Abstract 1286P
Background
Non-small cell lung cancer (NSCLC) with ALK rearrangement accounts for around 5% of lung adenocarcinomas. Due the growing number of ALK inhibitors used in first line setting in advanced stage, real-word data are needed.
Methods
Explore ALK GFPC 03-2019 study is a national prospective, non-interventional, multicenter real-world cohort of patients with advanced ALK-rearranged NSCLC. The inclusion period started in july 2020 and the study is still recruiting. A follow-up period of five years is planned. The aims of the study are to better characterize these patients, to assess therapeutic sequences, the efficacy and safety of different lines of treatment, and current practice regarding the search for resistance mechanisms.
Results
For this first interim analysis (cut-off date: April 12, 2024), 242 patients were included by 37 centers. Median age, 65 (29-91) years, 43.6% men, 90.7% PS 0/1, no, former, current smoker, 56.6%, 31.8%, 8.3%; 97.5% adenocarcinoma, 76.4% metastatic at diagnosis (31.9% with brain metastasis (BM)). Alectinib, brigatinib, and lorlatinib were initiated as first-line treatment in 146 (60.3%), 77 (31.8%), 8 (3.3%) pts, respectively. After a median follow up of 16.5 months (95%IC, 13.9-19,2) for the entire cohort, median real world progression free survival (rwmPFS) was 35.8 (95%CI, 23.2-50.3) months), median overall survival (mOS) was 50.3 (95%CI, 50.3-NR) months, and objective response rate (ORR) was 81%. After a median follow-up of 18,4 (95%CI, 15-21.7) months for alectinib, 13.9 (95%CI, 11.5-16.6) for brigatinib and 16.6 (95%CI, 3.4-23.5) for lorlatinib, the rwmPFS and mOS were respectively 35,8 (95% CI : 21,3-50,3) and 50,3 (95%CI : 50,3-NR), NR (95%CI 24,8-NR) and NR (95%CI : NR-NR), 19.3 (95%CI : 1.1-NR) and NR (95%CI : 4.1-NR) months. At time of progression, 20/51 (39.2%) of pts had a new biopsy (86% tissue biopsy). Outcomes according to BM at diagnosis, treatment sequences, details on progression mecanisms, and safety datas will be presented during the meeting.
Conclusions
We present here the preliminary results of Explore ALK project, a large ongoing real world cohort, assessing efficacy and safety of therapeutic management of ALK NSCLC.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Groupe Français de Pneumo-Cancerologie (GFPC).
Funding
Takeda and Pfizer.
Disclosure
C. Decroisette: Financial Interests, Personal, Advisory Board: BMS, MSD, Pfizer, Roche, Janssen Cilag; Financial Interests, Personal, Invited Speaker: Takeda, Sanofi, AstraZeneca, Amgen. R. Descourt: Financial Interests, Personal, Advisory Board: Takeda, Roche, Pfizer, AstraZeneca; Financial Interests, Personal, Invited Speaker: Sanofi. G. Rousseau Bussac: Financial Interests, Personal, Invited Speaker: Takeda, BMS; Financial Interests, Personal, Advisory Board: Roche, AZ; Other, congress: Pfizer; Other, hospitality: Boehringer Ingelheim, Lilly, Sanofi. A. Swalduz: Financial Interests, Personal, Advisory Board: Ipsen, AstraZeneca, Boehringer Ingelheim, Janssen, Lilly, MSD, Pfizer, Roche, Takeda; Financial Interests, Personal, Advisory Role: AstraZeneca, BMS, Daiichi Sankyo, Janssen, Roche, Pfizer, Sanofi. O. Bylicki: Financial Interests, Personal, Advisory Board, Expert BOARD: BMS, Roche, Takeda; Financial Interests, Personal, Other, Travel congress: MSD; Financial Interests, Personal, Advisory Board, expert board: AstraZeneca, Janssen; Financial Interests, Personal, Advisory Board, Board: MSD; Financial Interests, Personal, Other, Travel Congress: AstraZeneca. L. Bigay-Game: Financial Interests, Personal, Speaker, Consultant, Advisor: MSD, BMS, AstraZeneca, Takeda, Janssen, Roche, Pfizer, Sanofi, Leopharma, Viatris. H. Doubre: Financial Interests, Personal, Invited Speaker: Leo Pharma; Financial Interests, Personal, Advisory Board: Amgen; Financial Interests, Institutional, Local PI: Bristol Myers Squibb Foundation, Merck. A.B. Cortot: Financial