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Pazopanib as a possible option for the treatment of metastatic non-clear cell renal carcinoma patients: a systematic review

BACKGROUND: Effective systemic treatment of non-clear cell renal carcinoma (nccRCC) is still an unmet clinical need, with few studies to support an evidence-based approach. To date, the only recommended standard first-line treatment is sunitinib. Pazopanib may also be used in nccRCC but its place in...

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Autores principales: Bersanelli, Melissa, Brunelli, Matteo, Gnetti, Letizia, Maestroni, Umberto, Buti, Sebastiano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278098/
https://www.ncbi.nlm.nih.gov/pubmed/32550862
http://dx.doi.org/10.1177/1758835920915303
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author Bersanelli, Melissa
Brunelli, Matteo
Gnetti, Letizia
Maestroni, Umberto
Buti, Sebastiano
author_facet Bersanelli, Melissa
Brunelli, Matteo
Gnetti, Letizia
Maestroni, Umberto
Buti, Sebastiano
author_sort Bersanelli, Melissa
collection PubMed
description BACKGROUND: Effective systemic treatment of non-clear cell renal carcinoma (nccRCC) is still an unmet clinical need, with few studies to support an evidence-based approach. To date, the only recommended standard first-line treatment is sunitinib. Pazopanib may also be used in nccRCC but its place in therapy is not clearly established. It has comparable efficacy and better tolerability than sunitinib in clear cell renal carcinoma. Our objective was to review the use of pazopanib in metastatic nccRCC. METHODS: We conducted a systematic review according to PRISMA guidelines. Any type of study reporting the use of pazopanib in metastatic renal cell carcinoma including cases with non-clear cell histology was eligible. RESULTS: In all, 15 studies were included in our analysis, including a total of 318 nccRCC patients treated with pazopanib. Most studies were retrospective (n = 12); three were prospective trials. The specific outcomes of nccRCC patients were reported by four studies. Pazopanib alone as first-line treatment gave overall response rates ranging from 27% to 33%, disease control rates of 81–89%, median progression free survival of 8.1–16.5 months and median overall survival of 17.3–31.0 months. Grade 3–4 adverse events rates were 21–55%. CONCLUSION: The present review provides for the first time a systematic summary of evidence about the possible use of pazopanib as first-line treatment for nccRCC, with a favorable outcome despite the low strength of evidence. Pazopanib could be considered as a possible therapeutic option in this setting.
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spelling pubmed-72780982020-06-17 Pazopanib as a possible option for the treatment of metastatic non-clear cell renal carcinoma patients: a systematic review Bersanelli, Melissa Brunelli, Matteo Gnetti, Letizia Maestroni, Umberto Buti, Sebastiano Ther Adv Med Oncol Systematic Review BACKGROUND: Effective systemic treatment of non-clear cell renal carcinoma (nccRCC) is still an unmet clinical need, with few studies to support an evidence-based approach. To date, the only recommended standard first-line treatment is sunitinib. Pazopanib may also be used in nccRCC but its place in therapy is not clearly established. It has comparable efficacy and better tolerability than sunitinib in clear cell renal carcinoma. Our objective was to review the use of pazopanib in metastatic nccRCC. METHODS: We conducted a systematic review according to PRISMA guidelines. Any type of study reporting the use of pazopanib in metastatic renal cell carcinoma including cases with non-clear cell histology was eligible. RESULTS: In all, 15 studies were included in our analysis, including a total of 318 nccRCC patients treated with pazopanib. Most studies were retrospective (n = 12); three were prospective trials. The specific outcomes of nccRCC patients were reported by four studies. Pazopanib alone as first-line treatment gave overall response rates ranging from 27% to 33%, disease control rates of 81–89%, median progression free survival of 8.1–16.5 months and median overall survival of 17.3–31.0 months. Grade 3–4 adverse events rates were 21–55%. CONCLUSION: The present review provides for the first time a systematic summary of evidence about the possible use of pazopanib as first-line treatment for nccRCC, with a favorable outcome despite the low strength of evidence. Pazopanib could be considered as a possible therapeutic option in this setting. SAGE Publications 2020-05-26 /pmc/articles/PMC7278098/ /pubmed/32550862 http://dx.doi.org/10.1177/1758835920915303 Text en © The Author(s), 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Systematic Review
Bersanelli, Melissa
Brunelli, Matteo
Gnetti, Letizia
Maestroni, Umberto
Buti, Sebastiano
Pazopanib as a possible option for the treatment of metastatic non-clear cell renal carcinoma patients: a systematic review
title Pazopanib as a possible option for the treatment of metastatic non-clear cell renal carcinoma patients: a systematic review
title_full Pazopanib as a possible option for the treatment of metastatic non-clear cell renal carcinoma patients: a systematic review
title_fullStr Pazopanib as a possible option for the treatment of metastatic non-clear cell renal carcinoma patients: a systematic review
title_full_unstemmed Pazopanib as a possible option for the treatment of metastatic non-clear cell renal carcinoma patients: a systematic review
title_short Pazopanib as a possible option for the treatment of metastatic non-clear cell renal carcinoma patients: a systematic review
title_sort pazopanib as a possible option for the treatment of metastatic non-clear cell renal carcinoma patients: a systematic review
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278098/
https://www.ncbi.nlm.nih.gov/pubmed/32550862
http://dx.doi.org/10.1177/1758835920915303
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