作者
Giannis Mountzios,Anna Koumarianou,Helena Linardou,Anastasios Boutis,Dimitriοs Mavroudis,E. Samantas,Ippokratis Korantzis,Elias Athanasiadis,Evangelos Fergadis,Sofia Lampaki,Vassilis Georgoulias,Sofia Baka,Michalis V. Karamouzis,Ioannis Boukovinas,C. Andreadis,Aggeliki Rapti,Νikolaos Koulouris,George Pentheroudakis,Marios Froudarakis,Alvertos Somarakis,Eleftheria A. Anastasopoulou,Alexandra Karadimou,Foteini Papageorgiou,Zoe Paparepa,Aristeidis Nikolaou,Christina Papista,Konstantinos Syrigos
摘要
Real-world data on the EGFR mutational profile upon progression after first/second-generation EGFR-TKI treatment in patients with advanced non-small-cell lung cancer (NSCLC) and treatment strategies employed thereon are needed.This observational study was conducted in 23 hospital-based lung cancer Centers in Greece (protocol code: D133FR00126). Ninety-six eligible patients were consecutively enrolled between July-2017 and September-2019. Re-biopsy was performed in 18 of 79 patients who tested T790M-negative in liquid biopsy after progression in the first-line (1L) setting.Of the study population, 21.9% tested T790M-positive, while 72.9% proceeded to 2L treatment, mainly comprising of a third-generation EGFR-TKI (48.6%), a switch to chemotherapy (30.0%), or chemo-immunotherapy (17.1%). The objective response rate (ORR) in 2L was 27.9% in T790M-negative and 50.0% in T790M-positive patients. Of evaluable patients, 67.2% experienced disease progression; median progression-free survival (PFS) was 5.7 and 10.0 months among T790M-negative and positive patients, respectively. Among T790M-negative patients, longer median PFS and post-progression survival were observed with third-generation EGFR-TKI treatment.Mutational status and treatment strategy were identified as critical determinants of clinical outcomes in the 2L-setting of EGFR-mutated NSCLC patients in real-world settings in Greece, with early diagnosis, appropriate molecular testing and high-efficacy treatments at first lines positively affecting ORR and PFS.