Effects of pre-operative enteral immunonutrition for esophageal cancer patients treated with neoadjuvant chemoradiotherapy: protocol for a multicenter randomized controlled trial (point trial, pre-operative immunonutrition therapy)

  • Yun Yun Cao (Creator)
  • D. Han (Creator)
  • Su Geun Yang (Creator)
  • Yuan Yuan Shi (Creator)
  • S. W. Zhao (Creator)
  • Qianwen Jin (Creator)
  • Jian Jian Li (Creator)
  • C. Li (Creator)
  • Yajie Zhang (Creator)
  • W. Shen (Creator)
  • J. He (Creator)
  • M. Wang (Creator)
  • Gang Ji (Creator)
  • Zhigang Li (Creator)
  • Yi He (Creator)
  • Q. Chen (Creator)
  • Wei Wei (Creator)
  • Chun-Liang Chen (Creator)
  • Xueqian Gong (Creator)
  • J. Wang (Creator)
  • L. B. Tan (Creator)
  • Hao Wang (Creator)
  • H. H. Li (Creator)



Abstract Background Neoadjuvant chemoradiation followed by esophagectomy has been established as the first-line treatment for locally advanced esophageal cancer. Postoperative enteral nutrition has been widely used to improve perioperative outcomes. However, whether to implement preoperative nutritional intervention during neoadjuvant therapy is yet to be verified by prospective studies. Methods POINT trial is a multicenter, open-labeled, randomized controlled trial. A total of 244 patients with surgically resectable esophageal cancer are randomly assigned to nutritional therapy group (arm A) or control group (arm B) with a 2:1 ratio. Both groups receive neoadjuvant chemotherapy with concurrent radiotherapy based on the CROSS regimen followed by minimally invasive esophagectomy. The primary endpoint is the rate of nutrition and immune-related complications after surgery. Secondary endpoints include completion rate of neoadjuvant chemoradiation and related adverse events, rate of pathological complete response, perioperative outcomes, nutritional status, overall survival, progression-free survival and quality of life. Discussion This trial aims to verify whether immunonutrition during neoadjuvant chemoradiation can reduce the rate of complications and improve perioperative outcomes. Frequent communication and monitoring are essential for a multicenter investigator-initiated trial. Trial registration: ClinicalTrials.gov: NCT04513418. The trial was prospectively registered on 14 August 2020, https://www.clinicaltrials.gov/ct2/show/NCT04513418 .
Datos disponibles2022

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