# Blood glucose variability in early-onset adrenocorticotropic hormone deficiency induced by immune checkpoint inhibitor therapy with continuous blood glucose monitoring: a case report

**Authors:** Yuta Nanao, Gentaro Egusa, Ryuta Baba, Takaya Kodama, Tsuguka Matsuda, Gaku Nagano, Haruya Ohno

PMC · DOI: 10.1007/s13340-025-00870-6 · Diabetology international · 2026-01-12

## TL;DR

This case report shows how blood glucose monitoring helped detect early-onset hormone deficiency in a diabetic patient undergoing cancer treatment.

## Contribution

Demonstrates the use of continuous glucose monitoring to identify endocrine issues caused by immune checkpoint inhibitors in diabetic patients.

## Key findings

- The patient experienced unstable blood glucose levels after ICI treatment, with nocturnal hypoglycemia detected via CGM.
- Endocrine testing revealed hypopituitarism, highlighting the need for monitoring hormone function in such cases.
- CGM proved valuable in detecting subtle glucose fluctuations and guiding treatment adjustments.

## Abstract

Early diagnosis and treatment of immune-related adverse events (irAEs) associated with immune checkpoint inhibitors (ICIs) are essential because they directly impact patient quality of life. This report describes the case of an 85-year-old woman with type 2 diabetes on insulin therapy, whose glycemic fluctuations became highly unstable following irAE development. During treatment for refractory hepatocellular carcinoma with tremelimumab and durvalumab, she developed hyperglycemia and was hospitalized. Endogenous insulin secretion remained intact, and hyperglycemia improved after admission. Continuous glucose monitoring (CGM) revealed nocturnal and early-morning hypoglycemia from the fourth day of admission. Insulin requirements were tapered off; however, persistent anorexia and dyspnea led to the diagnosis of hypopituitarism through endocrine testing. For patients with diabetes who experience abnormal blood glucose fluctuations after ICI therapy, clinicians should monitor changes in endogenous insulin secretion and consider the possibility of hypoadrenocorticism. CGM may be valuable for detecting these endocrine abnormalities.

## Linked entities

- **Chemicals:** insulin (PubChem CID 70678557)
- **Diseases:** type 2 diabetes (MONDO:0005148), hepatocellular carcinoma (MONDO:0007256), hypopituitarism (MONDO:0005152)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}, GAD1 (glutamate decarboxylase 1) [NCBI Gene 2571] {aka CPSQ1, DEE89, GAD, GAD-67, SCP}, GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}, TRH (thyrotropin releasing hormone) [NCBI Gene 7200] {aka Pro-TRH, TRF}, PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, GNRH1 (gonadotropin releasing hormone 1) [NCBI Gene 2796] {aka GNRH, GRH, LHRH, LNRH}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, POR (cytochrome p450 oxidoreductase) [NCBI Gene 5447] {aka CPR, CYPOR, P450R}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, CRH (corticotropin releasing hormone) [NCBI Gene 1392] {aka CRF, CRH1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}, ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, S100A6 (S100 calcium binding protein A6) [NCBI Gene 6277] {aka 2A9, 5B10, CABP, CACY, PRA, S10A6}, GGTLC1 (gamma-glutamyltransferase light chain 1) [NCBI Gene 92086] {aka GGTL6, GGTLA3, GGTLA4, dJ831C21.1, dJ831C21.2}, AVP (arginine vasopressin) [NCBI Gene 551] {aka ADH, ARVP, AVP-NPII, AVRP, VP}
- **Diseases:** irAEs (MESH:D002318), Hypopituitarism (MESH:D007018), primary adrenal insufficiency (MESH:D000224), hepatic and renal dysfunction (MESH:D008107), weight loss (MESH:D015431), HD (MESH:D003428), diabetes (MESH:D003920), chronic fatigue (MESH:D015673), Type 1 diabetes (MESH:D003922), impaired insulin secretion (MESH:D007333), diabetic ketoacidosis (MESH:D016883), weakness (MESH:D018908), headache (MESH:D006261), mental disturbances (MESH:D008607), impaired consciousness (MESH:D003244), anorexia (MESH:D000855), hyperglycemic (MESH:D006944), impaired renal function (MESH:D007674), adrenal insufficiency (MESH:D000309), Pneumonia (MESH:D011014), polyuria (MESH:D011141), inflammation (MESH:D007249), ACTH deficiency (MESH:C535668), chronic kidney disease (MESH:D051436), fever (MESH:D005334), thyrotoxicosis (MESH:C566386), gastrointestinal symptoms (MESH:D012817), Hyperglycemia (MESH:D006943), vomiting (MESH:D014839), hypoglycemic symptoms (MESH:C000721848), dyspnea (MESH:D004417), appetite loss (MESH:D001068), Endocrine disorders (MESH:D004700), visual field disturbances (MESH:D014786), adrenocortical hypofunction (MESH:C562711), hyperinsulinemia (MESH:D006946), Hypoglycemia (MESH:D007003), hypotension (MESH:D007022), polydipsia (MESH:D059606), hypoadrenocorticism (MESH:D000075262), type 2 diabetes (MESH:D003924), Fatigue (MESH:D005221), arthralgia (MESH:D018771), cirrhosis (MESH:D005355), cancer (MESH:D009369), hepatocellular carcinoma (MESH:D006528)
- **Chemicals:** linagliptin (MESH:D000069476), Asp (MESH:D001224), potassium (MESH:D011188), repaglinide (MESH:C072379), Aldosterone (MESH:D000450), Blood glucose (MESH:D001786), Cortisol (MESH:D006854), IDeg/Asp (MESH:C578220), glucose (MESH:D005947), SU (MESH:D013453), tremelimumab (MESH:C520704), triiodothyronine (MESH:D014284), durvalumab (MESH:C000613593), E2 (MESH:D004958), sodium (MESH:D012964), thyroxine (MESH:D013974), mitiglinide (MESH:C087255), FT3 (-)
- **Species:** Hepatitis B virus (no rank) [taxon 10407], Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12796047/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12796047/full.md

---
Source: https://tomesphere.com/paper/PMC12796047