B7-H3 Inhibitors in Oncology Clinical Trials: A Review

Kavanya Feustel, Jared Martin, G. Falchook
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Abstract

B7-H3 is a transmembrane receptor highly prevalent on malignant cells and plays an important role in adaptive immunity that is not fully elucidated. Targeted B7-H3 inhibitors, including antibody-drug conjugates, radioimmunotherapy, and monoclonal antibodies, are a new class of antineoplastic agents showing promising preliminary clinical efficacy, observed with several of these agents against multiple tumor types. Particularly promising treatments are enoblituzumab for prostate cancer, 131I-omburtamab for central nervous system malignancies, and HS-20093 for small-cell lung cancer but further studies are warranted. There are clinical trials on the horizon that have not yet enrolled patients examining chimeric antigen receptor T-cell therapies, bi- and tri-specific killer engagers, and dual-affinity retargeting proteins. These data will be telling of the efficacy of B7-H3 inhibitors in both hematologic and solid malignancies. This study aimed to compile available results of B7-H3 inhibitors in oncology clinical trials.
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肿瘤临床试验中的 B7-H3 抑制剂:综述
B7-H3 是一种跨膜受体,在恶性细胞中非常普遍,在适应性免疫中发挥着尚未完全阐明的重要作用。靶向 B7-H3 抑制剂,包括抗体-药物共轭物、放射免疫疗法和单克隆抗体,是一类新型抗肿瘤药物,对多种肿瘤类型都有初步临床疗效。治疗前列腺癌的依诺布珠单抗、治疗中枢神经系统恶性肿瘤的 131I-omburtamab 和治疗小细胞肺癌的 HS-20093,尤其具有治疗前景,但仍需进一步研究。还有一些尚未招募患者的临床试验正在进行中,这些临床试验包括嵌合抗原受体 T 细胞疗法、双特异性和三特异性杀伤性参与因子以及双亲和再靶向蛋白。这些数据将说明B7-H3抑制剂在血液和实体恶性肿瘤中的疗效。本研究旨在汇编B7-H3抑制剂在肿瘤临床试验中的现有结果。
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CiteScore
2.40
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0.00%
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17
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