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Long-term efficacy and safety of osilodrostat in patients with Cushing's disease: results from the LINC 4 study extension.
Gadelha, Mônica; Snyder, Peter J; Witek, Przemyslaw; Bex, Marie; Belaya, Zhanna; Turcu, Adina F; Feelders, Richard A; Heaney, Anthony P; Paul, Michaela; Pedroncelli, Alberto M; Auchus, Richard J.
Afiliação
  • Gadelha M; Neuroendocrinology Research Center, Endocrinology Section, Medical School and Hospital Universitário Clementino Fraga Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Snyder PJ; Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
  • Witek P; Department of Internal Medicine, Endocrinology and Diabetes, Medical University of Warsaw, Warsaw, Poland.
  • Bex M; Department of Endocrinology, University Hospitals Leuven, Leuven, Belgium.
  • Belaya Z; Department of Neuroendocrinology and Bone Disease, Endocrinology Research Centre, Moscow, Russia.
  • Turcu AF; Division of Metabolism, Endocrinology and Diabetes, University of Michigan, Ann Arbor, MI, United States.
  • Feelders RA; Department of Internal Medicine, Endocrine Section, Erasmus Medical Center, Rotterdam, Netherlands.
  • Heaney AP; Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States.
  • Paul M; Novartis Pharma AG, Basel, Switzerland.
  • Pedroncelli AM; Recordati AG, Basel, Switzerland.
  • Auchus RJ; Division of Metabolism, Endocrinology and Diabetes, University of Michigan, Ann Arbor, MI, United States.
Front Endocrinol (Lausanne) ; 14: 1236465, 2023.
Article em En | MEDLINE | ID: mdl-37680892
Objective: To evaluate the long-term efficacy and safety of osilodrostat in patients with Cushing's disease. Methods: The multicenter, 48-week, Phase III LINC 4 clinical trial had an optional extension period that was initially intended to continue to week 96. Patients could continue in the extension until a managed-access program or alternative treatment became available locally, or until a protocol amendment was approved at their site that specified that patients should come for an end-of-treatment visit within 4 weeks or by week 96, whichever occurred first. Study outcomes assessed in the extension included: mean urinary free cortisol (mUFC) response rates; changes in mUFC, serum cortisol and late-night salivary cortisol (LNSC); changes in cardiovascular and metabolic-related parameters; blood pressure, waist circumference and weight; changes in physical manifestations of Cushing's disease; changes in patient-reported outcomes for health-related quality of life; changes in tumor volume; and adverse events. Results were analyzed descriptively; no formal statistical testing was performed. Results: Of 60 patients who entered, 53 completed the extension, with 29 patients receiving osilodrostat for more than 96 weeks (median osilodrostat duration: 87.1 weeks). The proportion of patients with normalized mUFC observed in the core period was maintained throughout the extension. At their end-of-trial visit, 72.4% of patients had achieved normal mUFC. Substantial reductions in serum cortisol and LNSC were also observed. Improvements in most cardiovascular and metabolic-related parameters, as well as physical manifestations of Cushing's disease, observed in the core period were maintained or continued to improve in the extension. Osilodrostat was generally well tolerated; the safety profile was consistent with previous reports. Conclusion: Osilodrostat provided long-term control of cortisol secretion that was associated with sustained improvements in clinical signs and physical manifestations of hypercortisolism. Osilodrostat is an effective long-term treatment for patients with Cushing's disease. Clinical trial registration: ClinicalTrials.gov, identifier NCT02180217.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperfunção Adrenocortical / Hipersecreção Hipofisária de ACTH Tipo de estudo: Clinical_trials / Guideline Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperfunção Adrenocortical / Hipersecreção Hipofisária de ACTH Tipo de estudo: Clinical_trials / Guideline Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article