Key result
Each 1-point increase in a risk prediction score increased the odds of cisplatin-induced nephrotoxicity by 26.5% (OR 1.27; 95% CI 1.02-1.57; p=0.034) in outpatients.
Why the study?
It was unclear whether a risk prediction score could effectively predict the development of nephrotoxicity throughout all cycles of cisplatin therapy among outpatients.
Does a risk prediction score predict the development of cisplatin-induced nephrotoxicity in adult outpatients?
Observational (n=186)
Yes
Does a risk prediction score predict the development of cisplatin-induced nephrotoxicity in adult outpatients?
A risk prediction score incorporating age, cisplatin dose, hypertension, and serum albumin successfully predicts cisplatin-induced nephrotoxicity in outpatients.
The score may aid outpatient cisplatin risk stratification; leaves open whether prospective validation or implementation improves outcomes.
BACKGROUND: The use of cisplatin is limited by the development of nephrotoxicity, with an incidence approaching 30%. It is unclear if a risk prediction score can effectively predict the development of nephrotoxicity throughout all cycles of cisplatin therapy among outpatients. METHODS: Retrospective, observational study evaluating adult patients receiving cisplatin in outpatient infusion centers from January 2009 to November 2019 (n = 186). A risk prediction score consisting of patient age, cisplatin dose, hypertension, and serum albumin was calculated to predict the risk of cisplatin-induced nephrotoxicity. RESULTS: The incidence of nephrotoxicity was 23.7% overall, with 8.1% of patients developing cisplatin-induced nephrotoxicity after the first dose. Patients who developed nephrotoxicity had a higher mean risk prediction score compared to patients who did not have nephrotoxicity (4.0 ± 2.0 versus 2.9 ± 2.1, p = 0.004, respectively). Multivariate logistic regression demonstrated each 1-point increase in the risk prediction score increased the odds of nephrotoxicity by 26.5% (OR: 1.27; 95% CI: 1.02-1.57, p = 0.034). Presence of diabetes mellitus increased the odds of cisplatin-induced nephrotoxicity (OR 3.66; 95% CI: 1.43-9.33, p = 0.007), whereas receipt of greater than or equal to 1 liter of 0.9% sodium chloride was protective, decreasing the odds of developing nephrotoxicity by 25%. CONCLUSION: By identifying patients at the highest risk of cisplatin-induced nephrotoxicity, providers can individualize risk reduction strategies. The use of a risk prediction model successfully predicted the risk of nephrotoxicity throughout all cycles of cisplatin in an outpatient setting.
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Burns et al. (2021) conducted an observational in Cisplatin-induced nephrotoxicity (n=186). Risk prediction score was evaluated on Cisplatin-induced nephrotoxicity (OR 1.27, 95% CI 1.02-1.57, p=0.034). Each 1-point increase in a risk prediction score increased the odds of cisplatin-induced nephrotoxicity by 26.5% (OR 1.27; 95% CI 1.02-1.57; p=0.034) in outpatients.
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