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This is a combination regimen consisting of four drugs: - **Tislelizumab** is a humanized IgG4 monoclonal antibody that targets programmed death receptor 1 (PD-1), blocking its interaction with PD-L1 and PD-L2 to restore T-cell function and promote immune-mediated antitumor activity. Developed by BeiGene, it is approved in several indications including urothelial carcinoma and esophageal squamous cell carcinoma[6][9]. - **Cisplatin** is a platinum-based chemotherapy agent that forms DNA crosslinks, leading to apoptosis of rapidly dividing cells. - **Gemcitabine** is a nucleoside analog used as chemotherapy; it inhibits DNA synthesis by incorporation into DNA strands during replication. - **Trilaciclib** is an intravenous cyclin-dependent kinase 4/6 (CDK4/6) inhibitor developed by G1 Therapeutics; it transiently arrests hematopoietic stem/progenitor cells in the G1 phase to protect them from chemotherapy-induced damage. The three-drug combination of tislelizumab, cisplatin, and gemcitabine has been studied extensively as first-line or adjuvant therapy for muscle-invasive urothelial carcinoma (MIUC), upper tract urothelial carcinoma (UTUC), and metastatic bladder cancer[1][2][3][4][8]. The addition of trilaciclib aims to reduce myelosuppression caused by cytotoxic agents but has not been widely reported in published clinical trials with this exact quadruple regimen.
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