CDK4/6 inhibitors have led to an improvement of both progression free survival (PFS) and overall survival (OS) in patients with advanced estrogen positive (ER+)/HER2- breast cancer when applied in the first or second line of treatment. Despite the advantages of CDK4/6 inhibitors, these medications can lead to adverse effects. One of the adverse events observed across all types of CDK4/6 inhibitors is an elevation in creatinine levels. An elevation in plasma creatinine during treatment with abemaciclib is not always indicative of a reduction in renal function; it can also be attributed to the inhibition of active tubular secretion of creatinine. This phenomenon is known as pseudo acute kidney injury (pseudo-AKI). The incidence of pseudo-AKI in patients using CDK4/6 inhibitors is currently unknown. A method to distinguish pseudo-AKI from AKI is measuring the level of an alternative filtration marker in blood, for example cystatin C. Cystatin C is also filtered at the glomerulus but not secreted intro the renal tubulus or reabsorbed into the bloodstream. Also, there is no affection by muscle mass or diet. In this study the investigators will explore the incidence of both AKI and pseudo-AKI in patients who are treated with CDK4/6 inhibitor treatment by assessing both creatinine and cystatin C in plasma.
Study Type
OBSERVATIONAL
Enrollment
40
no intervention
Erasmus Medical Center
Rotterdam, Netherlands
Pseudo-AKI in patients on CDK4/6 inhibitors
Percentage of patients with pseudo-AKI (%), i.e. patients with creatinin plasma levels (mmol/L) indicating AKI, but normal cystatin C levels (mg/mL)
Time frame: jan-april 2024
Pseudo-AKI in patients on CDK4/6 inhibitors per drug
The percentage of patients (%) per CDK4/6 inhibitor with creatinin plasma levels indicating AKI
Time frame: jan-april 2024
AKI in patients
The percentage of patients (%) on CDK4/6 inhibitors with cystatin C plasma levels indicating AKI
Time frame: jan-april 2024
Influencing factors cystatin C levels
The number of patients with influencing factors on cystatin C levels
Time frame: jan-april 2024
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