Henri Azaïs , Simon Garinet , Louise Benoit , Julie de Jesus , Mohamed Zizi , Samuel Landman , Anne-Sophie Bats , Valérie Taly , Pierre Laurent-Puig , Hélène Blons
{"title":"BRCA1 启动子甲基化对上皮性卵巢癌患者的预后价值。","authors":"Henri Azaïs , Simon Garinet , Louise Benoit , Julie de Jesus , Mohamed Zizi , Samuel Landman , Anne-Sophie Bats , Valérie Taly , Pierre Laurent-Puig , Hélène Blons","doi":"10.1016/j.jogoh.2024.102796","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>BRCA1 promoter methylation (BRCA1<em>pm</em>) is suspected to alter prognosis of patients with epithelial ovarian cancer (EOC). We aimed to evaluate the prognostic impact of this epigenetic modification.</p></div><div><h3>Methods</h3><p>We conducted a retrospective, monocentric study from 11/2006 to 08/2018. Patients with EOC and available status concerning somatic BRCA1/2 mutation and BRCA1<em>pm</em> were included. Three groups were defined: patients without BRCA1/2 mutation or BRCA1<em>pm</em>, patients with BRCA1/2 mutation and patients with BRCA1<em>pm</em>. BRCA1/2 mutations were analyzed in current care settings by next-generation sequencing (NGS). BRCA1<em>pm</em> analysis was assessed and quantified from bisulfite converted DNAs using fluorescent methylation specific polymerase chain reaction (PCR) and fragment analysis. All patients signed a consent form and the study was authorized by a Personal Protection Committee. Descriptive statistics were used to describe groups. Multivariate analysis was performed using the logistic regression model and including the variables that could be known at the time of diagnosis and that were significant at univariate analysis. Survival was compared between the groups. Kaplan-Mayer curves were used to express the differences in survival that were compared using log rank tests.</p></div><div><h3>Results</h3><p>145 patients were included: 95 (65.5 %) patients without BRCA1/2 mutation or BRCA1<em>pm</em>, 32 (22.1 %) patients with BRCA1/2 mutation, 18 (12.4 %) patients with BRCA1<em>pm</em>. Median survival was decreased in patients with BRCA1<em>pm</em>. Comparison of survival revealed a significant difference in overall survival (<em>p</em> = 0.0078) with a worse prognosis for patients with a BRCA1<em>pm</em>.</p></div><div><h3>Conclusion</h3><p>BRCA1<em>pm</em> in patients with EOC is an independent factor associated with a decreased overall survival.</p></div><div><h3>Synopsis</h3><p>BRCA1 promotor methylation in patients with epithelial ovarian cancer is an independent factor associated with a decreased overall survival.</p></div>","PeriodicalId":15871,"journal":{"name":"Journal of gynecology obstetrics and human reproduction","volume":"53 7","pages":"Article 102796"},"PeriodicalIF":1.7000,"publicationDate":"2024-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2468784724000746/pdfft?md5=4303178ec0dd9dee4b3db55556bf9d9c&pid=1-s2.0-S2468784724000746-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Prognostic value of BRCA1 promoter methylation for patients with epithelial ovarian cancer\",\"authors\":\"Henri Azaïs , Simon Garinet , Louise Benoit , Julie de Jesus , Mohamed Zizi , Samuel Landman , Anne-Sophie Bats , Valérie Taly , Pierre Laurent-Puig , Hélène Blons\",\"doi\":\"10.1016/j.jogoh.2024.102796\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><p>BRCA1 promoter methylation (BRCA1<em>pm</em>) is suspected to alter prognosis of patients with epithelial ovarian cancer (EOC). We aimed to evaluate the prognostic impact of this epigenetic modification.</p></div><div><h3>Methods</h3><p>We conducted a retrospective, monocentric study from 11/2006 to 08/2018. Patients with EOC and available status concerning somatic BRCA1/2 mutation and BRCA1<em>pm</em> were included. Three groups were defined: patients without BRCA1/2 mutation or BRCA1<em>pm</em>, patients with BRCA1/2 mutation and patients with BRCA1<em>pm</em>. BRCA1/2 mutations were analyzed in current care settings by next-generation sequencing (NGS). BRCA1<em>pm</em> analysis was assessed and quantified from bisulfite converted DNAs using fluorescent methylation specific polymerase chain reaction (PCR) and fragment analysis. All patients signed a consent form and the study was authorized by a Personal Protection Committee. Descriptive statistics were used to describe groups. Multivariate analysis was performed using the logistic regression model and including the variables that could be known at the time of diagnosis and that were significant at univariate analysis. Survival was compared between the groups. Kaplan-Mayer curves were used to express the differences in survival that were compared using log rank tests.