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A real or apparent decrease in glomerular filtration rate in patients using olaparib?
- Source :
-
European journal of clinical pharmacology [Eur J Clin Pharmacol] 2021 Feb; Vol. 77 (2), pp. 179-188. Date of Electronic Publication: 2020 Dec 14. - Publication Year :
- 2021
-
Abstract
- 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).<br />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).<br />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 <superscript>2</superscript> before/off treatment to 75 (IQR: 29) mL/min/1.73 m <superscript>2</superscript> 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).<br />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.
- Subjects :
- Adult
Aged
Aged, 80 and over
Biomarkers blood
Biomarkers metabolism
Creatinine blood
Creatinine metabolism
Cystatin C blood
Cystatin C metabolism
Dose-Response Relationship, Drug
Drug Administration Schedule
Drug Monitoring methods
Female
Glomerular Filtration Rate physiology
Humans
Kidney Glomerulus drug effects
Kidney Glomerulus physiology
Kidney Tubules, Proximal drug effects
Kidney Tubules, Proximal physiology
Male
Middle Aged
Neoplasms blood
Netherlands
Phthalazines administration & dosage
Piperazines administration & dosage
Poly(ADP-ribose) Polymerase Inhibitors administration & dosage
Renal Elimination drug effects
Renal Elimination physiology
Retrospective Studies
Glomerular Filtration Rate drug effects
Neoplasms drug therapy
Phthalazines adverse effects
Piperazines adverse effects
Poly(ADP-ribose) Polymerase Inhibitors adverse effects
Subjects
Details
- Language :
- English
- ISSN :
- 1432-1041
- Volume :
- 77
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- European journal of clinical pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 33319340
- Full Text :
- https://doi.org/10.1007/s00228-020-03070-0