Serial evaluation of serum thymidine kinase activity is prognostic in women with newly diagnosed metastatic breast cancer
Autor: | Anna Maria Larsson, Kristina Aaltonen, Sara Jansson, Lisa Rydén, Pär-Ola Bendahl, Carina Forsare, Charlotte Jørgensen, Mattias Bergqvist |
---|---|
Rok vydání: | 2020 |
Předmět: |
Adult
0301 basic medicine Oncology Thymidine kinase activity medicine.medical_specialty Prognostic factor lcsh:Medicine Breast Neoplasms Kaplan-Meier Estimate Newly diagnosed Thymidine Kinase Article Tumour biomarkers 03 medical and health sciences Breast cancer 0302 clinical medicine Internal medicine Antineoplastic Combined Chemotherapy Protocols Biomarkers Tumor Overall survival Humans Medicine Molecular Targeted Therapy Neoplasm Metastasis lcsh:Science skin and connective tissue diseases Thymidine kinase 1 Aged Neoplasm Staging Proportional Hazards Models Aged 80 and over Multidisciplinary business.industry Proportional hazards model lcsh:R Cancer Middle Aged Prognosis medicine.disease Metastatic breast cancer Treatment Outcome 030104 developmental biology 030220 oncology & carcinogenesis Female lcsh:Q business Follow-Up Studies |
Zdroj: | Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020) Scientific Reports |
ISSN: | 2045-2322 |
Popis: | 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 1st 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. |
Databáze: | OpenAIRE |
Externí odkaz: |