Long-Term Treatment with First-Line Amivantamab Plus Lazertinib: Impact of Treatment Discontinuation, Maintenance, and Early Adverse Event Management on Duration of Therapy
Recommended Citation
Nguyen D, Spira AI, Hayashi H, Owen S, Korbenfeld E, Rodriguez Cid JR, Martin C, Sethi S, Shah S, Johnson AL, Fennema E, Xia Y, Gadgeel SM. Long-Term Treatment with First-Line Amivantamab Plus Lazertinib: Impact of Treatment Discontinuation, Maintenance, and Early Adverse Event Management on Duration of Therapy. J Thorac Oncol 2026; 21(5):2.
Document Type
Conference Proceeding
Publication Date
5-1-2026
Publication Title
J Thorac Oncol
Keywords
Oncology, Respiratory System
Abstract
In MARIPOSA, first-line amivantamab-lazertinib significantly improved overall survival (OS) versus osimertinib, with a projected median OS of >4 years (Yang NEJM 2025). Since approval, the amivantamab-lazertinib safety profile has been further optimized using prophylactic regimens as demonstrated in the SKIPPirr (IRR reduction 2-fold) and COCOON (dermatologic adverse event [AE] reduction ∼2-fold) trials. In MARIPOSA, first onset of key AEs mostly occurred during the first 4 months (Spira NACLC 2023). Nearly half (49%) of dose interruptions occurred in the first 4 months, and these did not impact PFS (Campelo ELCC 2024). Here, we present an analysis of long-term treatment duration of amivantamab-lazertinib and osimertinib, including assessing characteristics of participants who remained on therapy for ≥ 3 years.
Volume
21
Issue
5
First Page
2
