemo-naive NSCLC published in English full papers. The platinum doublets should be either Cisplatin (CDDP), Carboplatin (CBDCA), or Nedaplatin (CDGP) plus one of the third-generation agents. The platinum triplet should be the doublet plus bevacizumab (BEV). The data were independently extracted and cross-checked by two investigators. We did not observed heterogeneity (whole network level Q = 28.9, df = 34, P = 0.717) among 59 pairwise comparisons from 45 studies with 16141 cases for the primary outcome, hazard ratio for overall survival (HRos). Using CBDCA + Paclitaxel (PTX) + BEV as a common comparator, CDGP + Docetaxel (DTX) (HRos = 0.98, 95%CI: 0.75-1.29, P = 0.884), CDDP + Tegafur gimeracil oteracil (S1) (HRos = 1.23, 95%CI: 0.96-1.57, P = 0.099), CBDCA + S1 (HRos = 1.23, 95%CI: 0.99-1.53, P = 0.062), and CDGP + Gemcitabine (GEM) (HRos = 1.24, 95%CI: 0.71-2.17, P = 0.45) did not have significantly poorer HRos. We suggest that these regimens as acceptable first-choice regimens.

摘要

铂类方案在不可治愈的非小细胞肺癌(NSCLC)的化疗中仍发挥着关键作用。尽管指南列出了许多铂类方案,但最佳方案尚未明确。我们于 2016 年 11 月 26 日至 28 日进行了电子检索。我们纳入了比较两种或更多铂类方案治疗不可治愈的初治 NSCLC 的个体随机试验,这些试验以英文全文发表。铂类双联方案应为顺铂(CDDP)、卡铂(CBDCA)或奈达铂(CDGP)加一种第三代药物。铂类三联方案应为双联方案加贝伐单抗(BEV)。数据由两名研究者独立提取和交叉核对。我们未观察到 45 项研究中的 59 项两两比较(共 16141 例)的主要结局(总生存期的风险比 [HRos])存在异质性(整个网络水平 Q=28.9,df=34,P=0.717)。以 CBDCA+紫杉醇(PTX)+BEV 作为共同比较,CDGP+多西他赛(DTX)(HRos=0.98,95%CI:0.75-1.29,P=0.884)、CDDP+替加氟吉美嘧啶(S1)(HRos=1.23,95%CI:0.96-1.57,P=0.099)、CBDCA+S1(HRos=1.23,95%CI:0.99-1.53,P=0.062)和 CDGP+吉西他滨(GEM)(HRos=1.24,95%CI:0.71-2.17,P=0.45)的 HRos 均无显著差异。我们建议这些方案为可接受的一线治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aac/5640659/c1b04473e713/41598_2017_13724_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aac/5640659/bbfb9063fc25/41598_2017_13724_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aac/5640659/89ca055f57a9/41598_2017_13724_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aac/5640659/c1b04473e713/41598_2017_13724_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aac/5640659/bbfb9063fc25/41598_2017_13724_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aac/5640659/89ca055f57a9/41598_2017_13724_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aac/5640659/c1b04473e713/41598_2017_13724_Fig3_HTML.jpg

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