Short-Course RT Plus CAPOX and Tislelizumab vs Long-Course CRT Plus Tislelizumab for Locally Advanced Rectal Cancer

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorFujian Cancer Hospital

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

Treatment groups

130 Participants
are divided into 2 treatment groups

Sponsors and collaborators