Interests, Personal, Invited Speaker: AstraZeneca, BMS, AstraZeneca, MSD, Pfizer, Novartis, Takeda, Roche; Financial Interests, Personal, Advisory Board: Novartis, Roche, Pfizer, Janssen, Exeliom, Amgen; Financial Interests, Institutional, Research Grant: Merck, Roche, AbbVie, Exeliom; Financial Interests, Institutional, Coordinating PI: AstraZeneca; Financial Interests, Institutional, Local PI: Janssen, Roche, Sparta, Amgen, Mirati, AbbVie; Non-Financial Interests, Member of Board of Directors: French Thoracic Intergroup. S. Hominal: Financial Interests, Personal, Non financial benefits: Pfizer. F. Guisier: Financial Interests, Personal, Advisory Board: Amgen, AstraZeneca, BMS, MSD, Roche, Sanofi, Janssen, Pfizer, Takeda; Financial Interests, Institutional, Research Grant: Pfizer, Roche, Takeda. C. Ricordel: Financial Interests, Personal, Advisory Board: Roche, Takeda, MSD, BMS, Janssen, Sanofi, AstraZeneca. S. Martinez: Financial Interests, Personal, Non financial benefits: Pfizer, Roche. G. Justeau: Non-Financial Interests, Advisory Role: BMS. C. Chouaid: Financial Interests, Personal, Advisory Board: AZ, BI, GSK, Roche, Sanofi Aventis, BMS, MSD, Lilly, Novartis, Pfizer, Takeda, Bayer, Janssen and Amgen; Financial Interests, Institutional, Funding: AZ, BI, GSK, Roche, Sanofi Aventis, BMS, MSD, Lilly, Novartis, Pfizer, Takeda, Bayer, Janssen and Amgen. L. Greillier: Financial Interests, Personal, Advisory Board: AbbVie, AstraZeneca, BMS, MSD, Novartis, Sanofi, Takeda, Roche; Financial Interests, Personal, Invited Speaker: Lilly, Pfizer; Financial Interests, Institutional, Local PI: AstraZeneca, AbbVie, BMS, MSD, Novartis, Takeda, Pfizer, Roche, PharmaMar; Financial Interests, Institutional, Coordinating PI: Sanofi. All other authors have declared no conflicts of interest.
Resources from the same session
1324P - Durvalumab in treatment-naive, stage IV non-small cell lung cancer (NSCLC) patients (pts), with ECOG performance status (PS) 2-3 and high PD-L1 tumour expression: Results of IFCT-1802 SAVIMMUNE phase II trial
Presenter: Valerie Gounant
Session: Poster session 05
1325P - TRIDENT: Machine learning (ML) multimodal signatures to identify patients that would benefit most from tremelimumab (T) addition to durvalumab (D) + chemotherapy (CT) with data from the POSEIDON trial
Presenter: Ferdinandos Skoulidis
Session: Poster session 05
1326P - Clinical and genomic characteristics of advanced non-small cell lung cancer (aNSCLC) patients (pts) with long-term response to first-line (1L) immunotherapy: A real-world study
Presenter: Sameh Daher
Session: Poster session 05
1327P - Lung immune prognostic index (LIPI) as a guide for addition of chemotherapy in immunotherapy in elderly patients (Pts) with non-small cell lung cancer (NSCLC): NEJ057
Presenter: OSAMU HONJO
Session: Poster session 05
1328P - Dynamic blood immune-inflammatory and radiomic profiling to decode distinct patterns of acquired resistance to immunotherapy in NSCLC patients
Presenter: Giulia Mazzaschi
Session: Poster session 05
1330P - Phase II study of pembrolizumab (pemb) plus plinabulin (plin) and docetaxel (doc) for patients (pts) with metastatic NSCLC after failure on first-line immune checkpoint inhibitor alone or combination therapy: Initial efficacy and safety results on Immune Re-sensitization
Presenter: Yan Xu
Session: Poster session 05
1331P - Efficacy, innovativeness, clinical trials, endpoints, and price of drugs with FDA approval for non-small cell lung cancer (NSCLC)
Presenter: Christoph Michaeli
Session: Poster session 05
1332P - Effects of immune checkpoint inhibitors for EGFR-wild/ALK-negative NSCLC patients with untreated brain metastases
Presenter: Toshihiko Iuchi
Session: Poster session 05
1333P - Prognostic value of circulating nucleosomes during treatment with or without immunotherapy in non-small lung cancer (NSCLC): Results from the NUCLEO-lung study
Presenter: Léa Payen
Session: Poster session 05