抗体-药物偶联物在弥漫性大b细胞淋巴瘤有效治疗中的潜力。

IF 3.6 3区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Gulrayz Ahmed, Mehdi Hamadani, Taha Al-Juhaishi
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引用次数: 0

摘要

抗体-药物偶联物(adc)是一类快速发展的抗癌药物,对包括弥漫性大b细胞淋巴瘤(DLBCL)在内的血液系统恶性肿瘤的治疗有重要影响。adc将细胞毒性药物(又称有效载荷)通过连接物与特定癌症抗原的单克隆抗体结合在一起。有效载荷包括微管干扰物或破坏DNA的化学物质。在与抗原结合后,ADC被内化,有效载荷被溶菌酶从ADC解离,并递送到预期的部位发挥细胞毒性作用。这种独特的分子设计可以更好地平衡功效和安全性。Loncastuximab tesirine和polatuzumab vedotin是美国批准用于治疗DLBCL的两种adc。涉及领域:本综述涵盖了这两种药物的疗效和安全性数据。我们将回顾新的基于adc的联合方案和正在开发的新结构。专家意见:adc对改善DLBCL患者的预后有显著影响。polatuzumab vedotin和loncastuximab tesirine都被确定为有用的治疗选择,polatuzumab vedotin目前被批准用于一线和复发/难治性环境,而loncastuximab tesirine被批准用于复发环境。adc具有良好的安全性,目前有更多的adc正在进行临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The potential of antibody-drug conjugates for effective therapy in diffuse large B-cell lymphoma.

Introduction: Antibody-drug conjugates (ADCs) are a rapidly evolving class of anti-cancer drugs with a significant impact on management of hematological malignancies including diffuse large B-cell lymphoma (DLBCL). ADCs combine a cytotoxic drug (a.k.a. payload) attached through a linker to a monoclonal antibody specific to a particular cancer antigen. Payloads include microtubule disruptors or DNA damaging chemicals. After attaching to the antigen, the ADCs are internalized, and the payload is dissociated from ADC by lysozymes and delivered to the intended site for exerting cytotoxic effects. This unique molecular design permits a better balance of efficacy and safety. Loncastuximab tesirine and polatuzumab vedotin are two ADCs approved in the U.S.A. for treatment of DLBCL.

Areas covered: This review covers the efficacy and safety data of these two drugs. We will review new ADC-based combination regimens and novel constructs in development.

Expert opinion: ADCs have made a significant impact in improving outcomes of DLBCL patients. Both polatuzumab vedotin and loncastuximab tesirine are established as useful therapeutics options, with polatuzumab vedotin currently approved in first line and relapsed/refractory setting, while loncastuximab tesirine is approved in relapsed setting. ADCs are effective with tolerable safety profile and currently many more ADCs are undergoing clinical trials.

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来源期刊
Expert Opinion on Biological Therapy
Expert Opinion on Biological Therapy 医学-生物工程与应用微生物
CiteScore
8.60
自引率
0.00%
发文量
96
审稿时长
3-8 weeks
期刊介绍: Expert Opinion on Biological Therapy (1471-2598; 1744-7682) is a MEDLINE-indexed, international journal publishing peer-reviewed research across all aspects of biological therapy. Each article is structured to incorporate the author’s own expert opinion on the impact of the topic on research and clinical practice and the scope for future development. The audience consists of scientists and managers in the healthcare and biopharmaceutical industries and others closely involved in the development and application of biological therapies for the treatment of human disease. The journal welcomes: Reviews covering therapeutic antibodies and vaccines, peptides and proteins, gene therapies and gene transfer technologies, cell-based therapies and regenerative medicine Drug evaluations reviewing the clinical data on a particular biological agent Original research papers reporting the results of clinical investigations on biological agents and biotherapeutic-based studies with a strong link to clinical practice Comprehensive coverage in each review is complemented by the unique Expert Collection format and includes the following sections: Expert Opinion – a personal view of the data presented in the article, a discussion on the developments that are likely to be important in the future, and the avenues of research likely to become exciting as further studies yield more detailed results; Article Highlights – an executive summary of the author’s most critical points.
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