BRCA 功能缺失(包括 BRCA1 DNA 甲基化)而非 BRCA 非相关同源重组缺失与高级别卵巢癌的铂超敏反应有关。

IF 4.8 2区 医学 Q1 GENETICS & HEREDITY Clinical Epigenetics Pub Date : 2024-11-27 DOI:10.1186/s13148-024-01781-0
Heidelinde Fiegl, Simon Schnaiter, Daniel U Reimer, Katharina Leitner, Petra Nardelli, Irina Tsibulak, Verena Wieser, Katharina Wimmer, Esther Schamschula, Christian Marth, Alain G Zeimet
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One hundred thirty-one HGOC tissues were tested for BRCA DNA-methylation, BRCA mutations, HRD and BRCA1 mRNA expression, followed by a comprehensive survival analysis.</p><p><strong>Results: </strong>BRCA1-methylation was detected in 11% of the tumors, exclusively in BRCA1-wild-type (wt) HGOCs. BRCA1-methylated tumors (BRCA1-meth) had HRD-scores similar to those of BRCA-mutated (mut) tumors, and higher compared to unmethylated-BRCA-wt tumors (BRCA-wt-unmeth; P < 0.001). Platinum-refractory or -resistant HGOCs at first recurrence were all BRCA-unmeth cancers. Only one of the BRCA-mut cancers had a platinum-resistant recurrence. Thus, 99% of relapses in cancers with epigenetic or genetic BRCA-alterations were platinum-sensitive. Multivariate analysis confirmed BRCA-LOF as an independent predictor of progression-free survival (PFS) and overall survival (OS), whereas HRD-status had no predictive value for PFS and OS. 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引用次数: 0

摘要

背景:在高级别卵巢癌(HGOC)中,同源重组缺陷(HRD)状态的测定通常用于预测对铂类疗法或多(ADP-核糖)聚合酶抑制剂(PARPi)的反应。在这里,我们测试了一个假设,即与HRD相比,表观遗传学或基因畸变导致的BRCA功能缺失(LOF)更能预测临床结果。我们对 131 例 HGOC 组织进行了 BRCA DNA 甲基化、BRCA 基因突变、HRD 和 BRCA1 mRNA 表达检测,然后进行了综合生存分析:结果:在11%的肿瘤中检测到了BRCA1甲基化,这些肿瘤只存在于BRCA1-wild型(wt)HGOC中。BRCA1甲基化肿瘤(BRCA1-meth)的HRD评分与BRCA突变(mut)肿瘤相似,高于未甲基化的BRCA-wt肿瘤(BRCA-wt-unmeth;P 结论:BRCA1甲基化肿瘤的HRD评分与BRCA突变肿瘤的HRD评分相似,高于未甲基化的BRCA-wt肿瘤(BRCA-wt-unmeth):在HGOC中,BRCA突变状态和BRCA1甲基化对良好的临床预后具有最佳预测力,因此对铂类药物治疗具有高度敏感性,而与BRCA无关的HRD阳性与铂类药物敏感性的提高无关。
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BRCA loss of function including BRCA1 DNA-methylation, but not BRCA-unrelated homologous recombination deficiency, is associated with platinum hypersensitivity in high-grade ovarian cancer.

Background: In high-grade ovarian cancer (HGOC), determination of homologous recombination deficiency (HRD) status is commonly used in routine practice to predict response to platinum-based therapy or poly (ADP-ribose) polymerase inhibitors (PARPi). Here we tested the hypothesis that BRCA loss of function (LOF) due to epigenetic or genetic aberrations is a better predictor for the clinical outcome than HRD. One hundred thirty-one HGOC tissues were tested for BRCA DNA-methylation, BRCA mutations, HRD and BRCA1 mRNA expression, followed by a comprehensive survival analysis.

Results: BRCA1-methylation was detected in 11% of the tumors, exclusively in BRCA1-wild-type (wt) HGOCs. BRCA1-methylated tumors (BRCA1-meth) had HRD-scores similar to those of BRCA-mutated (mut) tumors, and higher compared to unmethylated-BRCA-wt tumors (BRCA-wt-unmeth; P < 0.001). Platinum-refractory or -resistant HGOCs at first recurrence were all BRCA-unmeth cancers. Only one of the BRCA-mut cancers had a platinum-resistant recurrence. Thus, 99% of relapses in cancers with epigenetic or genetic BRCA-alterations were platinum-sensitive. Multivariate analysis confirmed BRCA-LOF as an independent predictor of progression-free survival (PFS) and overall survival (OS), whereas HRD-status had no predictive value for PFS and OS. Patients with BRCA-wt-unmeth cancers had the worst outcome compared to patients with cancers harboring epigenetic or genetic BRCA-alterations (PFS: P = 0.007; OS: P = 0.022). Most importantly, the BRCA-wt-unmeth subfraction of HRD-positive HGOCs exhibited the same poor survival as the entire HRD-negative cohort.

Conclusion: In HGOC BRCA mutational status together with BRCA1-methylation exhibit the best predictive power for favorable clinical outcome and thus high sensitivity to platinum-based therapy, whereas BRCA-unrelated HRD positivity was not associated with improved platinum sensitivity.

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来源期刊
自引率
5.30%
发文量
150
期刊介绍: Clinical Epigenetics, the official journal of the Clinical Epigenetics Society, is an open access, peer-reviewed journal that encompasses all aspects of epigenetic principles and mechanisms in relation to human disease, diagnosis and therapy. Clinical trials and research in disease model organisms are particularly welcome.
期刊最新文献
BRCA loss of function including BRCA1 DNA-methylation, but not BRCA-unrelated homologous recombination deficiency, is associated with platinum hypersensitivity in high-grade ovarian cancer. Methylation changes and INS-IGF2 expression predict progression in early-stage Wilms tumor. Road traffic noise and breast cancer: DNA methylation in four core circadian genes. Methylation assay in KMT2B-related dystonia: a novel diagnostic validation tool. Exploratory DNA methylation analysis in post-mortem heart tissue of sudden unexplained death.
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