Zytiga (Abiraterone)
is a hormonal chemotherapy agent used to treat prostate cancer. It selectively and irreversibly inhibits
CYP17 (17 alpha-hydroxylase/C17,20-lyase), an enzyme required for androgen
biosynthesis which is expressed in testicular, adrenal, and prostatic tumor
tissues. Inhibits the formation of the testosterone precursors dehydroepiandrosterone
(DHEA) and androstenedione.
Interestingly. it has
a high rate of hypernatremia as a known renal complication. In several studies,
hypernatremia (33%), hypokalemia (17% to 30%) were reported as known
complications. Why? It is postulated that it can increase mineralocorticoids due
to CYP17 inhibition may result in hypertension, hypokalemia, and fluid
retention (including grade 3 and 4 events) and perhaps some component of
hypernatremia as well- almost like a Cushing's state. Per package insert, concomitant administration
with corticosteroids reduces the incidence and severity of these adverse events.
In the LATITUDE trial, which
used prednisone 5 mg daily in combination with 1000 mg abiraterone acetate
daily, grades 3-4 hypokalemia were detected in 10% of patients on the zytiga arm and 1% of patients on the placebo arm, grades 3-4 hypertension were
observed in 20% of patients on the zytiga arm and 10% of patients on the
placebo arm. Grades 3-4 fluid retention occurred in 1% of patients each arm.
It is
recommended that patients get monitored for hypertension, hypokalemia, and
fluid retention at least once a month. Treatment of hypertension is recommended, choice
of drug is not defined.
This is an
interesting toxicity that as nephrologist seeing prostate cancer with CKD and
perhaps new onset hypertension, hypokalemia or hypernatremia should consider in the
differential diagnosis.
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