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Cutaneous toxicity from epidermal growth factor receptor inhibitors: would a subcutaneous desensitization be helpful?
Andrea D'Alessio1, Sara Cecchini1, Daniela Di Mauro1
1Medical Oncology and Internal Medicine, Policlinico San Marco - Istituti Ospedalieri Bergamaschi, Osio Sotto (Bergamo) - Italy.
Purpose:
Cetuximab and panitumumab are monoclonal antibody inhibitors that bind the epidermal growth factor receptor (EGFR) currently used in the treatment of metastatic colorectal cancer. The main adverse event related to EGFR inhibitors (EGFR-Is) is cutaneous toxicity, which can cause dosage reduction and interruption of treatment. State-of-the-art management of skin toxicity associated with EGFR-Is therapy involves the topical administration of corticosteroids and oral antibiotics, but is not completely effective in the management of toxicity. Subcutaneous desensitization with increasing concentrations of monoclonal antibodies can induce a tolerance to drug administration and reduce cutaneous adverse effects. To our knowledge, this is the first case in which a reduction or a disappearance of skin toxicity caused by EGFR-Is through subcutaneous desensitization has been achieved.
Case Report:
We present cases of 2 Caucasian patients with adenocarcinoma of the colon treated with EGFR-Is who developed severe cutaneous toxicity. A 73-year-old man presented grade 4 skin toxicity of the face and grade 3 skin toxicity of the trunk during treatment with cetuximab. A 68-year-old woman developed G2 rash on the face after the first administration of cetuximab. These patients underwent subcutaneous desensitization with increasing concentrations of EGFR-Is. After this procedure, patients restarted therapy at the optimal dosage with reduction or disappearance of skin toxicity.
Conclusions:
These cases suggest that by giving rising doses of antibody it is possible to obtain desensitization able to prevent severe cutaneous adverse events in patients treated with EGFR-Is.
Insights
Subcutaneous desensitization with epidermal growth factor receptor inhibitors (EGFR-Is) can reduce severe skin toxicity in metastatic colorectal cancer patients. This novel approach may prevent treatment interruptions and improve patient outcomes.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Cetuximab and panitumumab are monoclonal antibody epidermal growth factor receptor inhibitors (EGFR-Is) used for metastatic colorectal cancer.
- Cutaneous toxicity is a common adverse event of EGFR-Is, often necessitating treatment dose reduction or interruption.
- Current management strategies for EGFR-Is-induced skin toxicity, including topical corticosteroids and oral antibiotics, have limited efficacy.
Observation:
- Two patients with colorectal adenocarcinoma treated with EGFR-Is experienced severe cutaneous toxicity.
- One patient developed grade 4 facial and grade 3 truncal skin toxicity during cetuximab treatment.
- Another patient developed grade 2 facial rash after initial cetuximab administration.
Findings:
- Subcutaneous desensitization with escalating concentrations of EGFR-Is was administered to both patients.
- Following desensitization, patients resumed EGFR-Is therapy at optimal dosages.
- Both patients experienced a reduction or complete resolution of their skin toxicity after the procedure.
Implications:
- Subcutaneous desensitization represents a potential new strategy for managing severe cutaneous adverse events associated with EGFR-Is.
- This approach may enable continued treatment with EGFR-Is, potentially improving therapeutic outcomes in metastatic colorectal cancer.
- Further research is warranted to validate the efficacy and safety of subcutaneous desensitization for EGFR-Is-related skin toxicity.
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