What’s the latest with investigational drugs for soft tissue sarcoma?

医学 软组织肉瘤 内科学 粘液样脂肪肉瘤 肿瘤科 滑膜肉瘤 临床试验 蒽环类 肉瘤 病理 癌症 脂肪肉瘤 乳腺癌
作者
Elena Cojocaru,Andrea Napolitano,Cyril Fisher,Paul H. Huang,Robin L. Jones,Khin Thway
出处
期刊:Expert Opinion on Investigational Drugs [Taylor & Francis]
卷期号:31 (11): 1239-1253 被引量:4
标识
DOI:10.1080/13543784.2022.2152324
摘要

Introduction Despite extensive research undertaken in the past 20–30 years, the treatment for soft tissue sarcoma (STS) has remained largely the same, with anthracycline-based chemotherapy remaining the first choice for treating advanced or metastatic STS.Areas covered This review focuses on newly approved drugs for STS and current research directions, including recent results of late-phase trials in patients with STS. We cover several different histological subtypes, and we discuss the role of adoptive cell transfer (ACT) therapies for the treatment of synovial and myxoid/round cell (high-grade myxoid) liposarcoma, one of the most promising areas of treatment development to date. We searched clinicaltrials.gov and pubmed.ncbi.nih.gov, as well as recent year proceedings from the annual conferences of the American Society of Clinical Oncology (ASCO), European Society for Medical Oncology (ESMO), and Connective Tissue Oncology Society (CTOS).Expert opinion Immune-oncology drugs (IOs) show promise in certain subtypes of STS, but it is recognized that PD-1/PD-L1 axis inhibition is not enough on its own. Better trial stratifications based on the molecular categorization of different subtypes of STS are needed, and more evidence suggests that ‘one size fits all’ treatment is no longer sustainable in this heterogeneous and aggressive group of tumors.
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