About this trial
To explore the complete response (CR) rate of modified short-course radiotherapy plus CAPOX and Tislelizumab versus Long-course Chemoradiotherapy plus Tislelizumab for locally advanced rectal cancer.
Eligibility criteria
Qualifiers
Age 18-75 years, any gender.
Pathologically confirmed rectal adenocarcinoma.
Baseline MR stage T3-4/N+.
Distance from anal verge ≤12cm.
Disqualifiers
Pregnant or lactating women.
Pathological diagnosis of signet ring cell carcinoma.
History of other malignancies within the past 5 years, except cured skin cancer and cervical carcinoma in situ.
Uncontrolled epilepsy, central nervous system disorders, or history of psychiatric disorders that, in the opinion of the investigator, may interfere with signing the informed consent form or affect patient compliance with oral medication.
Trial design
Treatments tested in this trial
- Modified Short-course radiotherapy
- Long-course radiotherapy
- Oxaliplatin
- Capecitabine
- Tislelizumab
- Capecitabine
- Tislelizumab