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Pemetrexed-induced acute kidney failure following irreversible renal damage: two case reports and literature review

BACKGROUND: Pemetrexed (PEM) is a new-generation multitargeted antifolate agent with a demonstrated broad-spectrum activity in several types of human cancers, including non-small cell lung cancer (NSCLC) and mesothelioma. Major side effects include dose-limiting hematologic toxicities. PEM nephrotox...

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Autores principales: Zattera, Tito, Londrino, Francesco, Trezzi, Matteo, Palumbo, Roberto, Granata, Antonio, Tatangelo, Paola, Corbani, Valentina, Falqui, Valeria, Chiappini, Nadia, Mathiasen, Lisa, Cavallini, Marco, Rolla, Davide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Diabetic Nephropathy Prevention 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418068/
https://www.ncbi.nlm.nih.gov/pubmed/28491851
http://dx.doi.org/10.15171/jnp.2017.07
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author Zattera, Tito
Londrino, Francesco
Trezzi, Matteo
Palumbo, Roberto
Granata, Antonio
Tatangelo, Paola
Corbani, Valentina
Falqui, Valeria
Chiappini, Nadia
Mathiasen, Lisa
Cavallini, Marco
Rolla, Davide
author_facet Zattera, Tito
Londrino, Francesco
Trezzi, Matteo
Palumbo, Roberto
Granata, Antonio
Tatangelo, Paola
Corbani, Valentina
Falqui, Valeria
Chiappini, Nadia
Mathiasen, Lisa
Cavallini, Marco
Rolla, Davide
author_sort Zattera, Tito
collection PubMed
description BACKGROUND: Pemetrexed (PEM) is a new-generation multitargeted antifolate agent with a demonstrated broad-spectrum activity in several types of human cancers, including non-small cell lung cancer (NSCLC) and mesothelioma. Major side effects include dose-limiting hematologic toxicities. PEM nephrotoxicity is well known; however, its frequency is considered to be low. CASE PRESENTATION: Here we report two cases of acute kidney injury (AKI) related to PEM administration (500 mg/m2) in patients with NSCLC. The first patient required hemodialysis treatment and was submitted to renal biopsy which showed acute tubular damage and interstitial edema without acute tubular necrosis. No other potential nephrotoxic agents were identified. The second patient developed AKI, not proven by biopsy and did not require renal replacement therapy. Both patients, on regular supplementation with folic acid and vitamin B12, concomitantly developed myelosuppression and even several months after PEM withdrawal, showed only a modest improvement of renal function. CONCLUSIONS: PEM is an antifolate antineoplastic agent with a broad-spectrum activity in locally advanced or metastatic NSCLC. It has been shown that PEM allows longer survival. The risk of acute or chronic kidney disease may be one of the prices to be paid for this success.
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spelling pubmed-54180682017-05-10 Pemetrexed-induced acute kidney failure following irreversible renal damage: two case reports and literature review Zattera, Tito Londrino, Francesco Trezzi, Matteo Palumbo, Roberto Granata, Antonio Tatangelo, Paola Corbani, Valentina Falqui, Valeria Chiappini, Nadia Mathiasen, Lisa Cavallini, Marco Rolla, Davide J Nephropathol Case Report BACKGROUND: Pemetrexed (PEM) is a new-generation multitargeted antifolate agent with a demonstrated broad-spectrum activity in several types of human cancers, including non-small cell lung cancer (NSCLC) and mesothelioma. Major side effects include dose-limiting hematologic toxicities. PEM nephrotoxicity is well known; however, its frequency is considered to be low. CASE PRESENTATION: Here we report two cases of acute kidney injury (AKI) related to PEM administration (500 mg/m2) in patients with NSCLC. The first patient required hemodialysis treatment and was submitted to renal biopsy which showed acute tubular damage and interstitial edema without acute tubular necrosis. No other potential nephrotoxic agents were identified. The second patient developed AKI, not proven by biopsy and did not require renal replacement therapy. Both patients, on regular supplementation with folic acid and vitamin B12, concomitantly developed myelosuppression and even several months after PEM withdrawal, showed only a modest improvement of renal function. CONCLUSIONS: PEM is an antifolate antineoplastic agent with a broad-spectrum activity in locally advanced or metastatic NSCLC. It has been shown that PEM allows longer survival. The risk of acute or chronic kidney disease may be one of the prices to be paid for this success. Society of Diabetic Nephropathy Prevention 2017-03 2016-10-27 /pmc/articles/PMC5418068/ /pubmed/28491851 http://dx.doi.org/10.15171/jnp.2017.07 Text en © 2017 The Author(s) Published by Society of Diabetic Nephropathy Prevention. This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Zattera, Tito
Londrino, Francesco
Trezzi, Matteo
Palumbo, Roberto
Granata, Antonio
Tatangelo, Paola
Corbani, Valentina
Falqui, Valeria
Chiappini, Nadia
Mathiasen, Lisa
Cavallini, Marco
Rolla, Davide
Pemetrexed-induced acute kidney failure following irreversible renal damage: two case reports and literature review
title Pemetrexed-induced acute kidney failure following irreversible renal damage: two case reports and literature review
title_full Pemetrexed-induced acute kidney failure following irreversible renal damage: two case reports and literature review
title_fullStr Pemetrexed-induced acute kidney failure following irreversible renal damage: two case reports and literature review
title_full_unstemmed Pemetrexed-induced acute kidney failure following irreversible renal damage: two case reports and literature review
title_short Pemetrexed-induced acute kidney failure following irreversible renal damage: two case reports and literature review
title_sort pemetrexed-induced acute kidney failure following irreversible renal damage: two case reports and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418068/
https://www.ncbi.nlm.nih.gov/pubmed/28491851
http://dx.doi.org/10.15171/jnp.2017.07
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