Experimental Medicine Unit, Oncology R&D, GlaxoSmithKline, Collegeville, Pennsylvania.
Immuno-Oncology and Combinations RU, Oncology R&D, GlaxoSmithKline, Collegeville, Pennsylvania.
Mol Cancer Ther. 2021 Oct;20(10):1941-1955. doi: 10.1158/1535-7163.MCT-21-0035. Epub 2021 Jul 12.
B-cell maturation antigen (BCMA) is an attractive therapeutic target highly expressed on differentiated plasma cells in multiple myeloma and other B-cell malignancies. GSK2857916 (belantamab mafodotin, BLENREP) is a BCMA-targeting antibody-drug conjugate approved for the treatment of relapsed/refractory multiple myeloma. We report that GSK2857916 induces immunogenic cell death in BCMA-expressing cancer cells and promotes dendritic cell activation and GSK2857916 treatment enhances intratumor immune cell infiltration and activation, delays tumor growth, and promotes durable complete regressions in immune-competent mice bearing EL4 lymphoma tumors expressing human BCMA (EL4-hBCMA). Responding mice are immune to rechallenge with EL4 parental and EL4-hBCMA cells, suggesting engagement of an adaptive immune response, immunologic memory, and tumor antigen spreading, which are abrogated upon depletion of endogenous CD8 T cells. Combinations with OX40/OX86, an immune agonist antibody, significantly enhance antitumor activity and increase durable complete responses, providing a strong rationale for clinical evaluation of GSK2857916 combinations with immunotherapies targeting adaptive immune responses, including T-cell-directed checkpoint modulators.
B 细胞成熟抗原(BCMA)是一种在多发性骨髓瘤和其他 B 细胞恶性肿瘤中高度表达的分化浆细胞上的有吸引力的治疗靶点。GSK2857916(belantamab mafodotin,BLENREP)是一种针对 BCMA 的抗体药物偶联物,已被批准用于治疗复发性/难治性多发性骨髓瘤。我们报告 GSK2857916 在表达 BCMA 的癌细胞中诱导免疫原性细胞死亡,并促进树突状细胞激活和 GSK2857916 治疗增强肿瘤内免疫细胞浸润和激活,延迟肿瘤生长,并促进在表达人 BCMA(EL4-hBCMA)的免疫活性小鼠中产生持久的完全消退。应答小鼠对 EL4 亲本和 EL4-hBCMA 细胞的再挑战具有免疫力,表明适应性免疫反应、免疫记忆和肿瘤抗原扩散的参与,而在耗尽内源性 CD8 T 细胞后则被阻断。与 OX40/OX86(一种免疫激动剂抗体)联合使用可显著增强抗肿瘤活性并增加持久的完全缓解率,为临床评估 GSK2857916 与针对适应性免疫反应的免疫疗法(包括 T 细胞定向检查点调节剂)的联合治疗提供了强有力的依据。