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HER2 相关生物标志物预测曲妥珠单抗 deruxtecan 治疗 HER2 表达转移性结直肠癌患者的临床结局:DESTINY-CRC01 的生物标志物分析。

HER2-related biomarkers predict clinical outcomes with trastuzumab deruxtecan treatment in patients with HER2-expressing metastatic colorectal cancer: biomarker analyses of DESTINY-CRC01.

机构信息

Department of Oncology and Hemato-Oncology, Università degli Studi di Milano and Niguarda Cancer Center, Grande Ospedale Metropolitano Niguarda, Milan, Italy.

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Nat Commun. 2024 Nov 25;15(1):10213. doi: 10.1038/s41467-024-53223-3.

Abstract

DESTINY-CRC01 (NCT03384940) was a multicentre, open-label, phase 2 study that investigated the safety and efficacy of trastuzumab deruxtecan (T-DXd) in patients with human epidermal growth factor receptor 2 (HER2)-expressing metastatic colorectal cancer (CRC). The present exploratory biomarker analysis aims to investigate relationships between biomarkers and clinical outcomes in patients with HER2-positive (immunohistochemistry [IHC] 3+ or IHC 2+ and in situ hybridization [ISH] positive) Cohort A (N = 53) of DESTINY-CRC01. Higher levels of HER2 biomarkers in baseline tissue and liquid biopsies, including HER2 status (IHC/ISH), HER2/CEP17 ratio, HER2 ISH signals, HER2 H-score, plasma HER2 (ERBB2) amplification status, HER2 adjusted plasma copy number, and HER2 extracellular domain correlate with antitumor activity (indicated by objective response rate, progression-free survival, and overall survival) of T-DXd. Baseline circulating tumor DNA (ctDNA) analysis suggests antitumor activity of T-DXd in patients who had baseline activating RAS, PIK3CA, or HER2 mutations detected in ctDNA.

摘要

DESTINY-CRC01(NCT03384940)是一项多中心、开放标签、2 期研究,旨在评估曲妥珠单抗-德鲁替康(T-DXd)在人表皮生长因子受体 2(HER2)表达的转移性结直肠癌(CRC)患者中的安全性和疗效。本探索性生物标志物分析旨在研究 DESTINY-CRC01 中 HER2 阳性(免疫组织化学[IHC] 3+或 IHC 2+且原位杂交[ISH]阳性)队列 A(N=53)患者的生物标志物与临床结局之间的关系。基线组织和液体活检中更高水平的 HER2 生物标志物,包括 HER2 状态(IHC/ISH)、HER2/CEP17 比值、HER2 ISH 信号、HER2 H 评分、血浆 HER2(ERBB2)扩增状态、HER2 调整后的血浆拷贝数和 HER2 细胞外结构域,与 T-DXd 的抗肿瘤活性(由客观缓解率、无进展生存期和总生存期表示)相关。基线循环肿瘤 DNA(ctDNA)分析表明,在基线时 ctDNA 中检测到激活的 RAS、PIK3CA 或 HER2 突变的患者中,T-DXd 具有抗肿瘤活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bbb/11589615/4c1b279d89eb/41467_2024_53223_Fig1_HTML.jpg

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