Drug Eruptions
Recent clinical, regulatory, research and industry developments relating to this disease.
Dermatologic Reactions to Immune Checkpoint Inhibitors : Skin Toxicities and Immunotherapy.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Research activity
Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.
Major themes3
- Cytokines1
- Immune Checkpoint Inhibitors1
- Patch Tests1
Leading journals4
- American journal of clinical dermatology2
- Clinical cancer research : an official journal of the American Association for Cancer Research1
- Contact dermatitis1
- Journal of clinical oncology : official journal of the American Society of Clinical Oncology1
Leading researchers8
- Sibaud V2
- Aalto-Korte K1
- Agner T1
- Andersen KE1
- Bang A1
- Bauml JM1
- Berdyshev E1
- Bircher A1
Affiliations (unnormalised)6
- Asan Medical Center1
- Bispebjerg Hospital1
- Centre for Occupational and Environmental Medicine1
- Chungbuk National University Hospital1
- City of Hope Comprehensive Cancer Center1
- Columbia University Medical Center1
Related conditions
Diseases frequently studied alongside this one. Number shows shared papers.
Disease profile
A grounded synthesis of the condition — overview, causes, mechanism, risk factors and current standard of care.
Drug eruptions are adverse cutaneous reactions that occur after a drug is taken, given parenterally, or applied locally. They can present with a wide range of morphologic patterns and lesion types.
They are caused by exposure to a drug through ingestion, parenteral administration, or local application. The grounding also identifies immune checkpoint inhibitors and other targeted therapies as drug classes associated with cutaneous adverse reactions.
The mechanism varies by drug and eruption pattern. For immune checkpoint inhibitors, cutaneous toxicities are described as immune-related adverse events mediated by activation of cytotoxic CD4+/CD8+ T cells, and targeted therapies can produce dermatologic toxicity through effects on signaling pathways involved in normal epidermal and dermal homeostasis.
Exposure to drugs known to cause cutaneous adverse reactions increases risk. The grounding specifically notes immune checkpoint inhibitors and targeted therapies as associated with dermatologic toxicities, and patch testing guidance highlights patients with suspected allergic contact dermatitis or other delayed-type hypersensitivity skin and mucosal conditions as special groups.
Management is described at the modality level as diagnostic patch testing for suspected allergic contact dermatitis or other delayed-type hypersensitivity skin and mucosal conditions. For drug-associated cutaneous toxicities, the literature emphasizes recognition and classification of the eruption and the use of supportive dermatologic management rather than a single disease-specific drug class.
AI-generated summary grounded in MeSH and 3 peer-reviewed sources. Informational only — not medical advice. Generated 2026-07-07.
Reference
Authoritative identity, definition & identifiers.
Adverse cutaneous reactions caused by ingestion, parenteral use, or local application of a drug. These may assume various morphologic patterns and produce various types of lesions.
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
- Related entities are derived from literature co-mention (studied together) — associative, not causal.