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        <titl xml:lang="FR">Cohorte de familles françaises avec une mutation d’un gène MMR identifiée : estimation des risques de cancers</titl>
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        <altTitl xml:lang="FR">ERISCAM</altTitl>
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        <parTitl xml:lang="EN">Cohort of French Families with Identified MMR Gene Mutation: Assessment of Cancer Risk</parTitl>
        <IDNo>PEF73086</IDNo>
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        <AuthEnty affiliation="ITMO Santé Publique, Aviesan">Portail Épidémiologie-France</AuthEnty>
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        <copyright>Portail Épidémiologie-France 2026</copyright>
        <prodDate date="2026-04-13">13/04/2026</prodDate>
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        <contact email="portail-epidemiologie@inserm.fr">Portail Epidemiologie-France</contact>
        <depositr>Christine Lasset</depositr>
        <depDate xml:lang="FR">18/05/2015</depDate>
        <depDate xml:lang="EN">20/06/2016</depDate>
        <distDate>01/01/2019</distDate>
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        <version xml:lang="EN" date="01/01/2019">1</version>
        <verResp>Christine Lasset</verResp>
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        <altTitl xml:lang="FR">ERISCAM</altTitl>
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        <parTitl xml:lang="EN">Cohort of French Families with Identified MMR Gene Mutation: Assessment of Cancer Risk</parTitl>
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        <AuthEnty affiliation="CNRS">Christine Lasset</AuthEnty>
        <AuthEnty affiliation="CNRS">Valérie Bonadona</AuthEnty>
        <AuthEnty affiliation="Inserm">Catherine  Bonaiti-Pellie </AuthEnty>
        <AuthEnty affiliation="Inserm">Sylviane  Olschwang </AuthEnty>
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        <prodPlac>Prevention and genetics epidemiology - CNRS - </prodPlac>
        <prodPlac> - CNRS - </prodPlac>
        <prodPlac>Genetics epidemiology and human population structures - Inserm - </prodPlac>
        <prodPlac>Medical Genetics and Functional Genomics - Inserm - </prodPlac>
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        <fundAg xml:lang="FR" role="Privé">Fondation de France</fundAg>
        <fundAg xml:lang="EN" role="Private">Fondation de France</fundAg>
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        <distrbtr>CNRS</distrbtr>
        <distrbtr>CNRS</distrbtr>
        <distrbtr>Inserm</distrbtr>
        <distrbtr>Inserm</distrbtr>
        <contact affiliation="CNRS" email="christine.lasset@lyon.unicancer.fr">Christine Lasset</contact>
        <contact affiliation="CNRS" email="valerie.bonadona@lyon.unicancer.fr">Valérie Bonadona</contact>
        <contact affiliation="Inserm" email="catherine.bonaiti@inserm.fr">Catherine  Bonaiti-Pellie </contact>
        <contact affiliation="Inserm" email="sylviane.olschwang@inserm.fr">Sylviane  Olschwang </contact>
        <depositr>Christine Lasset</depositr>
        <depDate xml:lang="FR">18/05/2015</depDate>
        <depDate xml:lang="EN">20/06/2016</depDate>
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        <distDate xml:lang="EN">01/01/2019</distDate>
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        <verResp>Christine Lasset</verResp>
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      <subject>
        <keyword xml:lang="FR">Syndrome de Lynch</keyword>
        <keyword xml:lang="FR">gynécologie</keyword>
        <keyword xml:lang="FR">gènes MMR</keyword>
        <keyword xml:lang="FR">MLH1</keyword>
        <keyword xml:lang="FR">MSH2</keyword>
        <keyword xml:lang="FR">MSH6</keyword>
        <keyword xml:lang="FR">risque cumulé</keyword>
        <keyword xml:lang="FR">cancer</keyword>
        <keyword xml:lang="FR">colorectal</keyword>
        <keyword xml:lang="FR">génétique</keyword>
        <keyword xml:lang="FR">mutation</keyword>
        <keyword xml:lang="EN">Lynch syndrome</keyword>
        <keyword xml:lang="EN">gynaecology</keyword>
        <keyword xml:lang="EN">MMR genes</keyword>
        <keyword xml:lang="EN">cumulative risk</keyword>
        <keyword xml:lang="EN">MLH1</keyword>
        <keyword xml:lang="EN">MSH2</keyword>
        <keyword xml:lang="EN">MSH6</keyword>
        <keyword xml:lang="EN">colorectal</keyword>
        <keyword xml:lang="EN">cancer</keyword>
        <keyword xml:lang="EN">genetic</keyword>
        <keyword xml:lang="EN">mutation</keyword>
        <topcClas xml:lang="FR">Cancérologie</topcClas>
        <topcClas xml:lang="FR">Gastro-entérologie et hépatologie</topcClas>
        <topcClas xml:lang="FR">Gynécologie obstétrique</topcClas>
        <topcClas xml:lang="EN">Cancer research</topcClas>
        <topcClas xml:lang="EN">Gastroenterology et hepatology</topcClas>
        <topcClas xml:lang="EN">Gynecology/ obstetrics</topcClas>
