Targeting the FGFR Pathway in Patients with Advanced Solid Tumors.

IF 10 1区医学 Q1 ONCOLOGY

Clinical Cancer Research Pub Date : 2024-10-15 DOI:10.1158/1078-0432.CCR-24-1711

Chadi Hage Chehade, Zeynep Irem Ozay, Neeraj Agarwal

引用次数: 0

Abstract

In the phase II FUZE trial targeting the FGFR pathway, Debio 1347 showed limited antitumor activity and manageable toxicity in patients with advanced solid tumors. Results from transcriptome-based analysis enhanced our understanding of the genomic landscape of FGFR fusion-driven tumors, informing clinical trial design and generating hypotheses for resistance mechanisms. See related article by Grivas et al., p. 4572.

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针对晚期实体瘤患者的表皮生长因子受体通路。

在针对表皮生长因子受体（FGFR）通路的 FUZE II 期试验中，Debio 1347 对晚期实体瘤患者显示出有限的抗肿瘤活性和可控的毒性。基于转录组学的分析结果增强了我们对表皮生长因子受体融合驱动的肿瘤基因组图谱的了解，为临床试验设计提供了依据，并为耐药机制提出了假设。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Clinical Cancer Research 医学-肿瘤学

CiteScore

20.10

自引率

1.70%

发文量

1207

审稿时长

2.1 months

期刊介绍： Clinical Cancer Research is a journal focusing on groundbreaking research in cancer, specifically in the areas where the laboratory and the clinic intersect. Our primary interest lies in clinical trials that investigate novel treatments, accompanied by research on pharmacology, molecular alterations, and biomarkers that can predict response or resistance to these treatments. Furthermore, we prioritize laboratory and animal studies that explore new drugs and targeted agents with the potential to advance to clinical trials. We also encourage research on targetable mechanisms of cancer development, progression, and metastasis.