Literature DB >> 24499195

Complete resolution of hypercortisolism with sorafenib in a patient with advanced medullary thyroid carcinoma and ectopic ACTH (adrenocorticotropic hormone) syndrome.

Romualdo Barroso-Sousa1, Antonio Marcondes Lerario, Joao Evangelista, Carla Papadia, Delmar M Lourenço, Chin Shien Lin, Marco Antonio Kulcsar, Maria Candida Fragoso, Ana O Hoff.   

Abstract

BACKGROUND: The treatment of advanced medullary thyroid carcinoma (MTC) has evolved significantly over the past decade. The discovery of genetic abnormalities in MTC has led to the development of targeted therapies such as vandetanib and cabozantinib. Other kinase inhibitors (KI), such as sorafenib, have been investigated in this setting and are an alternative therapeutic option. The lack of specificity of these KIs to a single target may result in additional, unexpected effects. In this report, we describe a patient with metastatic MTC and Ectopic ACTH (adrenocorticotropic hormone) Syndrome in whom treatment with sorafenib resulted in complete resolution of hypercortisolism.
SUMMARY: A 45-year-old male with progressive metastatic MTC presented with clinical manifestations suspicious for Cushing's syndrome. Investigation revealed ACTH-dependent hypercortisolism suggestive of Ectopic ACTH Syndrome. Treatment with sorafenib 400 mg twice a day was initiated resulting in a rapid and significant reduction of cortisol and ACTH levels associated with dramatic clinical improvement. The rapid and effective control of hypercortisolism in the absence of a significant tumor reduction raises the question of whether sorafenib may have a direct effect on ACTH or cortisol hypersecretion.
CONCLUSIONS: This report suggests a previously unknown potential effect of sorafenib on the pituitary-adrenal axis. Further studies will be necessary to investigate the role of sorafenib in other cases of ACTH excess and to understand the mechanisms by which it alters steroid synthesis, action, or secretion.

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Year:  2014        PMID: 24499195     DOI: 10.1089/thy.2013.0571

Source DB:  PubMed          Journal:  Thyroid        ISSN: 1050-7256            Impact factor:   6.568


  7 in total

1.  Ectopic cushing in a patient with medullary thyroid carcinoma: hypercortisolism control and tumor reduction with Sunitinib.

Authors:  Pedro Marques; Margarida da Silva Vieira; Maria João Bugalho
Journal:  Endocrine       Date:  2014-07-15       Impact factor: 3.633

2.  Rapid and long-lasting response to selpercatinib of paraneoplastic Cushing's syndrome in medullary thyroid carcinoma.

Authors:  Marine Sitbon; Porhuoy Chou; Seydou Bengaly; Brigitte Poirot; Marie Laloi-Michelin; Laure Deville; Atanas Pachev; Ahouefa Kowo-Bille; Clement Dumont; Cécile N Chougnet
Journal:  Eur Thyroid J       Date:  2022-09-28

3.  Treatment of Cushing's Syndrome: An Endocrine Society Clinical Practice Guideline.

Authors:  Lynnette K Nieman; Beverly M K Biller; James W Findling; M Hassan Murad; John Newell-Price; Martin O Savage; Antoine Tabarin
Journal:  J Clin Endocrinol Metab       Date:  2015-07-29       Impact factor: 5.958

Review 4.  Aggressive pituitary adenomas--diagnosis and emerging treatments.

Authors:  Antonio Di Ieva; Fabio Rotondo; Luis V Syro; Michael D Cusimano; Kalman Kovacs
Journal:  Nat Rev Endocrinol       Date:  2014-05-13       Impact factor: 43.330

5.  Case report of severe Cushing's syndrome in medullary thyroid cancer complicated by functional diabetes insipidus, aortic dissection, jejunal intussusception, and paraneoplastic dysautonomia: remission with sorafenib without reduction in cortisol concentration.

Authors:  Muhammad M Hammami; Najla Duaiji; Ghazi Mutairi; Sabah Aklabi; Nasser Qattan; Mohei El-Din M Abouzied; Mohamed W Sous
Journal:  BMC Cancer       Date:  2015-09-09       Impact factor: 4.430

Review 6.  Targeted Therapy for Medullary Thyroid Cancer: A Review.

Authors:  S R Priya; Chandra Shekhar Dravid; Raghunadharao Digumarti; Mitali Dandekar
Journal:  Front Oncol       Date:  2017-10-06       Impact factor: 6.244

7.  Sporadic Medullary Thyroid Carcinoma with Paraneoplastic Cushing Syndrome.

Authors:  Aleksandra I Pivovarova; Stephanie Patrick; Punuru J Reddy
Journal:  Case Rep Endocrinol       Date:  2019-12-08
  7 in total

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