Efficacy and Safety of SBRT Followed by Tislelizumab Plus Cetuximab and Irinotecan in Patients With Previously Treated RAS Wild-type Advanced Refractory Colorectal Cancer

• Status: Not yet recruiting
• Trial end date: 2025-04-05
• Target enrollment: 0
• Participant gender: All

Summary

To evaluate the efficacy and safety of SBRT followed by tislelizumab plus cetuximab and irinotecan in patients with previously treated RAS wild-type advanced refractory colorectal cancer

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Fujian Cancer Hospital
• Treatments: Cetuximab; Irinotecan

Criteria

Inclusion Criteria:

• Aged 18-75 years

• Physical Condition Score (ECOG PS) of the Eastern Cancer Cooperative Group (USA) 0 or 1;

• Colorectal cancer diagnosed histologically and/or cytologically has metastases or relapses that are not curable by surgery

• Have received first - and second-line systemic antitumor therapy for mCRC (chemotherapy drugs may include fluorouracil, oxaliplatin, irinotecan, e.g. XELOX, FOLFOX, FOLFIRI, FOLFOXIRI, XELIRI; Can be combined with or without targeted drugs, such as cetuximab, bevacizumab);And disease progression after second-line treatment;

• Evaluation of lung or liver metastases can be evaluated, with stereotactic radiotherapy maneuverability;

• At least one measurable lesion as defined in RECIST version 1.1;

• Fertile patients must be willing to take effective pregnancy avoidance measures during the study period and ≥120 days after the last dose; Female patients with negative urine or serum pregnancy test results within 7 days or less before the first administration of the study drug;

• Have fully understood this study and voluntarily signed informed consent.

• Adequate organ and bone marrow function, meeting the following definitions:

1. Blood routine (no blood transfusion, no granulocyte colony stimulating factor [G-CSF], no other drug correction within 14 days before treatment);Absolute count of neutrophils (ANC) ≥1.5×109/L;Hemoglobin (HB) ≥9.0 g/dL;Platelet count (PLT) ≥80×109/L;

2. Blood biochemistry, serum creatinine (Cr) ≤ 1.5× upper limit of normal (ULN) or creatinine clearance ≥60 mL/min;Serum albumin ≥2.8g/dL, for patients with poor nutritional status before neoadjuvant therapy, patients who met the requirements through parenteral nutrition could also be included in the group;Total bilirubin (TBIL) ≤ 1.5×ULN;Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) level ≤2.5×ULN;

Exclusion Criteria:

• 1. Pregnant or lactating women;

• Patients with a known history of allergy to any investigative drug, similar drug or excipient;

• Patients with risk of massive gastrointestinal bleeding or gastrointestinal obstruction;

• Patients with a history of thromboembolism, except thrombosis caused by PICC;

• There are patients with active infection;

• Patients with unmanageable hypertension (systolic blood pressure ≥160 mmHg and diastolic blood pressure ≥90mmHg);

• Patients with brain metastases with clinical symptoms or imaging evidence;

• Contraindications exist in treatment with other chronic diseases;

• Patients with a history of immunotherapy-related myocarditis, pneumonia, colitis, hepatitis, nephritis, etc., with current AE ≥ grade 2;

• According to the evaluation criteria of NCI CTCAE version 5.0, there are patients with all kinds of toxicities ≥ grade 2 due to previous treatment;

• Other conditions that the researchers determined were not suitable for inclusion in the study.

• Received any antitumor therapy and participated in other clinical studies within 4 weeks before enrollment.