Locally Advanced Resectable Rectal Cancer
Conditions
Brief summary
The study is being conducted to evaluate the safety and efficacy of Adebrelimab and SHR-8068 in combination with chemoradiotherapy in subjects with rectal cancer.
Interventions
DRUGAdebrelimab in combination with SHR-8068 and chemotherapy
Adebrelimab in combination with SHR-8068 and chemotherapy.
Adebrelimab combined with chemotherapy.
DRUGChemotherapy
Chemotherapy.
Sponsors
Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
1. Subjects must voluntarily agree to participate in the trial and sign a written informed consent form. 2. Male or female ≥ 18 years old and ≤75 years old. 3. ECOG performance status of 0-1. 4. An assessment of resectable locally advanced rectal. 5. Has not received any anti-tumor treatment for rectal cancer. 6. With a life expectancy of ≥2 years. 7. Male participants whose partners are fertile women and fertile female participants must take effective contraceptive measures together with their partners from the time of signing the informed consent form until 6 months after the last administration of the investigational drug or the last radiotherapy. Female participants with fertility must have a negative serum or urine test for human chorionic gonadotropin (HCG) within 7 days before the first administration of the drug (if the serum HCG test is positive, pregnancy should be ruled out and further discussion with the sponsor should be conducted), and they must be not in the lactation period.
Exclusion criteria
1. Patients with rectal cancer who have experienced local recurrence after previous treatment. 2. Patients with concurrent colon tumors. 3. Patients with initially unresectable colorectal cancer as evaluated by researchers or those whose condition is determined by researchers to be intolerant to surgery. 4. Clinical or imaging examinations suggest the presence of intestinal obstruction or perforation, or those assessed by researchers as having a relatively high risk of perforation or bleeding. 5. With distant metastases. 6. Imaging examination of rectal cancer indicated positive lateral lymph nodes. 7. Having received surgery, radiotherapy, chemotherapy, targeted therapy, immunotherapy, etc. for tumors. 8. Female participants who are pregnant, breastfeeding or planning to become pregnant during the study period. 9. There are uncontrollable mental illnesses and other circumstances known to affect the completion of the research procedures, such as alcohol abuse, drug abuse or drug abuse, and criminal detention. 10. Any other factors that may increase the risk of participating in the study, interfere with the study results, or make participation in the study inappropriate as judged by investigators.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Phase II: pCR (Pathological Complete Response) rate | 12 months | Evaluated by investigators. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Phase II: Clinical complete response (cCR) rate | 60 months | Evaluated by investigators per RECIST v1.1. |
| Phase II: Disease-free survival (DFS) | 60 months | Evaluated by investigators per RECIST v1.1. |
| Phase II: EFS (Event Free Survival) | 60 months | Evaluated by investigators per RECIST v1.1. |
| Phase II: Tumor regression grade (TRG) | 60 months | Evaluated by investigators per RECIST v1.1. |
| Phase II: R0 resection rate | 60 months | Evaluated by investigators per RECIST v1.1. |
| Phase II: length of hospital stay | 60 months | Evaluated by investigators per RECIST v1.1. |
| Phase II: Overall survival (OS) | 60 months | Evaluated by investigators per RECIST v1.1. |
| Phase II: Perioperative mortality (within 30 days and 90 days after surgery) | 60 months | Evaluated by investigators per RECIST v1.1. |
Countries
China
Contacts
CONTACTChuanpei Huang
Outcome results
None listed