2022
DOI: 10.1002/ajh.26823
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Belantamab mafodotin induces immunogenic cell death within 24 h post‐administration in newly diagnosed multiple myeloma patients

Abstract: Despite the outstanding progress in the clinical management of Multiple Myeloma (MM) over the last decades, the disease remains incurable with unavoidable patients' relapses. In this context, there is

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Cited by 6 publications
(5 citation statements)
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“…GSK2857916 is an FDA-approved agent available for MM, which has been found to activate the PERK and increase phosphorylation of elF2 α to induce ER stress, exposing CRT, HSP70, HSP90, and IL8 with increased ATP and HMGB1 to trigger ICD in NCI-H929 cells, improving MM therapy in vitro and in vivo 436 . Similarly, belantamab mafodotin, a recent FDA-approved agent available for MM, has been found to increase CRT and HMGB1 to trigger ICD, improving MM therapy 437 . Imiquimod, an FDA-approved agent available for skin malignancies and viral warts, has been reported to produce ROS and activate the PERK/elF2 α axis to induce ER stress, leading to the release of CRT, ATP, and HMGB1 to trigger ICD in B16F10 cells, and slowing tumor growth in the B16F10 syngeneic model 438 .…”
Section: Targeting Non-apoptotic Rcd Subroutines With Small-molecule ...mentioning
confidence: 99%
“…GSK2857916 is an FDA-approved agent available for MM, which has been found to activate the PERK and increase phosphorylation of elF2 α to induce ER stress, exposing CRT, HSP70, HSP90, and IL8 with increased ATP and HMGB1 to trigger ICD in NCI-H929 cells, improving MM therapy in vitro and in vivo 436 . Similarly, belantamab mafodotin, a recent FDA-approved agent available for MM, has been found to increase CRT and HMGB1 to trigger ICD, improving MM therapy 437 . Imiquimod, an FDA-approved agent available for skin malignancies and viral warts, has been reported to produce ROS and activate the PERK/elF2 α axis to induce ER stress, leading to the release of CRT, ATP, and HMGB1 to trigger ICD in B16F10 cells, and slowing tumor growth in the B16F10 syngeneic model 438 .…”
Section: Targeting Non-apoptotic Rcd Subroutines With Small-molecule ...mentioning
confidence: 99%
“…The production of ROS not only facilitates the direct eradication of tumor cells but also enhances the release of antigens, including calreticulin (CRT), heat shock proteins (HSPs), adenosine triphosphate (ATP), and high-mobility group box 1 (HMGB1). These antigens are then recognized by the immune system, further stimulating an immune reaction against the tumor [54][55][56][57].…”
Section: Photodynamic Therapymentioning
confidence: 99%
“… 18 DAMPs enhance the immunogenicity of tumor cells, promote the recognition and antigen-presenting ability of DCs to cancer cells, stimulate DCs maturation, and mature DCs activate specific T cells to attack cancer cells. Currently, merely a few clinically relevant drugs have been demonstrated to trigger true ICD, such as adriamycin and onioncyclines, oxaliplatin, 19 lurbinectedin, 20 and belantamab mafodotin, 21 , 22 which have been employed in the treatment of several malignancies. Previous studies demostrated that Oxaliplatin causes ICD in HCC and has a synergistic impact when combined with anti-PD-1 antibodies.…”
Section: Introductionmentioning
confidence: 99%