About this trial
This study adopts a prospective randomized controlled design to evaluate the efficacy and safety of short-course radiotherapy followed by sequential PD-1 inhibitor and FOLFOX chemotherapy versus conventional regimens in high-risk locally advanced pMMR/MSS lower rectal adenocarcinoma, aiming to provide high-level evidence supporting a novel treatment paradigm.
Eligibility criteria
Qualifiers
Before implementing any procedures related to the study protocol rather than routine clinical care, a signed and dated informed consent form must be obtained from the subject voluntarily, in accordance with regulatory requirements and institutional guidelines.
Age 18-75 years.
Histologically or cytologically confirmed pMMR/MSS rectal adenocarcinoma.
The lower edge of the rectal tumor is located below the peritoneal reflection.
Disqualifiers
Patients with a history of severe drug allergy (including allergy to platinum agents, 5-FU, and 5-HT3 receptor antagonists).
Patients who have participated in or are currently participating in another clinical trial within 4 weeks prior to enrollment.
History of prior treatment with anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CTLA-4, or any other therapy specifically targeting T-cell co-stimulation or checkpoint pathways.
Severe electrolyte abnormalities.
Trial design
Treatments tested in this trial
- Short-course Radiotherapy, SCRT
- Toripalimab
Treatment groups
Sponsors and collaborators
Sixth Affiliated Hospital, Sun Yat-sen University
Lead sponsor
Junshi Biosciences
Collaborator