Belantamab Mafodotin (GSK2857916) Drives Immunogenic Cell Death and Immune-mediated Antitumor Responses In Vivo.
Rocio Montes de OcaAlireza S AlaviNick VitaliSabyasachi BhattacharyaChristina BlackwellKrupa PatelLaura Seestaller-WehrHeather KaczynskiHong ShiEric DobrzynskiLeslie A ObertLyuben TsvetkovDavid C CooperHeather JacksonPaul BojczukSabrina ForveilleOliver KeppAllan SauvatGuido KroemerMark Creighton-GutteridgeJingsong YangChris HopsonNiranjan YanamandraChristopher SheltonPatrick MayesJoanna OpalinskaMary BarnetteRoopa SrinivasanJames SmothersAxel HoosPublished in: Molecular cancer therapeutics (2021)
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 in vitro and in vivo 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.
Keyphrases
- cell cycle arrest
- pi k akt
- cell death
- multiple myeloma
- immune response
- signaling pathway
- induced apoptosis
- dendritic cells
- cancer therapy
- endothelial cells
- cell proliferation
- diffuse large b cell lymphoma
- clinical trial
- acute lymphoblastic leukemia
- small molecule
- type diabetes
- insulin resistance
- oxidative stress
- inflammatory response
- induced pluripotent stem cells
- cell cycle