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Patterns of thyroid hormone levels in pediatric medullary thyroid carcinoma patients on vandetanib therapy
BACKGROUND: Tyrosine kinase inhibitors (TKIs) have been associated with elevated TSH as a drug class effect. Prior studies of vandetanib in adults with medullary thyroid carcinoma (MTC) described an increase in levothyroxine (LT) requirement. We studied TSH, free T4, and LT dosing in children and ad...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429462/ https://www.ncbi.nlm.nih.gov/pubmed/25972901 http://dx.doi.org/10.1186/1687-9856-2015-3 |
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author | Lodish, Maya Gkourogianni, Alexandra Bornstein, Ethan Sinaii, Ninet Fox, Elizabeth Chuk, Meredith Marcus, Leigh Akshintala, Srivandana Balis, Frank Widemann, Brigitte Stratakis, Constantine A |
author_facet | Lodish, Maya Gkourogianni, Alexandra Bornstein, Ethan Sinaii, Ninet Fox, Elizabeth Chuk, Meredith Marcus, Leigh Akshintala, Srivandana Balis, Frank Widemann, Brigitte Stratakis, Constantine A |
author_sort | Lodish, Maya |
collection | PubMed |
description | BACKGROUND: Tyrosine kinase inhibitors (TKIs) have been associated with elevated TSH as a drug class effect. Prior studies of vandetanib in adults with medullary thyroid carcinoma (MTC) described an increase in levothyroxine (LT) requirement. We studied TSH, free T4, and LT dosing in children and adolescents enrolled in the phase I/II trial of vandetanib for medullary thyroid cancer (MTC) METHODS: Data from 13 patients with multiple endocrine neoplasia type 2B (MEN 2B) and MTC were analyzed [6 M, 7 F, median age 13.0 y (9.1-17.3)] Eleven patients (85%) had undergone prior thyroidectomy and all received single-drug therapy with vandetanib for > 6 months. Confirmed compliance with vandetanib (67–150 mg/m(2)/day) and LT was a necessary inclusion criterion. RESULTS: While on vandetanib treatment, all 11 athyerotic patients exhibited significantly increased TSH levels. The baseline TSH level was 4.37 mclU/ml (0.08 - 23.30); in comparison, the first peak TSH concentration on vandetanib was 15.70 mclU/ml (12.50 - 137.00, p = 0.0010). The median time to reach the initial peak of elevated TSH was 1.8 months (0.3 - 9.3). Free T4 levels remained within the normal reference range. An increase from a baseline LT dose of 91 mcg/m(2)/day (±24) to 116 mcg/m(2)/day (±24) was required in order to resume normative TSH levels (p = 0.00005), equal to an increase of 36.6% (±16.56) in the dosage of LT in mcg/day. For the 2 patients with intact thyroid glands, free T4 and TSH remained normal over a combined 6 patient years of follow up. CONCLUSIONS: In our cohort of pediatric MTC patients, athyreotic patients with preexisting hypothyroidism developed increased TSH and reduced free T4 during the first few months of treatment with vandetanib, necessitating an increase in LT dosage. Additional patients with normal thyroid function before treatment and intact glands (n = 2) maintained normal thyroid function tests during treatment. Elevated TSH in athyreotic patients may be due to an indirect effect of vandetanib on the metabolism of thyroid hormone, or to altered TSH sensitivity at the pituitary. Proper recognition and management of abnormal thyroid hormone levels is critical in growing children on TKIs. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT00514046 |
format | Online Article Text |
id | pubmed-4429462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44294622015-05-14 Patterns of thyroid hormone levels in pediatric medullary thyroid carcinoma patients on vandetanib therapy Lodish, Maya Gkourogianni, Alexandra Bornstein, Ethan Sinaii, Ninet Fox, Elizabeth Chuk, Meredith Marcus, Leigh Akshintala, Srivandana Balis, Frank Widemann, Brigitte Stratakis, Constantine A Int J Pediatr Endocrinol Research BACKGROUND: Tyrosine kinase inhibitors (TKIs) have been associated with elevated TSH as a drug class effect. Prior studies of vandetanib in adults with medullary thyroid carcinoma (MTC) described an increase in levothyroxine (LT) requirement. We studied TSH, free T4, and LT dosing in children and adolescents enrolled in the phase I/II trial of vandetanib for medullary thyroid cancer (MTC) METHODS: Data from 13 patients with multiple endocrine neoplasia type 2B (MEN 2B) and MTC were analyzed [6 M, 7 F, median age 13.0 y (9.1-17.3)] Eleven patients (85%) had undergone prior thyroidectomy and all received single-drug therapy with vandetanib for > 6 months. Confirmed compliance with vandetanib (67–150 mg/m(2)/day) and LT was a necessary inclusion criterion. RESULTS: While on vandetanib treatment, all 11 athyerotic patients exhibited significantly increased TSH levels. The baseline TSH level was 4.37 mclU/ml (0.08 - 23.30); in comparison, the first peak TSH concentration on vandetanib was 15.70 mclU/ml (12.50 - 137.00, p = 0.0010). The median time to reach the initial peak of elevated TSH was 1.8 months (0.3 - 9.3). Free T4 levels remained within the normal reference range. An increase from a baseline LT dose of 91 mcg/m(2)/day (±24) to 116 mcg/m(2)/day (±24) was required in order to resume normative TSH levels (p = 0.00005), equal to an increase of 36.6% (±16.56) in the dosage of LT in mcg/day. For the 2 patients with intact thyroid glands, free T4 and TSH remained normal over a combined 6 patient years of follow up. CONCLUSIONS: In our cohort of pediatric MTC patients, athyreotic patients with preexisting hypothyroidism developed increased TSH and reduced free T4 during the first few months of treatment with vandetanib, necessitating an increase in LT dosage. Additional patients with normal thyroid function before treatment and intact glands (n = 2) maintained normal thyroid function tests during treatment. Elevated TSH in athyreotic patients may be due to an indirect effect of vandetanib on the metabolism of thyroid hormone, or to altered TSH sensitivity at the pituitary. Proper recognition and management of abnormal thyroid hormone levels is critical in growing children on TKIs. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT00514046 BioMed Central 2015-02-16 2015 /pmc/articles/PMC4429462/ /pubmed/25972901 http://dx.doi.org/10.1186/1687-9856-2015-3 Text en © Lodish et al.; licensee BioMed Central. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Lodish, Maya Gkourogianni, Alexandra Bornstein, Ethan Sinaii, Ninet Fox, Elizabeth Chuk, Meredith Marcus, Leigh Akshintala, Srivandana Balis, Frank Widemann, Brigitte Stratakis, Constantine A Patterns of thyroid hormone levels in pediatric medullary thyroid carcinoma patients on vandetanib therapy |
title | Patterns of thyroid hormone levels in pediatric medullary thyroid carcinoma patients on vandetanib therapy |
title_full | Patterns of thyroid hormone levels in pediatric medullary thyroid carcinoma patients on vandetanib therapy |
title_fullStr | Patterns of thyroid hormone levels in pediatric medullary thyroid carcinoma patients on vandetanib therapy |
title_full_unstemmed | Patterns of thyroid hormone levels in pediatric medullary thyroid carcinoma patients on vandetanib therapy |
title_short | Patterns of thyroid hormone levels in pediatric medullary thyroid carcinoma patients on vandetanib therapy |
title_sort | patterns of thyroid hormone levels in pediatric medullary thyroid carcinoma patients on vandetanib therapy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429462/ https://www.ncbi.nlm.nih.gov/pubmed/25972901 http://dx.doi.org/10.1186/1687-9856-2015-3 |
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