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Ιmpact of sunitinib-induced hypothyroidism on survival of patients with metastatic renal cancer

BACKGROUND: Sunitinib plays an important role in managing the metastatic renal cell cancer (mRCC). Sunitinib-induced hypothyroidism is a common side-effect of the drug. There have been attempts to link hypothyroidism with a better clinical outcome in sunitinib-treated (mRCC) patients. Our aim was to...

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Autores principales: Vasileiadis, Theofanis, Chrisofos, Michail, Safioleas, Michail, Kontzoglou, Konstantinos, Papazisis, Konstantinos, Sdrolia, Athina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492389/
https://www.ncbi.nlm.nih.gov/pubmed/31039771
http://dx.doi.org/10.1186/s12885-019-5610-8
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author Vasileiadis, Theofanis
Chrisofos, Michail
Safioleas, Michail
Kontzoglou, Konstantinos
Papazisis, Konstantinos
Sdrolia, Athina
author_facet Vasileiadis, Theofanis
Chrisofos, Michail
Safioleas, Michail
Kontzoglou, Konstantinos
Papazisis, Konstantinos
Sdrolia, Athina
author_sort Vasileiadis, Theofanis
collection PubMed
description BACKGROUND: Sunitinib plays an important role in managing the metastatic renal cell cancer (mRCC). Sunitinib-induced hypothyroidism is a common side-effect of the drug. There have been attempts to link hypothyroidism with a better clinical outcome in sunitinib-treated (mRCC) patients. Our aim was to relate the impact of hypothyroidism to the survival of these patients. METHODS: We have evaluated 70 patients with mRCC that received sunitinib as a first line treatment. Thyroid-stimulating hormone (TSH) was measured at baseline, after 15 days of treatment (day-15) and at the end of the second cycle (day-75). Biomarker data and correlations with response were analysed with Microsoft Excel. Comparison results from Student’s t-test with a p less than 0.05 were considered statistically significant. Kaplan-Meyer and log-rank tests were performed using GraphPad Prism 5 for Windows. RESULTS: Regarding the response to treatment, a progression-free survival (PFS) of 9.47 months and an overall survival (OS) of 22.03 months were demonstrated. Our data are consistent with published data by other authors. On day-15 from the beginning of the treatment an important number of patients exhibited a TSH elevation. On day-15 42.86% had a TSH over the upper normal limit and 50.0% at the end of the second cycle (day-75). TSH increased earlier in patients that exhibited an objective response (× 3.33 times the baseline values on day-15) than patients that exhibited disease stabilisation (× 2.18) or disease progression (× 1.59). Early increases in TSH were associated with a longer PFS (11.92 vs. 8.82 months, p = 0.0476) and a longer OS (3.10 vs. 1.08 years, p = 0.0011). CONCLUSIONS: Early TSH-increase is associated with a clinical benefit. The patients that showed at least a twofold increase of their baseline TSH, responded to therapy by stabilisation or by regression of disease. This is the only study to our knowledge which shows that early increases - 2 weeks from starting the treatment - in TSH levels have a prognostic value. Both PFS and OS of the patients who demonstrated a higher than a twofold rise were significantly longer than the PFS and the OS of the patients that presented a lower or no TSH-increase.
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spelling pubmed-64923892019-05-08 Ιmpact of sunitinib-induced hypothyroidism on survival of patients with metastatic renal cancer Vasileiadis, Theofanis Chrisofos, Michail Safioleas, Michail Kontzoglou, Konstantinos Papazisis, Konstantinos Sdrolia, Athina BMC Cancer Research Article BACKGROUND: Sunitinib plays an important role in managing the metastatic renal cell cancer (mRCC). Sunitinib-induced hypothyroidism is a common side-effect of the drug. There have been attempts to link hypothyroidism with a better clinical outcome in sunitinib-treated (mRCC) patients. Our aim was to relate the impact of hypothyroidism to the survival of these patients. METHODS: We have evaluated 70 patients with mRCC that received sunitinib as a first line treatment. Thyroid-stimulating hormone (TSH) was measured at baseline, after 15 days of treatment (day-15) and at the end of the second cycle (day-75). Biomarker data and correlations with response were analysed with Microsoft Excel. Comparison results from Student’s t-test with a p less than 0.05 were considered statistically significant. Kaplan-Meyer and log-rank tests were performed using GraphPad Prism 5 for Windows. RESULTS: Regarding the response to treatment, a progression-free survival (PFS) of 9.47 months and an overall survival (OS) of 22.03 months were demonstrated. Our data are consistent with published data by other authors. On day-15 from the beginning of the treatment an important number of patients exhibited a TSH elevation. On day-15 42.86% had a TSH over the upper normal limit and 50.0% at the end of the second cycle (day-75). TSH increased earlier in patients that exhibited an objective response (× 3.33 times the baseline values on day-15) than patients that exhibited disease stabilisation (× 2.18) or disease progression (× 1.59). Early increases in TSH were associated with a longer PFS (11.92 vs. 8.82 months, p = 0.0476) and a longer OS (3.10 vs. 1.08 years, p = 0.0011). CONCLUSIONS: Early TSH-increase is associated with a clinical benefit. The patients that showed at least a twofold increase of their baseline TSH, responded to therapy by stabilisation or by regression of disease. This is the only study to our knowledge which shows that early increases - 2 weeks from starting the treatment - in TSH levels have a prognostic value. Both PFS and OS of the patients who demonstrated a higher than a twofold rise were significantly longer than the PFS and the OS of the patients that presented a lower or no TSH-increase. BioMed Central 2019-04-30 /pmc/articles/PMC6492389/ /pubmed/31039771 http://dx.doi.org/10.1186/s12885-019-5610-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Article
Vasileiadis, Theofanis
Chrisofos, Michail
Safioleas, Michail
Kontzoglou, Konstantinos
Papazisis, Konstantinos
Sdrolia, Athina
Ιmpact of sunitinib-induced hypothyroidism on survival of patients with metastatic renal cancer
title Ιmpact of sunitinib-induced hypothyroidism on survival of patients with metastatic renal cancer
title_full Ιmpact of sunitinib-induced hypothyroidism on survival of patients with metastatic renal cancer
title_fullStr Ιmpact of sunitinib-induced hypothyroidism on survival of patients with metastatic renal cancer
title_full_unstemmed Ιmpact of sunitinib-induced hypothyroidism on survival of patients with metastatic renal cancer
title_short Ιmpact of sunitinib-induced hypothyroidism on survival of patients with metastatic renal cancer
title_sort ιmpact of sunitinib-induced hypothyroidism on survival of patients with metastatic renal cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492389/
https://www.ncbi.nlm.nih.gov/pubmed/31039771
http://dx.doi.org/10.1186/s12885-019-5610-8
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