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dc.contributor.authorFernández Velasco, Pablo
dc.contributor.authorPeciña Melgosa, Paula
dc.contributor.authorTorres Torres, Beatriz 
dc.contributor.authorTorres Morientes, Luis Miguel
dc.contributor.authorFernández Rodríguez, Ana
dc.contributor.authorAlonso Mesonero, Marta
dc.contributor.authorUribe Viloria, Marta de
dc.contributor.authorÁlvarez Quiñones, María
dc.contributor.authorSantos Pérez, Jaime 
dc.contributor.authorLuis Ramón, Daniel de
dc.contributor.authorDíaz Soto, Gonzalo 
dc.date.accessioned2026-02-23T07:23:39Z
dc.date.available2026-02-23T07:23:39Z
dc.date.issued2026
dc.identifier.citationEndocrine, 2026, vol. 91 (Version of record)es
dc.identifier.issn1559-0100es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/82986
dc.descriptionProducción Científicaes
dc.description.abstractPurpuse. To compare dynamic risk stratification (DRS) according to the 2015 American Thyroid Association-Momesso et al. 2016 extension (ATA2015-M) and the 2025 ATA update in low-risk differentiated thyroid cancer (DTC) managed without radioactive iodine (I-131), and to explore the role of an intermediate thyroglobulin (Tg) cutoff of 1 ng/mL. Methods. We conducted a retrospective analysis of a prospectively collected cohort of 74 low-risk DTC patients treated with total thyroidectomy (n = 55) or hemithyroidectomy (n = 19) between 2020 and 2024. Clinical, histopathological, and biochemical data were collected. DRS was assessed at the first follow-up visit (6 months after surgery) and at the last visit (median follow-up 27 months [IQR 16–41]) using ATA2015-M and ATA2025 criteria. An exploratory analysis applying a Tg cutoff of 1 ng/mL was performed. Results. According to ATA2015-M, excellent response (ER) rates in total thyroidectomy patients increased from 49.2% at baseline to 52.8% at final follow-up. In contrast, ATA2025 classified 89.1% as ER at baseline and 98.2% at final follow-up (p < 0.001). Using the intermediate cutoff of 1 ng/mL, ER rates were 80.0% and 89.1%, respectively. Reclassification to ER under ATA2025 was primarily driven by anti-thyroglobulin antibody (TgAb) negativization, as Tg values remained stable and below the new 2.5 ng/mL threshold. No structural incomplete responses were observed. Conclusion. ATA2025 criteria substantially increase ER classification in low-risk DTC patients managed without I-131 compared with ATA2015-M. A 1 ng/mL Tg cutoff may provide a more realistic representation of clinical practice. The dynamic trend of TgAb, rather than their presence alone, is a key determinant for reclassification during follow-up.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherSpringer Naturees
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectEndocrinologíaes
dc.subjectOncologíaes
dc.subjectPatologíaes
dc.subject.classificationCarcinoma diferenciado de tiroideses
dc.subject.classificationEstratificación dinámica del riesgoes
dc.subject.classificationDirectrices de la ATAes
dc.subject.classificationTiroglobulinaes
dc.subject.classificationAnticuerpos antitiroglobulinaes
dc.subject.classificationCáncer de tiroides de bajo riesgoes
dc.titleComparative evaluation of dynamic risk stratification according to ATA 2015 and ATA 2025 in low-risk differentiated thyroid cancer without radioiodine ablationes
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2026 The Author(s)es
dc.identifier.doi10.1007/s12020-025-04548-6es
dc.relation.publisherversionhttps://link.springer.com/article/10.1007/s12020-025-04548-6es
dc.identifier.publicationissue1es
dc.identifier.publicationtitleEndocrinees
dc.identifier.publicationvolume91es
dc.peerreviewedSIes
dc.description.projectOpen access funding provided by FEDER European Funds and the Junta de Castilla y León under the Research and Innovation Strategy for Smart Specialization (RIS3) of Castilla y León 2021- 2027.es
dc.identifier.essn1559-0100es
dc.rightsAtribución 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones
dc.subject.unesco3205.02 Endocrinologíaes
dc.subject.unesco3207.13 Oncologíaes


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