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Renal-limited thrombotic microangiopathy after switching from bevacizumab to ramucirumab: a case report
BACKGROUND: It is well known that vascular endothelial growth factor (VEGF) inhibitors can cause proteinuria. The incidence of proteinuria is high for bevacizumab, a humanized monoclonal antibody directed against VEGF, but the range of proteinuria rarely becomes nephrotic (2.2% occurrence according...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329058/ https://www.ncbi.nlm.nih.gov/pubmed/30634936 http://dx.doi.org/10.1186/s12882-018-1194-9 |
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author | Yamada, Ryo Okawa, Takao Matsuo, Ken Suzuki, Makoto Mori, Noriko Mori, Kiyoshi |
author_facet | Yamada, Ryo Okawa, Takao Matsuo, Ken Suzuki, Makoto Mori, Noriko Mori, Kiyoshi |
author_sort | Yamada, Ryo |
collection | PubMed |
description | BACKGROUND: It is well known that vascular endothelial growth factor (VEGF) inhibitors can cause proteinuria. The incidence of proteinuria is high for bevacizumab, a humanized monoclonal antibody directed against VEGF, but the range of proteinuria rarely becomes nephrotic (2.2% occurrence according to a meta-analysis). In such cases, renal pathology shows thrombotic microangiopathy (TMA). Ramucirumab, anti-VEGF receptor 2 (VEGFR2) monoclonal antibody, can also cause proteinuria, but it is not yet reported whether the drug may induce TMA. CASE PRESENTATION: Here, we report a case who immediately developed TMA by ramucirumab after multiple courses of bevacizumab treatment. This is the first case of pathologically-proved TMA by ramucirumab. After cessation of the drug, symptoms of TMA improved gradually. CONCLUSIONS: This case demonstrates that not only blockade of VEGF but also VEGFR2 antagonism may result in TMA, which is a rare but life-threatening complication of cancer treatment drug. |
format | Online Article Text |
id | pubmed-6329058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63290582019-01-16 Renal-limited thrombotic microangiopathy after switching from bevacizumab to ramucirumab: a case report Yamada, Ryo Okawa, Takao Matsuo, Ken Suzuki, Makoto Mori, Noriko Mori, Kiyoshi BMC Nephrol Case Report BACKGROUND: It is well known that vascular endothelial growth factor (VEGF) inhibitors can cause proteinuria. The incidence of proteinuria is high for bevacizumab, a humanized monoclonal antibody directed against VEGF, but the range of proteinuria rarely becomes nephrotic (2.2% occurrence according to a meta-analysis). In such cases, renal pathology shows thrombotic microangiopathy (TMA). Ramucirumab, anti-VEGF receptor 2 (VEGFR2) monoclonal antibody, can also cause proteinuria, but it is not yet reported whether the drug may induce TMA. CASE PRESENTATION: Here, we report a case who immediately developed TMA by ramucirumab after multiple courses of bevacizumab treatment. This is the first case of pathologically-proved TMA by ramucirumab. After cessation of the drug, symptoms of TMA improved gradually. CONCLUSIONS: This case demonstrates that not only blockade of VEGF but also VEGFR2 antagonism may result in TMA, which is a rare but life-threatening complication of cancer treatment drug. BioMed Central 2019-01-11 /pmc/articles/PMC6329058/ /pubmed/30634936 http://dx.doi.org/10.1186/s12882-018-1194-9 Text en © The Author(s). 2019 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 Yamada, Ryo Okawa, Takao Matsuo, Ken Suzuki, Makoto Mori, Noriko Mori, Kiyoshi Renal-limited thrombotic microangiopathy after switching from bevacizumab to ramucirumab: a case report |
title | Renal-limited thrombotic microangiopathy after switching from bevacizumab to ramucirumab: a case report |
title_full | Renal-limited thrombotic microangiopathy after switching from bevacizumab to ramucirumab: a case report |
title_fullStr | Renal-limited thrombotic microangiopathy after switching from bevacizumab to ramucirumab: a case report |
title_full_unstemmed | Renal-limited thrombotic microangiopathy after switching from bevacizumab to ramucirumab: a case report |
title_short | Renal-limited thrombotic microangiopathy after switching from bevacizumab to ramucirumab: a case report |
title_sort | renal-limited thrombotic microangiopathy after switching from bevacizumab to ramucirumab: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329058/ https://www.ncbi.nlm.nih.gov/pubmed/30634936 http://dx.doi.org/10.1186/s12882-018-1194-9 |
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