<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>207(3)</volume><submitter>Johnstone P</submitter><pubmed_abstract>Large-cell transformation of mycosis fungoides (LCTMF) is rare, histologically distinct, with an aggressive clinical course; yet is not recognised as an independent entity in classification systems nor in staging systems for mycosis fungoides and Sézary syndrome (MF/SS). Herein, the patterns of care and survival outcomes for patients with LCTMF are described, with prognosis compared to published data of non-transformed MF/SS. Eligibility required clinicopathological diagnosis of LCTMF (1/1/1990-31/10/2021), managed at Peter MacCallum Cancer Centre. Eighty-three patients were eligible. Median follow-up was 8.0 years. At the time of LCTMF, 36% had early-stage MF (IA-IIA), 76% had cutaneous-only LCTMF. The most common first-line treatments were localised radiotherapy (48%) and multiagent chem</pubmed_abstract><journal>British journal of haematology</journal><pagination>824-833</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12436213</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Large-cell transformation of mycosis fungoides: Patterns of care and patient outcomes.</pubmed_title><pmcid>PMC12436213</pmcid><pubmed_authors>Higgins M</pubmed_authors><pubmed_authors>Prince HM</pubmed_authors><pubmed_authors>van der Weyden C</pubmed_authors><pubmed_authors>Blombery P</pubmed_authors><pubmed_authors>McCormack C</pubmed_authors><pubmed_authors>Bhabha F</pubmed_authors><pubmed_authors>Johnstone P</pubmed_authors><pubmed_authors>Buelens O</pubmed_authors><pubmed_authors>Campbell BA</pubmed_authors><pubmed_authors>Lade S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Large-cell transformation of mycosis fungoides: Patterns of care and patient outcomes.</name><description>Large-cell transformation of mycosis fungoides (LCTMF) is rare, histologically distinct, with an aggressive clinical course; yet is not recognised as an independent entity in classification systems nor in staging systems for mycosis fungoides and Sézary syndrome (MF/SS). Herein, the patterns of care and survival outcomes for patients with LCTMF are described, with prognosis compared to published data of non-transformed MF/SS. Eligibility required clinicopathological diagnosis of LCTMF (1/1/1990-31/10/2021), managed at Peter MacCallum Cancer Centre. Eighty-three patients were eligible. Median follow-up was 8.0 years. At the time of LCTMF, 36% had early-stage MF (IA-IIA), 76% had cutaneous-only LCTMF. The most common first-line treatments were localised radiotherapy (48%) and multiagent chem</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-01T14:01:40.446Z</modification><creation>2026-04-08T13:17:54.402Z</creation></dates><accession>S-EPMC12436213</accession><cross_references><pubmed>40557623</pubmed><doi>10.1111/bjh.20225</doi></cross_references></HashMap>