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Optimal first-line and second-line treatments for metastatic renal cell carcinoma: current evidence
Since 2005, an abundance of targeted agents has been approved for the treatment of metastatic renal cell carcinoma (mRCC), without any specification as to what may be the most optimal first-line and second-line sequence. Hence, our objective was to critically examine the evidence supporting the use...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219683/ https://www.ncbi.nlm.nih.gov/pubmed/25378943 http://dx.doi.org/10.2147/IJNRD.S48496 |
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author | Sun, Maxine Larcher, Alessandro Karakiewicz, Pierre I |
author_facet | Sun, Maxine Larcher, Alessandro Karakiewicz, Pierre I |
author_sort | Sun, Maxine |
collection | PubMed |
description | Since 2005, an abundance of targeted agents has been approved for the treatment of metastatic renal cell carcinoma (mRCC), without any specification as to what may be the most optimal first-line and second-line sequence. Hence, our objective was to critically examine the evidence supporting the use of first-line and second-line agents in the management of mRCC. Our review suggests that in first line, sunitinib and pazopanib represent treatment options for patients with favorable or intermediate-risk features and clear cell histology. Unfortunately, the Phase III trial cannot conclusively prove the noninferiority of pazopanib relative to sunitinib. Hence, the use of sunitinib as first-line standard of care remains justified. Pazopanib represents an option for specific patients in whom sunitinib might not be tolerated. In patients with poor-risk features, temsirolimus represents the only option supported with level 1 evidence. Less optimal alternatives include sunitinib and bevacizumab combined with interferon, based on the minimal inclusion of poor-risk patients in pivotal Phase III studies of these two molecules. In patients with non-clear cell mRCC, the use of temsirolimus is supported by Phase III data, unlike for any other molecule. In second line, the options consist of everolimus and axitinib. However, the axitinib data are substantially more robust given the inclusion of more patients considered as true second-line, and validly justify the choice of axitinib over everolimus. Nonetheless, the Phase III trial of everolimus may be considered as level 1 evidence for use as third-line or subsequent lines of therapy. |
format | Online Article Text |
id | pubmed-4219683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42196832014-11-06 Optimal first-line and second-line treatments for metastatic renal cell carcinoma: current evidence Sun, Maxine Larcher, Alessandro Karakiewicz, Pierre I Int J Nephrol Renovasc Dis Review Since 2005, an abundance of targeted agents has been approved for the treatment of metastatic renal cell carcinoma (mRCC), without any specification as to what may be the most optimal first-line and second-line sequence. Hence, our objective was to critically examine the evidence supporting the use of first-line and second-line agents in the management of mRCC. Our review suggests that in first line, sunitinib and pazopanib represent treatment options for patients with favorable or intermediate-risk features and clear cell histology. Unfortunately, the Phase III trial cannot conclusively prove the noninferiority of pazopanib relative to sunitinib. Hence, the use of sunitinib as first-line standard of care remains justified. Pazopanib represents an option for specific patients in whom sunitinib might not be tolerated. In patients with poor-risk features, temsirolimus represents the only option supported with level 1 evidence. Less optimal alternatives include sunitinib and bevacizumab combined with interferon, based on the minimal inclusion of poor-risk patients in pivotal Phase III studies of these two molecules. In patients with non-clear cell mRCC, the use of temsirolimus is supported by Phase III data, unlike for any other molecule. In second line, the options consist of everolimus and axitinib. However, the axitinib data are substantially more robust given the inclusion of more patients considered as true second-line, and validly justify the choice of axitinib over everolimus. Nonetheless, the Phase III trial of everolimus may be considered as level 1 evidence for use as third-line or subsequent lines of therapy. Dove Medical Press 2014-10-29 /pmc/articles/PMC4219683/ /pubmed/25378943 http://dx.doi.org/10.2147/IJNRD.S48496 Text en © 2014 Sun et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Sun, Maxine Larcher, Alessandro Karakiewicz, Pierre I Optimal first-line and second-line treatments for metastatic renal cell carcinoma: current evidence |
title | Optimal first-line and second-line treatments for metastatic renal cell carcinoma: current evidence |
title_full | Optimal first-line and second-line treatments for metastatic renal cell carcinoma: current evidence |
title_fullStr | Optimal first-line and second-line treatments for metastatic renal cell carcinoma: current evidence |
title_full_unstemmed | Optimal first-line and second-line treatments for metastatic renal cell carcinoma: current evidence |
title_short | Optimal first-line and second-line treatments for metastatic renal cell carcinoma: current evidence |
title_sort | optimal first-line and second-line treatments for metastatic renal cell carcinoma: current evidence |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219683/ https://www.ncbi.nlm.nih.gov/pubmed/25378943 http://dx.doi.org/10.2147/IJNRD.S48496 |
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