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A Multicenter Study by the DENO Research Group on the Use of Denosumab in Giant-Cell Tumors of the Bone

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dc.contributor.author de-la-Calva-Ceinos, Carolina
dc.contributor.author Angulo, Manuel
dc.contributor.author González-Rojo, Paula
dc.contributor.author Peiró, Ana
dc.contributor.author Machado, Pau
dc.contributor.author Cebrian, Juan-Luis
dc.contributor.author García-Maroto, Roberto
dc.contributor.author Valcárcel, Antonio
dc.contributor.author Puertas, Pablo
dc.contributor.author Valero-Cifuentes, Gregorio
dc.contributor.author Pablos, Oscar
dc.contributor.author Maireles, Miriam
dc.contributor.author Fontalva, María-Luisa
dc.contributor.author Chaves, Iván
dc.contributor.author Orce, Aida
dc.contributor.author Coll-Mesa, Luis
dc.contributor.author Pérez, Israel
dc.contributor.author González, Fausto
dc.contributor.author Sanz, María-del-Carmen
dc.contributor.author Gracia, Isidro
dc.date.accessioned 2026-03-09T08:39:15Z
dc.date.available 2026-03-09T08:39:15Z
dc.date.issued 2025-05-07
dc.identifier.citation DENO Research Group, Calva CDL, Angulo M, González-Rojo P, Peiró A, Machado P, et al. A Multicenter Study by the DENO Research Group on the Use of Denosumab in Giant-Cell Tumors of the Bone. JCM. 7 de mayo de 2025;14(9):3242. doi:10.3390/jcm14093242
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/25085
dc.description.abstract Background/Objectives: Despite the therapeutic potential of denosumab for the treatment of giant-cell tumors of the bone (GCTBs), there is a lack of standardization in treatment protocols. Methods: We present a multicenter, retrospective, descriptive study conducted across the seven hospitals in Spain affiliated with the DENO Research Group. Seventy-three patients diagnosed with GCTB and treated with denosumab were included and stratified according to treatment strategy-neoadjuvant (n = 38), adjuvant (n = 8), and single treatment (n = 27). Results: Patients in the neoadjuvant group received denosumab for a median of 6.1 months, with reintroduction after surgery in 25.8% of all cases. Among the neoadjuvant patients treated with curettage, recurrence was 35.5%, with no association with denosumab treatment duration (p = 0.274) nor with denosumab reintroduction after surgery (p = 0.405). In the adjuvant group, those who completed treatment received denosumab for 15.3 months, while those still undergoing therapy received it for a median of 12.8 months; only one case (12.5%) recurred. Recurrence rates in neoadjuvant and adjuvant treatment strategies were not different (p = 0.394). Patients treated only with denosumab and no longer on treatment had received it for 34.2 months, with 31.3% recurrence; those still on treatment had received it for 51.8 months, with 25.0% recurrence. Across all strategies, more than 85% of patients reported favorable clinical outcomes, and only 43.8% presented adverse events. No deaths occurred during this study. Conclusions: Although patients who experienced recurrence during neoadjuvant treatment had longer durations of denosumab administration, the difference was not statistically significant. Similarly, recurrence rates did not differ significantly, whether denosumab was reintroduced after surgery or not. Among the patients treated with curettage, recurrence rates were comparable between neoadjuvant and adjuvant strategies. Discontinuation of the single treatment did not necessarily result in disease progression.
dc.language.iso eng
dc.publisher MDPI
dc.rights Atribución/Reconocimiento 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by/4.0/deed.es
dc.title A Multicenter Study by the DENO Research Group on the Use of Denosumab in Giant-Cell Tumors of the Bone
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 40364272
dc.relation.publisherversion https://www.mdpi.com/2077-0383/14/9/3242
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.3390/jcm14093242
dc.journal.title Journal of Clinical Medicine
dc.identifier.essn 2077-0383


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