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HER2阳性乳腺癌中mRNA表达及对ado-曲妥珠单抗-恩坦辛(T-DM1)的反应

mRNA Expression and Response to Ado-Trastuzumab Emtansine (T-DM1) in HER2-Positive Breast Cancer.

作者信息

Griguolo Gaia, Brasó-Maristany Fara, González-Farré Blanca, Pascual Tomás, Chic Núria, Saurí Tamara, Kates Ronald, Gluz Oleg, Martínez Débora, Paré Laia, Tsvetkova Vassilena, Pesantez David, Vidal Maria, Adamo Barbara, Muñoz Montserrat, Galván Patricia, Barberá Laura, Cuatrecasas Miriam, Christgen Mathias, Kreipe Hans, Monge-Escartín Inés, Villagrasa Patricia, Soy Dolors, Giarratano Tommaso, Dieci Maria Vittoria, Conte Pierfranco, Harbeck Nadia, Guarneri Valentina, Prat Aleix

机构信息

Division of Medical Oncology 2, Istituto Oncologico Veneto IOV-IRCCS, 35128 Padova, Italy.

Department of Surgery, Oncology and Gastroenterology, University of Padova, 35124 Padova, Italy.

出版信息

Cancers (Basel). 2020 Jul 14;12(7):1902. doi: 10.3390/cancers12071902.

Abstract

Trastuzumab emtansine (T-DM1) is approved for the treatment of human epidermal growth factor receptor 2 (HER2)-positive (HER2+) metastatic breast cancer (BC) and for residual disease after neoadjuvant therapy; however, not all patients benefit. Here, we hypothesized that the heterogeneity in the response seen in patients is partly explained by the levels of human epidermal growth factor receptor 2 gene mRNA. We analyzed expression using a clinically applicable assay in formalin-fixed paraffin-embedded (FFPE) tumors (primary or metastatic) from a retrospective series of 77 patients with advanced HER2+ BC treated with T-DM1. The association of levels and response was further validated in 161 baseline tumors from the West German Study (WGS) Group ADAPT phase II trial exploring neoadjuvant T-DM1 and 9 in vitro BC cell lines. Finally, expression was explored in 392 BCs from an in-house dataset, 368 primary BCs from The Cancer Genome Atlas (TCGA) dataset and 10,071 tumors representing 33 cancer types from the PanCancer TCGA dataset. High mRNA was found associated with better response and progression-free survival in the metastatic setting and higher rates of pathological complete response in the neoadjuvant setting. expression also correlated with in vitro response to T-DM1. Finally, our assay identified 0.20-8.41% of tumors across 15 cancer types as -high, including gastric and esophagus adenocarcinomas, urothelial carcinoma, cervical squamous carcinoma and pancreatic cancer. In particular, we identified high mRNA in a patient with HER2+ advanced gastric cancer who achieved a long-lasting partial response to T-DM1. Our study demonstrates that the heterogeneity in response to T-DM1 is partly explained by levels and provides a clinically applicable assay to be tested in future clinical trials of breast cancer and other cancer types.

摘要

曲妥珠单抗-美坦新(T-DM1)被批准用于治疗人表皮生长因子受体2(HER2)阳性(HER2+)转移性乳腺癌(BC)以及新辅助治疗后的残留病灶;然而,并非所有患者都能从中获益。在此,我们推测患者反应的异质性部分可由人表皮生长因子受体2基因mRNA水平来解释。我们使用一种临床适用的检测方法,对来自77例接受T-DM1治疗的晚期HER2+ BC患者的回顾性系列福尔马林固定石蜡包埋(FFPE)肿瘤(原发性或转移性)进行了表达分析。在探索新辅助T-DM1的西德研究(WGS)组ADAPT II期试验的161个基线肿瘤以及9种体外BC细胞系中,进一步验证了水平与反应之间的关联。最后,在一个内部数据集的392例BC、癌症基因组图谱(TCGA)数据集的368例原发性BC以及泛癌症TCGA数据集中代表33种癌症类型的10,071个肿瘤中探索了表达情况。发现高mRNA与转移性环境中更好的反应和无进展生存期以及新辅助环境中更高的病理完全缓解率相关。表达也与对T-DM1的体外反应相关。最后,我们的检测方法确定了15种癌症类型中0.20 - 8.41%的肿瘤为高,包括胃和食管腺癌、尿路上皮癌、宫颈鳞状癌和胰腺癌。特别是,我们在一名HER2+晚期胃癌患者中发现了高mRNA,该患者对T-DM1取得了持久的部分缓解。我们的研究表明,对T-DM1反应的异质性部分可由水平来解释,并提供了一种临床适用的检测方法,有待在未来的乳腺癌和其他癌症类型的临床试验中进行测试。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/008e/7409149/d19ffaa0f161/cancers-12-01902-g001.jpg

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