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Response to post-axitinib treatment in patients with metastatic renal cell carcinoma

BACKGROUND: Axitinib is a potent inhibitor of the vascular endothelial growth factor (VEGF) receptor family with clinical activity in patients with metastatic renal cell carcinoma (mRCC). Given this biochemical potency, the clinical activity of subsequent treatment with targeted therapies in patient...

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Autores principales: Chittoria, Namita, Haddad, Housam, Elson, Paul, Tannir, Nizar M., Wood, Laura S., Dreicer, Robert, Garcia, Jorge A., Rini, Brian I., Jonasch, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810513/
https://www.ncbi.nlm.nih.gov/pubmed/27026229
http://dx.doi.org/10.1186/s12885-016-2282-5
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author Chittoria, Namita
Haddad, Housam
Elson, Paul
Tannir, Nizar M.
Wood, Laura S.
Dreicer, Robert
Garcia, Jorge A.
Rini, Brian I.
Jonasch, Eric
author_facet Chittoria, Namita
Haddad, Housam
Elson, Paul
Tannir, Nizar M.
Wood, Laura S.
Dreicer, Robert
Garcia, Jorge A.
Rini, Brian I.
Jonasch, Eric
author_sort Chittoria, Namita
collection PubMed
description BACKGROUND: Axitinib is a potent inhibitor of the vascular endothelial growth factor (VEGF) receptor family with clinical activity in patients with metastatic renal cell carcinoma (mRCC). Given this biochemical potency, the clinical activity of subsequent treatment with targeted therapies in patients progressing on axitinib is of interest. METHODS: Patients with advanced renal cell carcinoma of any pathologic subtype treated with at least one cycle (four weeks) of axitinib followed by at least one subsequent targeted therapy were investigated in a retrospective analysis. Patient characteristics, duration of treatment and clinical outcomes were analyzed for axitinib and each subsequent line of therapy by Response Evaluation Criteria in Solid Tumors (RECIST). RESULTS: Twenty-five mRCC patients who received at least one approved targeted agent following axitinib were identified. Eight percent of patients achieved a partial response (one patient each to sunitinib and pazopanib) and 42 % had a best response of stable disease to the first therapy after axitinib. The estimated median duration of therapy was 4.4 months (range, 0.2–27.5+). Twelve patients received a second post-axitinib targeted therapy. Six out of 11 evaluable patients (55 %) had a best response of SD. The estimated median duration of treatment was 4.8 months (range, 0.7–19.1+). CONCLUSION: Objective responses and stable disease is observed to post-axitinib targeted therapies and prospective studies are needed for validating role of predictive biomarkers.
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spelling pubmed-48105132016-03-30 Response to post-axitinib treatment in patients with metastatic renal cell carcinoma Chittoria, Namita Haddad, Housam Elson, Paul Tannir, Nizar M. Wood, Laura S. Dreicer, Robert Garcia, Jorge A. Rini, Brian I. Jonasch, Eric BMC Cancer Research Article BACKGROUND: Axitinib is a potent inhibitor of the vascular endothelial growth factor (VEGF) receptor family with clinical activity in patients with metastatic renal cell carcinoma (mRCC). Given this biochemical potency, the clinical activity of subsequent treatment with targeted therapies in patients progressing on axitinib is of interest. METHODS: Patients with advanced renal cell carcinoma of any pathologic subtype treated with at least one cycle (four weeks) of axitinib followed by at least one subsequent targeted therapy were investigated in a retrospective analysis. Patient characteristics, duration of treatment and clinical outcomes were analyzed for axitinib and each subsequent line of therapy by Response Evaluation Criteria in Solid Tumors (RECIST). RESULTS: Twenty-five mRCC patients who received at least one approved targeted agent following axitinib were identified. Eight percent of patients achieved a partial response (one patient each to sunitinib and pazopanib) and 42 % had a best response of stable disease to the first therapy after axitinib. The estimated median duration of therapy was 4.4 months (range, 0.2–27.5+). Twelve patients received a second post-axitinib targeted therapy. Six out of 11 evaluable patients (55 %) had a best response of SD. The estimated median duration of treatment was 4.8 months (range, 0.7–19.1+). CONCLUSION: Objective responses and stable disease is observed to post-axitinib targeted therapies and prospective studies are needed for validating role of predictive biomarkers. BioMed Central 2016-03-29 /pmc/articles/PMC4810513/ /pubmed/27026229 http://dx.doi.org/10.1186/s12885-016-2282-5 Text en © Chittoria et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Chittoria, Namita
Haddad, Housam
Elson, Paul
Tannir, Nizar M.
Wood, Laura S.
Dreicer, Robert
Garcia, Jorge A.
Rini, Brian I.
Jonasch, Eric
Response to post-axitinib treatment in patients with metastatic renal cell carcinoma
title Response to post-axitinib treatment in patients with metastatic renal cell carcinoma
title_full Response to post-axitinib treatment in patients with metastatic renal cell carcinoma
title_fullStr Response to post-axitinib treatment in patients with metastatic renal cell carcinoma
title_full_unstemmed Response to post-axitinib treatment in patients with metastatic renal cell carcinoma
title_short Response to post-axitinib treatment in patients with metastatic renal cell carcinoma
title_sort response to post-axitinib treatment in patients with metastatic renal cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810513/
https://www.ncbi.nlm.nih.gov/pubmed/27026229
http://dx.doi.org/10.1186/s12885-016-2282-5
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