AI Article Synopsis

  • Pembrolizumab, nivolumab, and the combination therapies have emerged as first-line treatments for advanced esophageal cancer, although their efficacy on primary tumors was previously unclear.
  • In a study of 23 patients experiencing esophageal dysphagia, significant improvement in swallowing was noted in 82.6%, with a median time to improvement of about 26 days.
  • While 10 patients experienced immune-related adverse events, the treatments provided high response rates and prolonged survival, indicating promising effectiveness against primary tumors.

Article Abstract

Recently, pembrolizumab plus 5-fluorouracil and cisplatin (FP), nivolumab plus FP, and nivolumab plus ipilimumab have become the first-line treatments for patients with advanced esophageal cancer. However, the treatment efficacy in primary tumors has not been reported. We assessed the outcomes of these treatments in advanced esophageal cancer, specifically focusing on esophageal dysphagia improvements and the primary tumor response. This retrospective study was conducted between October 2021 and November 2023. We investigated 23 patients with esophageal cancer and dysphagia who received an immune checkpoint inhibitor (ICI) plus FP or nivolumab plus ipilimumab. The median progression-free survival (PFS) was 10.6 months (95% confidence interval [CI]: 9.0-12.5), and the median overall survival was not reached (95%CI: 13.0-NA). Improvement in dysphagia was observed in 19/23 (82.6%) patients, with a median time to improvement of 26 days (range: 15-77 days) and a median dysphagia PFS of 12.6 months (range: 8.1-NA months). Ten patients experienced immune-related adverse events (irAEs): seven had interstitial pneumonia, and three had thyroid dysfunction, pituitary dysfunction, and rash, respectively. Although there was a high frequency of irAEs, ICI for esophageal cancer achieved high response rates and prolonged survival. The observed improvement in dysphagia suggests the potential efficacy of the treatment against primary tumors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11355245PMC
http://dx.doi.org/10.3390/jcm13164806DOI Listing

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