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从治疗到癌症预防:对高级别卵巢癌患者进行HRD检测的应用

From Therapy to Cancer Prevention Using HRD Testing on Patients with High-grade Ovarian Cancer.

作者信息

Tibiletti Maria Grazia, Carnevali Ileana, Facchi Sofia, Pensotti Valeria, Formenti Giorgio, Sahnane Nora, Libera Laura, Ronchi Susanna, Volorio Sara, Pierotti Marco Alessandro, La Rosa Stefano, Sessa Fausto

机构信息

Hereditary Cancer Research Center, University of Insubria, Varese, Italy.

Unit of Pathology, Ospedale di Circolo, ASST Sette Laghi, Varese, Italy.

出版信息

Cancer Prev Res (Phila). 2025 Jul 1;18(7):393-400. doi: 10.1158/1940-6207.CAPR-24-0474.

Abstract

UNLABELLED

Approximately half of high-grade ovarian cancers are characterized by genetic and epigenetic alterations in genes involved in homologous recombination repair (HRR), most commonly BRCA1 and BRCA2. HRR defects (HRD) identified by tests of genomic instability confer PARP inhibitor sensitivity in ovarian cancers. Commercial tests that combine tumor BRCA testing with a genomic instability score (HRD test) are available in clinical practice. We seek to determine the performance of three different HRD tests to improve therapy management and prevention of ovarian cancer. Tumor samples from 50 patients with high-grade ovarian cancers were investigated for tumoral BRCA status, genomic instability, and BRCA1 promoter methylation for treatment purposes. Patients with ovarian cancer that tested positive for BRCA variants and/or genomic instability defect were referred to the Cancer Genetics Service for germline testing. A positive HRD status was observed in 54% of cases, and pathogenic variants in BRCA genes were identified in 41% of cases presenting genomic instability. BRCA1 methylation assay revealed promoter hypermethylation in 20% of ovarian cancers that tested positive for HRD and negative for BRCA1/2 variants. Among 26 women referred to cancer genetic counseling, 10 carried germline variants in HRR genes. HRD status determined eligibility for PARP inhibitor treatment in all but two ovarian cancers. This study outlines that determining genomic instability helps identify inherited ovarian cancers. HRD testing, crucial for making high-grade ovarian cancer treatment choices, must be linked to an established path of cancer genetic counseling and management of individuals at high cancer risk.

PREVENTION RELEVANCE

Genomic instability status (HRD testing), which is essential for making therapy choices, is useful to identify inherited ovarian cancers. Identifying these families with high cancer risk is critical for implementing targeted cancer prevention strategies.

摘要

未标注

大约一半的高级别卵巢癌的特征是参与同源重组修复(HRR)的基因发生遗传和表观遗传改变,最常见的是BRCA1和BRCA2。通过基因组不稳定性检测确定的HRR缺陷(HRD)赋予卵巢癌对PARP抑制剂的敏感性。临床实践中已有将肿瘤BRCA检测与基因组不稳定性评分相结合的商业检测(HRD检测)。我们试图确定三种不同HRD检测的性能,以改善卵巢癌的治疗管理和预防。为了治疗目的,对50例高级别卵巢癌患者的肿瘤样本进行了肿瘤BRCA状态、基因组不稳定性和BRCA1启动子甲基化的研究。检测出BRCA变异和/或基因组不稳定性缺陷呈阳性的卵巢癌患者被转介至癌症遗传学服务部门进行种系检测。54%的病例观察到HRD状态呈阳性,在出现基因组不稳定性的病例中,41%鉴定出BRCA基因的致病性变异。BRCA1甲基化检测显示,在HRD检测呈阳性且BRCA1/2变异检测呈阴性的卵巢癌中,20%存在启动子高甲基化。在转介至癌症遗传咨询的26名女性中,10名携带HRR基因的种系变异。除两例外,所有卵巢癌中HRD状态均决定了是否适合接受PARP抑制剂治疗。这项研究概述了确定基因组不稳定性有助于识别遗传性卵巢癌。HRD检测对于做出高级别卵巢癌治疗选择至关重要,必须与既定的癌症遗传咨询途径以及对癌症高风险个体的管理相联系。

预防相关性

基因组不稳定性状态(HRD检测)对于做出治疗选择至关重要,有助于识别遗传性卵巢癌。识别这些癌症高风险家庭对于实施针对性的癌症预防策略至关重要。

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