Abstract 76P
Background
While ICIs demonstrate improved clinical trial outcomes in patients with NSCLC, little is known about real-world ICI retreatment patterns and outcomes after 2L+ nivo therapy. This analysis aimed to understand these endpoints in a real-world patient group in France.
Methods
Patients with locally advanced/metastatic NSCLC who initiated 2L+ nivo from 2015–2020 were included from ESME-AMLC, a retrospective observational cohort involving 39 centres in France (NCT03848052). Patient demographics, clinical and retreatment characteristics and outcomes were determined. Patients were followed from 2L+ nivo start date to last medical information date. Retreatment patterns were defined as: rechallenge (any ICI following an intervening non-ICI anticancer treatment after 2L+ nivo discontinuation); resumption (any ICI post-treatment break >6 weeks), ICI switch (any non-nivo ICI post-treatment break <6 weeks).
Results
After a median follow-up of 24 weeks, 2985/4001 (74.6%) patients discontinued 2L+ nivo treatment, 1604 received chemotherapy (CT) or targeted therapy (40.1%), 800 (20%) had no further treatment, and 226 (7.6%) were retreated with ICI. Of these: 110 (48.7%) were rechallenged (median treatment duration 2.1 months), 102 (45.1%) resumed (median treatment duration 3.3 months), and 14 (6.2%) switched ICI. Most patients retreated with ICI had non-squamous histology (80 [72.7%] patients with rechallenge, 76 [74.5%] with resumption, and 12 [85.7%] with ICI switch). Median duration of initial nivo treatment was 5.5 months for rechallenge, 7 months for resumption and 7 months for ICI switch. Median overall survival (OS) from retreatment date was 16.6 months vs 8.3 months for patients who resumed or were rechallenged. Patients who received initial 2L+ nivo for >26 weeks had higher ICI retreatment rates (15.8% overall) than patients who received 2L+ nivo for <13 weeks (3.6% overall).
Conclusions
Following 2L+ nivo discontinuation, most patients received CT. Few received ICI retreatment, although this increased with 2L+ nivo duration. Patients resuming ICI had longer OS than those with rechallenge.
Clinical trial identification
NCT03848052.
Editorial acknowledgement
Medical writing support was provided by Latitude (Powered by AXON).
Legal entity responsible for the study
Bristol Myers Squibb.
Funding
Bristol Myers Squibb.
Disclosure
G. Justeau: Non-Financial Interests, Personal, Advisory Role: BMS. 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. C. Audigier Valette: Financial Interests, Personal, Advisory Board: Roche, BMS, MSD, AstraZeneca, Sanofi, Janssen; Financial Interests, Personal, Invited Speaker: Pfizer. 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. X. Quantin: Financial Interests, Institutional, Invited Speaker: Sanofi; Financial Interests, Institutional, Advisory Board: BMS; Financial Interests, Institutional, Other, Educational support: AstraZeneca. H. Lena: Non-Financial Interests, Personal, Research Funding: Bristol Myers Squibb; Non-Financial Interests, Personal, Coordinating PI: Regeneron Pharmaceuticals, Sanofi Aventis, GSK, Pfizer; Financial Interests, Personal, Advisory Board: Sanofi Aventis, Pfizer, Takeda, Roche, Amgen. P. Macouillard: Financial Interests, Institutional, Full or part-time Employment: Unicancer. L. Bosquet: Financial Interests, Institutional, Full or part-time Employment, In charge of scientific projects at Unicancer, Health Data and Partnership Department: Unicancer. M.J. Schoemaker, M. Mella, B. Correia: Financial Interests, Personal, Full or part-time Employment: IQVIA. C. Rault: Financial Interests, Personal, Speaker, Consultant, Advisor: Bristol Myers Squibb; Financial Interests, Personal, Full or part-time Employment: Data Gnosis. M.J. Daumont: Financial Interests, Personal, Full or part-time Employment: Bristol Myers Squibb; Financial Interests, Personal, Stocks or ownership: Bristol Myers Squibb. J. Penrod: Financial Interests, Personal, Full or part-time Employment: Bristol Myers Squibb; Financial Interests, Personal, Stocks or ownership: Bristol Myers Squibb. 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.
Resources from the same session
1P - Integrated Data Analysis within IMMUcan Identifies Prognostic Features of Early NSCLC
Presenter: Daniel Schulz
Session: Poster Display
3P - Exploratory efficacy analysis by smoking status in PD-L1 high patients in the phase III, non-small cell lung cancer (NSCLC) IMpower110 study
Presenter: Luis Paz-Ares
Session: Poster Display
4P - Immune exoproteome, soluble proteome and immune-related gene expression profiles of anti-PD-1 therapy in stage IIIB/IV Non-Small Cell Lung Cancer: relevance of immunosuppressive factors
Presenter: Paulo Santos
Session: Poster Display
5P - Blood immune-inflammatory dynamic unveils distinctive irAE features in ICI treated NSCLC
Presenter: Giulia Mazzaschi
Session: Poster Display
6P - CD161+CD127+CD8+ T cells as a critical predictor of the efficacy of anti-PD-1 immunotherapy in diabetic patients with non-small cell lung cancer
Presenter: Jingjing Qu
Session: Poster Display
7P - A T-cell-derived circulating DNA as a biomarker for response to anti-PD(L)1 immunotherapy in advanced stage non-small cell lung cancer
Presenter: Nuthchaya Mejun
Session: Poster Display
9P - Primary NSCLC patient-derived microtumors (PMTs) for clinical-relvant prediction of immunotherapy efficacy
Presenter: Fabienne Nocera
Session: Poster Display
11P - Decreased monocyte-to-lymphocyte ratio was associated with satisfied outcomes of first-line PD-1 inhibitors plus chemotherapy in stage IIIB-IV non-small cell lung cancer
Presenter: Liang Zheng
Session: Poster Display
12P - Spatially preserved multi-region transcriptomic subtyping and biomarkers associated with long-term benefit with chemoimmunotherapy in extensive-stage small cell lung cancer (ES-SCLC)
Presenter: Melina Peressini Álvarez
Session: Poster Display