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胸膜间皮瘤:新兴药物靶点的快照及非手术治疗进展的机会。

Pleural mesothelioma: a snapshot of emerging drug targets and opportunities for non-surgical therapeutic advancement.

机构信息

Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, Université Paris Cité, Functional Genomics of Solid Tumors Laboratory, Paris, France.

GRC OncoThoParisEst, Service de Pneumologie, Centre Hospitalier IntercommunaI, UPEC, Créteil, France.

出版信息

Expert Opin Ther Targets. 2023 Jul-Dec;27(11):1059-1069. doi: 10.1080/14728222.2023.2277224. Epub 2023 Dec 7.

Abstract

INTRODUCTION

Pleural mesothelioma is a rare and aggressive cancer originating in the pleura, with a devastating prognosis and limited treatment options. There have been significant advancements in the management of this disease in recent years. Since 2021, nivolumab and ipilimumab immune checkpoint inhibitors have become the new standard of care for first-line treatment of pleural mesothelioma.

AREAS COVERED

While a combination of chemotherapy and immune checkpoint inhibitors appears to be the next step, targeted therapies are emerging thanks to our understanding of the oncogenesis of pleural mesothelioma. Moreover, several new strategies are currently being investigated, including viral therapy, antibody-drug conjugates, and even cell therapies with CAR-T cells or dendritic cells. In this review, we will explore the various future opportunities that could potentially transform patients' lives in light of the clinical trials that have been conducted.

EXPERT OPINION

Future clinical studies aim to rebiopsy patients after disease progression to identify new molecular alterations and to be associated with ancillary studies, guiding subsequent therapy decisions. Predicting and investigating treatment resistance mechanisms will lead to innovative approaches and improved treatment outcomes.

摘要

简介

胸膜间皮瘤是一种罕见且侵袭性的癌症,起源于胸膜,预后极差,治疗选择有限。近年来,胸膜间皮瘤的治疗取得了重大进展。自 2021 年以来,纳武利尤单抗和伊匹单抗免疫检查点抑制剂已成为治疗胸膜间皮瘤一线治疗的新标准。

涵盖领域

虽然化疗和免疫检查点抑制剂的联合似乎是下一步,但由于我们对胸膜间皮瘤发生机制的理解,靶向疗法正在出现。此外,目前正在研究几种新策略,包括病毒疗法、抗体药物偶联物,甚至使用 CAR-T 细胞或树突状细胞的细胞疗法。在这篇综述中,我们将探讨根据已进行的临床试验,未来可能改变患者生活的各种机会。

专家意见

未来的临床研究旨在在疾病进展后对患者进行再次活检,以识别新的分子改变,并与辅助研究相结合,指导后续的治疗决策。预测和研究治疗耐药机制将导致创新方法和改善治疗结果。

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