Publication:
Nivolumab for relapsed or refractory Hodgkin lymphoma: Real-life experience

dc.contributor.buuauthorDemirkaya, Metin
dc.contributor.departmentMühendislik Fakültesi
dc.contributor.departmentMakine Mühendisliği
dc.contributor.researcheridGAF-3538-2022
dc.contributor.scopusid24331130000
dc.date.accessioned2024-02-05T06:52:14Z
dc.date.available2024-02-05T06:52:14Z
dc.date.issued2020-05
dc.descriptionÇalışmada 21 yazar bulunmaktadır. Bu yazarlardan sadece Bursa Uludağ Üniversitesi mensuplarının girişleri yapılmıştır.
dc.description.abstractClassical Hodgkin lymphoma (cHL) is considered a curable disease; however, in approximately one-third of the responding patients, the disease relapses following completion of therapy. One of the drugs that have been approved for the treatment of relapsed/refractory cHL is nivolumab, an immune check point inhibitor that shows its effects by blocking the programmed death 1 (PD-1) receptor. In this study, we present a retrospective “real-life” analysis of the usage of nivolumab in patients with relapsed/refractory cHL that have joined the named patient program (NPP) for nivolumab, reflecting 4 years of experience in the treatment of relapsed/refractory cHL. We present a retrospective analysis of 87 patients (median age, 30) that participated in the NPP in 24 different centers, who had relapsed/refractory cHL and were consequently treated with nivolumab. The median follow-up was 29 months, and the median number of previous treatments was 5 (2–11). In this study, the best overall response rate was 70% (CR, 36%; PR, 34%). Twenty-eight of the responding patients underwent subsequent stem cell transplantation (SCT). Among 15 patients receiving allogeneic stem cell transplantation, 9 patients underwent transplantation with objective response, of which 8 of them are currently alive with ongoing response. At the time of analysis, 23 patients remained on nivolumab treatment and the rest discontinued therapy. The main reason for discontinuing nivolumab was disease progression (n = 23). The safety profile was acceptable, with only nine patients requiring cessation of nivolumab due to serious adverse events. The 24-month progression-free and overall survival rates were 58.5% (95% CI, 0.47–0.68) and 78.7% (95% CI, 0.68–0.86), respectively. Eighteen patients died during the follow-up and only one of these was regarded to be treatment-related. With its efficacy and its safety profile, PD-1 blockers became an important treatment option in the heavily pretreated cHL patients.
dc.identifier.citationBeköz, S. vd. (2020). "Nivolumab for relapsed or refractory Hodgkin lymphoma: Real-life experience". Annals of Hematology, 99(11), 2565-2576.
dc.identifier.doihttps://doi.org/10.1007/s00277-020-04077-4
dc.identifier.endpage2576
dc.identifier.issn0939-5555
dc.identifier.issn1432-0584
dc.identifier.issue11
dc.identifier.pubmed32507911
dc.identifier.scopus2-s2.0-85086129098
dc.identifier.startpage2565
dc.identifier.urihttps://link.springer.com/article/10.1007/s00277-020-04077-4
dc.identifier.urihttps://hdl.handle.net/11452/39491
dc.identifier.volume99
dc.identifier.wos000538693900001
dc.indexed.scopusScopus
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/closedAccess
dc.subjectHodgkin lymphoma
dc.subjectResistant
dc.subjectRelapsed disease
dc.subjectProgrammed death 1 (PD-1) blocker
dc.subjectNivolumab
dc.subjectBrentuximab vedotin
dc.subjectPhase-II
dc.subjectCell transplantation
dc.subjectResponse criteria
dc.subjectPembrolizumab
dc.subjectMulticohort
