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Predictive Markers of First Line Pazopanib Treatment in Kidney Cancer

Real-world evidence from clinical practices is fundamental for understanding the efficacy and tolerability of medicinal products. Patients with renal cell cancer were studied to gain data not represented by analyses conducted on highly selected patients participating in clinical trials. Our goal was...

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Autores principales: Küronya, Zsófia, Szőnyi, Mihály Dániel, Nagyiványi, Krisztián, Gyergyay, Fruzsina, Géczi, Lajos, Budai, Barna, Martin, Tamás, Ladányi, Andrea, Kiss, Edina, Biró, Krisztina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471165/
https://www.ncbi.nlm.nih.gov/pubmed/32572819
http://dx.doi.org/10.1007/s12253-020-00853-9
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author Küronya, Zsófia
Szőnyi, Mihály Dániel
Nagyiványi, Krisztián
Gyergyay, Fruzsina
Géczi, Lajos
Budai, Barna
Martin, Tamás
Ladányi, Andrea
Kiss, Edina
Biró, Krisztina
author_facet Küronya, Zsófia
Szőnyi, Mihály Dániel
Nagyiványi, Krisztián
Gyergyay, Fruzsina
Géczi, Lajos
Budai, Barna
Martin, Tamás
Ladányi, Andrea
Kiss, Edina
Biró, Krisztina
author_sort Küronya, Zsófia
collection PubMed
description Real-world evidence from clinical practices is fundamental for understanding the efficacy and tolerability of medicinal products. Patients with renal cell cancer were studied to gain data not represented by analyses conducted on highly selected patients participating in clinical trials. Our goal was to retrospectively collect data from patients with advanced renal tumours treated with pazopanib (PZ) to investigate the efficacy, frequency of side effects, and searching for predictive markers. Eighty-one patients who had received PZ therapy as first-line treatment were retrospectively evaluated. Overall survival (OS), progression-free survival (PFS) were assessed as endpoints. Median PFS and OS were 11.8 months (95% CI: 8.8–22.4); and 30.2 months (95% CI: 20.3–41.7) respectively. Severe side effects were only encountered in 11 (14%) patients. The presence of liver metastasis shortened the median PFS (5.5 vs. 14.8 months, p = 0.003). Median PFS for patients with or without side effects was 25.6 vs. 7.3 months, respectively (p = 0.0001). Patients younger than 65 years had a median OS of 41.7 months vs. 25.2 months for those over 65 years of age (p = 0.008). According to our results absence of liver metastases, younger age (<65 years) and presence of side effects proved to be independent predictive markers of better PFS and OS.
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spelling pubmed-74711652020-09-16 Predictive Markers of First Line Pazopanib Treatment in Kidney Cancer Küronya, Zsófia Szőnyi, Mihály Dániel Nagyiványi, Krisztián Gyergyay, Fruzsina Géczi, Lajos Budai, Barna Martin, Tamás Ladányi, Andrea Kiss, Edina Biró, Krisztina Pathol Oncol Res Original Article Real-world evidence from clinical practices is fundamental for understanding the efficacy and tolerability of medicinal products. Patients with renal cell cancer were studied to gain data not represented by analyses conducted on highly selected patients participating in clinical trials. Our goal was to retrospectively collect data from patients with advanced renal tumours treated with pazopanib (PZ) to investigate the efficacy, frequency of side effects, and searching for predictive markers. Eighty-one patients who had received PZ therapy as first-line treatment were retrospectively evaluated. Overall survival (OS), progression-free survival (PFS) were assessed as endpoints. Median PFS and OS were 11.8 months (95% CI: 8.8–22.4); and 30.2 months (95% CI: 20.3–41.7) respectively. Severe side effects were only encountered in 11 (14%) patients. The presence of liver metastasis shortened the median PFS (5.5 vs. 14.8 months, p = 0.003). Median PFS for patients with or without side effects was 25.6 vs. 7.3 months, respectively (p = 0.0001). Patients younger than 65 years had a median OS of 41.7 months vs. 25.2 months for those over 65 years of age (p = 0.008). According to our results absence of liver metastases, younger age (<65 years) and presence of side effects proved to be independent predictive markers of better PFS and OS. Springer Netherlands 2020-06-22 2020 /pmc/articles/PMC7471165/ /pubmed/32572819 http://dx.doi.org/10.1007/s12253-020-00853-9 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Küronya, Zsófia
Szőnyi, Mihály Dániel
Nagyiványi, Krisztián
Gyergyay, Fruzsina
Géczi, Lajos
Budai, Barna
Martin, Tamás
Ladányi, Andrea
Kiss, Edina
Biró, Krisztina
Predictive Markers of First Line Pazopanib Treatment in Kidney Cancer
title Predictive Markers of First Line Pazopanib Treatment in Kidney Cancer
title_full Predictive Markers of First Line Pazopanib Treatment in Kidney Cancer
title_fullStr Predictive Markers of First Line Pazopanib Treatment in Kidney Cancer
title_full_unstemmed Predictive Markers of First Line Pazopanib Treatment in Kidney Cancer
title_short Predictive Markers of First Line Pazopanib Treatment in Kidney Cancer
title_sort predictive markers of first line pazopanib treatment in kidney cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471165/
https://www.ncbi.nlm.nih.gov/pubmed/32572819
http://dx.doi.org/10.1007/s12253-020-00853-9
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