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Drugs. 2022 Oct;82(15):1557-1564. doi: 10.1007/s40265-022-01787-z.
Pucotenlimab (Puyouheng™) is a humanised immunoglobulin (Ig) G4 monoclonal antibody (mAb) being developed by Lepu Biopharma for the treatment of solid tumours, including gastrointestinal cancer, metastatic melanoma, liver cancer, bladder cancer, non-small cell lung cancer and breast cancer. Pucotenlimab binds to PD-1 and blocks its interaction with its ligands, PD-L1 and PD-L2, thereby restoring the ability of immune cells to target cancer cells. In July 2022, pucotenlimab received conditional first approval in China for the treatment of patients with unresectable or metastatic microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) solid tumours, including patients with advanced colorectal cancer who have experienced disease progression after previous therapy with fluorouracil, oxaliplatin and irinotecan, as well as patients with other advanced solid tumours who have experienced disease progression after previous first-line therapy and have no satisfactory treatment alternatives. In September 2022, pucotenlimab was approved in China for the treatment of unresectable or metastatic melanomas after the failure of previous systemic therapy. This article summarizes the milestones in the development of pucotenlimab leading to the first approval for the treatment of MSI-H/dMMR advanced solid tumours.
普特利单抗(Puyouheng™)是由丽珠单抗开发的一种人源化 IgG4 单克隆抗体(mAb),用于治疗实体瘤,包括胃肠道癌、转移性黑色素瘤、肝癌、膀胱癌、非小细胞肺癌和乳腺癌。普特利单抗与 PD-1 结合并阻断其与配体 PD-L1 和 PD-L2 的相互作用,从而恢复免疫细胞靶向癌细胞的能力。2022 年 7 月,普特利单抗在中国获得有条件的首次批准,用于治疗不可切除或转移性微卫星不稳定高(MSI-H)或错配修复缺陷(dMMR)的实体瘤患者,包括既往氟尿嘧啶、奥沙利铂和伊立替康治疗后疾病进展的晚期结直肠癌患者,以及既往一线治疗后疾病进展且无满意治疗选择的其他晚期实体瘤患者。2022 年 9 月,普特利单抗在中国获得批准,用于治疗既往全身治疗失败的不可切除或转移性黑色素瘤。本文总结了普特利单抗开发的里程碑事件,导致其首次批准用于治疗 MSI-H/dMMR 晚期实体瘤。