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Cutaneous Adverse Events in Children Receiving Mitogen-Activated Protein Kinase Pathway Inhibitors
Yuong Chin Tan1, Santosh Valvi2, Nicholas G Gottardo2
1Department of Paediatric Dermatology, Perth Children's Hospital, Perth, Western Australia, Australia.
Background/Objective:
Mitogen-activated protein kinase pathway inhibitors (MAPKi) are increasingly used as targeted therapies for paediatric central nervous system tumours and other malignancies. Cutaneous toxicities, including xerosis, dermatitis, follicular-based infections, acne, and paronychia, are common and may result in significant morbidity and treatment interruption.
Method:
In this 18-month ambispective observational cohort study, 24 consecutive children receiving MAPKi at a tertiary paediatric centre were included. Patients were followed prospectively, with retrospective data collected for those already receiving therapy at study commencement. The incidence and spectrum of cutaneous adverse events (AE), predisposing factors and management strategies were documented.
Results:
Overall, 21/24 (87.5%) patients developed at least one cutaneous AE, most commonly xerosis, dermatitis, hair changes, paronychia, and pustular skin infections. Most events were Common Terminology Criteria for Adverse Events (CTCAE) grade 1-2; however, a small number of patients required dose modification or temporary treatment interruption.
Conclusion:
These findings support early dermatologic assessment and proactive management of MAPKi-associated cutaneous toxicities. We propose practical caregiver-directed skin care recommendations to be introduced at treatment initiation to reduce morbidity and improve treatment tolerability.
Insights
Mitogen-activated protein kinase inhibitors (MAPKi) commonly cause skin issues in children. Early skin care and assessment can reduce side effects and improve treatment tolerance.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Mitogen-activated protein kinase inhibitors (MAPKi) are vital targeted therapies for pediatric cancers.
- Cutaneous toxicities like xerosis, dermatitis, and infections are frequent side effects of MAPKi treatment.
- These skin toxicities can lead to significant patient morbidity and treatment interruptions.
Purpose of the Study:
- To investigate the incidence, spectrum, and predisposing factors of cutaneous adverse events (AE) in children treated with MAPKi.
- To document management strategies for MAPKi-associated skin toxicities.
- To propose practical skin care recommendations for caregivers to improve treatment tolerability.
Main Methods:
- An 18-month ambispective observational cohort study.
- Inclusion of 24 consecutive pediatric patients receiving MAPKi at a tertiary center.
- Prospective follow-up with retrospective data collection for ongoing therapies.
Main Results:
- A high incidence of cutaneous AE was observed, with 87.5% of patients developing at least one.
- Common AEs included xerosis, dermatitis, hair changes, paronychia, and pustular skin infections.
- Most events were low-grade (CTCAE grade 1-2), but some necessitated dose modification or treatment interruption.
Conclusions:
- Early dermatologic assessment is crucial for managing MAPKi-associated skin toxicities.
- Proactive management strategies and caregiver-directed skin care recommendations can reduce morbidity.
- Implementing these recommendations at treatment initiation can improve patient outcomes and treatment adherence.
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