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. 2019 Jul 7;36(9):1075–1081. doi: 10.1111/dme.14050

Table 1.

Clinical, metabolic and immunological characteristics of anti‐programmed cell death protein‐1 or anti‐programmed cell death protein‐1 ligand inhibitor‐induced Type 1 diabetes

  All cases (n=71) Nivolumab (n=38) Pembrolizumab (n=26) anti‐PD‐L1a (n=7)
Age, years
Mean (sd) 61.7 (12.2) 61.4 (12.8) 61.1 (11.4) 65.7 (10.8)
Median 62.0 62.5 61.0 66.5
Range 23–84 28–83 23–82 50–84
Gender
Female, % 45.0 50.0 38.5 42.8
Cancer type, % ( n)
Melanoma 53.5 (38) 50.0 (19) 73.0 (19) 0 (0)
Lung 26.8 (19) 34.2 (13) 15.4 (4) 28.5 (2)
Renal cell 5.7 (4) 10.6 (4) 0 (0) 0 (0)
Head and neck 7.0 (5) 2.6 (1) 7.7 (2) 28.5 (2)
Urothelial carcinoma 4.2 (3) 0 (0) 0 (0) 43.0 (3)
Other 2.8 (2) 2.6 (1) 3.9 (1) 0 (0)
Duration to diabetes, days
Mean (sd) 83.5 (88.5) 98.0 (102.1) 65.9 (72.1) 75.0 (39.7)
Median 49 73.5 42 84
Range 5‐448 5‐448 14‐365 21‐126
Diabetic ketoacidosis, % ( n)
Present 76.0 (54) 71.0 (27) 80.7 (21) 85.7 (6)
Severe 38.9 (21) 33.3 (9) 52.4 (11) 16.6 (1)
Moderate 20.4 (11) 22.2 (6) 14.3 (3) 33.3 (2)
Mild 11.1 (6) 3.7 (1) 14.3 (3) 33.3 (2)
Not able to assess 29.6 (16) 40.8 (11) 19.0 (4) 16.6 (1)
Blood glucose, mmol/l
Mean (sd) 33.4 (11.5) 33.8 (12.1) 34.1 (9.5) 29.4 (13.8)
Median 32.2 31.7 34.2 22.8
Range 13.7–67.3 13.7–67.3 15.0–50.5 18.1–56.4
HbA 1c , mmol/mol
Mean (sd) 62 (0.3) 60 (0.3) 64 (0.3) 66 (0.4)
Median 61 56 62 66
Range 40–93 40–88 40–93 46–84
Type 1 diabetes‐associated antibodies, % ( n)
Present 50.7 (36) 44.7 (17) 57.7 (15) 57.1 (4)
Absent 49.3 (35) 55.3 (21) 42.3 (11) 42.9 (3)
Type 1 diabetes risk HLA genes b , % ( n)
Present 38.0 (27) 39.5 (15) 38.5 (10) 28.5 (2)
Absent 7.0 (5) 13.1 (5) 0 (0) 0 (0)
Not Reported 55.0 (39) 47.4 (18) 61.5 (16) 71.5 (5)
Ipilimumab (anti‐CTLA‐4) use c , % ( n)
Present 31.0 (22) 31.5 (12) 38.5 (10) 0 (0)
Absent 69.0 (49) 68.5 (26) 61.5 (16) 100.0 (7)

HLA, human leukocyte antigen; PD‐1, programmed cell death protein; PD‐L1, programmed cell death protein‐1 ligand.

a

Atezolizumab, avelumab and durvalumab.

b

HLA‐DQ‐DR risk genes include DR3, DR4, DQ2, DQ8.

c

Prior or concurrent use of ipilimumab with anti‐PD‐1/PD‐L1 treatment.