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Metformin Use and the Outcome of Metastatic Renal Cell Carcinoma Treated with Sunitinib or Pazopanib

BACKGROUND: The anticancer properties of metformin have been suggested in numerous experimental studies and several retrospective clinical studies show that its use is associated with improved outcome of patients with cancer. However, limited data are available for patients with metastatic renal cel...

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Autores principales: Fiala, Ondřej, Ostašov, Pavel, Rozsypalová, Aneta, Hora, Milan, Šorejs, Ondřej, Šustr, Jan, Bendová, Barbora, Trávníček, Ivan, Filipovský, Jan, Fínek, Jindřich, Büchler, Tomáš
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153069/
https://www.ncbi.nlm.nih.gov/pubmed/34054309
http://dx.doi.org/10.2147/CMAR.S305321
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author Fiala, Ondřej
Ostašov, Pavel
Rozsypalová, Aneta
Hora, Milan
Šorejs, Ondřej
Šustr, Jan
Bendová, Barbora
Trávníček, Ivan
Filipovský, Jan
Fínek, Jindřich
Büchler, Tomáš
author_facet Fiala, Ondřej
Ostašov, Pavel
Rozsypalová, Aneta
Hora, Milan
Šorejs, Ondřej
Šustr, Jan
Bendová, Barbora
Trávníček, Ivan
Filipovský, Jan
Fínek, Jindřich
Büchler, Tomáš
author_sort Fiala, Ondřej
collection PubMed
description BACKGROUND: The anticancer properties of metformin have been suggested in numerous experimental studies and several retrospective clinical studies show that its use is associated with improved outcome of patients with cancer. However, limited data are available for patients with metastatic renal cell carcinoma (mRCC) treated with targeted therapy. The aim of this retrospective study was to assess the impact of the metformin use on survival of mRCC patients treated with sunitinib or pazopanib. METHODS: Clinical data from 343 patients with mRCC treated with sunitinib or pazopanib in the first line were analyzed. Progression-free survival (PFS) and overall survival (OS) were compared according to the use of metformin. RESULTS: The median PFS and OS for patients using metformin was 31.1 (95% CI 20.6–35.1) and 51.6 (95% CI 44.7-NR) months compared to 9.3 (95% CI 8.0–12.0) and 22.4 (95% CI 19.4–26.8) months for patients not using metformin (p<0.0001 and p=0.0002, respectively). Cox multivariate analysis shows that the use of metformin remains a significant factor for PFS (HR=0.55 [95% CI 0.343–0.883], p=0.013) and also for OS (HR=0.45 [95% CI 0.256–0.794], p=0.006). CONCLUSION: The present study results suggest that the use of metformin was associated with favorable outcome of mRCC patients treated with sunitinib or pazopanib.
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spelling pubmed-81530692021-05-27 Metformin Use and the Outcome of Metastatic Renal Cell Carcinoma Treated with Sunitinib or Pazopanib Fiala, Ondřej Ostašov, Pavel Rozsypalová, Aneta Hora, Milan Šorejs, Ondřej Šustr, Jan Bendová, Barbora Trávníček, Ivan Filipovský, Jan Fínek, Jindřich Büchler, Tomáš Cancer Manag Res Original Research BACKGROUND: The anticancer properties of metformin have been suggested in numerous experimental studies and several retrospective clinical studies show that its use is associated with improved outcome of patients with cancer. However, limited data are available for patients with metastatic renal cell carcinoma (mRCC) treated with targeted therapy. The aim of this retrospective study was to assess the impact of the metformin use on survival of mRCC patients treated with sunitinib or pazopanib. METHODS: Clinical data from 343 patients with mRCC treated with sunitinib or pazopanib in the first line were analyzed. Progression-free survival (PFS) and overall survival (OS) were compared according to the use of metformin. RESULTS: The median PFS and OS for patients using metformin was 31.1 (95% CI 20.6–35.1) and 51.6 (95% CI 44.7-NR) months compared to 9.3 (95% CI 8.0–12.0) and 22.4 (95% CI 19.4–26.8) months for patients not using metformin (p<0.0001 and p=0.0002, respectively). Cox multivariate analysis shows that the use of metformin remains a significant factor for PFS (HR=0.55 [95% CI 0.343–0.883], p=0.013) and also for OS (HR=0.45 [95% CI 0.256–0.794], p=0.006). CONCLUSION: The present study results suggest that the use of metformin was associated with favorable outcome of mRCC patients treated with sunitinib or pazopanib. Dove 2021-05-21 /pmc/articles/PMC8153069/ /pubmed/34054309 http://dx.doi.org/10.2147/CMAR.S305321 Text en © 2021 Fiala et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Fiala, Ondřej
Ostašov, Pavel
Rozsypalová, Aneta
Hora, Milan
Šorejs, Ondřej
Šustr, Jan
Bendová, Barbora
Trávníček, Ivan
Filipovský, Jan
Fínek, Jindřich
Büchler, Tomáš
Metformin Use and the Outcome of Metastatic Renal Cell Carcinoma Treated with Sunitinib or Pazopanib
title Metformin Use and the Outcome of Metastatic Renal Cell Carcinoma Treated with Sunitinib or Pazopanib
title_full Metformin Use and the Outcome of Metastatic Renal Cell Carcinoma Treated with Sunitinib or Pazopanib
title_fullStr Metformin Use and the Outcome of Metastatic Renal Cell Carcinoma Treated with Sunitinib or Pazopanib
title_full_unstemmed Metformin Use and the Outcome of Metastatic Renal Cell Carcinoma Treated with Sunitinib or Pazopanib
title_short Metformin Use and the Outcome of Metastatic Renal Cell Carcinoma Treated with Sunitinib or Pazopanib
title_sort metformin use and the outcome of metastatic renal cell carcinoma treated with sunitinib or pazopanib
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153069/
https://www.ncbi.nlm.nih.gov/pubmed/34054309
http://dx.doi.org/10.2147/CMAR.S305321
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