Methods
In this retrospective, observational study, routinely collected data from 2010 to 2023 were pooled from 4 databases (NCRAS England, ESME France, and COTA, Concert AI US). Pts aged ≥ 18 years with locally advanced/metastatic NSCLC, without prior systemic tx, with ECOG PS 0-1 (when available), and confirmed exon20ins were included. Objectives were to describe 1L tx patterns and outcomes, and compare time to next tx (TTNT; as a proxy for progression-free survival) and overall survival (OS) of amivantamab + CP (from PAPILLON) vs RW tx options (alternatives to platinum (P)-based chemotherapy) using inverse probability weighting of the average tx effect in the treated (IPW-ATT) adjustment for potential confounders.
Results
A total of 232 RW pts were included in the analysis. Median follow-up was 50.5 months; 65.5% of pts were female, 57.8% were aged > 65 years, 40.5% reported a history of smoking, 40.1% had ≥ 3 metastasis locations, 21.6% had liver metastases (mets), and 30.2% had brain mets. Observed 1L txs were: P-based chemotherapies (31.5%), P + immunotherapy (IO) (24.1%), EGFR TKI alone (15.5%), IO alone (9.1%), or other txs (19.8%). Amivantamab + CP demonstrated better comparative effectiveness (TTNT and OS) vs RW txs other than P-based chemotherapy (Table).
Conclusions
In RW practice, P-based chemotherapies were the most commonly used 1L tx in NSCLC pts with EGFR exon20ins. 1L amivantamab + CP demonstrated superior effectiveness vs other commonly used RW txs