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Successful Treatment with Selpercatinib for Ectopic Cushing's Syndrome Due to Medullary Thyroid Cancer.

Authors :
Ragnarsson, Oskar
Piasecka, Marta
Hallqvist, Andreas
Source :
Current Oncology; May2022, Vol. 29 Issue 5, p3494-N.PAG3498, 5p, 1 Black and White Photograph, 1 Diagram
Publication Year :
2022

Abstract

Selpercatinib, a RET kinase inhibitor, is an effective treatment for patients with medullary thyroid cancer with RET mutations. In this paper, we present the case of a 62-year-old man with ectopic Cushing's syndrome due to medullary thyroid cancer who received treatment with selpercatinib. Six months later, all the cushingoid features had resolved, and s-calcitonin had decreased from 580 pmol/L to 3.5 pmol/L (normal < 3). After further 6 months, s-calcitonin had normalized (1.5 pmol/L), and radiological evaluation showed a profound tumour volume reduction. We are aware of two other cases where treatment with selpercatinib has also been successful. Thus, selpercatinib may be a promising treatment alternative in patients with ectopic Cushing's syndrome due to medullary thyroid cancer, especially when other treatment options are ineffective or not tolerated. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
11980052
Volume :
29
Issue :
5
Database :
Complementary Index
Journal :
Current Oncology
Publication Type :
Academic Journal
Accession number :
157188029
Full Text :
https://doi.org/10.3390/curroncol29050282