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Renal function during rofecoxib therapy in patients with metastatic cancer: retrospective analysis of a prospective phase II trial
BACKGROUND: Angiostatic/antiinflammatory therapy with COX-II inhibitors and pioglitazone seems to be a well tolerated and promising regimen in patients with metastatic cancer. COX-II inhibitors may have less gastrointestinal side effects than conventional non-steroidal antiinflammatory drugs, but th...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038926/ https://www.ncbi.nlm.nih.gov/pubmed/21208422 http://dx.doi.org/10.1186/1756-0500-4-2 |
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author | Reinhold, Stephan W Reichle, Albrecht Leiminger, Sonja Bergler, Tobias Hoffmann, Ute Krüger, Bernd Banas, Bernhard Krämer, Bernhard K |
author_facet | Reinhold, Stephan W Reichle, Albrecht Leiminger, Sonja Bergler, Tobias Hoffmann, Ute Krüger, Bernd Banas, Bernhard Krämer, Bernhard K |
author_sort | Reinhold, Stephan W |
collection | PubMed |
description | BACKGROUND: Angiostatic/antiinflammatory therapy with COX-II inhibitors and pioglitazone seems to be a well tolerated and promising regimen in patients with metastatic cancer. COX-II inhibitors may have less gastrointestinal side effects than conventional non-steroidal antiinflammatory drugs, but their impact on renal function seems to be similar. METHODS: 87 patients with metastatic/advanced cancer were treated up to 12 months (mean 19.5 weeks) with rofecoxib, pioglitazone and either capecitabine (group A with gastrointestinal and urological cancer, n = 50) or trofosfamide (group B with non-gastrointestinal/non-urological cancer, n = 37) and followed for further 6 months. RESULTS: Baseline serum creatinine concentration was 0.81 ± 0.28 mg/dl, and increased by about 0.15 mg/dl during months 1-3. Accordingly estimated glomerular filtration rate (eGFR) decreased from 90.3 ml/min ± 3.6 ml/min at baseline by about 10 ml/min during months 1-3. Renal function decreased in 75 patients (86%) in the first month (p < 0.0001). This decrease went along with clinical signs of volume expansion. Renal function tended to recover after discontinuation of the study medication. CONCLUSIONS: Therapy with rofecoxib in an antiangiogenic/antiinflammatory setting results in a decrease of renal function in nearly every patient. TRIAL REGISTRATION NUMBER: German Clinical Trials Register DRKS: DRKS00000119 |
format | Text |
id | pubmed-3038926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30389262011-02-15 Renal function during rofecoxib therapy in patients with metastatic cancer: retrospective analysis of a prospective phase II trial Reinhold, Stephan W Reichle, Albrecht Leiminger, Sonja Bergler, Tobias Hoffmann, Ute Krüger, Bernd Banas, Bernhard Krämer, Bernhard K BMC Res Notes Research Article BACKGROUND: Angiostatic/antiinflammatory therapy with COX-II inhibitors and pioglitazone seems to be a well tolerated and promising regimen in patients with metastatic cancer. COX-II inhibitors may have less gastrointestinal side effects than conventional non-steroidal antiinflammatory drugs, but their impact on renal function seems to be similar. METHODS: 87 patients with metastatic/advanced cancer were treated up to 12 months (mean 19.5 weeks) with rofecoxib, pioglitazone and either capecitabine (group A with gastrointestinal and urological cancer, n = 50) or trofosfamide (group B with non-gastrointestinal/non-urological cancer, n = 37) and followed for further 6 months. RESULTS: Baseline serum creatinine concentration was 0.81 ± 0.28 mg/dl, and increased by about 0.15 mg/dl during months 1-3. Accordingly estimated glomerular filtration rate (eGFR) decreased from 90.3 ml/min ± 3.6 ml/min at baseline by about 10 ml/min during months 1-3. Renal function decreased in 75 patients (86%) in the first month (p < 0.0001). This decrease went along with clinical signs of volume expansion. Renal function tended to recover after discontinuation of the study medication. CONCLUSIONS: Therapy with rofecoxib in an antiangiogenic/antiinflammatory setting results in a decrease of renal function in nearly every patient. TRIAL REGISTRATION NUMBER: German Clinical Trials Register DRKS: DRKS00000119 BioMed Central 2011-01-05 /pmc/articles/PMC3038926/ /pubmed/21208422 http://dx.doi.org/10.1186/1756-0500-4-2 Text en Copyright ©2011 Reinhold et al; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Reinhold, Stephan W Reichle, Albrecht Leiminger, Sonja Bergler, Tobias Hoffmann, Ute Krüger, Bernd Banas, Bernhard Krämer, Bernhard K Renal function during rofecoxib therapy in patients with metastatic cancer: retrospective analysis of a prospective phase II trial |
title | Renal function during rofecoxib therapy in patients with metastatic cancer: retrospective analysis of a prospective phase II trial |
title_full | Renal function during rofecoxib therapy in patients with metastatic cancer: retrospective analysis of a prospective phase II trial |
title_fullStr | Renal function during rofecoxib therapy in patients with metastatic cancer: retrospective analysis of a prospective phase II trial |
title_full_unstemmed | Renal function during rofecoxib therapy in patients with metastatic cancer: retrospective analysis of a prospective phase II trial |
title_short | Renal function during rofecoxib therapy in patients with metastatic cancer: retrospective analysis of a prospective phase II trial |
title_sort | renal function during rofecoxib therapy in patients with metastatic cancer: retrospective analysis of a prospective phase ii trial |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038926/ https://www.ncbi.nlm.nih.gov/pubmed/21208422 http://dx.doi.org/10.1186/1756-0500-4-2 |
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