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Dacomitinib-Induced Paronychia Associated With PRIDE Syndrome in a Patient With Non-Small Cell Lung Cancer
Geethanjali Sahadevan1, Divyashanthi Cm2, Kalaimani Sivamani3
1Dermatology, Jawaharlal Institute of Postgraduate Medical Education & Research, Karaikal, IND.
This case study highlights a patient with non-small cell lung cancer (NSCLC) who experienced early-onset, toe-predominant paronychia and rash from epidermal growth factor receptor (EGFR) inhibitors. These side effects were successfully managed, allowing continued treatment.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Epidermal growth factor receptor (EGFR) inhibitors are crucial for treating non-small cell lung cancer (NSCLC) with EGFR mutations.
- These therapies often induce cutaneous toxicities, including papulopustules, paronychia, hair growth abnormalities, itching, and dryness, collectively termed PRIDE syndrome.
Observation:
- A 55-year-old male with advanced NSCLC developed toe-predominant paronychia, a papulopustular rash on the trunk and limbs, and diarrhea 4-8 weeks after starting dacomitinib.
- Causality assessment using Naranjo, WHO-UMC, and Liverpool tools indicated a probable relationship between dacomitinib and the observed adverse events.
Findings:
- Adverse effects were managed symptomatically, enabling uninterrupted dacomitinib therapy and dose maintenance.
- This case documents an atypical presentation of PRIDE syndrome with early onset and a unique toe-predominant distribution.
Implications:
- Early recognition and symptomatic management of EGFR inhibitor-induced toxicities are vital for patient adherence and treatment success.
- This case underscores the importance of pharmacovigilance and reporting to optimize the safe use of EGFR inhibitors in NSCLC treatment.
- Successful management of these adverse events without dose modification or discontinuation can improve patient outcomes in EGFR-mutated NSCLC.
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