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Adjuvant therapy for locally advanced renal cell cancer: A systematic review with meta-analysis

BACKGROUND: Many adjuvant trials have been undertaken in an attempt to reduce the risk of recurrence among patients who undergo surgical resection for locally advanced renal cancer. However, no clear benefit has been identified to date. This systematic review was conducted to examine the exact role...

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Autores principales: Scherr, Adolfo JO, Lima, Joao Paulo SN, Sasse, Emma C, Lima, Carmen SP, Sasse, André D
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080342/
https://www.ncbi.nlm.nih.gov/pubmed/21453469
http://dx.doi.org/10.1186/1471-2407-11-115
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author Scherr, Adolfo JO
Lima, Joao Paulo SN
Sasse, Emma C
Lima, Carmen SP
Sasse, André D
author_facet Scherr, Adolfo JO
Lima, Joao Paulo SN
Sasse, Emma C
Lima, Carmen SP
Sasse, André D
author_sort Scherr, Adolfo JO
collection PubMed
description BACKGROUND: Many adjuvant trials have been undertaken in an attempt to reduce the risk of recurrence among patients who undergo surgical resection for locally advanced renal cancer. However, no clear benefit has been identified to date. This systematic review was conducted to examine the exact role of adjuvant therapy in renal cancer setting. METHODS: Randomized controlled trials were searched comparing adjuvant therapy (chemotherapy, vaccine, immunotherapy, biochemotherapy) versus no active treatment after surgery among renal cell cancer patients. Outcomes were overall survival (OS), disease-free survival (DFS), and severe toxicities. Risk ratios (RR), hazard ratios (HR) and 95% confidence intervals were calculated using a fixed-effects meta-analysis. Heterogeneity was measured by I(2). Different strategies of adjuvant treatment were evaluated separately. RESULTS: Ten studies (2,609 patients) were included. Adjuvant therapy provided no benefits in terms of OS (HR 1.07; 95%CI 0.89 to 1.28; P = 0.48 I(2 )= 0%) or DFS (HR 1.03; 95%CI 0.87 to 1.21; P = 0.77 I(2 )= 15%) when compared to no treatment. No subgroup analysis (immunotherapy, vaccines, biochemotherapy and hormone therapy) had relevant results. Toxicity evaluation depicted a significantly higher frequency of serious adverse events in the adjuvant group. CONCLUSIONS: This analysis provided no support for the hypothesis that the agents studied provide any clinical benefit for renal cancer patients although they increase the risk of toxic effects. Randomized trials are underway to test targeted therapies, which might open a new therapeutic frontier. Until these trials yield results, no adjuvant therapy can be recommended for patients who undergo surgical resection for renal cell cancer.
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spelling pubmed-30803422011-04-21 Adjuvant therapy for locally advanced renal cell cancer: A systematic review with meta-analysis Scherr, Adolfo JO Lima, Joao Paulo SN Sasse, Emma C Lima, Carmen SP Sasse, André D BMC Cancer Research Article BACKGROUND: Many adjuvant trials have been undertaken in an attempt to reduce the risk of recurrence among patients who undergo surgical resection for locally advanced renal cancer. However, no clear benefit has been identified to date. This systematic review was conducted to examine the exact role of adjuvant therapy in renal cancer setting. METHODS: Randomized controlled trials were searched comparing adjuvant therapy (chemotherapy, vaccine, immunotherapy, biochemotherapy) versus no active treatment after surgery among renal cell cancer patients. Outcomes were overall survival (OS), disease-free survival (DFS), and severe toxicities. Risk ratios (RR), hazard ratios (HR) and 95% confidence intervals were calculated using a fixed-effects meta-analysis. Heterogeneity was measured by I(2). Different strategies of adjuvant treatment were evaluated separately. RESULTS: Ten studies (2,609 patients) were included. Adjuvant therapy provided no benefits in terms of OS (HR 1.07; 95%CI 0.89 to 1.28; P = 0.48 I(2 )= 0%) or DFS (HR 1.03; 95%CI 0.87 to 1.21; P = 0.77 I(2 )= 15%) when compared to no treatment. No subgroup analysis (immunotherapy, vaccines, biochemotherapy and hormone therapy) had relevant results. Toxicity evaluation depicted a significantly higher frequency of serious adverse events in the adjuvant group. CONCLUSIONS: This analysis provided no support for the hypothesis that the agents studied provide any clinical benefit for renal cancer patients although they increase the risk of toxic effects. Randomized trials are underway to test targeted therapies, which might open a new therapeutic frontier. Until these trials yield results, no adjuvant therapy can be recommended for patients who undergo surgical resection for renal cell cancer. BioMed Central 2011-03-31 /pmc/articles/PMC3080342/ /pubmed/21453469 http://dx.doi.org/10.1186/1471-2407-11-115 Text en Copyright ©2011 Scherr et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Scherr, Adolfo JO
Lima, Joao Paulo SN
Sasse, Emma C
Lima, Carmen SP
Sasse, André D
Adjuvant therapy for locally advanced renal cell cancer: A systematic review with meta-analysis
title Adjuvant therapy for locally advanced renal cell cancer: A systematic review with meta-analysis
title_full Adjuvant therapy for locally advanced renal cell cancer: A systematic review with meta-analysis
title_fullStr Adjuvant therapy for locally advanced renal cell cancer: A systematic review with meta-analysis
title_full_unstemmed Adjuvant therapy for locally advanced renal cell cancer: A systematic review with meta-analysis
title_short Adjuvant therapy for locally advanced renal cell cancer: A systematic review with meta-analysis
title_sort adjuvant therapy for locally advanced renal cell cancer: a systematic review with meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080342/
https://www.ncbi.nlm.nih.gov/pubmed/21453469
http://dx.doi.org/10.1186/1471-2407-11-115
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