Acute kidney injury in acute promyelocytic leukemia: a possible adverse effect of high dose arsenic trioxide in obese patients.
Wei-Ying JenKoiji SasakiCaitlin R RauschCourtney D D DiNardoTapan Mahendra KadiaMusa YlimazGautam BorthakurYesid AlvaradoDavid McCueDeborah MccueHagop M KantarjianFarhad RavandiPublished in: Leukemia & lymphoma (2023)
Arsenic trioxide (ATO)-based regimens are standard in acute promyelocytic leukemia (APL). ATO-related nephrotoxicity has not been reported. We reviewed APL patients treated with ATO to identify cases of acute kidney injury (AKI). Clinically significant cases were characterized. Multivariate analysis was performed to identify predictors of idiopathic, clinically significant AKI. One hundred and eight patients were included. ATO dose was 0.15 mg/kg/day using actual body weight with no dose cap. Thirty-one (28.7%) AKI cases were identified, 10 (32.3%) clinically significant. Six were idiopathic; five required dialysis. The proportion with significant, idiopathic AKI was 15.8% in patients receiving >15mg ATO versus 0% in those receiving ≤15mg ( p = 0.001). On multivariate analysis, only ATO dose was a significant predictor of clinically significant AKI (odds ratio of 1.91, 95%CI, 1.19-3.07, p = 0.007). High-dose ATO may be associated with significant nephrotoxicity. We recommend that ATO dose be capped at 15 mg to minimize toxicity for this curable disease.
Keyphrases
- acute kidney injury
- high dose
- cardiac surgery
- end stage renal disease
- body weight
- obese patients
- chronic kidney disease
- drug induced
- liver failure
- bariatric surgery
- low dose
- acute myeloid leukemia
- emergency department
- newly diagnosed
- bone marrow
- ejection fraction
- peritoneal dialysis
- stem cell transplantation
- hepatitis b virus
- roux en y gastric bypass
- acute respiratory distress syndrome
- electronic health record