<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Holte H</submitter><funding>NCI NIH HHS</funding><pagination>225-234</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6530911</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>183(2)</volume><pubmed_abstract>Patients with mantle cell lymphoma (MCL) generally have a dismal prognosis. Intensified induction treatment with rituximab and high dose cytarabine (R_HDAC), and consolidation with high-dose therapy with autologous stem cell support has resulted in 10-year overall survival (OS) higher than 60%. However, the clinical course varies. Diagnostic tools capable of stratifying patients include the MCL International Prognostic Index (MIPI), gene expression-based proliferation signature, Ki-67 proliferation index or tumour cell morphology. Here, we tested the performance of a newly developed Nanostring-based RNA expression-based proliferation assay (MCL35) on formalin-fixed paraffin-embedded tumour tissue from younger patients recruited in or treated according to Nordic MCL protocols compared to th</pubmed_abstract><journal>British journal of haematology</journal><pubmed_title>The MCL35 gene expression proliferation assay predicts high-risk MCL patients in a Norwegian cohort of younger patients given intensive first line therapy.</pubmed_title><pmcid>PMC6530911</pmcid><funding_grant_id>UH2 CA217847</funding_grant_id><pubmed_authors>Beiske K</pubmed_authors><pubmed_authors>Myklebust J</pubmed_authors><pubmed_authors>Smeland EB</pubmed_authors><pubmed_authors>Holte H</pubmed_authors><pubmed_authors>Blaker YN</pubmed_authors><pubmed_authors>Kvaloy S</pubmed_authors><pubmed_authors>Lingjaerde OC</pubmed_authors><pubmed_authors>Kolstad A</pubmed_authors><pubmed_authors>Boyle M</pubmed_authors><pubmed_authors>Rimsza LM</pubmed_authors><pubmed_authors>Rosenwald A</pubmed_authors><pubmed_authors>Scott DW</pubmed_authors><pubmed_authors>Troen G</pubmed_authors></additional><is_claimable>false</is_claimable><name>The MCL35 gene expression proliferation assay predicts high-risk MCL patients in a Norwegian cohort of younger patients given intensive first line therapy.</name><description>Patients with mantle cell lymphoma (MCL) generally have a dismal prognosis. Intensified induction treatment with rituximab and high dose cytarabine (R_HDAC), and consolidation with high-dose therapy with autologous stem cell support has resulted in 10-year overall survival (OS) higher than 60%. However, the clinical course varies. Diagnostic tools capable of stratifying patients include the MCL International Prognostic Index (MIPI), gene expression-based proliferation signature, Ki-67 proliferation index or tumour cell morphology. Here, we tested the performance of a newly developed Nanostring-based RNA expression-based proliferation assay (MCL35) on formalin-fixed paraffin-embedded tumour tissue from younger patients recruited in or treated according to Nordic MCL protocols compared to th</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Oct</publication><modification>2025-05-29T20:30:47.902Z</modification><creation>2025-05-29T20:30:47.902Z</creation></dates><accession>S-EPMC6530911</accession><cross_references><pubmed>30080252</pubmed><doi>10.1111/bjh.15518</doi></cross_references></HashMap>