Publication:
Endocrine adverse events in patients treated with immune checkpoint inhibitors: a comprehensive analysis

dc.contributor.coauthorDokmetas, Meric
dc.contributor.coauthorMuglu, Harun
dc.contributor.coauthorOzcan, Erkan
dc.contributor.coauthorHelvaci, Kaan
dc.contributor.coauthorKalaci, Ender
dc.contributor.coauthorKahraman, Seda
dc.contributor.coauthorAykan, Musa Baris
dc.contributor.coauthorCicin, Irfan
dc.contributor.coauthorOlmez, Omer Fatih
dc.contributor.coauthorBilici, Ahmet
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorKuvvet, Fadime Buket Bayram
dc.contributor.kuauthorSelçukbiricik, Fatih
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2025-05-22T10:36:26Z
dc.date.available2025-05-22
dc.date.issued2025
dc.description.abstractBackground and Objectives: Immune checkpoint inhibitors (ICIs) have revolutionized cancer therapy, but their use is associated with a spectrum of immune-related adverse events (irAEs), including endocrine disorders. This study aims to investigate the incidence, timing, treatment modalities, and impact of ICI-related endocrine side effects in cancer patients. Materials and Methods: This retrospective study analyzed 139 cancer patients treated with ICIs between 2016 and 2022. Data regarding endocrine irAEs, including hypothyroidism, hyperthyroidism, hypophysitis, and diabetes mellitus, were collected. The study examined the timing of irAE onset, management approaches, and the association between irAEs and treatment outcomes. Results: The most common endocrine irAE was hypothyroidism (65.5%), followed by hyperthyroidism (2.3%), hypophysitis (8.6%), and diabetes mellitus (0.7%). These disorders typically emerged within the first six months of ICI therapy. Most cases were managed conservatively or with hormone replacement therapy. Patients who developed endocrine irAEs exhibited a higher objective response rate (ORR) and clinical benefit rate (CBR) compared to those without irAEs. Conclusions: Endocrine dysfunction is a significant toxicity of ICI therapy. Early recognition, prompt diagnosis, and appropriate management are crucial to minimize their impact on patient health and quality of life. This study highlights the potential association between irAEs and improved clinical outcomes. Further research is needed to elucidate the underlying mechanisms and identify predictive biomarkers for irAE development.
dc.description.fulltextYes
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyPubMed
dc.description.indexedbyScopus
dc.description.openaccessGold OA
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.versionPublished Version
dc.identifier.doi10.3390/medicina61010123
dc.identifier.eissn1648-9144
dc.identifier.embargoNo
dc.identifier.filenameinventorynoIR06322
dc.identifier.issn1010-660X
dc.identifier.issue1
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85216877987
dc.identifier.urihttps://doi.org/10.3390/medicina61010123
dc.identifier.urihttps://hdl.handle.net/20.500.14288/29575
dc.identifier.volume61
dc.identifier.wos001404273800001
dc.keywordsImmune checkpoint inhibitors (ICIs)
dc.keywordsImmune-related adverse events (irAEs)
dc.keywordsEndocrine dysfunction
dc.keywordsCancer therapy
dc.language.isoeng
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofMedicina
dc.relation.openaccessYes
dc.rightsCC BY (Attribution)
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectGeneral and internal medicine
dc.titleEndocrine adverse events in patients treated with immune checkpoint inhibitors: a comprehensive analysis
dc.typeJournal Article
dspace.entity.typePublication
person.familyNameKuvvet
person.familyNameSelçukbiricik
person.givenNameFadime Buket Bayram
person.givenNameFatih
relation.isOrgUnitOfPublicationd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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