</p></div><div><h3>Results</h3><p>145 patients were included: 95 (65.5 %) patients without BRCA1/2 mutation or BRCA1<em>pm</em>, 32 (22.1 %) patients with BRCA1/2 mutation, 18 (12.4 %) patients with BRCA1<em>pm</em>. Median survival was decreased in patients with BRCA1<em>pm</em>. Comparison of survival revealed a significant difference in overall survival (<em>p</em> = 0.0078) with a worse prognosis for patients with a BRCA1<em>pm</em>.</p></div><div><h3>Conclusion</h3><p>BRCA1<em>pm</em> in patients with EOC is an independent factor associated with a decreased overall survival.</p></div><div><h3>Synopsis</h3><p>BRCA1 promotor methylation in patients with epithelial ovarian cancer is an independent factor associated with a decreased overall survival.</p></div>\",\"PeriodicalId\":15871,\"journal\":{\"name\":\"Journal of gynecology obstetrics and human reproduction\",\"volume\":\"53 7\",\"pages\":\"Article 102796\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-05-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2468784724000746/pdfft?md5=4303178ec0dd9dee4b3db55556bf9d9c&pid=1-s2.0-S2468784724000746-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of gynecology obstetrics and human reproduction\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2468784724000746\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"OBSTETRICS & GYNECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of gynecology obstetrics and human reproduction","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468784724000746","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"OBSTETRICS & GYNECOLOGY","Score":null,"Total":0}
Prognostic value of BRCA1 promoter methylation for patients with epithelial ovarian cancer
Objective
BRCA1 promoter methylation (BRCA1pm) is suspected to alter prognosis of patients with epithelial ovarian cancer (EOC). We aimed to evaluate the prognostic impact of this epigenetic modification.
Methods
We conducted a retrospective, monocentric study from 11/2006 to 08/2018. Patients with EOC and available status concerning somatic BRCA1/2 mutation and BRCA1pm were included. Three groups were defined: patients without BRCA1/2 mutation or BRCA1pm, patients with BRCA1/2 mutation and patients with BRCA1pm. BRCA1/2 mutations were analyzed in current care settings by next-generation sequencing (NGS). BRCA1pm analysis was assessed and quantified from bisulfite converted DNAs using fluorescent methylation specific polymerase chain reaction (PCR) and fragment analysis. All patients signed a consent form and the study was authorized by a Personal Protection Committee. Descriptive statistics were used to describe groups. Multivariate analysis was performed using the logistic regression model and including the variables that could be known at the time of diagnosis and that were significant at univariate analysis. Survival was compared between the groups. Kaplan-Mayer curves were used to express the differences in survival that were compared using log rank tests.
Results
145 patients were included: 95 (65.5 %) patients without BRCA1/2 mutation or BRCA1pm, 32 (22.1 %) patients with BRCA1/2 mutation, 18 (12.4 %) patients with BRCA1pm. Median survival was decreased in patients with BRCA1pm. Comparison of survival revealed a significant difference in overall survival (p = 0.0078) with a worse prognosis for patients with a BRCA1pm.
Conclusion
BRCA1pm in patients with EOC is an independent factor associated with a decreased overall survival.
Synopsis
BRCA1 promotor methylation in patients with epithelial ovarian cancer is an independent factor associated with a decreased overall survival.
期刊介绍:
Formerly known as Journal de Gynécologie Obstétrique et Biologie de la Reproduction, Journal of Gynecology Obstetrics and Human Reproduction is the official Academic publication of the French College of Obstetricians and Gynecologists (Collège National des Gynécologues et Obstétriciens Français / CNGOF).
J Gynecol Obstet Hum Reprod publishes monthly, in English, research papers and techniques in the fields of Gynecology, Obstetrics, Neonatology and Human Reproduction: (guest) editorials, original articles, reviews, updates, technical notes, case reports, letters to the editor and guidelines.
Original works include clinical or laboratory investigations and clinical or equipment reports. Reviews include narrative reviews, systematic reviews and meta-analyses.