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This neoadjuvant chemotherapy regimen is a combination therapy being evaluated for the treatment of locally advanced or fertility-desiring cervical cancer. It consists of the bifunctional biologic QL1706 (iparomlimab and tuvonralimab), which simultaneously targets the immune checkpoint proteins PD-1 and CTLA-4, combined with the standard chemotherapy agents paclitaxel and cisplatin. QL1706, developed by Qilu Pharmaceutical, is designed to enhance tumor-specific immune activation by dual blockade of inhibitory pathways on T-lymphocytes. Paclitaxel acts as a microtubule stabilizer, while cisplatin is a platinum-based DNA-damaging agent. The regimen is currently being studied in a Phase 2 umbrella trial (NCT06878222) sponsored by the Obstetrics & Gynecology Hospital of Fudan University to shrink tumors prior to surgery and potentially improve fertility-sparing outcomes.
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