<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>121(12)</volume><submitter>Darlix A</submitter><funding>This work was supported by R&amp;amp;D UNICANCER. The ESME MBC database is supported by an industrial consortium</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Metastatic breast cancer (MBC) behaviour differs depending on hormone receptors (HR) and human epidermal growth factor receptor (HER2) statuses.&lt;h4>Methods&lt;/h4>The kinetics of central nervous system (CNS) metastases (CNS metastasis-free survival, CNSM-FS) and subsequent patient's prognosis (overall survival, OS) according to the molecular subtype were retrospectively assessed in 16703 MBC patients of the ESME nationwide multicentre MBC database (Kaplan-Meier method).&lt;h4>Results&lt;/h4>CNS metastases occurred in 4118 patients (24.6%) (7.2% at MBC diagnosis and 17.5% later during follow-up). Tumours were HER2-/HR+ (45.3%), HER2+/HR+ (14.5%), HER2+/HR- (14.9%) and triple negative (25.4%). Median age at CNS metastasis diagnosis was 58.1 years (range: 22.8-92.0). The median CNSM</pubmed_abstract><journal>British journal of cancer</journal><pagination>991-1000</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6964671</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Impact of breast cancer molecular subtypes on the incidence, kinetics and prognosis of central nervous system metastases in a large multicentre real-life cohort.</pubmed_title><pmcid>PMC6964671</pmcid><pubmed_authors>Chevrot M</pubmed_authors><pubmed_authors>Levy C</pubmed_authors><pubmed_authors>Louvel G</pubmed_authors><pubmed_authors>Pasquier D</pubmed_authors><pubmed_authors>Ferrero JM</pubmed_authors><pubmed_authors>Uwer L</pubmed_authors><pubmed_authors>Brain E</pubmed_authors><pubmed_authors>Robain M</pubmed_authors><pubmed_authors>Leheurteur M</pubmed_authors><pubmed_authors>Cottu P</pubmed_authors><pubmed_authors>Darlix A</pubmed_authors><pubmed_authors>Campone M</pubmed_authors><pubmed_authors>Lecouillard I</pubmed_authors><pubmed_authors>Augereau P</pubmed_authors><pubmed_authors>Goncalves A</pubmed_authors><pubmed_authors>Dalenc F</pubmed_authors><pubmed_authors>Dieras V</pubmed_authors><pubmed_authors>Jacot W</pubmed_authors><pubmed_authors>Fraisse J</pubmed_authors><pubmed_authors>Debled M</pubmed_authors><pubmed_authors>Mouret-Reynier MA</pubmed_authors><pubmed_authors>Fumet JD</pubmed_authors><pubmed_authors>Bachelot T</pubmed_authors><pubmed_authors>Petit T</pubmed_authors><pubmed_authors>Jouannaud C</pubmed_authors><pubmed_authors>Delaloge S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of breast cancer molecular subtypes on the incidence, kinetics and prognosis of central nervous system metastases in a large multicentre real-life cohort.</name><description>&lt;h4>Background&lt;/h4>Metastatic breast cancer (MBC) behaviour differs depending on hormone receptors (HR) and human epidermal growth factor receptor (HER2) statuses.&lt;h4>Methods&lt;/h4>The kinetics of central nervous system (CNS) metastases (CNS metastasis-free survival, CNSM-FS) and subsequent patient's prognosis (overall survival, OS) according to the molecular subtype were retrospectively assessed in 16703 MBC patients of the ESME nationwide multicentre MBC database (Kaplan-Meier method).&lt;h4>Results&lt;/h4>CNS metastases occurred in 4118 patients (24.6%) (7.2% at MBC diagnosis and 17.5% later during follow-up). Tumours were HER2-/HR+ (45.3%), HER2+/HR+ (14.5%), HER2+/HR- (14.9%) and triple negative (25.4%). Median age at CNS metastasis diagnosis was 58.1 years (range: 22.8-92.0). The median CNSM</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Dec</publication><modification>2026-05-07T02:55:27.67Z</modification><creation>2020-11-19T11:38:10Z</creation></dates><accession>S-EPMC6964671</accession><cross_references><pubmed>31719684</pubmed><doi>10.1038/s41416-019-0619-y</doi></cross_references></HashMap>