Cargando…
A real or apparent decrease in glomerular filtration rate in patients using olaparib?
PURPOSE: Olaparib is a poly (ADP-ribose) polymerase (PARP) inhibitor indicated for ovarian and metastatic breast cancer. Increased serum creatinine levels have been observed in patients taking olaparib, but the underlying mechanism is unknown. This study aimed to investigate if patients receiving ol...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803870/ https://www.ncbi.nlm.nih.gov/pubmed/33319340 http://dx.doi.org/10.1007/s00228-020-03070-0 |
_version_ | 1783636037303533568 |
---|---|
author | Bruin, M. A. C. Korse, C. M. van Wijnen, B. de Jong, V. M. T. Linn, S. C. van Triest, B. Rosing, H. Beijnen, J. H. van den Broek, D. Huitema, A. D. R. |
author_facet | Bruin, M. A. C. Korse, C. M. van Wijnen, B. de Jong, V. M. T. Linn, S. C. van Triest, B. Rosing, H. Beijnen, J. H. van den Broek, D. Huitema, A. D. R. |
author_sort | Bruin, M. A. C. |
collection | PubMed |
description | PURPOSE: Olaparib is a poly (ADP-ribose) polymerase (PARP) inhibitor indicated for ovarian and metastatic breast cancer. Increased serum creatinine levels have been observed in patients taking olaparib, but the underlying mechanism is unknown. This study aimed to investigate if patients receiving olaparib have increased creatinine levels during olaparib treatment and whether this actually relates to a declined glomerular filtration rate (GFR). METHODS: We retrospectively identified patients using olaparib at the Netherlands Cancer Institute – Antoni van Leeuwenhoek (NKI-AVL) from 2012 until 2020. Patients with at least one plasma or serum sample available at baseline/off treatment and during olaparib treatment were included. Cystatin C levels were measured, creatinine levels were available and renal function was determined by calculating the estimated glomerular filtration rate (eGFR) using the Creatinine Equation (CKD-EPI 2009) and the Cystatin C Equation (CKD-EPI 2012). RESULTS: In total, 66 patients were included. Olaparib treatment was associated with a 14% increase in median creatinine from 72 (inter quartile range (IQR): 22) μmol/L before/off treatment to 82 (IQR: 20) μmol/L during treatment (p < 0.001) and a 13% decrease in median creatinine-derived eGFR from 86 (IQR: 26) mL/min/1.73 m(2) before/off treatment to 75 (IQR: 29) mL/min/1.73 m(2) during treatment (p < 0.001). Olaparib treatment had no significant effect on median cystatin C levels (p = 0.520) and the median cystatin C–derived eGFR (p = 0.918). CONCLUSIONS: This study demonstrates that olaparib likely causes inhibition of renal transporters leading to a reversible and dose-dependent increase in creatinine and does not affect GFR, since the median cystatin C–derived eGFR was comparable before/off treatment and during treatment of olaparib. Using the creatinine-derived eGFR can give an underestimation of GFR in patients taking olaparib. Therefore, an alternative renal marker such as cystatin C should be used to accurately calculate eGFR in patients taking olaparib. |
format | Online Article Text |
id | pubmed-7803870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-78038702021-01-21 A real or apparent decrease in glomerular filtration rate in patients using olaparib? Bruin, M. A. C. Korse, C. M. van Wijnen, B. de Jong, V. M. T. Linn, S. C. van Triest, B. Rosing, H. Beijnen, J. H. van den Broek, D. Huitema, A. D. R. Eur J Clin Pharmacol Pharmacodynamics PURPOSE: Olaparib is a poly (ADP-ribose) polymerase (PARP) inhibitor indicated for ovarian and metastatic breast cancer. Increased serum creatinine levels have been observed in patients taking olaparib, but the underlying mechanism is unknown. This study aimed to investigate if patients receiving olaparib have increased creatinine levels during olaparib treatment and whether this actually relates to a declined glomerular filtration rate (GFR). METHODS: We retrospectively identified patients using olaparib at the Netherlands Cancer Institute – Antoni van Leeuwenhoek (NKI-AVL) from 2012 until 2020. Patients with at least one plasma or serum sample available at baseline/off treatment and during olaparib treatment were included. Cystatin C levels were measured, creatinine levels were available and renal function was determined by calculating the estimated glomerular filtration rate (eGFR) using the Creatinine Equation (CKD-EPI 2009) and the Cystatin C Equation (CKD-EPI 2012). RESULTS: In total, 66 patients were included. Olaparib treatment was associated with a 14% increase in median creatinine from 72 (inter quartile range (IQR): 22) μmol/L before/off treatment to 82 (IQR: 20) μmol/L during treatment (p < 0.001) and a 13% decrease in median creatinine-derived eGFR from 86 (IQR: 26) mL/min/1.73 m(2) before/off treatment to 75 (IQR: 29) mL/min/1.73 m(2) during treatment (p < 0.001). Olaparib treatment had no significant effect on median cystatin C levels (p = 0.520) and the median cystatin C–derived eGFR (p = 0.918). CONCLUSIONS: This study demonstrates that olaparib likely causes inhibition of renal transporters leading to a reversible and dose-dependent increase in creatinine and does not affect GFR, since the median cystatin C–derived eGFR was comparable before/off treatment and during treatment of olaparib. Using the creatinine-derived eGFR can give an underestimation of GFR in patients taking olaparib. Therefore, an alternative renal marker such as cystatin C should be used to accurately calculate eGFR in patients taking olaparib. Springer Berlin Heidelberg 2020-12-14 2021 /pmc/articles/PMC7803870/ /pubmed/33319340 http://dx.doi.org/10.1007/s00228-020-03070-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Pharmacodynamics Bruin, M. A. C. Korse, C. M. van Wijnen, B. de Jong, V. M. T. Linn, S. C. van Triest, B. Rosing, H. Beijnen, J. H. van den Broek, D. Huitema, A. D. R. A real or apparent decrease in glomerular filtration rate in patients using olaparib? |
title | A real or apparent decrease in glomerular filtration rate in patients using olaparib? |
title_full | A real or apparent decrease in glomerular filtration rate in patients using olaparib? |
title_fullStr | A real or apparent decrease in glomerular filtration rate in patients using olaparib? |
title_full_unstemmed | A real or apparent decrease in glomerular filtration rate in patients using olaparib? |
title_short | A real or apparent decrease in glomerular filtration rate in patients using olaparib? |
title_sort | real or apparent decrease in glomerular filtration rate in patients using olaparib? |
topic | Pharmacodynamics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803870/ https://www.ncbi.nlm.nih.gov/pubmed/33319340 http://dx.doi.org/10.1007/s00228-020-03070-0 |
work_keys_str_mv | AT bruinmac arealorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT korsecm arealorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT vanwijnenb arealorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT dejongvmt arealorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT linnsc arealorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT vantriestb arealorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT rosingh arealorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT beijnenjh arealorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT vandenbroekd arealorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT huitemaadr arealorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT bruinmac realorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT korsecm realorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT vanwijnenb realorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT dejongvmt realorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT linnsc realorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT vantriestb realorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT rosingh realorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT beijnenjh realorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT vandenbroekd realorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib AT huitemaadr realorapparentdecreaseinglomerularfiltrationrateinpatientsusingolaparib |