AI Article Synopsis

  • The study compared the effectiveness and safety of various immune checkpoint inhibitors for treating advanced or metastatic esophageal squamous cell carcinoma (ESCC).
  • A systematic review included ten trials with 5250 patients, using Bayesian network meta-analysis to evaluate overall survival and progression-free survival among different treatments.
  • The findings indicated that Toripalimab and Camrelizumab with chemotherapy were the most effective first-line treatment options, while Sintilimab and Camrelizumab showed promise for patients with refractory cases, with manageable toxicity levels.

Article Abstract

Background: The study aimed to compare efficacy and safety of various immune checkpoint inhibitors for patients with advanced or metastatic esophageal squamous cell carcinoma (ESCC).

Methods: 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.

Results: 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.

Conclusions: 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.

Trial Registration: PROSPERO registration number: (CRD 42021261554).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482734PMC
http://dx.doi.org/10.1186/s12885-022-10086-5DOI Listing

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