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. 2023 Jul 24;14:1213225. doi: 10.3389/fendo.2023.1213225

Table 2.

Characteristics of patients with ICI-DM.

Characteristic Value
Interval to onset after ICIs therapy initiation
 Number of cycles of therapy, n 10 (5–12)
 Duration to onset, weeks 44.1 (18.4–52.3)
Glucose at diagnosis, mmol/L 28.6 (18.5–33.3)
HbA1c at diagnosis, % 8.5 (7.5–10.0)
CTCAE level at diagnosis(n)
II 3
III 8
IV 12
DKA (n, yes/no) 15/8
C-peptide at diagnosis, pmol/L 8.62 (3.33–46.05)
Fulminant type 1 diabetes mellitus (n, yes/no) 14/9
β-cell antibodies, n positive/n tested (%)
 GADA* 4/1/20
 ICA 0/20
 IA-2A 0/20
 IAA 0/20
Increased amylase (n, yes/no/untested) 2/9/12
History of DM (n, yes/no) 2/21
Best response of ICIs treatment(n, CR/PR/SD/PD) 1/5/14/3
Combined other endocrine glands irAE(n)
 Thyroid 8
 Hypophysitis 3
 Thyroid + Adrenal gland 1
 Thyroid + Hypophysitis 1
Combined non-endocrine SAE (n)
 Myocarditis 1
 AKI 1
 AKI, AMI 1
 Cerebral demyelinating lesions 1
 Dermatological AE 1
Treatment interrupt/withdrawal/continue (n) 3/12/8

* Four cases were positive for GADAs, and one case had uncertain GADA positivity.

IAA, insulin antibody; IA-2A, insulinoma-associated protein 2 antibody; GADA, glutamic acid decarboxylase antibody; ICA, islet cell autoantibody; CR, complete response; PR, partial response; SD, stable disease; PD, progressive disease; DKA, diabetic ketoacidosis; HbA1c, hemoglobin A1c; CTCAE, Common Terminology Criteria for Adverse Events; irAE, immune-related adverse event; SAE, serious adverse event; AKI, acute kidney injury; AMI, acute myocardial infarction.