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Iatrogenic Pituitary Shutdown: A Rare Adverse Event of Programmed Cell Death-Ligand 1 Inhibitor
Mohammed Al-Hiari1, Anthony Workman1, Ebubechukwu Ezeh1
1School of Medicine Internal Residency Program, Marshall University, Huntington, WV 25701, USA.
Immune checkpoint inhibitors (ICIs) can cause rare central adrenal insufficiency. Early diagnosis and pituitary hormone monitoring are crucial for patients on ICIs, especially those with hypothyroidism.
Area of Science:
- Endocrinology
- Oncology
- Immunology
Background:
- Immune checkpoint inhibitors (ICIs) represent a significant advancement in cancer therapy.
- Immune-related adverse events (irAEs) are known complications of ICI treatment.
- Adrenal insufficiency is a rare irAE, more commonly associated with CTLA-4 inhibitors than PD-L1 inhibitors.
Observation:
- A 74-year-old male patient with hepatocellular carcinoma developed symptoms of central adrenal insufficiency after 33 weeks of atezolizumab (a PD-L1 inhibitor).
- Brain imaging revealed no apparent cause for the adrenal insufficiency.
- The patient had pre-existing incidentally discovered central hypothyroidism (low TSH and thyroxine) for which he had initiated replacement therapy.
Findings:
- This case highlights a rare instance of central adrenal insufficiency potentially linked to PD-L1 inhibitor therapy.
- The co-occurrence with central hypothyroidism warrants careful evaluation of pituitary function in patients receiving ICIs.
Implications:
- Clinicians should maintain a high index of suspicion for adrenal insufficiency in patients treated with ICIs, even those on PD-L1 inhibitors.
- Regular monitoring of pituitary hormones is recommended for patients on ICIs.
- It is essential to investigate pituitary hormonal deficiencies, including central hypothyroidism, before initiating hormone replacement therapy.
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