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解析多发性骨髓瘤对 SINE、T 细胞衔接疗法及 CELMoDs 的耐药机制复杂性:综合综述

英文原题:Unraveling the complexity of drug resistance mechanisms to SINE, T cell-engaging therapies and CELMoDs in multiple myeloma: a comprehensive review.

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Unraveling the complexity of drug resistance mechanisms to SINE, T cell-engaging therapies and CELMoDs in multiple myeloma: a comprehensive review.

PubMed 2024/06/26(内容时间) Cancer Drug Resist Q1 · IF 7.6(JCR 2025)

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中文摘要

尽管过去二十年对多发性骨髓瘤生物学认识加深并开发了新疗法,该病仍不可治愈。选择性核输出抑制剂、调节泛素通路的CELMoD药物及T细胞重定向治疗等新机制显著改善患者结局,但耐药仍是主要问题。本文总结这些治疗的现有数据及其耐药机制。理解耐药对于开发克服治疗失败的策略、进一步改善疗效至关重要。

展开英文摘要原文

Despite significant advances in the understanding of multiple myeloma (MM) biology and the development of novel treatment strategies in the last two decades, MM is still an incurable disease. Novel drugs with alternative mechanisms of action, such as selective inhibitors of nuclear export (SINE), modulators of the ubiquitin pathway [cereblon E3 ligase modulatory drugs (CELMoDs)], and T cell redirecting (TCR) therapy, have led to significant improvement in patient outcomes.

However, resistance still emerges, posing a major problem for the treatment of myeloma patients. This review summarizes current data on treatment with SINE, TCR therapy, and CELMoDs and explores their mechanism of resistance. Understanding these resistance mechanisms is critical for developing strategies to overcome treatment failure and improve therapeutic outcomes.

论文信息

作者
Schütt J、Brinkert K、Plis A、Schenk T、Brioli A
单位
Clinic for Hematology, Hemostasis, Oncology and Stem cell transplantation, Hannover Medical School, Hannover 30625, Germany.Germany
文献类型
综述
期刊
Cancer drug resistance (Alhambra, Calif.)2024
原文标识
PubMed 39050883 · DOI 10.20517/cdr.2024.39