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This drug combination is an investigational multi-agent regimen being evaluated for the treatment of metastatic colorectal cancer (mCRC), particularly in patients who have progressed after second-line standard therapies. The regimen consists of **fruquintinib**, a highly selective oral tyrosine kinase inhibitor of VEGFR 1, 2, and 3; an **immune checkpoint inhibitor** (typically targeting the PD-1/PD-L1 pathway); **trifluridine/tipiracil** (TAS-102), an oral cytotoxic chemotherapy; and **bevacizumab**, a monoclonal antibody that targets VEGF-A. The rationale behind this combination is to leverage the synergistic effects of anti-angiogenesis (via fruquintinib and bevacizumab) and cytotoxic chemotherapy (TAS-102) to modulate the tumor microenvironment, potentially converting 'cold' microsatellite stable (MSS) tumors into 'hot' tumors that are more responsive to immune checkpoint blockade. This specific regimen is being studied in a Phase Ib/II clinical trial sponsored by the Tianjin Medical University Cancer Institute and Hospital.
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