<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>187(4)</volume><submitter>Burman P</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>To describe clinical and pathological characteristics and treatment outcomes in a large cohort of aggressive pituitary tumours (APT)/pituitary carcinomas (PC).&lt;h4>Design&lt;/h4>Electronic survey August 2020-May 2021.&lt;h4>Results&lt;/h4>96% of 171 (121 APT, 50 PC), initially presented as macro/giant tumours, 6 were microadenomas (5 corticotroph). Ninety-seven tumours, initially considered clinically benign, demonstrated aggressive behaviour after 5.5 years (IQR: 2.8-12). Of the patients, 63% were men. Adrenocorticotrophic hormone (ACTH)-secreting tumours constituted 30% of the APT/PC, and the gonadotroph subtypes were under-represented. Five out of 13 silent corticotroph tumours and 2/6 silent somatotroph tumours became secreting. Metastases were observed after median 6.3 years (</pubmed_abstract><journal>European journal of endocrinology</journal><pagination>593-605</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9513638</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Aggressive pituitary tumours and carcinomas, characteristics and management of 171 patients.</pubmed_title><pmcid>PMC9513638</pmcid><pubmed_authors>Mantovani G</pubmed_authors><pubmed_authors>Otto Lunde Jorgensen J</pubmed_authors><pubmed_authors>Jublanc C</pubmed_authors><pubmed_authors>Garay IB</pubmed_authors><pubmed_authors>Usui T</pubmed_authors><pubmed_authors>Mazzuco TL</pubmed_authors><pubmed_authors>Vila G</pubmed_authors><pubmed_authors>Bach L</pubmed_authors><pubmed_authors>Toth M</pubmed_authors><pubmed_authors>Schillo F</pubmed_authors><pubmed_authors>Losa M</pubmed_authors><pubmed_authors>Berinder K</pubmed_authors><pubmed_authors>Jaffrain-Rea ML</pubmed_authors><pubmed_authors>Lasolle H</pubmed_authors><pubmed_authors>Pekic S</pubmed_authors><pubmed_authors>Ekman B</pubmed_authors><pubmed_authors>Kuhn E</pubmed_authors><pubmed_authors>Korbonits M</pubmed_authors><pubmed_authors>Hubalewska-Dydejezky A</pubmed_authors><pubmed_authors>Krogh Rasmussen A</pubmed_authors><pubmed_authors>Zatelli MC</pubmed_authors><pubmed_authors>Trouillas J</pubmed_authors><pubmed_authors>Castinetti F</pubmed_authors><pubmed_authors>Syro L</pubmed_authors><pubmed_authors>Whitelaw B</pubmed_authors><pubmed_authors>Ragnarsson O</pubmed_authors><pubmed_authors>Ragonese M</pubmed_authors><pubmed_authors>Reincke M</pubmed_authors><pubmed_authors>Guenego A</pubmed_authors><pubmed_authors>Garcia C</pubmed_authors><pubmed_authors>Micko A</pubmed_authors><pubmed_authors>Christ E</pubmed_authors><pubmed_authors>Criniere L</pubmed_authors><pubmed_authors>McCormack A</pubmed_authors><pubmed_authors>Maiter D</pubmed_authors><pubmed_authors>Ritzel K</pubmed_authors><pubmed_authors>Bourcigaux N</pubmed_authors><pubmed_authors>Mallea-Gil S</pubmed_authors><pubmed_authors>Theodoropoulou M</pubmed_authors><pubmed_authors>Chanson P</pubmed_authors><pubmed_authors>Batisse-Lignier M</pubmed_authors><pubmed_authors>Bresson D</pubmed_authors><pubmed_authors>Laws ER</pubmed_authors><pubmed_authors>Hoybye C</pubmed_authors><pubmed_authors>Cortet Rudelli C</pubmed_authors><pubmed_authors>Petersenn S</pubmed_authors><pubmed_authors>Ortiz LD</pubmed_authors><pubmed_authors>Feldt-Rasmussen U</pubmed_authors><pubmed_authors>Ceccato F</pubmed_authors><pubmed_authors>ESE survey collaborators †</pubmed_authors><pubmed_authors>Larrieu-Ciron D</pubmed_authors><pubmed_authors>Dusek T</pubmed_authors><pubmed_authors>Raverot G</pubmed_authors><pubmed_authors>Popovic V</pubmed_authors><pubmed_authors>Kralievic I</pubmed_authors><pubmed_authors>Deutschbein T</pubmed_authors><pubmed_authors>Henley D</pubmed_authors><pubmed_authors>Dekkers OM</pubmed_authors><pubmed_authors>Greenman Y</pubmed_authors><pubmed_authors>Burman P</pubmed_authors><pubmed_authors>Troendle A</pubmed_authors><pubmed_authors>Chevalier N</pubmed_authors><pubmed_authors>Decoudier B</pubmed_authors><pubmed_authors>Higham C</pubmed_authors><pubmed_authors>Engstrom BE</pubmed_authors><pubmed_authors>Haissaguerre M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Aggressive pituitary tumours and carcinomas, characteristics and management of 171 patients.</name><description>&lt;h4>Objective&lt;/h4>To describe clinical and pathological characteristics and treatment outcomes in a large cohort of aggressive pituitary tumours (APT)/pituitary carcinomas (PC).&lt;h4>Design&lt;/h4>Electronic survey August 2020-May 2021.&lt;h4>Results&lt;/h4>96% of 171 (121 APT, 50 PC), initially presented as macro/giant tumours, 6 were microadenomas (5 corticotroph). Ninety-seven tumours, initially considered clinically benign, demonstrated aggressive behaviour after 5.5 years (IQR: 2.8-12). Of the patients, 63% were men. Adrenocorticotrophic hormone (ACTH)-secreting tumours constituted 30% of the APT/PC, and the gonadotroph subtypes were under-represented. Five out of 13 silent corticotroph tumours and 2/6 silent somatotroph tumours became secreting. Metastases were observed after median 6.3 years (</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-05-28T00:35:19.031Z</modification><creation>2025-04-07T12:26:48.047Z</creation></dates><accession>S-EPMC9513638</accession><cross_references><pubmed>36018781</pubmed><doi>10.1530/EJE-22-0440</doi></cross_references></HashMap>