Table 2

Characteristics of initial episode of ICPi-AKI

VariableShorter duration
(n=56)
Longer duration
(n=109)
P value
Time to ICPi-AKI, days, median (IQR)97 (63–188)112 (56–224)0.81
ICPi-AKI stage,* n (%)0.37
 Stage 18 (14.3)11 (10.1)
 Stage 220 (35.7)37 (33.9)
 Stage 328 (50.0)61 (56.0)
KRT, n (%)4 (7.1)5 (4.6)0.49
Hospitalized for AKI, n (%)33 (58.9)63 (57.8)0.99
Nephrologist involved, n (%)44 (78.6)94 (86.2)0.27
Urine studies
 Blood (≥2+) on UA, n (%)10 (17.9)11 (10.1)0.24
 Leukocyte esterase (≥2+) on UA, n (%)11 (19.6)18 (16.5)0.77
 Pyuria (≥5 WBCs per hpf on UA), n (%)25 (44.6)57 (51.4)0.44
 UPCR ≥0.3 g/g, n (%)16 (28.6)34 (31.2)0.87
Biopsied, n (%)13 (23.2)38 (34.9)0.16
 ATIN on kidney biopsy, n (%)13 (100)38 (100)0.99
Time to CS Initiation, days, median (IQR)3 (0–7)2 (0–5)0.43
Initial daily oral CS dose (prednisone equivalent units, mg), median (IQR)60 (58–60)60 (60–88)0.78
Received intravenous pulse CS, n (%)17 (30.4)26 (23.9)0.58
Non-CS immunosuppression,† n (%)1 (1.8)2 (1.8)0.99
Rechallenged, n (%)13 (23.2)15 (13.7)0.13
 Recurrent ICPi-AKI after rechallenge, n (%)1 (1.8)2 (1.8)0.99
  • A total of 28 patients (50%) were missing data on UPCR, and 8 (14.3%) were missing data on leukocyte esterase, blood, and pyuria on UA in the shorter duration group. A total of 52 patients (47.8%) were missing data on UPCR, and 28 (25.7%) were missing data on leukocyte esterase, blood, and pyuria on UA in the longer duration group.

  • *AKI stages are defined by Kidney Disease: Improving Global Outcomes criteria.

  • †One patient in the shorter duration group received tocilizumab. In the longer duration group, one patient received mycophenolate mofetil, and one received infliximab.

  • ATIN, acute tubulointerstitial nephritis; CS, corticosteroid; hpf, high power field; ICPi-AKI, immune checkpoint inhibitor-associated acute kidney injury; KRT, kidney replacement therapy; SCr, serum creatinine; UA, urinalysis; UPCR, urine protein:creatinine ratio; WBCs, white blood cells.