Publication: Brentuximab vedotin and bendamustine: an effective salvage therapy for relapsed or refractory Hodgkin lymphoma patients
dc.contributor.coauthor | Ulu, Bahar Uncu | |
dc.contributor.coauthor | Dal, Mehmet Sinan | |
dc.contributor.coauthor | Hindilerden, Ipek Yonal | |
dc.contributor.coauthor | Mehtap, Ozgur | |
dc.contributor.coauthor | Buyukkurt, Nurhilal | |
dc.contributor.coauthor | Hindilerden, Fehmi | |
dc.contributor.coauthor | Gunes, Ahmet Kursad | |
dc.contributor.coauthor | Yigenoglu, Tugce Nur | |
dc.contributor.coauthor | Basci, Semih | |
dc.contributor.coauthor | Cakar, Merih Kizil | |
dc.contributor.coauthor | Acik, Didar Yanardag | |
dc.contributor.coauthor | Korkmaz, Serdal | |
dc.contributor.coauthor | Ulas, Turgay | |
dc.contributor.coauthor | Ozet, Gulsum | |
dc.contributor.coauthor | Ferhanoglu, Burhan | |
dc.contributor.coauthor | Nalcaci, Meliha | |
dc.contributor.coauthor | Altuntas, Fevzi | |
dc.contributor.department | School of Medicine | |
dc.contributor.kuauthor | Akay, Olga Meltem | |
dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
dc.date.accessioned | 2024-11-09T23:11:20Z | |
dc.date.issued | 2022 | |
dc.description.abstract | The prognosis is poor for relapsed or refractory (R/R) classical Hodgkin Lymphoma (cHL) patients. The brentuximab vedotin (Bv) and bendamustine (B) combination has been used as a preferable salvage regimen in R/R cHL patient trials. We retrospectively evaluated response rates, toxicities, and the survival in R/R cHL patients treated with the BvB combination. In a multi-centre real-life study, 61 R/R HL patients received intravenous doses of 1.8 mg/kg Bv on the first day plus 90 mg/m(2) B on the first and second days of a 21-day cycle as a second-line or beyond-salvage regimen. Patients' median age at BvB initiation was 33 (range: 18-76 years). BvB was given as median third-line treatment for a median of four cycles (range: 2-11). The overall and complete response rates were 82% and 68.9%, respectively. After BvB initiation, the median follow-up was 14 months, and one- and two-year overall survival rates were 85% and 72%, respectively. Grade 3/4 toxicities included neutropenia (24.6%), lymphopenia (40%), thrombocytopenia (13%), anaemia (13%), infusion reactions (8.2%), neuropathy (6.5%), and others. The BvB combination could be given as salvage regimen aiming a bridge to autologous stem cell transplant (ASCT), in patients relapse after ASCT or to transplant-ineligible patients with manageable toxicity profiles. | |
dc.description.indexedby | WOS | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | PubMed | |
dc.description.issue | 3 | |
dc.description.openaccess | NO | |
dc.description.publisherscope | International | |
dc.description.sponsoredbyTubitakEu | N/A | |
dc.description.volume | 34 | |
dc.identifier.doi | 10.1080/1120009X.2021.1976912 | |
dc.identifier.eissn | 1973-9478 | |
dc.identifier.issn | 1120-009X | |
dc.identifier.quartile | Q4 | |
dc.identifier.scopus | 2-s2.0-85114844019 | |
dc.identifier.uri | https://doi.org/10.1080/1120009X.2021.1976912 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/9627 | |
dc.identifier.wos | 695425000001 | |
dc.keywords | Brentuximab vedotin | |
dc.keywords | Bendamustine | |
dc.keywords | Relapsed and refractory | |
dc.keywords | Hodgkin lymphoma | |
dc.keywords | Salvage therapy | |
dc.language.iso | eng | |
dc.publisher | TAYLOR & FRANCIS LTD | |
dc.relation.ispartof | JOURNAL of CHEMOTHERAPY | |
dc.subject | Oncology | |
dc.subject | Infectious diseases | |
dc.subject | Pathology | |
dc.subject | Pharmacology | |
dc.subject | Pharmacy | |
dc.title | Brentuximab vedotin and bendamustine: an effective salvage therapy for relapsed or refractory Hodgkin lymphoma patients | |
dc.type | Journal Article | |
dspace.entity.type | Publication | |
local.contributor.kuauthor | Akay, Olga Meltem | |
local.publication.orgunit1 | SCHOOL OF MEDICINE | |
local.publication.orgunit2 | School of Medicine | |
relation.isOrgUnitOfPublication | d02929e1-2a70-44f0-ae17-7819f587bedd | |
relation.isOrgUnitOfPublication.latestForDiscovery | d02929e1-2a70-44f0-ae17-7819f587bedd | |
relation.isParentOrgUnitOfPublication | 17f2dc8e-6e54-4fa8-b5e0-d6415123a93e | |
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