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Updated: Jan 13, 2026

Preparation of Mouse Pituitary Immunogen for the Induction of Experimental Autoimmune Hypophysitis
Published on: December 17, 2010
Immune Checkpoint Inhibitor-Related Hypophysitis and Pituitary Dysfunction: A Systematic Review of Diagnosis and
Pooja SirDeshpande1, Soorya Bavikeri Shivakumara Hegde2, Hassan Akhtar3
1Endocrinology, Diabetes and Metabolism, London Northwest University Healthcare NHS Trust, London, GBR.
Immune checkpoint inhibitors (ICPi) can cause hypophysitis, leading to pituitary dysfunction. Early diagnosis and management are crucial for reducing long-term endocrine issues in cancer patients.
Area of Science:
- Endocrinology
- Oncology
- Immunology
Background:
- Immune checkpoint inhibitors (ICPis) are vital cancer therapies.
- ICPi-associated hypophysitis is an emerging immune-related adverse event (irAE).
- Understanding its clinical spectrum is crucial for patient management.
Purpose of the Study:
- To systematically review the clinical presentation, diagnosis, and management of ICPi-associated hypophysitis and pituitary dysfunction.
- To evaluate pituitary irAEs linked to CTLA-4, PD-1/PD-L1 inhibitors, and combination therapies.
Main Methods:
- Systematic review of 84 studies (2005-2025) including 7,259 patients.
- Analysis of data on ICPi type, demographics, cancer, treatment, imaging, pituitary dysfunction, symptoms, and management.
- Statistical analysis of pooled data.
Main Results:
- Common symptoms include fatigue, headache, hyponatraemia, and neuropsychiatric changes.
- CTLA-4 inhibitors, especially ipilimumab, more frequently caused hypopituitarism.
- PD-1/PD-L1 inhibitors were linked to isolated ACTH deficiency; MRI may not detect early changes.
- Hypopituitarism is a frequent and persistent consequence.
Conclusions:
- ICPi-associated hypophysitis frequently leads to hypopituitarism.
- Early recognition via clinical, biochemical, and radiological assessment is essential.
- Timely management reduces long-term endocrine morbidity and optimizes outcomes.
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