Video content above is prompted by the following:
Amivantamab Plus Lazertinib in EGFR-Mutant NSCLC
Background
- Discussion between Alexander Spira, MD, PhD, FACP, FASCO, and Randi Rabin, MPH, MSc, PA-C
- Topic: Prevention of moderate to severe dermatologic adverse events in first-line EGFR-mutant advanced non–small cell lung cancer treated with amivantamab plus lazertinib
- Referenced data from the COCOON trial presented at the European Lung Cancer Congress 2025
Clinical Experience
- Practitioners have extensive experience with amivantamab and lazertinib across multiple clinical trials (COCOON, CHRYSALIS 2, SKIPPirr, PALOMA 2 and 3).
- Overall positive experience reported for both providers and patients
- “Fantastic overall survival data” noted
Evolving Treatment Focus
- Field shifting from solely focusing on response rates and survival metrics to also emphasizing:
- Management of adverse events
- Quality of life measures
- Rationale: Improved tolerability increases adherence, which is essential for drug efficacy.
Patient Outcomes
- Patients on these medications reportedly maintain active lifestyles (travel, community involvement, physical activities).
- Quality of life improvements allow patients to continue normal activities while undergoing treatment.
Current Research Direction
- Focus on optimizing management rather than just administering treatment
- Specifically discussing the COCOON trial’s findings on skin/dermatologic adverse event management
- Related research includes infusion-related reaction management from the SKIPPirr trial
This summary reflects a discussion about managing adverse effects to improve both efficacy and quality of life for patients receiving amivantamab plus lazertinib combination therapy.