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抗体药物偶联物:患者与治疗选择

Antibody-Drug Conjugates: Patient and Treatment Selection.

作者信息

Makawita Shalini, Meric-Bernstam Funda

机构信息

Division of Cancer Medicine, University of Texas MD Anderson Cancer Center, Houston, TX.

Department of Investigational Cancer Therapeutics, University of Texas MD Anderson Cancer Center, Houston, TX.

出版信息

Am Soc Clin Oncol Educ Book. 2020 Mar;40:1-10. doi: 10.1200/EDBK_280775.

Abstract

Antibody-drug conjugates (ADCs) are a promising drug platform designed to enhance the therapeutic index and minimize the toxicity of anticancer agents. ADCs have experienced substantial progress and technological growth over the past decades; however, several challenges to patient selection and treatment remain. Methods to optimally capture all patients who may benefit from a particular ADC are still largely unknown. Although target antigen expression remains a biomarker for patient selection, the impact of intratumor heterogeneity on antigen expression, as well as the dynamic changes in expression with treatment and disease progression, are important considerations in patient selection. Better understanding of these factors, as well as minimum levels of target antigen expression required to achieve therapeutic efficacy, will enable further optimization of selection strategies. Other important considerations include understanding mechanisms of primary and acquired resistance to ADCs. Ongoing efforts in the design of its constituent parts to possess the intrinsic ability to overcome these mechanisms, including use of the "bystander effect" to enhance efficacy in heterogeneous or low target antigen-expressing tumors, as well as modulation of the chemical and immunophenotypic properties of antibodies and linker molecules to improve payload sensitivity and therapeutic efficacy, are under way. These strategies may also lead to improved safety profiles. Similarly, combination strategies using ADCs with other cytotoxic or immunomodulatory agents are also under development. Great strides have been made in ADC technology. With further refinements, this therapeutic modality has the potential to make an important clinical impact on a wider range of tumor types.

摘要

抗体药物偶联物(ADCs)是一种很有前景的药物平台,旨在提高治疗指数并将抗癌药物的毒性降至最低。在过去几十年中,ADCs取得了显著进展和技术发展;然而,在患者选择和治疗方面仍存在一些挑战。如何最佳地筛选出所有可能从特定ADC中获益的患者的方法在很大程度上仍不为人知。尽管靶抗原表达仍然是患者选择的生物标志物,但肿瘤内异质性对抗原表达的影响,以及随着治疗和疾病进展表达的动态变化,是患者选择中的重要考虑因素。更好地理解这些因素以及实现治疗效果所需的靶抗原表达的最低水平,将有助于进一步优化选择策略。其他重要考虑因素包括了解对ADCs的原发性和获得性耐药机制。目前正在努力设计其组成部分,使其具有克服这些机制的内在能力,包括利用“旁观者效应”来提高在异质性或低靶抗原表达肿瘤中的疗效,以及调节抗体和连接分子的化学和免疫表型特性以提高有效载荷敏感性和治疗效果。这些策略也可能导致安全性的改善。同样,将ADCs与其他细胞毒性或免疫调节药物联合使用的策略也在开发中。ADCs技术已经取得了巨大进展。随着进一步完善,这种治疗方式有可能对更广泛的肿瘤类型产生重要的临床影响。

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