Abstract 1455P
Background
Nivo as monotherapy for the treatment of aNSCLC after prior chemotherapy (chemo) was approved by EMA in 2015 and has been used in clinical practice since. In this study, we describe RW survival outcomes of patients with aNSCLC who resumed nivo after interrupting an initial nivo treatment received as 2+ line-of-therapy (LOT).
Methods
This study leverages RWD collected in 2 prospective, non-interventional studies: EVIDENS (NCT03382496; France) and ENLARGE (NCT02910999; Germany) on patients with aNSCLC treated with nivo. Data were pooled and two cohorts were defined: 1) nivo resumption cohort (patients who re-started nivo after an interruption of ≥6 weeks) and 2) chemo cohort (patients who received chemo or other systemic anti-cancer therapy after nivo). Demographics and clinical characteristics were described, and overall survival (OS) was estimated using Kaplan-Meier methods from the start of the “index treatment” (LOT following the initial nivo treatment).
Results
Among 2,266 patients (1,397 from France and 869 from Germany), 210 (9.3%) resumed nivo after an initial interruption of ≥6 weeks. 697 (30.8%) started a chemo treatment after nivo, among which 171 - from the ENLARGE study - had data required for this analysis and constituted the chemo cohort. Median age was 67 (range: 41-89) in the nivo resumption cohort and 64 (21-83) in the chemo cohort. In both cohorts, majority of patients were male and received their index treatment as third LOT. Median OS was 19.6 months (mo) [95% CI: 16.2-25.2] for the nivo resumption cohort and 9.1 mo [7.1-10.0] for the chemo cohort. Nivo-resuming patients who had received an initial nivo treatment of ≥3 mo had a median OS of 22.8 mo, compared to 10.7 mo in patients with <3 mo initial nivo treatment. In the chemo cohort, patients with a duration of initial nivo therapy of ≥3 mo had a median OS of 9.9 mo in subsequent treatment, compared with 7.1 mo in patients with <3 mo of initial nivo treatment.
Conclusions
OS data show that patients with aNSCLC who interrupted their initial nivo treatment may benefit from resuming nivo, primarily when initial exposure to nivo lasted for more than three months.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Bristol Myers Squibb.
Funding
Bristol Myers Squibb.
Disclosure
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. M. Sebastian: Financial Interests, Personal, Other, Honoraria: Amgen, AstraZeneca, Boehringer Ingelheim, Bristol Myers Squibb, Janssen Oncology, Lilly, MSD, Novartis, Pfizer/EMD Serono, Roche/Genentech, Sanofi, Takeda; Financial Interests, Personal, Advisory Role: AstraZeneca, Boehringer Ingelheim, Bristol Myers Squibb, Janssen Oncology, Lilly, MSD, Novartis, Pfizer, Roche/Genentech, Sanofi, Takeda; Financial Interests, Institutional, Research Funding: AstraZeneca; Financial Interests, Personal, Other, Travel, Accommodations, Expenses: Pfizer, Takeda. F. Barlesi: Financial Interests, Institutional, Advisory Board: AstraZeneca, Bayer, Bristol Myers Squibb, Boehringer Ingelheim, Eli Lilly Oncology, F. Hoffmann–La Roche Ltd, Novartis, Merck, Mirati, MSD, Pierre Fabre, Pfizer, Sanofi Aventis, Seattle Genetics, Takeda, AbbVie, Acea, Amgen, Eisai, Ignyta; Non-Financial Interests, Principal Investigator: AstraZeneca, BMS, Merck, Pierre Fabre, F. Hoffmann-La Roche Ltd., Innate Pharma, Mirati. C. Schumann: Financial Interests, Personal, Invited Speaker: AstraZeneca, BMS, MSD; Financial Interests, Institutional, Advisory Board: AstraZeneca; Financial Interests, Personal, Writing Engagement: AstraZeneca; Financial Interests, Personal, Advisory Board: BMS, Roche; Financial Interests, Institutional, Invited Speaker: Lilly. D. Reynaud, D. Waldenberger, A. Lee, N. Varol, J.R. Penrod, F. Brellier: Financial Interests, Personal, Full or part-time Employment: Bristol Myers Squibb; Financial Interests, Personal, Stocks/Shares: Bristol Myers Squibb.
Resources from the same session
1452P - Factors associated with real-world (rw) outcomes among pts with metastatic NSCLC (mNSCLC) receiving select immuno-oncology (IO) regimens: CORRELATE
Presenter: Stephen Liu
Session: Poster session 20
1453P - Trends in treatment regimens and survival in the use of immune checkpoint inhibitors for lung cancer treatment in the Netherlands from 2016-2020
Presenter: Erick Suazo Zepeda
Session: Poster session 20
1454P - Radiomic analysis predicts response to immunotherapy in metastastic non-small cell lung cancer (mNSCLC): Preliminary results
Presenter: Salvatore Grisanti
Session: Poster session 20
1456P - Exploring biological and molecular factors as outcome predictors for pembrolizumab (Pem) or pembrolizumab-chemotherapy (Pem-CT) in advanced non-small cell lung cancer (NSCLC)
Presenter: Lodovica Zullo
Session: Poster session 20
1457P - Oligometastatic non-small cell lung cancer: Impact of local and systemic treatment approaches on clinical outcome
Presenter: Marcel Wiesweg
Session: Poster session 20
1459P - Preliminary efficacy and safety of KN046 (a bispecific anti-PD-L1/CTLA-4) in patients with metastatic non-small cell lung cancer who previously treated with immune checkpoint inhibitor(s)
Presenter: Caicun Zhou
Session: Poster session 20
1460P - GALLANT-1: GB1211 galectin-3 (Gal-3) inhibitor plus atezolizumab (atz) for first line treatment in patients (pts) with advanced/metastatic non-small cell lung cancer (NSCLC)
Presenter: Francisco Aparisi Aparisi
Session: Poster session 20
1461P - Predictive value of residual FDG-PET metabolic activity in metastatic non-small cell lung cancer (mNSCLC) patients (pts) with long-lasting response to immune checkpoint inhibitors (ICIs)
Presenter: Toublanc Anne-Claire
Session: Poster session 20
1463P - IL-6 triggers chemoimmunotherapy resistance by creating immunosuppressive tumor microenvironment in non-small cell lung cancer
Presenter: Yaning Yang
Session: Poster session 20