Abstract 103P
Background
Durability of response with immune checkpoint inhibitors is often associated with long-term survival benefits. This analysis explored the relationship between achieving objective response (OR) with nivolumab (NIVO) and the possibility of previously treated patients with aRCC being long-term survivors (LTS) in the phase 3 CheckMate 025 trial.
Methods
Mixture cure models (MCMs) were applied to analyze overall survival (OS) and duration of response (DoR) data with ≥7 years of follow-up separately for patients achieving confirmed OR (n=94, 22.9%) with NIVO. In both analyses, LTS were only subject to risk of non–disease-related (NDR) mortality. In the DoR analysis, LTS were also assumed to remain in response until death. OS/DoR outcomes for non-LTS were subject to both disease-related and NDR risk, and modeled by parametric distributions. NDR mortality rates were derived via publicly available World Health Organization lifetable data matched to the study population’s demographic characteristics. The fraction of LTS and OS/DoR for non-LTS were estimated simultaneously through maximum likelihood methods. Candidate MCMs were evaluated based on statistical fit criteria, visual fits to the observed OS/DoR data, and corresponding hazard trends.
Results
Across all clinically plausible candidate models, log-normal MCMs provided the best fit to the observed data for both endpoints, and estimated the fractions of LTS (95% CI) among responders as 31.5% (12.1%–60.5%) and 7% (1.1%–33.4%) from the OS and DoR data, respectively. The range of estimated fractions of LTS across all plausible models was narrower in the DoR analysis (5.7%–11.2%) than in the OS analysis (28.6%–41.1%). Projected 30-year mean OS and DoR for responders from the best-fitting MCMs were 9.35 and 3.30 years, respectively.
Conclusions
MCMs estimated the subgroup achieving OR with NIVO in the CheckMate 025 trial to have a higher fraction of LTS than those previously reported for the entire NIVO arm and a modest proportion of LTS to be in response until death. Even with long-term follow-up data, estimated fractions of LTS were subject to uncertainty due to the limited number of patients contributing to the formation of OS and DoR plateaus.
Clinical trial identification
NCT01668784.
Legal entity responsible for the study
Bristol Myers Squibb.
Funding
Bristol Myers Squibb.
Disclosure
S. George: Financial Interests, Personal, Advisory Board, advisor/consultant: BMS, Bayer, Pfizer, Exelixis, Sanofi/Genzyme, Seattle Genetics, EMD Serono, Eisai, Merck, Aveo, QED therapeutics; Financial Interests, Personal, Advisory Board, Advisor/consultant: Novartis, AstraZeneca; Financial Interests, Institutional, Local PI: Pfizer, Merck, Agensys, Novartis, BMS, Bayer, Eisai, Seattle Genetics, Surface Oncology, Exelixis, Aravive, Aveo, Gilead. J. Larkin: Financial Interests, Personal, Invited Speaker: BMS, Pfizer, Roche, Pierre Fabre, AstraZeneca, Novartis, EUSA Pharma, MSD, Merck, GSK, Ipsen, Aptitude, Eisai, Calithera, Ultimovacs, Seagen, Goldman Sachs, eCancer, Inselgruppe, Agence Unik; Financial Interests, Personal, Other, Consultancy: Incyte, iOnctura, Apple Tree, Merck, BMS, Eisai, Debipharm; Financial Interests, Personal, Other, Honorarium: touchIME, touchEXPERTS, VJOncology, RGCP, Cambridge Healthcare Research, Royal College of Physicians; Financial Interests, Institutional, Funding: BMS, MSD, Novartis, Pfizer, Achilles, Roche, Nektar, Covance, Immunocore, Pharmacyclics, Aveo. L.M. Garcia Fernandez: Financial Interests, Institutional, Advisory Role: Parexel International. J. May, M. Dyer, M. Kurt: Financial Interests, Personal, Full or part-time Employment: Bristol Myers Squibb; Financial Interests, Personal, Stocks or ownership: Bristol Myers Squibb. M. Patel: Financial Interests, Personal, Full or part-time Employment: Bristol Myers Squibb/Medarex, LEO Pharma; Other, Personal, Other, An Immediate Family Member: Pfizer, CVS Health; Financial Interests, Personal, Stocks or ownership: Sanofi, Bristol Myers Squibb/Medarex; Financial Interests, Personal, Stocks or ownership, An Immediate Family Member: CVS Health. All other authors have declared no conflicts of interest.
Resources from the same session
35P - Peripheral immunotype classification for monitoring Soft Tissue Sarcoma patients
Presenter: Jani Sofia Almeida
Session: Poster Display
36P - Expression of germinal center B cell- and Th17 cell-related transcripts are prognostic of soft-tissue sarcoma patient outcomes
Presenter: Giulia Petroni
Session: Poster Display
38P - Machine learning-based pathomics model to predict the infiltration of Treg and prognosis in IDH-wt GBM
Presenter: Shaoli Peng
Session: Poster Display
40P - The role of low avidity tumour-specific CD8+ T cells in immunotherapeutic response to anti-PD-1
Presenter: Doreen Lau
Session: Poster Display
41P - Contrasting drivers of response to immunotherapy across solid tumour types: results from analysis of >2500 cases
Presenter: Danwen Qian
Session: Poster Display
42P - TCCIA: A Comprehensive Resource for Exploring CircRNA in Cancer Immunotherapy
Presenter: Jian-Guo Zhou
Session: Poster Display
43P - Immune and tumor cells expression of VISTA in a panel of cancer indications: A strategy to inform selection of patients treated with anti-VISTA
Presenter: Pierre Launay
Session: Poster Display
44P - Exploratory Analysis of Peripheral Pharmacodynamic (PD) Biomarkers After Sitravatinib (Sitra) and Tislelizumab (TIS) in Advanced Solid Tumors: SAFFRON-103
Presenter: Yi-Long Wu
Session: Poster Display
45P - Protein biomarkers associated with organ-specific immune-related toxicity and response to management identified by proteome analysis of extracellular vesicles from plasma
Presenter: Anders Kverneland
Session: Poster Display