<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Miyao K</submitter><funding>Fifth District Eagles Cancer Telethon</funding><funding>Gerstner Family Foundation</funding><funding>National Institutes of Health</funding><funding>Henry J. Predolin Foundation for Research in Leukemia</funding><pubmed_abstract>Primary central nervous system lymphoma (PCNSL) is a rare form and aggressive type of diffuse large B-cell lymphoma (DLBCL) that occurs in both immunocompetent and immunocompromised adults. While adding rituximab to chemotherapeutic regimens resulted in dramatic improvement in both progression-free survival and overall survival in patients with non-central nervous system (CNS) DLBCL, the outcomes of PCNSL are generally poor due to the immune-privileged tumor microenvironment or suboptimal delivery of systemic agents into tumor tissues. Therefore, more effective therapy for PCNSL generally requires systemic therapy with sufficient CNS penetration, including high-dose intravenous methotrexate with rituximab or high-dose chemotherapy followed by autologous stem cell transplantation. However, </pubmed_abstract><journal>Frontiers in oncology</journal><pagination>1082235</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9850100</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Is CD19-directed chimeric antigen receptor T cell therapy a smart strategy to combat central nervous system lymphoma?</pubmed_title><pmcid>PMC9850100</pmcid><pubmed_authors>Miyao K</pubmed_authors><pubmed_authors>Sakemura RL</pubmed_authors><pubmed_authors>Yokota H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Is CD19-directed chimeric antigen receptor T cell therapy a smart strategy to combat central nervous system lymphoma?</name><description>Primary central nervous system lymphoma (PCNSL) is a rare form and aggressive type of diffuse large B-cell lymphoma (DLBCL) that occurs in both immunocompetent and immunocompromised adults. While adding rituximab to chemotherapeutic regimens resulted in dramatic improvement in both progression-free survival and overall survival in patients with non-central nervous system (CNS) DLBCL, the outcomes of PCNSL are generally poor due to the immune-privileged tumor microenvironment or suboptimal delivery of systemic agents into tumor tissues. Therefore, more effective therapy for PCNSL generally requires systemic therapy with sufficient CNS penetration, including high-dose intravenous methotrexate with rituximab or high-dose chemotherapy followed by autologous stem cell transplantation. However, </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T08:33:49.946Z</modification><creation>2025-04-04T08:33:49.946Z</creation></dates><accession>S-EPMC9850100</accession><cross_references><pubmed>36686821</pubmed><doi>10.3389/fonc.2022.1082235</doi></cross_references></HashMap>