<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>28(17)</volume><submitter>Palazon-Carrion N</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>New therapeutic options are needed in relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL). Lenalidomide-based schedules can reverse rituximab refractoriness in lymphoma.&lt;h4>Patients and methods&lt;/h4>In the phase II R2-GDP trial, 78 patients unsuitable for autologous stem cell transplant received treatment with the following schedule: lenalidomide 10 mg Days (D)1-14, rituximab 375 mg/m2 D1, cisplatin 60 mg/m2 D1, gemcitabine 750 mg/m2 D1 and D8, and dexamethasone 20 mg D1-3, up to 6 cycles (induction phase), followed by lenalidomide 10 mg (or last lenalidomide dose received) D1-21 every 28 days (maintenance phase). Primary endpoint was overall response rate (ORR). Secondary endpoints included progression-free survival (PFS), overall survival (OS), safety, and monito</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pagination>3658-3668</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9433956</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Lenalidomide plus R-GDP (R2-GDP) in Relapsed/Refractory Diffuse Large B-Cell Lymphoma: Final Results of the R2-GDP-GOTEL Trial and Immune Biomarker Subanalysis.</pubmed_title><pmcid>PMC9433956</pmcid><pubmed_authors>de la Cruz-Vicente F</pubmed_authors><pubmed_authors>Guirado-Risueno M</pubmed_authors><pubmed_authors>Espejo-Garcia P</pubmed_authors><pubmed_authors>Hontecillas-Prieto L</pubmed_authors><pubmed_authors>Jimenez-Cortegana C</pubmed_authors><pubmed_authors>Galvez-Carvajal L</pubmed_authors><pubmed_authors>Rueda-Dominguez A</pubmed_authors><pubmed_authors>Sanchez-Beato M</pubmed_authors><pubmed_authors>Navarro M</pubmed_authors><pubmed_authors>Fernandez-Roman I</pubmed_authors><pubmed_authors>Gomez-Codina J</pubmed_authors><pubmed_authors>Rios-Herranz E</pubmed_authors><pubmed_authors>Palazon-Carrion N</pubmed_authors><pubmed_authors>Garcia-Dominguez DJ</pubmed_authors><pubmed_authors>Sanchez-Margalet V</pubmed_authors><pubmed_authors>Martin Garcia-Sancho A</pubmed_authors><pubmed_authors>Salar-Silvestre A</pubmed_authors><pubmed_authors>Labrador J</pubmed_authors><pubmed_authors>Rodriguez-Garcia G</pubmed_authors><pubmed_authors>Nogales-Fernandez E</pubmed_authors><pubmed_authors>Rodriguez-Abreu D</pubmed_authors><pubmed_authors>Fernandez-Alvarez R</pubmed_authors><pubmed_authors>Alvaro-Naranjo T</pubmed_authors><pubmed_authors>de la Cruz-Merino L</pubmed_authors><pubmed_authors>Provencio-Pulla M</pubmed_authors><pubmed_authors>Guma-Padro J</pubmed_authors><pubmed_authors>Carnicero-Gonzalez F</pubmed_authors><pubmed_authors>Martinez-Banaclocha N</pubmed_authors><pubmed_authors>Casanova-Espinosa M</pubmed_authors><pubmed_authors>Marylene L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lenalidomide plus R-GDP (R2-GDP) in Relapsed/Refractory Diffuse Large B-Cell Lymphoma: Final Results of the R2-GDP-GOTEL Trial and Immune Biomarker Subanalysis.</name><description>&lt;h4>Purpose&lt;/h4>New therapeutic options are needed in relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL). Lenalidomide-based schedules can reverse rituximab refractoriness in lymphoma.&lt;h4>Patients and methods&lt;/h4>In the phase II R2-GDP trial, 78 patients unsuitable for autologous stem cell transplant received treatment with the following schedule: lenalidomide 10 mg Days (D)1-14, rituximab 375 mg/m2 D1, cisplatin 60 mg/m2 D1, gemcitabine 750 mg/m2 D1 and D8, and dexamethasone 20 mg D1-3, up to 6 cycles (induction phase), followed by lenalidomide 10 mg (or last lenalidomide dose received) D1-21 every 28 days (maintenance phase). Primary endpoint was overall response rate (ORR). Secondary endpoints included progression-free survival (PFS), overall survival (OS), safety, and monito</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2026-05-28T03:45:57.361Z</modification><creation>2025-04-06T00:51:45.978Z</creation></dates><accession>S-EPMC9433956</accession><cross_references><pubmed>35727601</pubmed><doi>10.1158/1078-0432.CCR-22-0588</doi></cross_references></HashMap>