解锁派姆单抗加维多单抗在尿路上皮癌患者中的活性机制

IF 4.9 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Matteo Santoni, Alessandro Rizzo, Francesco Massari
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引用次数: 0

摘要

导读:尿路上皮癌(UC)通常与晚期疾病患者预后不良相关。强有力的生物学原理支持将抗体-药物偶联物(adc)与免疫治疗相结合的研究,以克服耐药性的发生并改善患者的预后。所涵盖的领域:在这篇综述中,我们阐述了派姆单抗和维多汀(EV)的作用机制以及它们在mUC患者中协同作用的免疫和生物学原理。专家意见:EV联合派姆单抗的结果代表了mUC患者治疗方案中的一束光。深入了解这些药物协同作用的机制对于减少耐药和进一步改善mUC患者的预后至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unlocking the mechanisms underlying the activity of pembrolizumab plus enfortumab vedotin in patients with urothelial carcinoma.

Introduction: Urothelial carcinoma (UC) is frequently associated with a poor prognosis in patients with advanced disease. A strong biological rationale supports the investigation of combining antibody-drug conjugates (ADCs) with immunotherapy to overcome the occurrence of resistance and improve patient outcomes.

Areas covered: In this review, we illustrate the mechanisms of action of pembrolizumab and enfortumab vedotin (EV) and the immune and biological rationales underlying their synergy in mUC patients.

Expert opinion: The results of the combination of EV and pembrolizumab represent a ray of light in the therapeutic scenario of mUC patients. A deeper understanding of the mechanisms underlying the synergistic effects of these agents will be crucial to reduce drug-resistance and further improve the outcome of mUC patients.

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来源期刊
CiteScore
10.00
自引率
0.00%
发文量
71
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Investigational Drugs (ISSN 1354-3784 [print], 1744-7658 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles and original papers on drugs in preclinical and early stage clinical development, providing expert opinion on the scope for future development. The Editors welcome: Reviews covering preclinical through to Phase II data on drugs or drug classes for specific indications, and their potential impact on future treatment strategies Drug Evaluations reviewing the clinical and pharmacological data on a particular drug Original Research papers reporting the results of clinical investigations on agents that are in Phase I and II clinical trials The audience consists of scientists, managers and decision-makers in the pharmaceutical industry, and others closely involved in R&D.
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