Abstract 1407P
Background
KRAS G12C mutation is found in 14% of NSCLC. Pts with KRAS G12C AM NSCLC have not been well characterized in routine clinical setting. Our objective was to describe pts with KRAS G12C AM NSCLC and compare them to pts with other KRAS and non-KRAS AM NSCLC.
Methods
We performed a retrospective observational cohort study of AM NSCLC pts included in the Epidemio-Strategy and Medical Economics (ESME) Lung Cancer Database and diagnosed between 2015 and 2021. Pts tested for KRAS mutation before first-line treatment (L1 or during the disease for pts who didn’t receive any L1) were divided in 3 subgroups: KRAS G12C (positive KRAS G12C mutation), other KRAS (positive for KRAS mutation other than G12C) and non-KRAS (negative for all KRAS mutations).
Results
A total of 1073 pts carried KRAS G12C (15%), 1642 other KRAS (23%) and 4295 non-KRAS (61%). Among KRAS G12C pts, 58% were male, and the median age was 63 years. The majority (98%) had a smoking history. 68% had an ECOG PS of 0-1. 69% had de novo stage IV. The most frequent metastatic sites involved were bone (42%), brain (35%) and contralateral lung (27%). STK11 appears to be the most common co-mutation (54%) when tested. When PD-L1 status was screened (43%), one third had PD-L1≥50%, and one third had PD-L1<1%. In 2015, most pts received platinum-based chemotherapy (CT) alone (89%) in 1L; this proportion decreased to 55% in 2019 given the benefit of immunotherapy (IO) combined to CT or as monotherapy. In L2, treatments were evenly used in 2015 but IO monotherapy peaked in 2018 to 65%. In L3, IO and other treatments were quite stable over time. The patient and disease characteristics were similar in other KRAS and non-KRAS pts, except a higher proportion of non-smokers (20%) and a less frequent STK11 mutation (28%) in non-KRAS pts than in the 2 other groups. Treatments were similar in the 3 subgroups except the peak of IO observed in L2 in 2017 and in L3 in 2018 for other KRAS pts.
Conclusions
In real-world clinical practice, clinical characteristics and treatment sequences of pts with KRAS G12C AM NSCLC are similar to those of other KRAS mutations or wild-type KRAS pts except for the prevalence of STK11 co-mutation and the proportion of non-smokers.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Unicancer.
Funding
The ESME Lung Cancer Database receives financial support from industrial partners (AstraZeneca, Merck Sharp and Dohme, Bristol Myers Squibb, Roche, Janssen, Amgen) but Unicancer manages the database (data collection, analysis and publication) independently. This study was funded by Amgen Ltd.
Disclosure
N. Girard: Financial Interests, Personal, Invited Speaker: AstraZeneca, BMS, MSD, Roche, Pfizer, Mirati, Amgen, Novartis, Sanofi, Gilead; Financial Interests, Personal, Advisory Board: AstraZeneca, BMS, MSD, Roche, Pfizer, Janssen, Boehringer, Novartis, Sanofi, AbbVie, Amgen, Lilly, Grunenthal, Takeda, Owkin, Leo Pharma, Daiichi Sankyo, Ipsen; Financial Interests, Institutional, Research Grant, Local: Roche, Sivan, Janssen; Financial Interests, Institutional, Funding: BMS, Leo Pharma; Financial Interests, Institutional, Research Grant: MSD; Non-Financial Interests, Officer, International Thymic malignancy interest group, president: ITMIG; Other, Family member is an employee: AstraZeneca. M. Pérol: Financial Interests, Personal, Advisory Board: Roche, AstraZeneca, MSD, BMS, Lilly, Novartis, Takeda, Gritstone, Sanofi, Pfizer, Amgen, Janssen, GSK, Eisai, Ipsen; Financial