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Whole-course Immunonutrition Combined With Chemoradiotherapy±ICIs for Local Advanced Patients With Inoperable Esophageal Squamous Cell Carcinoma

U

University of Science and Technology of China (USTC)

Status and phase

Enrolling
Phase 2

Conditions

Chemoradiotherapy
Esophageal Squamous Cell Carcinoma
Immunonutrition
Inoperable

Treatments

Dietary Supplement: Whole-course Immunonutrition Combined With Chemoradiotherapy±ICIs

Study type

Observational

Funder types

Other

Identifiers

NCT05833594
2023WCIN001

Details and patient eligibility

About

Chemoradiotherapy has been a standard modality for inoperable locally advance esophageal carcinoma. The goal of this randomized control study is to compare the feasibility, and survival benefits of whole-course immunonutrition combined with chemoradiotherapy±ICIs for local advanced patients with inoperable esophageal squamous cell carcinoma. The main questions it aims to answer are: • If the feasibility and safety of whole-course immunonutrition combined with chemoradiotherapy±ICIs is better. • If the survival benefits (1, 2 and 3-years progression free survival) of whole-course immunonutrition combined with chemoradiotherapy±ICIs is longer. The Experimental group will receive a combination immunonutrition of omega-3 fatty acids, and glutamine, whereas the control group will receive standard formula.

Enrollment

70 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-85 years old;
  • Eastern Cooperative Oncology Group (ECOG) 0-2;
  • Esophageal squamous cell carcinoma;
  • cT2-4aN0-3M0 (AJCC 8th) confirmed by radiological examination;
  • initial unresectable at initial diagnosis confirmed by thoracic surgeons;
  • Treatment naive;
  • No contraindications for adjuvant chemoradiotherapy;
  • Signature of inform consent.

Exclusion criteria

  • younger than 18 years old or older than 85 years old;
  • ECOG>2;
  • Esophageal adenocarcinoma, small-cell cancer and other pathological types;
  • cT1anyNM0, cT4banyNM0, c anyTanyNM0 confirmed by radiological examination;
  • Resectable at initial diagnosis confirmed by thoracic surgeons;
  • Previous treatment of chemotherapy, radiotherapy, and other treatment;
  • Contraindications for chemoradiotherapy;
  • No signature of inform consent.

Trial design

70 participants in 2 patient groups

Experimental
Description:
Whole-course Immunonutrition Combined With Chemoradiotherapy±ICIs
Treatment:
Dietary Supplement: Whole-course Immunonutrition Combined With Chemoradiotherapy±ICIs
Comparator
Description:
Whole-course nutrition Combined With Chemoradiotherapy±ICIs
Treatment:
Dietary Supplement: Whole-course Immunonutrition Combined With Chemoradiotherapy±ICIs

Trial contacts and locations

1

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Central trial contact

dong qian, M.D.

Data sourced from clinicaltrials.gov

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