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dc.contributor.authorMoreno-Moreno, Paloma-
dc.contributor.authorIbáñez-Costa, Alejandro-
dc.contributor.authorVenegas-Moreno, Eva-
dc.contributor.authorFuentes-Fayos, Antonio C-
dc.contributor.authorAlhambra-Expósito, Maria R.-
dc.contributor.otherDepartamentos de la UMH::Medicina Clínicaes_ES
dc.date.accessioned2026-01-27T11:01:55Z-
dc.date.available2026-01-27T11:01:55Z-
dc.date.created2022-
dc.identifier.citationThe Journal of Clinical Endocrinology & Metabolism, 2022, 107, e2938–e2951es_ES
dc.identifier.issn1945-7197-
dc.identifier.urihttps://hdl.handle.net/11000/39026-
dc.description.abstractContext: Adrenocorticotropin (ACTH)-secreting pituitary tumors (ACTHomas) are associated with severe comorbidities and increased mortality. Current treatments mainly focus on remission and prevention of persistent disease and recurrence. However, there are still no useful biomarkers to accurately predict the clinical outcome after surgery, long-term remission, or disease relapse. Objectives: This work aimed to identify clinical, biochemical, and molecular markers for predicting long-term clinical outcome and remission in ACTHomas. Methods: A retrospective multicenter study was performed with 60 ACTHomas patients diagnosed between 2004 and 2018 with at least 2 years’ follow-up. Clinical/biochemical variables were evaluated yearly. Molecular expression profile of the somatostatin/ghrelin/dopamine regulatory systems components and of key pituitary factors and proliferation markers were evaluated in tumor samples after the first surgery. Results: Clinical variables including tumor size, time until diagnosis/first surgery, serum prolactin, and postsurgery cortisol levels were associated with tumor remission and relapsed disease. The molecular markers analyzed were distinctly expressed in ACTHomas, with some components (ie, SSTR1, CRHR1, and MKI67) showing instructive associations with recurrence and/or remission. Notably, an integrative model including selected clinical variables (tumor size/postsurgery serum cortisol), and molecular markers (SSTR1/CRHR1) can accurately predict the clinical evolution and remission of patients with ACTHomas, generating a receiver operating characteristic curve with an area under the curve of 1 (P < .001). Conclusion: This study demonstrates that the combination of a set of clinical and molecular biomarkers in ACTHomas is able to accurately predict the clinical evolution and remission of patients. Consequently, the postsurgery molecular profile represents a valuable tool for clinical evaluation and follow-up of patients with ACTHomas.es_ES
dc.formatapplication/pdfes_ES
dc.format.extent14es_ES
dc.language.isoenges_ES
dc.publisherOxfordes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectACTH-secreting pituitary tumorses_ES
dc.subjectCushing diseasees_ES
dc.subjectbiochemical variableses_ES
dc.subjectmolecular markerses_ES
dc.subjectpredictive biomarkerses_ES
dc.subject.otherCDU::6 - Ciencias aplicadas::61 - Medicinaes_ES
dc.titleIntegrative Clinical, Radiological, and Molecular Analysis for Predicting Remission and Recurrence of Cushing Diseasees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttps://doi.org/10.1210/clinem/dgac172es_ES
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