Interests, Personal, Invited Speaker: Roche, AstraZeneca, MSD, BMS, Boehringer Ingelheim, Takeda, Illumina, Pfizer, Medscape; Financial Interests, Institutional, Research Grant: AstraZeneca, Roche, Takeda, Boehringer Ingelheim; Financial Interests, Personal, Steering Committee Member: Roche; Financial Interests, Personal, Other, DMSB: Roche. D. Debieuvre: Financial Interests, Personal, Advisory Board: AstraZeneca, BMS, MSD, Janssen, Pfizer, Ose Immunotherapeutics, Novartis, SanofiAventis, Amgen, Roche, Ipsen; Financial Interests, Personal, Invited Speaker: Gilead, Takeda; Financial Interests, Personal, Coordinating PI: Pfizer; Financial Interests, Institutional, Funding: Roche, AstraZeneca, Janssen, MSD, Pfizer, BMS, Lilly, Boehringer Ingelheim, GSK, Chugaï, Chiesi, Novartis, Takeda, Bayer, SanofiAventis. L. Bosquet: Financial Interests, Institutional, Full or part-time Employment, In charge of scientific projects at Unicancer, Health Data and Partnership Department: Unicancer. C. Veillard: Financial Interests, Personal, Full or part-time Employment, Medical Advisor Amgen France: Amgen; Financial Interests, Personal, Stocks/Shares: Amgen. M. Caillon, L. Tzala, G. Desamericq: Financial Interests, Personal, Full or part-time Employment: Amgen; Financial Interests, Personal, Stocks/Shares: Amgen. C. Audigier Valette: Financial Interests, Personal, Advisory Board: Roche, BMS, MSD, AstraZeneca, Sanofi, Janssen; Financial Interests, Personal, Invited Speaker: Pfizer.
Resources from the same session
1390P - Real-world characteristics, treatment patterns and outcomes of patients with advanced HER2/ERBB2-mutant non-small cell lung cancer (NSCLC) in France and Germany
Presenter: Petros Christopoulos
Session: Poster session 20
1391P - Capmatinib vs docetaxel as second- or third-line (2/3L) therapy in patients (pts) with METex14-mutated advanced NSCLC (aNSCLC): The GeoMETry-III trial
Presenter: Oscar Jose Juan Vidal
Session: Poster session 20
1392P - Safety and efficacy of crizotinib in MET mutated (METmut) advanced non-small cell lung Cancer (aNSCLC): Results from the Drug Rediscovery Protocol (DRUP)
Presenter: Karlijn Verkerk
Session: Poster session 20
1393P - Characteristics of MET gene and its relationship with TMB/MMR genes in Chinese NSCLC population
Presenter: Hong Yi Zhang
Session: Poster session 20
1394P - Real-world experience in treatment of patients with non-small cell lung cancer with BRAF and cMET Exon 14 skipping mutations
Presenter: Urska Janzic
Session: Poster session 20
1396P - HER2 testing pattern, characteristics of locally advanced or metastatic NSCLC patients by HER2 testing in France
Presenter: Didier Debieuvre
Session: Poster session 20
1397P - Prevalence, molecular characterization, and prognosis of MET–overexpressing non-small cell lung cancer (NSCLC) in a real-world patient cohort
Presenter: Jair Bar
Session: Poster session 20
1398P - Hepatotoxicity in patients (pts) with KRASG12C-mutated non-small cell lung cancer (NSCLC) treated with sotorasib after prior immunotherapy (IO)
Presenter: Sophie Ernst
Session: Poster session 20
1399P - Tumor-immune microenvironment analysis of de novo and acquired KRAS-mutated non-small cell lung cancer
Presenter: Joshua Reuss
Session: Poster session 20
1400P - Real-world effectiveness and safety of sotorasib in patients with KRAS G12C mutated metastatic non-small cell lung cancer (NSCLC): Results of the IFCT-2102 Lung KG12Ci study
Presenter: Marie Wislez
Session: Poster session 20