<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>3(4)</volume><submitter>Zheng Y</submitter><pubmed_abstract>Diffuse large B-cell lymphoma (DLBCL), the most common subtype of non-Hodgkin lymphoma, is highly heterogeneous and invasive. Although the majority of DLBCL patients show a good response to rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone treatment, approximately one-third of patients still have a poor prognosis. Many immune-targeted drugs, such as bispecific T-cell engagers and CAR T-cell therapy, have been proven effective for refractory and relapsed patients. This article reviews the progress of immune targeted therapy for DLBCL.</pubmed_abstract><journal>Blood science (Baltimore, Md.)</journal><pagination>136-148</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8975004</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Immune targeted therapy for diffuse large B cell lymphoma.</pubmed_title><pmcid>PMC8975004</pmcid><pubmed_authors>Yuan T</pubmed_authors><pubmed_authors>Zheng Y</pubmed_authors><pubmed_authors>Ding S</pubmed_authors><pubmed_authors>Si J</pubmed_authors><pubmed_authors>Tian C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immune targeted therapy for diffuse large B cell lymphoma.</name><description>Diffuse large B-cell lymphoma (DLBCL), the most common subtype of non-Hodgkin lymphoma, is highly heterogeneous and invasive. Although the majority of DLBCL patients show a good response to rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone treatment, approximately one-third of patients still have a poor prognosis. Many immune-targeted drugs, such as bispecific T-cell engagers and CAR T-cell therapy, have been proven effective for refractory and relapsed patients. This article reviews the progress of immune targeted therapy for DLBCL.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2025-04-05T00:40:01.338Z</modification><creation>2025-04-05T00:40:01.338Z</creation></dates><accession>S-EPMC8975004</accession><cross_references><pubmed>35402846</pubmed><doi>10.1097/BS9.0000000000000095</doi></cross_references></HashMap>