Publication:
Brentuximab vedotin and bendamustine: an effective salvage therapy for relapsed or refractory Hodgkin lymphoma patients

dc.contributor.coauthorUncu Ulu, Bahar
dc.contributor.coauthorDal, Mehmet Sinan
dc.contributor.coauthorYönal Hindilerden, İpek
dc.contributor.coauthorMehtap, Özgür
dc.contributor.coauthorBüyükkurt, Nurhilal
dc.contributor.coauthorHindilerden, Fehmi
dc.contributor.coauthorGüneş, Ahmet Kürşad
dc.contributor.coauthorYiğenoğlu, Tuğçe Nur
dc.contributor.coauthorBaşçı, Semih
dc.contributor.coauthorKızıl Çakar, Merih
dc.contributor.coauthorYanardağ Açık, Didar
dc.contributor.coauthorKorkmaz, Serdal
dc.contributor.coauthorUlaş, Turgay
dc.contributor.coauthorÖzet, Gülsüm
dc.contributor.coauthorFerhanoğlu, Burhan
dc.contributor.coauthorNalçacı, Meliha
dc.contributor.coauthorAltuntaş, Fevzi
dc.contributor.departmentSchool of Medicine
dc.contributor.facultymemberYes
dc.contributor.kuauthorAkay, Olga Meltem
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:11:20Z
dc.date.issued2022
dc.description.abstractThe 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/m2 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.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessNO
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.studentonlypublicationNo
dc.description.studentpublicationNo
dc.description.versionN/A
dc.identifier.WoSQuartileQ4
dc.identifier.doi10.1080/1120009X.2021.1976912
dc.identifier.eissn1973-9478
dc.identifier.embargoN/A
dc.identifier.endpage198
dc.identifier.issn1120-009X
dc.identifier.issue3
dc.identifier.pubmed34514960
dc.identifier.scopus2-s2.0-85114844019
dc.identifier.startpage190
dc.identifier.urihttps://doi.org/10.1080/1120009X.2021.1976912
dc.identifier.urihttps://hdl.handle.net/20.500.14288/9627
dc.identifier.volume34
dc.identifier.wos000695425000001
dc.keywordsBrentuximab vedotin
dc.keywordsBendamustine
dc.keywordsRelapsed and refractory
dc.keywordsHodgkin lymphoma
dc.keywordsSalvage therapy
dc.language.isoeng
dc.publisherTaylor and Francis
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofJournal of Chemotherapy
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectHematology
dc.subjectMedical oncology
dc.subjectCancer chemotherapy
dc.subjectClinical pharmacology
dc.titleBrentuximab vedotin and bendamustine: an effective salvage therapy for relapsed or refractory Hodgkin lymphoma patients
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorAkay, Olga Meltem
relation.isGoalOfPublicationa9786601-9431-4553-9a46-013bb366fb87
relation.isGoalOfPublication.latestForDiscoverya9786601-9431-4553-9a46-013bb366fb87
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