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晚期胃癌三线治疗的疗效与安全性比较:一项系统评价与网状Meta分析

Comparison of the efficacy and safety of third-line treatments for advanced gastric cancer: A systematic review and network meta-analysis.

作者信息

Zhang Chan, Xiang Yaoxian, Wang Jing, Yan Dong

机构信息

Department of Oncology, Beijing Luhe Hospital Affiliated to Capital Medical University, Beijing, China.

出版信息

Front Oncol. 2023 Mar 1;13:1118820. doi: 10.3389/fonc.2023.1118820. eCollection 2023.

Abstract

BACKGROUND

Many options for third-line treatment of advanced gastric cancer (GC) or gastroesophageal junction carcinoma (GEJC) have been developed. Therapies including immunotherapy (nivolumab), chemotherapy (irinotecan, FTD/TPI), targeted therapy (apatinib), and antibody drug conjugates (ADC) have shown to increase the survival rates in patients, but few studies have compared the relative efficacy of these treatments. Here, we compared the efficacies of these regimens using network meta-analysis (NMA) to provide guides in selecting the best regimen and formulating a precise individualized treatment plan.

METHODS

The published RCTs of phase II/III in PubMed, the Cochrane Central Register of Controlled Trials, and Embase were searched. The median overall survival (mOS) was the primary outcome of NMA, and the other outcomes were median progression-free survival (mPFS), disease control rate (DCR) (proportion of patients with confirmed CR, PR, or stable disease (SD)) and incidence of grade 3 or above adverse events (≥3AEs).

RESULTS

Five phase II/III RCTs involving 1674 patients and 7 treatment regimens were analyzed. It showed that Trastuzumab Deruxtecan (DS-8201) prolonged the OS of patients significantly comparing with chemotherapy (HR: 0.59; 95% CI: 0.39-0.89) for the overall population. DS-8201 (HR: 0.27; 95% CI: 0.17-0.42) and chemotherapy (HR: 0.57; 95% CI: 0.47-0.7) improved the PFS significantly over nivolumab. Apatinib (RR: 3.04; 95% CI: 1.65-5.95) and DS-8201 (RR: 2.67; 95% CI: 1.51-4.83) were more effective than nivolumab in improving DCR. DS-8201 achieved greater OS benefits compared to chemotherapy (HR: 0.59; 95% CI: 0.39-0.88) for patients who were HER2-positive. We ranked the Bayesian surface under the cumulative ranking curve according to OS benefit, and showed that ADC ranked first for the general patient population and for patients with a HER2-positive diagnosis, intestinal histopathology, previous gastrectomy history, gastric origination cancer, ages over 65 and ECOG PS=0/1, followed by nivolumab and apatinib. For patients with GEJC, nivolumab ranked first.

CONCLUSIONS

Nivolumab, apatinib, chemotherapy, and ADC all improved the OS of GC/GEJC patients significantly. ADC may be the best option for the overall population of GC, as well as for patients with HER2-overexpression, intestinal histopathology, previous gastrectomy history, gastric origination cancer, ages over 65 and ECOG PS=0/1, followed by nivolumab and apatinib. Nivolumab may be the first treatment option for GEJC patients.

SYSTEMATIC REVIEW REGISTRATION

https://www.crd.york.ac.uk/prospero, identifier CRD42022364714.

摘要

背景

晚期胃癌(GC)或胃食管交界癌(GEJC)的三线治疗已出现多种选择。包括免疫疗法(纳武单抗)、化疗(伊立替康、FTD/TPI)、靶向疗法(阿帕替尼)和抗体药物偶联物(ADC)在内的疗法已显示可提高患者生存率,但很少有研究比较这些治疗的相对疗效。在此,我们使用网络荟萃分析(NMA)比较这些方案的疗效,为选择最佳方案和制定精确的个体化治疗计划提供指导。

方法

检索PubMed、Cochrane对照试验中心注册库和Embase中已发表的II/III期随机对照试验(RCT)。NMA的主要结局为中位总生存期(mOS),其他结局为中位无进展生存期(mPFS)、疾病控制率(DCR)(确诊为完全缓解、部分缓解或疾病稳定的患者比例)以及3级及以上不良事件(≥3AE)的发生率。

结果

分析了5项涉及1674例患者和7种治疗方案的II/III期RCT。结果显示,对于总体人群,与化疗相比,曲妥珠单抗德鲁替康(DS-8201)显著延长了患者的总生存期(HR:0.59;95%CI:0.39 - 0.89)。DS-8201(HR:0.27;95%CI:0.17 - 0.42)和化疗(HR:0.57;95%CI:0.47 - 0.7)在无进展生存期方面显著优于纳武单抗。阿帕替尼(RR:3.04;95%CI:1.65 - 5.95)和DS-8201(RR:2.67;95%CI:1.51 - 4.83)在改善疾病控制率方面比纳武单抗更有效。对于HER2阳性患者,与化疗相比,DS-8201在总生存期方面有更大获益(HR:0.59;95%CI:0.39 - 0.88)。我们根据总生存期获益对累积排序曲线下的贝叶斯曲面进行排序,结果显示,对于一般患者群体以及HER2阳性诊断、肠型组织病理学、既往胃切除史、原发于胃的癌症、年龄超过65岁且ECOG体能状态评分为0/1的患者,ADC排名第一,其次是纳武单抗和阿帕替尼。对于胃食管交界癌患者,纳武单抗排名第一。

结论

纳武单抗、阿帕替尼、化疗和ADC均显著改善了GC/GEJC患者的总生存期。ADC可能是GC总体人群以及HER2过表达、肠型组织病理学、既往胃切除史、原发于胃的癌症、年龄超过65岁且ECOG体能状态评分为0/1的患者的最佳选择,其次是纳武单抗和阿帕替尼。纳武单抗可能是胃食管交界癌患者的首选治疗方案。

系统评价注册

https://www.crd.york.ac.uk/prospero,标识符CRD42022364714。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0229/10016689/dfa136a937de/fonc-13-1118820-g001.jpg

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