Abstract 1448P
Background
The CheckMate 9LA study showed that NIVO + IPI with 2 cycles of chemotherapy (chemo) vs chemo alone significantly improved overall survival (OS) for patients (pts) with metastatic NSCLC. The FINN real-world study (NCT04794010) aims to evaluate this regimen in clinical practice in Germany.
Methods
Enrollment for the prospective, observational study is ongoing, with 90 sites and 650 pts planned in Germany. Pts ≥18 years old with metastatic NSCLC are eligible if they began first-line NIVO + IPI with 2 cycles of chemo according to the approved EMA label. During the planned ≤5-year follow-up period (from treatment [tx] initiation until death, withdrawal of consent, loss of follow-up, or end of study), assessments will be conducted per routine local clinical practice. The primary endpoint is OS. Secondary endpoints include progression-free survival, tx duration, patient characteristics, and safety.
Results
At the interim analysis (Jan 31, 2023), 256 pts were enrolled (median follow-up duration: 5.6 months). Median (range) age was 67 (43–86) years and 60.9% were male. Other patient characteristics are presented (Table). Tx-related adverse events (AEs) of all grades occurred in 53.9% of pts, and tx-related severe AEs occurred in 17.6% of pts. There was 1 tx-related death from immune-mediated hepatitis. We will present an update of the data with longer follow-up (data cutoff July 2023).
Table: 1448P
Patient characteristics∗ (N = 256), n (%) unless noted
Age group, years <66 66–75 >75 | 120 (46.9) 102 (39.8) 33 (12.9) |
Smoking status Current Former Never | 98 (38.3) 111 (43.4) 28 (10.9) |
Eastern Cooperative Oncology Group performance status 0 1 2 3 | 74 (28.9) 142 (55.5) 26 (10.2) 5 (2.0) |
Number of metastases, median (range) | 2 (0–12) |
Histology Squamous Non-squamous | 89 (34.8) 163 (63.7) |
Metastasis stage M1a (contralateral lung) M1b/M1c (extrathoracic metastasis) | 39 (15.2) 173 (67.6) |
Metastasis site Brain Liver | 51 (19.9) 49 (19.1) |
Radiotherapy No/yes | 204 (79.7)/48 (18.8) |
Surgery No/yes | 208 (81.2)/44 (17.2) |
Systemic therapy/chemo No/yes/unknown | 217 (84.8)/33 (12.9)/2 (0.8) |
∗ Excludes missing data.
Conclusions
The FINN study will describe patient characteristics, efficacy, safety profile, and tx patterns of first-line NIVO + IPI with 2 cycles of chemo in clinical practice in Germany. At interim analysis, pts had a manageable safety profile.
Clinical trial identification
NCT04794010.
Editorial acknowledgement
Writing and editorial assistance was provided by Christy Chao, PhD, of Evidence Scientific Solutions Inc., funded by Bristol Myers Squibb.
Legal entity responsible for the study
Bristol Myers Squibb, Princeton, NJ, USA.
Funding
Bristol Myers Squibb, Princeton, NJ, USA.
Disclosure
J.B. Kuon: Financial Interests, Personal, Speaker, Consultant, Advisor, Honoraria: BMS, AstraZeneca, Pfizer. E. von der Heyde: Financial Interests, Personal, Speaker, Consultant, Advisor, Honoraria: BMS, Novartis, AstraZeneca, Pierre Fabre; Financial Interests, Personal, Advisory Board: AstraZeneca, BeiGene. S. Wilop: Financial Interests, Personal, Advisory Board, Advisory Board Multiple Myeloma: Amgen. G. Huebner: Financial Interests, Personal, Speaker, Consultant, Advisor, Honoraria: Roche, Amgen, Servier, Pierre-Fabre; Financial Interests, Personal, Other, Travel/Accommodations: Roche, BeiGene, Octapharma; Financial Interests, Personal, Advisory Board: Alexion, AstraZeneca. D. Flieger: Financial Interests, Personal, Speaker, Consultant, Advisor, Honoraria - Roundtable Finn: BMS. H. Forstbauer: Financial Interests, Personal, Speaker, Consultant, Advisor, Honoraria: BMS, Roche, iOMEDICO. M. Groschek: Financial Interests, Institutional, Other, Study contract for present abstract: BMS; Financial Interests, Personal, Speaker, Consultant, Advisor, Honoraria: Ipsen; Financial Interests, Personal, Other, Travel/Accommodations: Roche, Ipsen, Onkovis, Gilead; Financial Interests, Personal, Advisory Board: Roche, BMS, Ipsen, GSK. H. Mueller-Huesmann: Financial Interests, Institutional, Research Grant: Roche, BMS, Janssen, MSD, Boehringer Ingelheim, Pfizer, Servier, AstraZeneca, Seagen, 420-Pharma; Financial Interests, Personal, Speaker, Consultant, Advisor, Honoraria: Roche, BMS, Janssen, MSD, Pfizer, AstraZeneca, Seagen, 420-Pharma; Financial Interests, Personal, Other, Travel/Accommodations: Roche, AstraZeneca; Financial Interests, Personal, Advisory Board: Roche, BMS, AstraZeneca, Seagen. C. Schumann: Financial Interests, Personal and Institutional, Speaker, Consultant, Advisor, Honoraria: BMS, AstraZeneca, Sanofi; Financial Interests, Personal, Other, Attending Meeting: BMS; Financial Interests, Personal, Other, Travel and Congress: AstraZeneca; Financial Interests, Personal, Other, Congress: Sanofi; Financial Interests, Personal and Institutional, Advisory Board: AstraZeneca, BMS, Roche, MSD; Financial Interests, Institutional, Advisory Board: DSMB. D. Waldenberger: Financial Interests, Personal, Full or part-time Employment: Bristol Myers Squibb. S. Gütz: Financial Interests, Personal, Other, Consulting: Bristol Myers Squibb, MSD, Sanofi Aventis Deutschland GmbH, Novartis Pharma GmbH; Financial Interests, Personal, Speaker, Consultant, Advisor, Honoraria: Bristol Myers Squibb, Amgen, AstraZeneca, Sanofi Aventis Deutschland GmbH, Roche Pharma, Pfizer, Lilly Deutschland, MSD, Takeda; Financial Interests, Personal, Expert Testimony: Roche Pharma, AstraZeneca; Financial Interests, Personal, Other, Travel/Accommodations: Takeda, Lilly, Roche; Non-Financial Interests, Personal, Leadership Role, Co-Coordinator S3-Guidelines Lung Cancer: Misc. All other authors have declared no conflicts of interest.
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