Real-World Outcomes of Belinostat in Relapsed Refractory T-Cell Lymphomas: A Report from the Lymphoma Study Group of Turkish Society of Hematology

dc.contributor.authorUlukoylu Menguc, Meral
dc.contributor.authorArikan, Fatma
dc.contributor.authorAytan, Pelin
dc.contributor.authorBekoz, Huseyin Saffet
dc.contributor.authorHunutlu, Fazil Cagri
dc.contributor.authorKeklik Karadag, Fatma
dc.contributor.authorToptas, Tayfur
dc.date.accessioned2026-09-08T07:11:44Z
dc.date.issued2026
dc.departmentFırat Üniveristesi
dc.description.abstractBackground: T-cell lymphomas (TCLs) constitute a heterogeneous group of mature T-cell neoplasms characterized by aggressive clinical behavior and poor outcomes, particularly in the relapsed/refractory (R/R) setting. Belinostat is a pan-HDAC inhibitor approved for R/R peripheral T-cell lymphomas. In this retrospective study, we analyze the real-world outcomes of single-agent belinostat in Turkish patients with R/R TCLs. Methods: Patients with R/R TCLs across Turkey who received at least one course of belinostat were included in the study. The primary end point was the overall response rate (ORR). The secondary end points included progression-free survival (PFS), overall survival (OS) and duration of response (DOR). Results: A total of 59 patients with R/R TCL were enrolled in the study, with a median age of 62 years. The median number of previous lines of therapy before belinostat was 2.5. The ORR for belinostat was 30.5% in the overall study cohort. Response assessment was available in 53 patients, among whom the ORR was 34% (18/53). The median PFS was 3 months. The median OS was 12 months, and the median DOR was not reached in responders. At least one adverse event occurred in 39.0% of patients. Conclusions: Belinostat produced objective responses in a subset of patients. These findings support belinostat as a potential individualized treatment option rather than a broadly effective standard for all patients with R/R TCLs. This multicenter real-world study demonstrates that the observed response rates closely mirror those reported in prospective clinical trials, confirming the reproducibility of belinostat efficacy in routine clinical practice.
dc.identifier.doi10.3390/jcm15166350
dc.identifier.issn2077-0383
dc.identifier.issue16
dc.identifier.scopus2-s2.0-105048443270
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.3390/jcm15166350
dc.identifier.urihttps://hdl.handle.net/11508/65123
dc.identifier.volume15
dc.identifier.wosWOS:001859207700001
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherMdpi
dc.relation.ispartofJournal of Clinical Medicine
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250903
dc.subjectT-Cell Lymphoma
dc.subjectRelapsed Refractory
dc.subjectBelinostat
dc.subjectHdac Inhibitors
dc.titleReal-World Outcomes of Belinostat in Relapsed Refractory T-Cell Lymphomas: A Report from the Lymphoma Study Group of Turkish Society of Hematology
dc.typeArticle

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