bcma暴露的复发/难治性多发性骨髓瘤的新疗法:抗bcma治疗难治性患者

E. Golden, S. Ingram, H. Schade, J. Matous, T. Gregory
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引用次数: 1

摘要

多发性骨髓瘤(MM)是一种由骨髓中单克隆浆细胞恶性过度生长引起的血液学恶性肿瘤。预计美国每年将有近3.5万例新病例。在过去的二十年里,随着许多新药及其组合的批准,有了许多临床进展,这提高了生存率。尽管如此,MM仍然无法治愈,复发/难治性MM患者仍然脆弱。嵌合抗原受体t细胞(CAR-T)疗法的发展已经显示出利用几种靶抗原的有希望的结果;值得注意的是,b细胞成熟抗原(BCMA)最为突出,因为它在恶性浆细胞表面普遍表达。虽然抗bcma CAR-T疗法令人鼓舞,但大多数患者最终会复发,需要进一步治疗。随着这些患者通过标准治疗取得进展,以及最近通过新型抗bcma CAR-T疗法,我们面临着探索新的治疗方案来挑战他们的疾病。在这篇综述中,我们讨论了抗bcma治疗的不同耐药机制,抗bcma靶向治疗在MM中的有效再治疗,以及利用其他新靶点治疗通过抗bcma治疗进展的患者的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel Therapies in BCMA-exposed Relapsed/Refractory Multiple Myeloma: The Anti-BCMA Therapy-refractory Patient
Multiple myeloma (MM) is a haematologic malignancy resulting from the malignant overgrowth of monoclonal plasma cells in the bone marrow. Nearly 35,000 new cases are expected in the USA each year. In the last two decades there have been many clinical advances with the approvals of many new drugs and their combinations, which have improved survival statistics. Despite this, MM remains incurable, and patients with relapsed/refractory MM remain vulnerable. The development of chimeric antigen receptor T-cell (CAR-T) therapy has shown promising results utilizing several target antigens; of note, B-cell maturation antigen (BCMA) is most prominent, due to its universal expression on the surface of malignant plasma cells. While anti-BCMA CAR-T therapies are inspiring, most patients eventually relapse and require further treatment. With these patients progressing through standard-of-care therapies, and more recently through novel anti-BCMA CAR-T therapies, we are faced with exploring novel treatment regimens to challenge their diseases. In this review, we discuss the different mechanisms of resistance to anti-BCMA therapies, effective retreatment with anti-BCMA-targeted therapies in MM, and advances in therapies utilizing other novel targets for patients who have progressed through anti-BCMA treatment.
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