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Efficacy and safety of short-course radiotherapy in total neoadjuvant therapy combined with enlonstobart for pMMR locally advanced rectal cancer
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| short-course radiotherapy and immunotherapy | Experimental | patients will receive 5*5Gy short-course radiotherapy, followed by 4 cycles of CAPOX chemotherapy and Enlonstobart |
|
| chemoradiotherapy | Active Comparator | Long-course radiotherapy +Capecitabine 825mg/m2 bid d1-d14, followed by 4 cycles of CAPOX chemotherapy |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Experimental: short-course radiotherapy and immunotherapy | Drug | patients will receive 5*5Gy short-course radiotherapy, followed by 4 cycles of CAPOX chemotherapy and Enlonstobart Enlonstobart 200mg IV every 3 weeks; Oxaliplatin 130mg/m2 IV Q3W d1 Capecitabine 1000mg/m2 bid d1-14 q3w |
| Measure | Description | Time Frame |
|---|---|---|
| complete response Rate (pCR+cCR ) | Clinical complete response or pathological complete response (cCR or pCR) | up to 2 year |
| Measure | Description | Time Frame |
|---|---|---|
| Major pathologic response rate | up to 2 year | |
| R0 resection rate | The R0 resection rate will be evaluated after surgery, an average of 4 weeks | |
| 3-year event-free survival (EFS) rate |
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Inclusion Criteria:
1.age >=18 years old, female and male. 2.Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. 3.Histologically confirmed adenocarcinoma of the colon, and umor biopsy immunohistochemistry (IHC) indicates pMMR .
4.Staged as T3-4 NanyM0 or T1-2N+ M0 according to the AJCC 8th edition. 5.Rectal cancer: <10 cm from the anal verge. 6.Adequate organ function:
Hematology : i. Absolute Neutrophil Count (ANC) ≥ 1.5 × 10⁹/L. ii. Platelet count ≥ 100 × 10⁹/L . iii. Hemoglobin ≥ 90 g/L.
Hepatic: i. Serum Total Bilirubin (TBil) ≤ 1.5 × ULN (Upper Limit of Normal). ii. AST and ALT ≤ 2.5 × ULN. iii. Creatinine ≤ 1.5 × ULN ; Renal: Calculated Creatinine Clearance (CrCl) ≥ 60 mL/min (calculated using the Cockcroft-Gault formula)
Coagulation: i. International Normalized Ratio (INR) and Activated Partial Thromboplastin Time (APTT) ≤ 1.5 × ULN.
7. Men and women of childbearing potential must agree to use effective contraceptive measures during the study and for 6 months after the last treatment.
8. Willing and able to voluntarily provide written informed consent and comply with all scheduled treatments and follow-up assessments.
Exclusion Criteria:
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|
| Chemoradiotherapy | Drug | Long-course radiotherapy +Capecitabine 825mg/m2 bid d1-d14, followed by 4 cycles of CAPOX chemotherapy |
|
| up to 3 years |
| 3-year overall survival (OS) | up to 3 years |
| Adverse Event | up to 2 year |
| ID | Term |
|---|---|
| D007167 | Immunotherapy |
| D059248 | Chemoradiotherapy |
| ID | Term |
|---|---|
| D056747 | Immunomodulation |
| D001691 | Biological Therapy |
| D013812 | Therapeutics |
| D003131 | Combined Modality Therapy |
| D004358 | Drug Therapy |
| D011878 | Radiotherapy |
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