Cutri-French Clare, Nasioudis Dimitrios, George Erin, Tanyi Janos L
Department of Obstetrics and Gynecology, University of Pennsylvania Health System, Philadelphia, PA 19104, USA.
Division of Gynecologic Oncology, University of Pennsylvania Health System, Philadelphia, PA 19104, USA.
Diagnostics (Basel). 2024 Apr 16;14(8):819. doi: 10.3390/diagnostics14080819.
The success of chimeric antigen receptor T-cell (CAR-T) therapies in the treatment of hematologic malignancies has led to the investigation of their potential in the treatment of solid tumors, including ovarian cancer. While the immunosuppressive microenvironment of ovarian cancer has been a barrier in their implementation, several early phase clinical trials are currently evaluating CAR-T cell therapies targeting mesothelin, folate receptor a, HER2, MUC16, and B7H3. Ongoing challenges include cytokine-associated and "on-target, off-tumor" toxicities, while most common adverse events include cytokine release syndrome, hemophagocytic lymphohistiocytosis/macrophage activation-like syndrome (HLH/MAS), and neurotoxicity. In the present review, we summarize the current status of CAR-T therapy in ovarian cancer and discuss future directions.
嵌合抗原受体T细胞(CAR-T)疗法在治疗血液系统恶性肿瘤方面的成功,引发了对其在治疗实体瘤(包括卵巢癌)中潜力的研究。虽然卵巢癌的免疫抑制微环境一直是其应用的障碍,但目前有几项早期临床试验正在评估靶向间皮素、叶酸受体α、HER2、MUC16和B7H3的CAR-T细胞疗法。持续存在的挑战包括细胞因子相关毒性和“靶向非肿瘤”毒性,而最常见的不良事件包括细胞因子释放综合征、噬血细胞性淋巴组织细胞增生症/巨噬细胞活化样综合征(HLH/MAS)和神经毒性。在本综述中,我们总结了CAR-T疗法在卵巢癌中的现状,并讨论了未来的方向。