Nature Communications (Aug 2024)

Toripalimab plus chemotherapy and radiotherapy for treatment-naive advanced esophageal squamous cell carcinoma: a single-arm phase 2 trial

  • Lei Wu,
  • Baisen Li,
  • Gang Wan,
  • Yi Wang,
  • Jie Zhu,
  • Long Liang,
  • Xuefeng Leng,
  • Wenwu He,
  • Lin Peng,
  • Yongtao Han,
  • Shuya He,
  • Dongsheng Wang,
  • Yehan Zhou,
  • Liang Yi,
  • Wencheng Zhang,
  • Qingsong Pang,
  • Wei Zhang,
  • Tao Li,
  • Jinyi Lang,
  • Yang Liu,
  • Bangrong Cao,
  • Qifeng Wang

DOI
https://doi.org/10.1038/s41467-024-51105-2
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 12

Abstract

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Abstract This single-arm phase 2 trial (ChiCTR2100046715) examined previously untreated patients with advanced esophageal squamous cell carcinoma (ESCC) who received four cycles of paclitaxel with carboplatin every 3 weeks. Toripalimab was infused intravenously every 3 weeks for 12 months, or until disease progression or intolerable toxicity. Radiotherapy that encompassed the primary lesions and metastases commenced in the third cycle. The median progression-free survival time was 9.8 months (95% confidence interval [CI]: 6.8–not estimable) in the intent-to-treat population, failing to meet the pre-specified primary endpoints. Secondary endpoints included an objective response rate of 45.5%, a disease control rate of 57.6%, and a median duration of response of 11.5 months (interquartile range, 6.4–15.0). The 1-year progression-free survival and overall survival rates were 41.9% (95% CI: 27.7–63.5) and 69.7% (95% CI: 55.7–87.3), respectively. Lymphopenia was the most frequent grade ≥3 adverse event (82%), and an esophageal fistula developed in three patients (9.1%). No treatment-related deaths occurred. In prespecified exploratory biomarker analysis, higher densities of CD8 + T cells, CD11c+ dendritic cells, and CD68+ macrophages correlated with improved tumor response and prognosis. Radiotherapy supplementation to first-line chemo-immunotherapy for treatment-naive advanced ESCC demonstrated some antitumor activity and manageable safety profiles, warranting further randomized controlled trials.