Actively Recruiting

Phase 2
Age: 18Years - 75Years
All Genders
NCT06787183

SCRT(Short Course Radiotherapy) Combined With CAPOX Plus QL1706 for Rectal Cancer Liver Metastases

Led by Fujian Cancer Hospital · Updated on 2026-03-03

42

Participants Needed

2

Research Sites

208 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To enhance the treatment efficacy of rectal cancer liver metastasis through a multidisciplinary approach of radiotherapy, immunotherapy, and chemotherapy, and to provide a new direction for the combination treatment strategy.

CONDITIONS

Official Title

SCRT(Short Course Radiotherapy) Combined With CAPOX Plus QL1706 for Rectal Cancer Liver Metastases

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 75 years, any gender
  • Pathologically confirmed rectal cancer with liver metastases (stage M1)
  • Karnofsky Performance Status of 70 or higher
  • Adequate organ function with no contraindications to radiotherapy or immunotherapy
  • Microsatellite stability or proficient mismatch repair status (MSS/pMMR)
  • No prior chemotherapy or other anti-tumor treatments before study entry
  • No prior immunotherapy
  • Ability to comply with the study protocol during the study period
  • Signed written informed consent
Not Eligible

You will not qualify if you...

  • Pregnant or lactating women
  • Diagnosis of signet ring cell carcinoma
  • History of other cancers within the past 5 years, except cured skin cancer and cervical carcinoma in situ
  • Uncontrolled epilepsy, central nervous system disorders, or psychiatric conditions affecting consent or medication compliance
  • Active significant cardiac disease or recent myocardial infarction within 12 months
  • Organ transplant recipients on immunosuppressive therapy or long-term steroid use
  • Presence of autoimmune diseases
  • Severe uncontrolled infections or other serious comorbidities
  • Abnormal baseline blood counts or liver/kidney function tests beyond specified limits
  • Known deficiency of dihydropyrimidine dehydrogenase (DPD)
  • Allergy to any investigational drug components

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Fuzhou First General Hospital

Fuzhou, Fujian, China, 350004

Not Yet Recruiting

2

Fujian Cancer Hospital

Fuzhou, Fujian, China, 350014

Actively Recruiting

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Research Team

H

Hui Li, MD

CONTACT

J

Jinluan Li, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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