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Published on: September 13, 2022
Bullous Pemphigoid Associated With a New Combination Checkpoint Inhibitor Immunotherapy
Abstract:
Novel immunotherapies including antibodies to programmed death ligand 1 (PD-1) and cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) have become common therapies for neoplasms including metastatic melanoma and non-small cell lung cancer (NSCLC). Dermatologic toxicity is the most common adverse event associated with these immunotherapies. We report a case of bullous pemphogoid (BP) in a patient receiving combination durvalumab and tremelimumab, two newer immunotherapy checkpoint inhibitors under investigation in phase III trials. J Drugs Dermatol. 2019;18(1):103-104.
Insights
Newer immunotherapies targeting programmed death ligand 1 (PD-1) and cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) can cause skin issues. This study details a rare case of bullous pemphigoid (BP) linked to combination immunotherapy.
Area of Science:
- Oncology
- Immunology
- Dermatology
Background:
- Immune checkpoint inhibitors (ICIs) targeting PD-1 and CTLA-4 are standard treatments for advanced cancers like melanoma and NSCLC.
- Dermatologic adverse events are the most frequent side effects of these immunotherapies.
- Bullous pemphigoid (BP) is an autoimmune blistering disease that can be triggered by various medications.
Observation:
- A patient undergoing combination therapy with durvalumab (anti-PD-1) and tremelimumab (anti-CTLA-4) developed bullous pemphigoid.
- Durvalumab and tremelimumab are novel immunotherapy checkpoint inhibitors currently under investigation in phase III clinical trials.
Findings:
- The development of bullous pemphigoid represents a rare but significant dermatologic toxicity associated with the combination of durvalumab and tremelimumab.
- This case underscores the potential for immune-related adverse events beyond common skin toxicities with novel ICI combinations.
Implications:
- Clinicians should maintain a high index of suspicion for autoimmune blistering diseases like BP in patients treated with novel ICI combinations.
- Early recognition and management of BP are crucial to mitigate potential morbidity and allow for continued oncologic treatment if appropriate.
- Further research is warranted to elucidate the mechanisms underlying ICI-induced BP and to develop predictive or preventative strategies.
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