Why does it matter? ICPi-AKI can lead to:
*Discontinuation of ICPi therapy
*Irreversible loss of kidney function
*Prolonged courses of immunosuppression (2/11)
We conducted a multicenter study of 429 patients with ICPi-AKI from 30 sites across 10 countries, along with 429 control patients who received ICPis contemporaneously but did not develop ICPi-AKI. This is the largest study to date on ICPi-AKI (3/11)
TIMING: ICPi-AKI developed at a median of 16 weeks (IQR 8-32) after ICPi initiation (4/11)
DIAGNOSIS: Urinary findings like leukocyte esterase, proteinuria, and hematuria were highly variable
Extrarenal immune-related adverse events (irAEs) occurred in 57% of patients
Among the 151 biopsied patients, 83% had ATIN (5/11)
RISK FACTORS: Lower baseline eGFR, PPI use, and prior or concomitant extrarenal irAEs were independent risk factors for ICPi-AKI (6/11)
TREATMENT/OUTCOMES: Early treatment with steroids (within 3 days) was associated with a greater likelihood of renal recovery (7/11)
RECHALLENGE: 121 patients were rechallenged, of whom only 16.5% had recurrent ICPi-AKI (8/11)
Our study is the largest to date, and generated important insights on ICPi-AKI, including the low risk of recurrent ICPi-AKI with ICPi rechallenge (9/11)