Trifluridine and Tipiracil Hydrochloride Tablets, Bevacizumab and Sintilimab With/Without Involved Lesions Irradiation as 3rd- or Later-line Therapy for Advanced MSS/pMMR Colorectal Cancer: a Phase 2, Double Cohort Clinical Trial

Brief Summary

Detailed Description

Colorectal cancer ranks among the top three in terms of incidence and mortality of tumors in the world, and it is a major load on the global and China's medical and health care services. In China, about 60% of the patients are in relatively advanced stage at the time of diagnosis, and the 5-year overall survival rate is less than 15%, which is a serious threat to people's life safety. The treatment of advanced metastatic colorectal cancer which comprises of chemotherapy, mainly including oxaliplatin, irinotecan and 5-fluorouracil drugs, and target therapy, mainly including anti-EGFR and anti-vascular drugs, has led to a significant prolongation of the overall survival of patients with advanced colorectal cancer, up to about 30 months. In terms of the chemotherapy regimens for advanced colorectal cancer, oxaliplatin and irinotecan based chemotherapy regimens are mutual first and second line, and third line and above after failure, there are some limited options available, but there are obvious limitations. Anti-VEGFR TKI-targeted therapies such as regorafenib and furaquintinib, although among the commonly available treatment options for third-line treatment of advanced colorectal cancer, have very limited efficacy rates, all less than 5%, and patients' survival time has been prolonged by only a very limited 1-2 months. Studies in the last two years have found that combining immunotherapy with an anti-VEGFR TKI can further improve efficacy, and the REGONIVO study assessed the efficacy and safety of regorafenib versus nabumab in patients with advanced colorectal cancer, and achieved an ORR of up to 36%. However, subsequent clinical studies could not achieve such favorable outcomes, and it is hypothesized that this may be related to the small percentage of liver metastases in the patients enrolled in this study. Several clinical studies have shown that anti-VEGFR TKIs combined with PD-1 monoclonal antibody have an efficacy rate of 10%-20%, which is still very limited, and more effective therapeutic strategies need to be determined. Trifluridine-tipyrimidine is a new oral cytotoxic chemotherapy drug. Trifluridine tepipiridine consists of FTD and TPI, FTD can replace thymine into the DNA double-stranded to play an anti-tumor effect, while TPI can inhibit thymidine phosphorylase activity, prevent FTD degradation to maintain sufficient blood concentration to play a potentiating role. Bevacizumab is a recombinant humanized immunoglobulin G1 monoclonal antibody, which can effectively neutralize the vascular endothelial cell growth factor (VEGF) and inhibit its binding to the receptor, thus inhibiting its biological effects and achieving the effect of inhibiting tumor angiogenesis. Bevacizumab in combination with chemotherapy is currently used in multiple lines of treatment for advanced colorectal cancer. Trifluridine tepicillin combined with bevacizumab can appropriately improve the survival time of colorectal cancer patients, Pfeiffer et al. conducted a phase II clinical trial showed that trifluridine tepicillin combined with bevacizumab significantly prolonged the survival of the patients compared with single-agent trifluridine tepicillin, but the survival time of the combination group was still limited, with the median progression-free survival of only 4.6 months, and the median overall survival was only 9.6 months. The median overall survival was only 9.4 months, which still needs further improvement. The most common sites of metastatic colorectal metastases are liver, lung, and bone, respectively, and some studies have found that intensive treatment of metastases improves overall survival. In surgically resected liver metastases, the 5-year overall survival rate for colorectal cancer patients ranges from 50% to 60%. However, in some cases, many patients with metastases cannot be treated with surgery due to the size and location of the tumor, and palliative radiotherapy can be used not only as an alternative to surgery, but also as a complementary treatment. In addition, radiotherapy can eliminate residual lesions or positive margins after surgical resection and reduce the risk of local recurrence. Besides, radiotherapy has been shown to activate the immune system, and the immunomodulation by radiotherapy is related to the dose and segmentation. In vitro studies have shown that a single high dose (10Gy) is more likely to induce cellular DNA damage and produce tumor neoantigens, and to activate the rapamycin pathway, which accelerates protein degradation and presentation, than a single low dose of radiation. High-dose exposures tend to induce the expression or release of immunogenic cell death-associated molecules. Compared with single high-dose irradiation, multiple high-divided radiotherapy is more likely to induce systemic immune effects. Several animal studies have found that high-divided irradiation of 8Gy×3F, 6Gy×5F, 5Gy×3F and 5Gy×4F is more likely to induce tumor growth inhibition in non-irradiated areas. Analysis of tumor-draining lymph nodes revealed that 5Gy×3F was more likely to stimulate immune cell activation than 15Gy×1F. Given that T cells are very sensitive to radiation, large fractionated radiotherapy is more favorable for lymphocyte protection. In summary, for patients with advanced colorectal cancer, this study proposes to use a three-drug combination of trifluorouracil tepidopyrimidine, bevacizumab, and sindilizumab. For patients who meet the indications for radiotherapy, this study proposes to combine palliative radiotherapy of the lesion with the three-drug treatment. And to explore the efficacy and safety of the new combination regimen in this type of patients.

Primary Outcomes

Secondary Outcomes

• Disease control rate (DCR)(Baseline, 6-8 weeks after treatment complete)
• Progression-free survival (PFS)(month 6, year 1, year 2)
• Overall survival (OS)(month 6, year 1, year 2)
• Treatment related toxicity(Baseline, 6-8 weeks after treatment complete)