dc.subjectEfficacy
dc.subjectBlockade
dc.subjectFailure
dc.subjectABVD
dc.subjectHematology
dc.subject.emtreeNivolumab
dc.subject.emtreeAbdominal pain
dc.subject.emtreeAdult
dc.subject.emtreeAllogeneic stem cell transplantation
dc.subject.emtreeAnemia
dc.subject.emtreeAppetite disorder
dc.subject.emtreeArthritis
dc.subject.emtreeArticle
dc.subject.emtreeAutoimmune liver disease
dc.subject.emtreeAutoimmune pneumonitis
dc.subject.emtreeCancer growth
dc.subject.emtreeCancer immunotherapy
dc.subject.emtreeCancer mortality
dc.subject.emtreeCancer pain
dc.subject.emtreeCancer recurrence
dc.subject.emtreeCatheter infection
dc.subject.emtreeClassical Hodgkin lymphoma
dc.subject.emtreeCohort analysis
dc.subject.emtreeCystitis
dc.subject.emtreeDermatitis
dc.subject.emtreeDiarrhea
dc.subject.emtreeDrug efficacy
dc.subject.emtreeDrug hypersensitivity
dc.subject.emtreeDrug safety
dc.subject.emtreeDrug withdrawal
dc.subject.emtreeEdema
dc.subject.emtreeEncephalitis
dc.subject.emtreeEncephalitis
dc.subject.emtreeFatigue
dc.subject.emtreeFever
dc.subject.emtreeFollow up
dc.subject.emtreeGraft versus host reaction
dc.subject.emtreeGynecomastia
dc.subject.emtreeHeadache
dc.subject.emtreeHeart infarction
dc.subject.emtreeHuman
dc.subject.emtreeHypercalcemia
dc.subject.emtreeHyperthyroidism
dc.subject.emtreeHypertransaminasemia
dc.subject.emtreeHypocalcemia
dc.subject.emtreeHypophosphatemia
dc.subject.emtreeHypothyroidism
dc.subject.emtreeImmunopathology
dc.subject.emtreeLymphocytopenia
dc.subject.emtreeMajor clinical study
dc.subject.emtreeMultiple cycle treatment
dc.subject.emtreeMuscle cramp
dc.subject.emtreeNamed patient program
dc.subject.emtreeNausea
dc.subject.emtreeNeutropenia
dc.subject.emtreeOverall response rate
dc.subject.emtreeOverall survival
dc.subject.emtreePain
dc.subject.emtreePancreatitis
dc.subject.emtreePeripheral neuropathy
dc.subject.emtreePhlebitis
dc.subject.emtreePneumonia
dc.subject.emtreePriority journal
dc.subject.emtreeProgression free survival
dc.subject.emtreePruritus
dc.subject.emtreeRash
dc.subject.emtreeRetrospective study
dc.subject.emtreeScrotal pain
dc.subject.emtreeSepsis
dc.subject.emtreeSide effect
dc.subject.emtreeStomatitis
dc.subject.emtreeThrombocytopenia
dc.subject.emtreeTreatment response
dc.subject.emtreeTreatment withdrawal
dc.subject.emtreeUpper respiratory tract infection
dc.subject.emtreeVisual disorder
dc.subject.emtreeAllograft
dc.subject.emtreeClinical trial
dc.subject.emtreeDisease free survival
dc.subject.emtreeFemale
dc.subject.emtreeHodgkin disease
dc.subject.emtreeMale
dc.subject.emtreeMiddle aged
dc.subject.emtreeMortality
dc.subject.emtreeMulticenter study
dc.subject.emtreeStem cell transplantation
dc.subject.emtreeSurvival rate
dc.subject.meshAdult
dc.subject.meshAllografts
dc.subject.meshDisease-free survival
dc.subject.meshFemale
dc.subject.meshFollow-up Studies
dc.subject.meshHodgkin disease
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMiddle aged
dc.subject.meshNivolumab
dc.subject.meshRetrospective studies
dc.subject.meshStem cell transplantation
dc.subject.meshSurvival rate
dc.subject.scopusBrentuximab Vedotin; Hodgkin's Disease; Refractory Materials
dc.subject.wosHematology
dc.titleNivolumab for relapsed or refractory Hodgkin lymphoma: Real-life experience
dc.typeArticle
dc.wos.quartileQ2
dc.wos.quartileQ2
dspace.entity.typePublication
local.contributor.departmentMühendislik Fakültesi/Makine Mühendisliği
local.indexed.atPubMed
local.indexed.atWOS
local.indexed.atScopus

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