Publication:
Brentuximab vedotin for relapsed or refractory Hodgkin lymphoma: Experience in Turkey

dc.contributor.authorSalihoğlu, Ayşe
dc.contributor.authorElverdi, Tuğrul
dc.contributor.authorKaradoğan, İhsan
dc.contributor.authorPaydaş, Semra
dc.contributor.authorÖzdemir, Evren
dc.contributor.authorErdem, Gökhan
dc.contributor.authorKaradurmuş, Nuri
dc.contributor.authorAkyol, Gülşah
dc.contributor.authorKaynar, L.
dc.contributor.authorYeğin, Zeynep Arzu
dc.contributor.authorŞucak, Gülsan Türköz
dc.contributor.authorTopçuoğlu, Pervin
dc.contributor.authorÖzcan, Muhit
dc.contributor.authorBirtaş, Elif
dc.contributor.authorGöker, Hakan
dc.contributor.authorBaşlar, Zafer
dc.contributor.authorFerhanoğlu, Burhan
dc.contributor.buuauthorÖzkocaman, Vildan
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentİç Hastalıkları Ana Bilim Dalı
dc.contributor.departmentHematoloji Bilim Dalı
dc.contributor.researcheridAAH-1854-2021
dc.contributor.scopusid6603145040
dc.date.accessioned2022-06-13T12:51:36Z
dc.date.available2022-06-13T12:51:36Z
dc.date.issued2015-03
dc.description.abstractCurrent treatment modalities can cure up to 70-80 % of patients with classical Hodgkin lymphoma. Approximately, 20-30 % of patients require further treatment options. Brentuximab vedotin has been approved for the treatment of relapsed and refractory Hodgkin lymphoma. In the present study, we report the experience with brentuximab vedotin as single agent in 58 patients with relapsed or refractory Hodgkin lymphoma. The objective response rate was 63.5 % with 13 complete responders (26.5 %) among 49 patients evaluated at the early phase of treatment (2-5 cycles). Upon treatment prolongation (a parts per thousand yen6 cycles), 37 patients achieved a final objective response rate of 32.4 % with 21.6 % of complete and 10.8 % of partial response. Overall survival at 12 months was 70.6 %, and progression-free survival at 12 months was 32.8 %. Median overall survival could not be reached and median progression-free survival was 7 months. While the median duration of response was 9 months in the whole cohort, it was 11.5 months in the complete responders. Complete response rates in patients treated with > 3 chemotherapy regimens before brentuximab vedotin were significantly lower (p = 0.016). Fourteen patients were subsequently transplanted. In conclusion, brentuximab vedotin provided a bridge to transplantation in approximately one quarter of the patients. The declining response rates during the course of treatment suggest that transplantation should be implemented early during brentuximab vedotin treatment.
dc.identifier.citationSalihoğlu, A. vd. (2015). "Brentuximab vedotin for relapsed or refractory Hodgkin lymphoma: Experience in Turkey". Annals of Hematology, 94(3), 415-420.
dc.identifier.endpage420
dc.identifier.issn0939-5555
dc.identifier.issue3
dc.identifier.pubmed25231929
dc.identifier.scopus2-s2.0-84925461571
dc.identifier.startpage415
dc.identifier.urihttps://doi.org/10.1007/s00277-014-2215-9
dc.identifier.urihttps://link.springer.com/article/10.1007/s00277-014-2215-9
dc.identifier.urihttp://hdl.handle.net/11452/27113
dc.identifier.volume94
dc.identifier.wos000349225200007
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherSpringer
dc.relation.collaborationYurt içi
dc.relation.collaborationSanayi
dc.relation.journalAnnals of Hematology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBrentuximab vedotin
dc.subjectHodgkin Lymphoma
dc.subjectRefractory
dc.subjectRelapsed
dc.subjectTransplantation
dc.subjectMalignancies
dc.subjectIntensity
dc.subjectHematology
dc.subject.emtreeBrentuximab vedotin
dc.subject.emtreeAntibody conjugate
dc.subject.emtreecAC10-vcMMAE
dc.subject.emtreeAdolescent
dc.subject.emtreeAdult
dc.subject.emtreeAlopecia
dc.subject.emtreeArticle
dc.subject.emtreeCancer regression
dc.subject.emtreeConstipation
dc.subject.emtreeCytopenia
dc.subject.emtreeDrug dose reduction
dc.subject.emtreeDrug efficacy
dc.subject.emtreeDrug safety
dc.subject.emtreeFatigue
dc.subject.emtreeFemale
dc.subject.emtreeFever
dc.subject.emtreeFollow up
dc.subject.emtreeHodgkin disease
dc.subject.emtreeHuman
dc.subject.emtreeLimb pain
dc.subject.emtreeMajor clinical study
dc.subject.emtreeMale
dc.subject.emtreeMultiple cycle treatment
dc.subject.emtreeMuscle spasm
dc.subject.emtreeMyalgia
dc.subject.emtreeNausea
dc.subject.emtreeNeuropathy
dc.subject.emtreeNeurotoxicity
dc.subject.emtreeNeutropenia
dc.subject.emtreeOphthalmoplegia
dc.subject.emtreeOutcome assessment
dc.subject.emtreeOverall survival
dc.subject.emtreePeripheral neuropathy
dc.subject.emtreePriority journal
dc.subject.emtreeProgression free survival
dc.subject.emtreePruritus
dc.subject.emtreeRetrospective study
dc.subject.emtreeSurvival time
dc.subject.emtreeTonic seizure
dc.subject.emtreeTreatment duration
dc.subject.emtreeTreatment response
dc.subject.emtreeTurkey (republic)
dc.subject.emtreeVomiting
dc.subject.emtreeClinical trial
dc.subject.emtreeDrug effects
dc.subject.emtreeDrug resistance
dc.subject.emtreeHodgkin disease
dc.subject.emtreeMiddle aged
dc.subject.emtreeMulticenter study
dc.subject.emtreePathology
dc.subject.emtreeRecurrent disease
dc.subject.emtreeTreatment outcome
dc.subject.emtreeTurkey
dc.subject.emtreeYoung adult
dc.subject.meshAdolescent
dc.subject.meshAdult
dc.subject.meshDrug resistance, neoplasm
dc.subject.meshFemale
dc.subject.meshHodgkin disease
dc.subject.meshHumans
dc.subject.meshImmunoconjugates
dc.subject.meshMale
dc.subject.meshMiddle aged
dc.subject.meshRecurrence
dc.subject.meshRetrospective studies
dc.subject.meshTreatment outcome
dc.subject.meshTurkey
dc.subject.meshYoung adult
dc.subject.scopusBrentuximab Vedotin; Hodgkin's Disease; Refractory Materials
dc.subject.wosHematology
dc.titleBrentuximab vedotin for relapsed or refractory Hodgkin lymphoma: Experience in Turkey
dc.typeArticle
dc.wos.quartileQ2
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/İç Hastalıkları Ana Bilim Dalı/Hematoloji Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

Files

Original bundle

Now showing 1 - 1 of 1
Thumbnail Image
Name:
Özkocaman_vd_2015.pdf
Size:
502.17 KB
Format:
Adobe Portable Document Format
Description:

License bundle

Now showing 1 - 1 of 1
Placeholder
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: