Amivantamab plus Lazertinib in Previously Untreated <i>EGFR</i> -Mutated Advanced NSCLC

Byoung Chul Cho(Harbin Medical University), Shun Lu(Harbin Medical University), Enriqueta Felip(Harbin Medical University), Alexander I. Spira(Harbin Medical University), Nicolas Girard(Harbin Medical University), Jong-Seok Lee(Harbin Medical University), Se-Hoon Lee(Harbin Medical University), Yurii Ostapenko(Harbin Medical University), Pongwut Danchaivijitr(Harbin Medical University), Baogang Liu(Harbin Medical University), Adlinda Alip(Harbin Medical University), Ernesto Korbenfeld(Harbin Medical University), Josiane Mourão Dias(Harbin Medical University), Benjamin Besse(Harbin Medical University), Ki-Hyeong Lee(Harbin Medical University), Hailin Xiong(Harbin Medical University), Soon-Hin How(Harbin Medical University), Ying Cheng(Harbin Medical University), Gee‐Chen Chang(Harbin Medical University), Hiroshige Yoshioka(Harbin Medical University), James Chih‐Hsin Yang(Harbin Medical University), Michael J. Thomas(Harbin Medical University), Danny Nguyen(Harbin Medical University), Sai‐Hong Ignatius Ou(Harbin Medical University), Sanjay Mukhedkar(Harbin Medical University), Kumar Prabhash(Harbin Medical University), M. D’Arcangelo(Harbin Medical University), Jorge Alatorre-Alexander(Harbin Medical University), Juan Carlos Vázquez Limón(Harbin Medical University), Sara Alves(Harbin Medical University), Daniil Stroyakovskiy(Harbin Medical University), Marina Peregudova(Harbin Medical University), Mehmet Alı Nahıt Şendur(Harbin Medical University), Ozan Yazıcı(Harbin Medical University), Raffaele Califano(Harbin Medical University), Vanesa Gutiérrez Calderón(Harbin Medical University), Filippo de Marinis(Harbin Medical University), Antonio Passaro(Harbin Medical University), Sang‐We Kim(Harbin Medical University), Shirish M. Gadgeel(Harbin Medical University), John Xie(Harbin Medical University), Tao Sun(Harbin Medical University), Melissa Martínez(Harbin Medical University), Mariah Ennis(Harbin Medical University), E. Fennema(Harbin Medical University), Mahesh Daksh(Harbin Medical University), Dawn Millington(Harbin Medical University), Isabelle Leconte(Harbin Medical University), Ryota Iwasawa(Harbin Medical University), Patricia Lorenzini(Harbin Medical University), Mahadi Baig(Harbin Medical University), Sujay Shah(Harbin Medical University), Joshua Bauml(Harbin Medical University), S. Martin Shreeve(Harbin Medical University), Seema Sethi(Harbin Medical University), R.E. Knoblauch(Harbin Medical University), Hidetoshi Hayashi(Harbin Medical University)
New England Journal of Medicine
June 26, 2024
Cited by 365Open Access
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Abstract

BACKGROUND: (epidermal growth factor receptor)-mutated advanced non-small-cell lung cancer (NSCLC). METHODS: -mutated (exon 19 deletion or L858R), locally advanced or metastatic NSCLC to receive amivantamab-lazertinib (in an open-label fashion), osimertinib (in a blinded fashion), or lazertinib (in a blinded fashion, to assess the contribution of treatment components). The primary end point was progression-free survival in the amivantamab-lazertinib group as compared with the osimertinib group, as assessed by blinded independent central review. RESULTS: -related toxic effects. The incidence of discontinuation of all agents due to treatment-related adverse events was 10% with amivantamab-lazertinib and 3% with osimertinib. CONCLUSIONS: -mutated advanced NSCLC. (Funded by Janssen Research and Development; MARIPOSA ClinicalTrials.gov number, NCT04487080.).


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