        <topcClas xml:lang="FR">Génétique</topcClas>
        <topcClas xml:lang="EN">Genetic</topcClas>
      </subject>
      <abstract xml:lang="FR">Objectif de la base de données : Objectif est d’estimer de façon fiable et précise les risques des différentes tumeurs chez les sujets porteurs d’une mutation d’un gène MMR</abstract>
      <abstract xml:lang="EN">Database objective : The aim is to reliably and accurately determine the risks of different tumours in subjects with MMR gene mutations.</abstract>
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        <collDate event="start">2007</collDate>
        <collDate event="end">2009</collDate>
        <collDate xml:lang="FR">Collecte des données terminée</collDate>
        <collDate xml:lang="EN">Data collection completed</collDate>
        <nation>France</nation>
        <geogCover xml:lang="FR">France</geogCover>
        <geogCover xml:lang="EN">France</geogCover>
        <geogUnit>National</geogUnit>
        <anlyUnit xml:lang="fr">individuel
                </anlyUnit>
        <anlyUnit xml:lang="en">individuals
                </anlyUnit>
        <universe xml:lang="FR" clusion="I">Familles françaises avec une mutation d’un gène MMR identifiée , recrutées par les 40 centres de consultation d’oncogénétique participants à l’étude, tous membres du Groupe Génétique et Cancer. </universe>
        <universe xml:lang="EN" clusion="I">French families with an identified MMR gene mutation recruited throughout 40 cancer genetic consultation centres participating in the study; all members of the Cancer and Genetics Network.</universe>
        <universe xml:lang="FR">Nombre d'individus : 537 familles/families (248 : MSH1 mutation, 256 MSH2 mutation, 33 MSH6 mutation). 2622 patients</universe>
        <universe xml:lang="EN">Number of individuals: 537 families (248: MSH1 mutation, 256 MSH2 mutation, 33 MSH6 mutation). 2,622 patients</universe>
        <universe xml:lang="FR">Recrutement via une base administrative ou un registre</universe>
        <universe xml:lang="EN">Recruiting through an administrative base or a register</universe>
        <universe xml:lang="FR" level="Tranche d'âge">Adulte (19 à 24 ans)</universe>
        <universe xml:lang="FR" level="Tranche d'âge">Adulte (25 à 44 ans)</universe>
        <universe xml:lang="FR" level="Tranche d'âge">Adulte (45 à 64 ans)</universe>
        <universe xml:lang="FR" level="Tranche d'âge">Personnes âgées (65 à 79 ans)</universe>
        <universe xml:lang="FR" level="Tranche d'âge">Grand âge (80 ans et plus)</universe>
        <universe xml:lang="EN" level="Age range">Adulthood (19 to 24 years)</universe>
        <universe xml:lang="EN" level="Age range">Adulthood (25 to 44 years)</universe>
        <universe xml:lang="EN" level="Age range">Adulthood (45 to 64 years)</universe>
        <universe xml:lang="EN" level="Age range">Elderly (65 to 79 years)</universe>
        <universe xml:lang="EN" level="Age range">Great age (80 years and more)</universe>
        <universe xml:lang="FR" level="Type de population">Sujets malades</universe>
        <universe xml:lang="EN" level="Population type">Sick population</universe>
        <universe xml:lang="FR" level="Sexe">Masculin</universe>
        <universe xml:lang="FR" level="Sexe">Féminin</universe>
        <universe xml:lang="EN" level="Sex">Male</universe>
        <universe xml:lang="EN" level="Sex">Female</universe>
        <dataKind xml:lang="FR">Bases de données issues d’enquêtes</dataKind>
        <dataKind xml:lang="EN">Study databases</dataKind>
        <dataKind xml:lang="FR">Etudes de cohortes</dataKind>
        <dataKind xml:lang="EN">Cohort study</dataKind>
        <dataKind xml:lang="FR">Données cliniques : Sexe, age, age du dernier suivi, histoire du cancer (site, age du diagnostice, mort), mutation statut, modalité de surveillance colonoscipic, chirurgie colorectal ou gynécologique</dataKind>
        <dataKind xml:lang="FR">Données déclaratives : Face à face</dataKind>
        <dataKind xml:lang="EN">Clinical data: Sex; age; age at last follow-up; cancer history (location, age at diagnosis, death); mutation status; colonoscopic surveillance method; colorectal or gynaecological surgery</dataKind>
        <dataKind xml:lang="EN">Declarative data: Face to face interview</dataKind>
        <dataKind xml:lang="FR"/>
        <dataKind xml:lang="EN"/>
        <dataKind xml:lang="FR"/>
        <dataKind xml:lang="EN"/>
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        <dataCollector affiliation="CNRS">Christine Lasset</dataCollector>
        <dataCollector affiliation="CNRS">Valérie Bonadona</dataCollector>
        <dataCollector affiliation="Inserm">Catherine  Bonaiti-Pellie </dataCollector>
        <dataCollector affiliation="Inserm">Sylviane  Olschwang </dataCollector>
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        <collMode xml:lang="EN">Face to face interview: Même information si dossier médical pas disponible</collMode>
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