Immunotherapy in Squamous Cell Cancer of the Esophagus.

Curr Oncol

Hematology-Oncology Practice Eppendorf (HOPE), 20249 Hamburg, Germany.

Published: March 2022

AI Article Synopsis

  • Treatment of esophageal carcinoma has evolved with immunotherapy, particularly highlighting the effectiveness of PD-1 inhibitors like nivolumab and pembrolizumab in improving patient outcomes.
  • Notable trials, such as CheckMate-577 and KEYNOTE-590, show these drugs enhance disease-free survival (DFS) and overall survival (OS) in various settings, including adjuvant therapy and first-line treatment for PD-L1 positive patients.
  • Additional studies in Asian populations further reinforce these findings, demonstrating significant survival benefits from other PD-1 inhibitors combined with chemotherapy in both first-line and second-line treatment scenarios.

Article Abstract

Treatment of esophageal carcinoma has changed dramatically following several landmark trials, which have proven the benefit of immunotherapy. The selective PD-1 (programmed cell death ligand-1)-inhibitor nivolumab has been shown to improve DFS in the adjuvant therapy setting (CheckMate-577). In the first-line treatment, PD-L1 positive (CPS ≥ 10) squamous cell carcinoma patients (pts) have been shown to have an increased OS following treatment with the PD-1-inhibitor pembrolizumab in combination with chemotherapy (KEYNOTE-590). Nivolumab also improved overall survival in the first line setting either combined with ipilimumab or with chemotherapy (CheckMate 648) compared to chemotherapy alone. In Asian first-line patients, phase III trials investigating camrelizumab (ESCORT 1), toripalimab (JUPITER 06), or sintilimab (ORIENT 15) in addition to chemotherapy also showed significant survival benefits. In the second-line setting, monotherapy with nivolumab (ATTRACTION-03), pembrolizumab (KEYNOTE-181), camrelizumab (ESCORT), and tislelizumab (RATIONALE 302) demonstrated a benefit in OS in comparison to chemotherapy. Here we will review these trials and integrate them into the current treatment algorithm.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026413PMC
http://dx.doi.org/10.3390/curroncol29040200DOI Listing

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