<HashMap><database>biostudies-literature</database><scores/><additional><submitter>de Pinieux G</submitter><funding>Ligue Contre le Cancer</funding><funding>Fondation ARC pour la Recherche sur le Cancer</funding><funding>Agence Nationale de la Recherche</funding><funding>Institut National Du Cancer</funding><funding>EUROPEAN COMMISSION (EU) EURACAN</funding><pagination>e0246958</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7906477</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(2)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Since 2010, nationwide networks of reference centers for sarcomas (RREPS/NETSARC/RESOS) collected and prospectively reviewed all cases of sarcomas and connective tumors of intermediate malignancy (TIM) in France.&lt;h4>Methods&lt;/h4>The nationwide incidence of sarcoma or TIM (2013-2016) was measured using the 2013 WHO classification and confirmed by a second independent review by expert pathologists. Simple clinical characteristics, yearly variations and correlation of incidence with published clinical trials are presented and analyzed.&lt;h4>Results&lt;/h4>Over 150 different histological subtypes are reported from the 25172 patients with sarcomas (n = 18712, 74,3%) or TIM (n = 6460, 25.7%), with n = 5838, n = 6153, n = 6654, and n = 6527 yearly cases from 2013 to 2016. Over these </pubmed_abstract><journal>PloS one</journal><pubmed_title>Nationwide incidence of sarcomas and connective tissue tumors of intermediate malignancy over four years using an expert pathology review network.</pubmed_title><pmcid>PMC7906477</pmcid><funding_grant_id>RESOS</funding_grant_id><funding_grant_id>Institut Convergence PLASCAN (17-CONV-0002)</funding_grant_id><funding_grant_id>RREPS</funding_grant_id><funding_grant_id>Unicancer</funding_grant_id><funding_grant_id>LabEx DEvweCAN (ANR-10-LABX-0061),</funding_grant_id><funding_grant_id>EC 739521</funding_grant_id><funding_grant_id>NETSARC</funding_grant_id><funding_grant_id>INTERSARC</funding_grant_id><funding_grant_id>Canopee</funding_grant_id><funding_grant_id>NETSARC+</funding_grant_id><pubmed_authors>Mesli N</pubmed_authors><pubmed_authors>Penel N</pubmed_authors><pubmed_authors>Mescam L</pubmed_authors><pubmed_authors>Angot E</pubmed_authors><pubmed_authors>Neuville A</pubmed_authors><pubmed_authors>Leroux A</pubmed_authors><pubmed_authors>Macagno N</pubmed_authors><pubmed_authors>Charon-Barra C</pubmed_authors><pubmed_authors>de Pinieux G</pubmed_authors><pubmed_authors>Moreau A</pubmed_authors><pubmed_authors>Jean-Denis M</pubmed_authors><pubmed_authors>Coindre JM</pubmed_authors><pubmed_authors>Toulmonde M</pubmed_authors><pubmed_authors>Gouin F</pubmed_authors><pubmed_authors>Ranchere D</pubmed_authors><pubmed_authors>Karanian M</pubmed_authors><pubmed_authors>Chateau MC</pubmed_authors><pubmed_authors>Collin F</pubmed_authors><pubmed_authors>Chemin-Airiau C</pubmed_authors><pubmed_authors>Rochaix P</pubmed_authors><pubmed_authors>Courreges JB</pubmed_authors><pubmed_authors>Le Guellec S</pubmed_authors><pubmed_authors>Demuret A</pubmed_authors><pubmed_authors>Bouvier C</pubmed_authors><pubmed_authors>Blay JY</pubmed_authors><pubmed_authors>Bazille C</pubmed_authors><pubmed_authors>Lae M</pubmed_authors><pubmed_authors>Croce S</pubmed_authors><pubmed_authors>Robin YM</pubmed_authors><pubmed_authors>Terrier P</pubmed_authors><pubmed_authors>Stock N</pubmed_authors><pubmed_authors>Emile JF</pubmed_authors><pubmed_authors>Mishellany F</pubmed_authors><pubmed_authors>Le Cesne A</pubmed_authors><pubmed_authors>Chabaud S</pubmed_authors><pubmed_authors>Birtwisle-Peyrottes I</pubmed_authors><pubmed_authors>Weinbreck N</pubmed_authors><pubmed_authors>Brouchet A</pubmed_authors><pubmed_authors>Ducimetiere F</pubmed_authors><pubmed_authors>Le Loarer F</pubmed_authors><pubmed_authors>NetSarc/RePPS/ResSos and French Sarcoma Group- Groupe d’Etude des Tumeurs Osseuses (GSF-GETO) networks</pubmed_authors><pubmed_authors>Berchoud J</pubmed_authors><pubmed_authors>Ghnassia JP</pubmed_authors><pubmed_authors>Larousserie F</pubmed_authors><pubmed_authors>Aubert S</pubmed_authors><pubmed_authors>Chetaille B</pubmed_authors><pubmed_authors>Italiano A</pubmed_authors><pubmed_authors>Quintin-Rouet I</pubmed_authors><pubmed_authors>Delfour C</pubmed_authors><pubmed_authors>Fayet Y</pubmed_authors><pubmed_authors>Pommepuy I</pubmed_authors><pubmed_authors>Ortonne N</pubmed_authors><pubmed_authors>Doucet L</pubmed_authors><pubmed_authors>Batistella M</pubmed_authors><pubmed_authors>Valo I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Nationwide incidence of sarcomas and connective tissue tumors of intermediate malignancy over four years using an expert pathology review network.</name><description>&lt;h4>Background&lt;/h4>Since 2010, nationwide networks of reference centers for sarcomas (RREPS/NETSARC/RESOS) collected and prospectively reviewed all cases of sarcomas and connective tumors of intermediate malignancy (TIM) in France.&lt;h4>Methods&lt;/h4>The nationwide incidence of sarcoma or TIM (2013-2016) was measured using the 2013 WHO classification and confirmed by a second independent review by expert pathologists. Simple clinical characteristics, yearly variations and correlation of incidence with published clinical trials are presented and analyzed.&lt;h4>Results&lt;/h4>Over 150 different histological subtypes are reported from the 25172 patients with sarcomas (n = 18712, 74,3%) or TIM (n = 6460, 25.7%), with n = 5838, n = 6153, n = 6654, and n = 6527 yearly cases from 2013 to 2016. Over these </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2026-05-09T08:54:26.726Z</modification><creation>2021-03-06T08:16:38Z</creation></dates><accession>S-EPMC7906477</accession><cross_references><pubmed>33630918</pubmed><doi>10.1371/journal.pone.0246958</doi></cross_references></HashMap>