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Renal failure during chemotherapy: renal biopsy for assessing subacute nephrotoxicity of pemetrexed
BACKGROUND: Pemetrexed, a multitargeted antifolate cytotoxic agent, is currently used primarily in combination with cisplatin for metastatic non-small cell lung cancer and for malignant mesothelioma. Acute renal toxicity of pemetrexed has been recently described with polychemotherapy, in which the i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689204/ https://www.ncbi.nlm.nih.gov/pubmed/29145816 http://dx.doi.org/10.1186/s12885-017-3705-7 |
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author | Assayag, Maureen Rouvier, Philippe Gauthier, Marion Costel, Ghania Cluzel, Philippe Mercadal, Lucile Deray, Gilbert Isnard Bagnis, Corinne |
author_facet | Assayag, Maureen Rouvier, Philippe Gauthier, Marion Costel, Ghania Cluzel, Philippe Mercadal, Lucile Deray, Gilbert Isnard Bagnis, Corinne |
author_sort | Assayag, Maureen |
collection | PubMed |
description | BACKGROUND: Pemetrexed, a multitargeted antifolate cytotoxic agent, is currently used primarily in combination with cisplatin for metastatic non-small cell lung cancer and for malignant mesothelioma. Acute renal toxicity of pemetrexed has been recently described with polychemotherapy, in which the individual responsibility of each drug is difficult to establish. Only one recent report documents renal involvement in long-term exposed patients. CASE PRESENTATION: We report on a case of rapidly progressive nephropathy leading to the cessation of platinum salts and the secondary interruption of pemetrexed and bevacizumab. Acute tubular necrosis shown on the renal biopsy could potentially be due to pemetrexed. Persistent severe renal failure after the resumption of all drugs led to new treatment lines with gemcitabine (while the glomerular filtration rate was below 30 ml/min/1.73m(2)), then followed by Taxol. CONCLUSIONS: The optimal strategy with regard to renal complications in cancer patients is not clear. Acute or chronic loss in renal function generally leads to a new treatment line, possibly impairing the overall success of the treatment. The use of chemotherapy in patients with a glomerular filtration rate below 30 ml/min/1.73m(2) is usually associated with an increased risk of side effects when not contraindicated by renal elimination of the drug. |
format | Online Article Text |
id | pubmed-5689204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56892042017-11-24 Renal failure during chemotherapy: renal biopsy for assessing subacute nephrotoxicity of pemetrexed Assayag, Maureen Rouvier, Philippe Gauthier, Marion Costel, Ghania Cluzel, Philippe Mercadal, Lucile Deray, Gilbert Isnard Bagnis, Corinne BMC Cancer Case Report BACKGROUND: Pemetrexed, a multitargeted antifolate cytotoxic agent, is currently used primarily in combination with cisplatin for metastatic non-small cell lung cancer and for malignant mesothelioma. Acute renal toxicity of pemetrexed has been recently described with polychemotherapy, in which the individual responsibility of each drug is difficult to establish. Only one recent report documents renal involvement in long-term exposed patients. CASE PRESENTATION: We report on a case of rapidly progressive nephropathy leading to the cessation of platinum salts and the secondary interruption of pemetrexed and bevacizumab. Acute tubular necrosis shown on the renal biopsy could potentially be due to pemetrexed. Persistent severe renal failure after the resumption of all drugs led to new treatment lines with gemcitabine (while the glomerular filtration rate was below 30 ml/min/1.73m(2)), then followed by Taxol. CONCLUSIONS: The optimal strategy with regard to renal complications in cancer patients is not clear. Acute or chronic loss in renal function generally leads to a new treatment line, possibly impairing the overall success of the treatment. The use of chemotherapy in patients with a glomerular filtration rate below 30 ml/min/1.73m(2) is usually associated with an increased risk of side effects when not contraindicated by renal elimination of the drug. BioMed Central 2017-11-16 /pmc/articles/PMC5689204/ /pubmed/29145816 http://dx.doi.org/10.1186/s12885-017-3705-7 Text en © The Author(s). 2017 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 | Case Report Assayag, Maureen Rouvier, Philippe Gauthier, Marion Costel, Ghania Cluzel, Philippe Mercadal, Lucile Deray, Gilbert Isnard Bagnis, Corinne Renal failure during chemotherapy: renal biopsy for assessing subacute nephrotoxicity of pemetrexed |
title | Renal failure during chemotherapy: renal biopsy for assessing subacute nephrotoxicity of pemetrexed |
title_full | Renal failure during chemotherapy: renal biopsy for assessing subacute nephrotoxicity of pemetrexed |
title_fullStr | Renal failure during chemotherapy: renal biopsy for assessing subacute nephrotoxicity of pemetrexed |
title_full_unstemmed | Renal failure during chemotherapy: renal biopsy for assessing subacute nephrotoxicity of pemetrexed |
title_short | Renal failure during chemotherapy: renal biopsy for assessing subacute nephrotoxicity of pemetrexed |
title_sort | renal failure during chemotherapy: renal biopsy for assessing subacute nephrotoxicity of pemetrexed |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5689204/ https://www.ncbi.nlm.nih.gov/pubmed/29145816 http://dx.doi.org/10.1186/s12885-017-3705-7 |
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