<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(18)</volume><submitter>Khan N</submitter><pubmed_abstract>&lt;h4>Abstract&lt;/h4>Patients with peripheral T-cell lymphoma (PTCL) have suboptimal outcomes. Autologous hematopoietic stem-cell transplantation (AHCT) is a therapeutic strategy for patients in first complete remission (CR1) or first partial remission (PR1), with median intent-to-treat progression-free survival (PFS) of 36% to 48%. Romidepsin is a histone deacetylase inhibitor used for treatment of relapsed/refractory PTCL. We present a multicenter study to evaluate the PFS of patients receiving maintenance therapy with romidepsin after AHCT. Twenty-six patients who underwent AHCT in CR1 or PR1 were evaluated for the primary end point of 2-year PFS. The exploratory cohort enrolled patients who underwent transplantation during or after CR/PR2 (n = 5) or high-risk histologies (n = 2). Patients underwent AHCT with carmustine, etoposide, cytarabine, and melphalan conditioning. Romidepsin 14 mg/m2 was started on days 42 to 80 after -AHCT every other week until 6 months of -AHCT, every 3 weeks between 6 months and 1-year of -AHCT, and every 4 weeks between 1 and 2 years of -AHCT. PFS was estimated using the Kaplan-Meier analysis. Forty-seven patients consented and 13 did not receive romidepsin. With a median progression-free follow-up of 32 months (range, 24-36), 15 of the first 25 patients in cohort 1 were progression-free after 2 years. The estimated 2-year PFS was 62% (95% confidence interval, 45-83). The most common toxicities were fatigue (n = 24, 73%), decreased platelets (n = 16, 48%), and anemia (n = 16, 48%). Although the study did not meet its desired primary efficacy end point, maintenance romidepsin was feasible, with a favorable estimated 2-year PFS of 62%. This trial was registered at www.ClinicalTrials.gov as #NCT01908777.</pubmed_abstract><journal>Blood advances</journal><pagination>4687-4692</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12466233</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Maintenance therapy with romidepsin after autologous stem-cell transplant for peripheral T-cell lymphoma.</pubmed_title><pmcid>PMC12466233</pmcid><pubmed_authors>Dahi PB</pubmed_authors><pubmed_authors>Moskowitz AJ</pubmed_authors><pubmed_authors>van Beisen K</pubmed_authors><pubmed_authors>Drullinsky P</pubmed_authors><pubmed_authors>Noy A</pubmed_authors><pubmed_authors>Sauter CS</pubmed_authors><pubmed_authors>Matasar MJ</pubmed_authors><pubmed_authors>Hancock H</pubmed_authors><pubmed_authors>Ganesan N</pubmed_authors><pubmed_authors>Shah GL</pubmed_authors><pubmed_authors>Drill E</pubmed_authors><pubmed_authors>Galasso N</pubmed_authors><pubmed_authors>Ruan J</pubmed_authors><pubmed_authors>Horwitz SM</pubmed_authors><pubmed_authors>Straus DJ</pubmed_authors><pubmed_authors>Zelenetz AD</pubmed_authors><pubmed_authors>Shadman M</pubmed_authors><pubmed_authors>Khan N</pubmed_authors><pubmed_authors>Hamilton A</pubmed_authors><pubmed_authors>Kumar A</pubmed_authors><pubmed_authors>Davey T</pubmed_authors><pubmed_authors>Khimani F</pubmed_authors><pubmed_authors>Shustov AR</pubmed_authors><pubmed_authors>Giralt S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Maintenance therapy with romidepsin after autologous stem-cell transplant for peripheral T-cell lymphoma.</name><description>&lt;h4>Abstract&lt;/h4>Patients with peripheral T-cell lymphoma (PTCL) have suboptimal outcomes. Autologous hematopoietic stem-cell transplantation (AHCT) is a therapeutic strategy for patients in first complete remission (CR1) or first partial remission (PR1), with median intent-to-treat progression-free survival (PFS) of 36% to 48%. Romidepsin is a histone deacetylase inhibitor used for treatment of relapsed/refractory PTCL. We present a multicenter study to evaluate the PFS of patients receiving maintenance therapy with romidepsin after AHCT. Twenty-six patients who underwent AHCT in CR1 or PR1 were evaluated for the primary end point of 2-year PFS. The exploratory cohort enrolled patients who underwent transplantation during or after CR/PR2 (n = 5) or high-risk histologies (n = 2). Patients underwent AHCT with carmustine, etoposide, cytarabine, and melphalan conditioning. Romidepsin 14 mg/m2 was started on days 42 to 80 after -AHCT every other week until 6 months of -AHCT, every 3 weeks between 6 months and 1-year of -AHCT, and every 4 weeks between 1 and 2 years of -AHCT. PFS was estimated using the Kaplan-Meier analysis. Forty-seven patients consented and 13 did not receive romidepsin. With a median progression-free follow-up of 32 months (range, 24-36), 15 of the first 25 patients in cohort 1 were progression-free after 2 years. The estimated 2-year PFS was 62% (95% confidence interval, 45-83). The most common toxicities were fatigue (n = 24, 73%), decreased platelets (n = 16, 48%), and anemia (n = 16, 48%). Although the study did not meet its desired primary efficacy end point, maintenance romidepsin was feasible, with a favorable estimated 2-year PFS of 62%. This trial was registered at www.ClinicalTrials.gov as #NCT01908777.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T21:26:18.409Z</modification><creation>2026-05-01T03:11:22.815Z</creation></dates><accession>S-EPMC12466233</accession><cross_references><pubmed>40179392</pubmed><doi>10.1182/bloodadvances.2024014263</doi></cross_references></HashMap>