Tepotinib plus osimertinib in patients with EGFR-mutated non-small-cell lung cancer with MET amplification following progression on first-line osimertinib (INSIGHT 2): a multicentre, open-label, phase 2 trial.
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Wu Yi-Long, Guarneri Valentina, Voon Pei Jye, Lim Boon Khaw, Yang Jin-Ji, Wislez Marie, Huang Cheng, Liam Chong Kin, Mazieres Julien, Tho Lye Mun, Hayashi Hidetoshi, Nhung Nguyen Viet, Chia Puey Ling, de Marinis Filippo, Raskin Jo, Zhou Qinghua, Finocchiaro Giovanna, Le Anh Tuan, Wang Jialei, Dooms Christophe, Kato Terufumi, Nadal Ernest, Hin How Soon, Smit Egbert F, Wermke Martin, Tan Daniel, Morise Masahiro, O'Brate Aurora, Adrian Svenja, Pfeiffer Boris M, Stroh Christopher, Juraeva Dilafruz, Strotmann Rainer, Goteti Kosalaram, Berghoff Karin, Ellers-Lenz Barbara, Karachaliou Niki, Le Xiuning, Kim Tae Min, INSIGHT 2 investigators
Аннотация
METHODS: This open-label, phase 2 study was conducted at 179 academic centres and community clinics in 17 countries. Eligible patients were aged 18 years or older with an Eastern Cooperative Oncology Group performance status of 0 or 1 and advanced or metastatic EGFR-mutated NSCLC of any histology, with MET amplification by tissue biopsy fluorescence in-situ hybridisation (FISH; MET gene copy number of ≥5 or MET-to-CEP7 ratio of ≥2) or liquid biopsy next-generation sequencing (MET plasma gene copy number of ≥2·3), following progression on first-line osimertinib. Patients received oral tepotinib 500 mg plus oral osimertinib 80 mg once daily. The primary endpoint was independently assessed objective response in patients with MET amplification by central FISH treated with tepotinib plus osimertinib with at least 9 months of follow-up. Safety was analysed in patients who received at least one study drug dose. This study is registered with ClinicalTrials.gov, NCT03940703 (enrolment complete).
FINDINGS: Between Feb 13, 2020, and Nov 4, 2022, 128 patients (74 [58%] female, 54 [42%] male) were enrolled and initiated tepotinib plus osimertinib. The primary activity analysis population included 98 patients with MET amplification confirmed by central FISH, previous first-line osimertinib and at least 9 months of follow-up (median 12·7 months [IQR 9·9-20·3]). The confirmed objective response rate was 50·0% (95% CI 39·7-60·3; 49 of 98 patients). The most common treatment-related grade 3 or worse adverse events were peripheral oedema (six [5%] of 128 patients), decreased appetite (five [4%]), prolonged electrocardiogram QT interval (five [4%]), and pneumonitis (four [3%]). Serious treatment-related adverse events were reported in 16 (13%) patients. Deaths of four (3%) patients were assessed as potentially related to either trial drug by the investigator due to pneumonitis (two [2%] patients), decreased platelet count (one [1%]), respiratory failure (one [1%]), and dyspnoea (one [1%]); one death was attributed to both pneumonitis and dyspnoea.
INTERPRETATION: Tepotinib plus osimertinib showed promising activity and acceptable safety in patients with EGFR-mutated NSCLC and MET amplification as a mechanism of resistance to first-line osimertinib, suggesting a potential chemotherapy-sparing oral targeted therapy option that should be further investigated.
FUNDING: Merck (CrossRef Funder ID: 10.13039/100009945).