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Serial evaluation of serum thymidine kinase activity is prognostic in women with newly diagnosed metastatic breast cancer

The rapid development of new therapies in metastatic breast cancer (MBC), entails a need for improved prognostic and monitoring tools. Thymidine kinase 1 (TK1) is involved in DNA synthesis and its activity correlates to outcome in cancer patients. The aim of this study was to evaluate serum TK1 acti...

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Autores principales: Larsson, Anna-Maria, Bendahl, Pär-Ola, Aaltonen, Kristina, Jansson, Sara, Forsare, Carina, Bergqvist, Mattias, Jørgensen, Charlotte Levin Tykjær, Rydén, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066186/
https://www.ncbi.nlm.nih.gov/pubmed/32161278
http://dx.doi.org/10.1038/s41598-020-61416-1
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author Larsson, Anna-Maria
Bendahl, Pär-Ola
Aaltonen, Kristina
Jansson, Sara
Forsare, Carina
Bergqvist, Mattias
Jørgensen, Charlotte Levin Tykjær
Rydén, Lisa
author_facet Larsson, Anna-Maria
Bendahl, Pär-Ola
Aaltonen, Kristina
Jansson, Sara
Forsare, Carina
Bergqvist, Mattias
Jørgensen, Charlotte Levin Tykjær
Rydén, Lisa
author_sort Larsson, Anna-Maria
collection PubMed
description The rapid development of new therapies in metastatic breast cancer (MBC), entails a need for improved prognostic and monitoring tools. Thymidine kinase 1 (TK1) is involved in DNA synthesis and its activity correlates to outcome in cancer patients. The aim of this study was to evaluate serum TK1 activity (sTK1) levels in MBC patients as a tool for prognostication and treatment monitoring. 142 women with MBC scheduled for 1(st) line systemic treatment were included in a prospective observational study. sTK1 was measured at baseline (BL) and at 1, 3 and 6 months and correlations to progression-free and overall survival (PFS, OS) evaluated. High sTK1 levels (above median) correlated to worse PFS and OS at BL, also after adjusting for other prognostic factors. sTK1 levels were significantly associated with PFS and OS measured from follow-up time points during therapy. Changes from 3 to 6 months during therapy significantly correlated to PFS and OS, whereas early changes did not. We could demonstrate sTK1 level as an independent prognostic factor in patients with newly diagnosed MBC. Changes in sTK1 levels from 3 to 6 months correlated to PFS and OS. Future studies of sTK1 are warranted to further define its clinical utility.
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spelling pubmed-70661862020-03-19 Serial evaluation of serum thymidine kinase activity is prognostic in women with newly diagnosed metastatic breast cancer Larsson, Anna-Maria Bendahl, Pär-Ola Aaltonen, Kristina Jansson, Sara Forsare, Carina Bergqvist, Mattias Jørgensen, Charlotte Levin Tykjær Rydén, Lisa Sci Rep Article The rapid development of new therapies in metastatic breast cancer (MBC), entails a need for improved prognostic and monitoring tools. Thymidine kinase 1 (TK1) is involved in DNA synthesis and its activity correlates to outcome in cancer patients. The aim of this study was to evaluate serum TK1 activity (sTK1) levels in MBC patients as a tool for prognostication and treatment monitoring. 142 women with MBC scheduled for 1(st) line systemic treatment were included in a prospective observational study. sTK1 was measured at baseline (BL) and at 1, 3 and 6 months and correlations to progression-free and overall survival (PFS, OS) evaluated. High sTK1 levels (above median) correlated to worse PFS and OS at BL, also after adjusting for other prognostic factors. sTK1 levels were significantly associated with PFS and OS measured from follow-up time points during therapy. Changes from 3 to 6 months during therapy significantly correlated to PFS and OS, whereas early changes did not. We could demonstrate sTK1 level as an independent prognostic factor in patients with newly diagnosed MBC. Changes in sTK1 levels from 3 to 6 months correlated to PFS and OS. Future studies of sTK1 are warranted to further define its clinical utility. Nature Publishing Group UK 2020-03-11 /pmc/articles/PMC7066186/ /pubmed/32161278 http://dx.doi.org/10.1038/s41598-020-61416-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Larsson, Anna-Maria
Bendahl, Pär-Ola
Aaltonen, Kristina
Jansson, Sara
Forsare, Carina
Bergqvist, Mattias
Jørgensen, Charlotte Levin Tykjær
Rydén, Lisa
Serial evaluation of serum thymidine kinase activity is prognostic in women with newly diagnosed metastatic breast cancer
title Serial evaluation of serum thymidine kinase activity is prognostic in women with newly diagnosed metastatic breast cancer
title_full Serial evaluation of serum thymidine kinase activity is prognostic in women with newly diagnosed metastatic breast cancer
title_fullStr Serial evaluation of serum thymidine kinase activity is prognostic in women with newly diagnosed metastatic breast cancer
title_full_unstemmed Serial evaluation of serum thymidine kinase activity is prognostic in women with newly diagnosed metastatic breast cancer
title_short Serial evaluation of serum thymidine kinase activity is prognostic in women with newly diagnosed metastatic breast cancer
title_sort serial evaluation of serum thymidine kinase activity is prognostic in women with newly diagnosed metastatic breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066186/
https://www.ncbi.nlm.nih.gov/pubmed/32161278
http://dx.doi.org/10.1038/s41598-020-61416-1
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