Belantamab Mafodotin 与复发/难治性多发性骨髓瘤:这不是游戏结束

IF 1.7 4区 医学 Q3 HEMATOLOGY
Acta Haematologica Pub Date : 2024-01-01 Epub Date: 2021-11-26 DOI:10.1159/000521112
Annalisa Condorelli, Bruno Garibaldi, Caterina Gagliano, Alessandra Romano, Vittorio Del Fabro, Nunziatina Laura Parrinello, Antonio Longo, Sebastiano Cosentino, Francesco Di Raimondo, Concetta Conticello
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引用次数: 0

摘要

虽然多发性骨髓瘤(MM)的治疗范围不断扩大,但这种疾病总是容易复发。为了获得深入持久的治疗效果,每次复发都需要采用新的治疗策略。近年来,即使是重症患者也出现了新的治疗方案。在复发/难治(RRMM)病例中,新型、耐受性好且高效的疗法目前代表着真正的希望。贝仑单抗-马福多汀(Belantamab mafodotin,BLENREP™)是一种首创的单克隆抗体-药物共轭物(ADC),其靶点是B细胞成熟抗原(BCMA)与细胞毒性微管抑制剂单甲基乌司他丁 F(MMAF)共轭。在这里,我们介绍两例接受过大量预处理的 RRMM 患者,他们接受了贝兰单抗马福多汀的治疗,至少获得了部分应答。患者耐受性良好,治疗仍在继续。这是贝仑单抗马福多汀在对照临床试验之外的实际临床应用的罕见报告,提供了这类抗骨髓瘤新药的疗效和安全性方面的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Belantamab Mafodotin and Relapsed/Refractory Multiple Myeloma: This Is Not Game Over.

Although the therapeutic landscape for multiple myeloma (MM) has expanded, the disease always tends to relapse. In an attempt to obtain deep and durable responses, each relapse requires the use of a new strategy. In recent years, new treatment options have emerged, even for heavily treated patients. Novel, well-tolerated, and highly effective therapies in the relapsed/refractory (RRMM) setting currently represent a real hope. Belantamab mafodotin (BLENREP™) is a first-in-class monoclonal antibody-drug conjugate whose target is B-cell maturation antigen conjugated to the cytotoxic microtubule inhibitor monomethyl auristatin F. Here, we present two cases of heavily pre-treated RRMM patients that were favorably treated with belantamab mafodotin, obtaining at least a partial response. Treatment was well tolerated and is ongoing. This is a rare report on real life clinical use of belantamab mafodotin outside of controlled clinical trials and provides information on efficacy and safety of this anti-myeloma new class of drugs.

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来源期刊
Acta Haematologica
Acta Haematologica 医学-血液学
CiteScore
4.90
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: ''Acta Haematologica'' is a well-established and internationally recognized clinically-oriented journal featuring balanced, wide-ranging coverage of current hematology research. A wealth of information on such problems as anemia, leukemia, lymphoma, multiple myeloma, hereditary disorders, blood coagulation, growth factors, hematopoiesis and differentiation is contained in first-rate basic and clinical papers some of which are accompanied by editorial comments by eminent experts. These are supplemented by short state-of-the-art communications, reviews and correspondence as well as occasional special issues devoted to ‘hot topics’ in hematology. These will keep the practicing hematologist well informed of the new developments in the field.
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