Chronic kidney disease and denosumab in metastatic bone disease: A multicenter Turkish cohort study on severe hypocalcemia, skeletal events, and survival

dc.contributor.authorEllez, Halil Ibrahim
dc.contributor.authorSemiz, Huseyin Salih
dc.contributor.authorEkinci, Ferhat
dc.contributor.authorErdogan, Atike Pinar
dc.contributor.authorKus, Fatih
dc.contributor.authorKaratas, Fatih
dc.contributor.authorTurhal, Nazim Serdar
dc.date.accessioned2026-08-12T17:27:30Z
dc.date.issued2025
dc.departmentFırat Üniversitesi
dc.description.abstractBackground Denosumab, a monoclonal antibody against receptor activator of nuclear factor kappa-B ligand (RANKL), is widely used to prevent skeletal-related events (SREs) in patients with bone metastases from solid tumours. However, its safety in individuals with advanced chronic kidney disease (CKD), particularly regarding severe hypocalcaemia and skeletal complications, is not well defined. Methods We conducted a retrospective, multicentre study within the Turkish Oncology Group including patients with breast, prostate, or lung cancer who received denosumab between January 2011 and December 2022. Demographic and clinical data, CKD stage, prior fractures, serum calcium levels, episodes of hypocalcaemia, concomitant medications, and adverse events were recorded. Primary endpoints were the incidences of grade >= 3 hypocalcaemia and other grade >= 3 toxicities; secondary endpoints included skeletal-related events and overall survival. Results We analysed 264 patients from 17 oncology centres. Overall, 18 patients (6.8 %) experienced grade >= 3 toxicity, including 16 cases of severe hypocalcaemia and two of renal function decline. Among 42 patients with baseline estimated glomerular filtration rate (eGFR) < 60 mL/min, 13 (31.0 %) developed grade >= 3 toxicity (11 hypocalcaemia, two renal decline), representing a significantly higher risk than in patients with eGFR >= 60 mL/min (p < 0.01). Pathological fractures occurred in 21 patients, six with eGFR < 60 mL/min (p = 0.035). Eight patients required surgery for skeletal-related events, four with eGFR < 60 mL/min (p = 0.012). Conclusion Cancer patients with CKD receiving denosumab have an increased risk of severe hypocalcaemia and skeletal complications. Close monitoring of calcium and renal function is essential, and clinicians should carefully balance the benefits of denosumab against these risks in this vulnerable population.
dc.identifier.doi10.1016/j.jbo.2025.100730
dc.identifier.issn2212-1374
dc.identifier.orcid0000-0001-8713-7613
dc.identifier.orcid0000-0002-9593-0942
dc.identifier.pmid41399765
dc.identifier.scopus2-s2.0-105022917124
dc.identifier.scopusqualityQ2
dc.identifier.urihttps://doi.org/10.1016/j.jbo.2025.100730
dc.identifier.urihttps://hdl.handle.net/11508/55234
dc.identifier.volume55
dc.identifier.wosWOS:001633498800001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofJournal of Bone Oncology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectBone metastases
dc.subjectChronic kidney disease
dc.subjectHypocalcemia
dc.subjectOverall survival
dc.subjectRenal impairment
dc.subjectSkeletal-related events
dc.titleChronic kidney disease and denosumab in metastatic bone disease: A multicenter Turkish cohort study on severe hypocalcemia, skeletal events, and survival
dc.typeArticle

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