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This combination neoadjuvant therapy regimen consists of **ipromlimab** (an anti-CTLA-4 monoclonal antibody), **tuvonralimab** (a bifunctional antibody targeting PD-1 and CTLA-4), **albumin-bound paclitaxel** (a microtubule inhibitor), and **nedaplatin** (a platinum-based DNA alkylating agent). The regimen is currently being investigated in a Phase II clinical trial sponsored by **Sun Yat-sen University** for the treatment of locally advanced resectable esophageal squamous cell carcinoma (ESCC). Ipromlimab enhances T-cell activation by blocking the CTLA-4 checkpoint, while tuvonralimab provides dual blockade of the PD-1 and CTLA-4 pathways. The addition of chemotherapy (paclitaxel and nedaplatin) is intended to provide synergistic anti-tumor activity, potentially increasing the pathological complete response (pCR) rate and improving surgical outcomes in the neoadjuvant setting.
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