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- Presentation
Toxic Erythema of Chemotherapy: Clinical Presentations, Subtypes, and Management
Description
Toxic erythema of chemotherapy (TEC) is an umbrella term for non-allergic, direct cytotoxic skin reactions caused by chemotherapy and related cancer therapies, affecting a large proportion of patients and accounting for a substantial share of dermatologic adverse events. The talk emphasizes that TEC is driven by drug accumulation in eccrine glands and sweat, leading to keratinocyte damage, and typically appears in high-sweat or friction areas such as the hands, feet, flexures, flanks, and medial thighs. Common culprit drugs include cytarabine, anthracyclines, 5-FU/capecitabine, and taxanes, with continuous infusions and liposomal formulations often increasing risk. Subtypes discussed include hand-foot syndrome, which progresses from dysesthesia to edema, erythema, and desquamation and may later cause nail shedding; palmar-plantar erythema/pateosin-like variants; neutrophilic eccrine hidradenitis, often painful and associated with fever/neutropenia; flexural/intertriginous eruptions often mistaken for fungal rashes; and severe TEN-like presentations that can mimic SJS-TEN, especially with mucositis. The talk also notes that some skin toxicities may correlate with better treatment response, and explains how antibody-drug conjugates such as enfortumab vedotin can cause TEC-like reactions because their target, Nectin-4, is present in normal skin as well as tumor cells.
View moreConclusions
- Toxic erythema of chemotherapy is a broad, non-allergic, direct cytotoxic skin toxicity rather than a hypersensitivity reaction.
- Chemotherapy-related skin adverse events are common, and chemotherapy remains a major contributor to severe cutaneous reactions despite greater attention to immunotherapy.
- TEC most often affects areas with high eccrine density or friction and commonly involves the hands, feet, flexures, flanks, medial thighs, groin, and axillae.
- Hand-foot syndrome is the best-known TEC subtype and typically progresses from pain or dysesthesia to edema, erythema, and desquamation.
- Drug exposure pattern matters, with continuous infusions and longer drug persistence generally increasing the risk of TEC.
- Certain chemotherapy classes, especially cytarabine, anthracyclines, 5-FU/capecitabine, taxanes, and methotrexate, are repeatedly implicated in TEC.
- Some TEC variants can mimic other diagnoses, including fungal intertrigo and Stevens-Johnson syndrome/toxic epidermal necrolysis, so distribution and clinical context are critical for recognition.
- More severe TEC presentations may include mucositis and widespread exfoliative or bullous changes, but biopsy and history can help distinguish them from true SJS/TEN.
- Biologic and antibody-drug conjugate therapies can also produce TEC-like eruptions when the target or payload affects normal skin structures.
- Recognizing TEC matters clinically because appropriate diagnosis can guide supportive care, chemotherapy modification, and avoidance of unnecessary discontinuation when reactions are manageable.
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