Department of Radiation Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center of Cancer Medicine, Guangzhou, China.
Department of Medicine, Qingdao University, Qingdao, Shandong, China.
BMC Cancer. 2022 Sep 17;22(1):992. doi: 10.1186/s12885-022-10086-5.
The study aimed to compare efficacy and safety of various immune checkpoint inhibitors for patients with advanced or metastatic esophageal squamous cell carcinoma (ESCC).
We searched Medline, Web of Science, Cochrane Central Register of Controlled Trials, Embase, Clinical Trials.gov and several international conference databases from January 1, 2000 to December 19, 2021. We conducted Bayesian network meta-analysis to assess the relative effects among treatments. Outcomes included overall survival (OS), progression-free survival (PFS), overall response rate and adverse events.
Ten eligible trials with 5250 patients were included. Toripalimab and Camrelizumab plus chemotherapy were preferred to rank first on OS (probability, 61%) and PFS (probability, 37%) in the first-line setting, respectively. In refractory patients, Sintilimab and Camrlizumab were most likely to be ranked first on OS (probability, 37%) and PFS (probability, 94%). The toxicity related to immunotherapy was manageable in clinical trials. Camrelizumab and Nivolumab had the less adverse events of grade 3 or higher in the first and refractory setting, respectively.
This study found that Toripalimab and Camrelizumab plus chemotherapy were likely to be the best option in terms of OS and PFS in the first-line setting for patients with advanced or metastatic ESCC respectively. Sintilimab and Camrelizumab were the preferred options for OS and PFS in refractory patients respectively. The toxicity of immunotherapy was different from conventional chemotherapy, but manageable in patients with ESCC.
PROSPERO registration number: (CRD 42021261554).
本研究旨在比较不同免疫检查点抑制剂治疗晚期或转移性食管鳞癌(ESCC)患者的疗效和安全性。
我们检索了 Medline、Web of Science、Cochrane 中央对照试验注册库、Embase、ClinicalTrials.gov 和几个国际会议数据库,检索时间为 2000 年 1 月 1 日至 2021 年 12 月 19 日。我们采用贝叶斯网状荟萃分析评估治疗方法之间的相对效果。主要终点包括总生存期(OS)、无进展生存期(PFS)、总缓解率和不良反应。
共纳入 10 项符合条件的试验,共 5250 例患者。在一线治疗中,特瑞普利单抗和卡瑞利珠单抗联合化疗在 OS(概率为 61%)和 PFS(概率为 37%)方面可能排名第一。在难治性患者中,信迪利单抗和卡瑞利珠单抗在 OS(概率为 37%)和 PFS(概率为 94%)方面最有可能排名第一。免疫治疗相关毒性在临床试验中是可控的。卡瑞利珠单抗和纳武利尤单抗在一线和难治性治疗中,3 级或以上不良反应发生率较低。
本研究发现,特瑞普利单抗和卡瑞利珠单抗联合化疗可能是晚期或转移性 ESCC 患者一线治疗中 OS 和 PFS 的最佳选择。信迪利单抗和卡瑞利珠单抗可能是难治性患者 OS 和 PFS 的首选方案。免疫治疗的毒性与传统化疗不同,但在 ESCC 患者中是可控的。
PROSPERO 注册号:(CRD 42021261554)。