<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li RC</submitter><funding>Clinical Research Plan of Shanghai Hospital Development Center</funding><funding>Chang Jiang Scholars Program, Shanghai Clinical Research Center for Cell Therapy</funding><funding>Multicenter Clinical Research Project by Shanghai Jiao Tong University School of Medicine</funding><funding>Shanghai Municipal Education Commission Gaofeng Clinical Medicine Grant Support</funding><funding>National Natural Science Foundation of China</funding><funding>National Key Research and Development Program of China</funding><pagination>131</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12553287</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Follicular lymphoma (FL) represents the most common subtype of indolent non-Hodgkin's lymphoma. Extranodal involvement (ENI) indicates a poor clinical outcome in patients who received rituximab-based immunochemotherapy. Recent studies indicate that genetic alterations and tumor microenvironment dysregulation drive extranodal dissemination and lymphoma progression. However, the molecular mechanisms underlying ENI in FL remain to be fully elucidated.&lt;h4>Methods&lt;/h4>Aiming to investigate the influence of oncogenic mutations and tumor microenvironment alterations on ENI in FL, the clinical features of 501 patients with newly diagnosed FL receiving rituximab-based therapy were analyzed, with DNA and RNA sequencing performed on 403 and 175 patients, respectively.&lt;h4>Results&lt;/h</pubmed_abstract><journal>Genome medicine</journal><pubmed_title>Clinical characteristics and molecular heterogeneity in Follicular lymphoma with extranodal involvement.</pubmed_title><pmcid>PMC12553287</pmcid><funding_grant_id>2022YFC2502600</funding_grant_id><funding_grant_id>81900193</funding_grant_id><funding_grant_id>DLY201601</funding_grant_id><funding_grant_id>SHDC2020CR1032B</funding_grant_id><funding_grant_id>82130004</funding_grant_id><funding_grant_id>23J41900100</funding_grant_id><funding_grant_id>20152206</funding_grant_id><pubmed_authors>Zheng Z</pubmed_authors><pubmed_authors>Chen SY</pubmed_authors><pubmed_authors>Yi HM</pubmed_authors><pubmed_authors>Xu TY</pubmed_authors><pubmed_authors>Feng Y</pubmed_authors><pubmed_authors>Dong L</pubmed_authors><pubmed_authors>Li RC</pubmed_authors><pubmed_authors>Zhao WL</pubmed_authors><pubmed_authors>Wang XH</pubmed_authors><pubmed_authors>Zhang HL</pubmed_authors><pubmed_authors>Xu PP</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Cheng S</pubmed_authors><pubmed_authors>Wang N</pubmed_authors><pubmed_authors>Sun R</pubmed_authors><pubmed_authors>Shen R</pubmed_authors><pubmed_authors>Tang W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical characteristics and molecular heterogeneity in Follicular lymphoma with extranodal involvement.</name><description>&lt;h4>Background&lt;/h4>Follicular lymphoma (FL) represents the most common subtype of indolent non-Hodgkin's lymphoma. Extranodal involvement (ENI) indicates a poor clinical outcome in patients who received rituximab-based immunochemotherapy. Recent studies indicate that genetic alterations and tumor microenvironment dysregulation drive extranodal dissemination and lymphoma progression. However, the molecular mechanisms underlying ENI in FL remain to be fully elucidated.&lt;h4>Methods&lt;/h4>Aiming to investigate the influence of oncogenic mutations and tumor microenvironment alterations on ENI in FL, the clinical features of 501 patients with newly diagnosed FL receiving rituximab-based therapy were analyzed, with DNA and RNA sequencing performed on 403 and 175 patients, respectively.&lt;h4>Results&lt;/h</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-06-05T04:52:01.597Z</modification><creation>2026-05-13T14:28:33.021Z</creation></dates><accession>S-EPMC12553287</accession><cross_references><pubmed>41137062</pubmed><doi>10.1186/s13073-025-01557-y</doi></cross_references></HashMap>