Abstract 153P
Background
The IMbrave150 study (Finn RS, NEJM 2020; Cheng AL, J Hepatol 2022) established atezolizumab (atezo) plus bevacizumab (bev) as the global standard of care in pts with unresectable HCC. Previously, tumour response by RECIST 1.1 was reported to be associated with OS in pts treated with atezo+bev (Ducreux M, ASCO 2021; Lim M, Hepatology 2023). Here, we report exploratory analyses investigating associations between OS and DpR or DoR.
Methods
DpR was defined as the maximum tumour shrinkage from baseline based on the sum of longest diameters as assessed by an independent review facility (IRF) per RECIST 1.1. DoR was defined as time from first documented complete or partial response by IRF assessment per RECIST 1.1 until disease progression or death, whichever occurred first. Associations between OS and DpR or DoR were evaluated by scatterplot. The Kaplan-Meier method and proportional hazard modelling were also used to estimate the survival distribution and hazard ratio (HR). The DpR analysis included pts who survived ≥6 mo to reduce immortal time bias.
Results
Of the 336 and 165 pts randomised to the atezo+bev and sorafenib arms, respectively, 264 and 99 pts who survived ≥6 mo were included in the DpR analysis, and 97 and 18 pts were included in the DoR analysis. The scatterplot of DpR-OS indicated that the association between DpR and OS was not conclusive. However, the 6-mo landmark analysis for the atezo+bev arm showed that the tumour shrinkage population (DpR <0%) had a better OS than the non-tumour shrinkage population (DpR ≥0%; HR, 0.29; 95% CI: 0.19, 0.44). A similar trend was observed for the 12-mo landmark analysis (HR, 0.31; 95% CI: 0.17, 0.55). For DoR, the scatterplot of DoR-OS showed that DoR was generally associated with OS, as expected by the definition of the endpoints. However, some pts had longer OS despite shorter DoR, and interpretation was limited due to censored pts.
Conclusions
Although these exploratory analyses have several limitations, including immortal time bias, DpR and DoR tend to be associated with OS, and tumour shrinkage may be an additional outcome measure of treatment efficacy.
Clinical trial identification
NCT03434379.
Editorial acknowledgement
Editorial assistance for this abstract was provided by Megan Zborowski of Health Interactions and funded by Chugai Pharmaceutical Co., Ltd.
Legal entity responsible for the study
F. Hoffmann-La Roche Ltd. and Chugai Pharmaceutical Co., Ltd.
Funding
F. Hoffmann-La Roche Ltd. and Chugai Pharmaceutical Co., Ltd.
Disclosure
M. Kudo: Financial Interests, Personal, Invited Speaker: Eisai, Chugai, Eli Liiy, Bayer, Takeda, AstraZeneca; Financial Interests, Institutional, Research Grant: Otsuka, EA Pharma, Taiho, Eisai, AbbVie, GE Healthcare, Chugai. T. Yamashita: Financial Interests, Personal, Speaker’s Bureau: Bayer, Chugai Pharmaceutical Co. Ltd. ; Financial Interests, Personal, Research Funding: F Hoffmann-La Roche Ltd. R.S. Finn: Financial Interests, Personal, Advisory Board: AstraZeneca, Bayer, BMS, CSTONE, Eisai, Exelixis, Eli Lilly, Merck, Pfizer, Roche, Genentech, Hengrui; Financial Interests, Personal, Invited Speaker: Pfizer, Roche, Bayer; Financial Interests, Institutional, Research Grant: Bayer, Eisai, Eli Lilly, BMS; Financial Interests, Institutional, Coordinating PI: Roche, Pfizer, Merck. P.R. Galle: Financial Interests, Personal, Sponsor/Funding: Adaptimmune, AstraZeneca, Bayer, Boston Scientific, BMS, Eisai, Eli Lilly, F. Hoffmann-La Roche Ltd, Guerbet, Ipsen, Merck, Sharp & Dohme, Sirtex Medical; Financial Interests, Personal, Other, Honoraria: Adaptimmune, AstraZeneca, Bayer, Boston Scientific, BMS, Eisai, Eli Lilly, F. Hoffmann-La Roche Ltd., Guerbet, Ipsen, Merck Sharp & Dohme, Sirtex Medical; Financial Interests, Personal, Advisory Role: Adaptimmune, AstraZeneca, Bayer, Boston Scientific, BMS, Eisai, Eli Lilly, F. Hoffmann-La Roche Ltd, Guerbet, Ipsen, Merck Sharp & Dohme, Sirtex Medical; Financial Interests, Institutional, Research Funding: F Hoffmann-La Roche Ltd, Bayer. M.P. Ducreux: Financial Interests, Personal, Advisory Role: Amgen, AstraZeneca, Bayer, Eli Lilly, F. Hoffmann-La Roche Ltd, Ipsen, Merck Serono, Pierre Fabre, Servier; Financial Interests, Personal, Other, travel: Bayer, Eli Lilly, F. Hoffmann-La Roche Ltd, Ipsen, Merck Sharp & Dohme, Servier; Financial Interests, Personal, Speaker’s Bureau: Amgen, Bayer, Eli Lilly, F Hoffmann-La Roche Ltd, Ipsen; Financial Interests, Personal, Speaker’s Bureau, F Hoffmann-La Roche Ltd: Merck Serono; Financial Interests, Institutional, Research Funding: F Hoffmann-La Roche Ltd, Bayer. A. Cheng: Financial Interests, Institutional, Research Funding: F Hoffmann-La Roche Ltd. K. Tsuchiya: Financial Interests, Personal, Advisory Role: Chugai Pharmaceutical Co. Ltd; Financial Interests, Personal, Advisory Board: Eisai; Financial Interests, Personal, Speaker’s Bureau: Chugai Pharmaceutical Co. Ltd, Eisai, Eli Lilly, Takeda; Financial Interests, Personal, Research Funding: F Hoffmann-La Roche Ltd. N. Sakamoto: Financial Interests, Personal, Financially compensated role, honoraria: AbbVie, Eisai, Gilead Sciences, Otsuka; Financial Interests, Institutional, Research Funding: Astellas Pharmaceutical, Bayer, Chugai Pharmaceutical Co., Ltd, Daiichi Sankyo, F. Hoffmann-La Roche Ltd., Gilead Sciences, Otsuka, Takeda. S. Hige: Financial Interests, Personal, Speaker, Consultant, Advisor: gilead sciences, AbbVie, Chugai Pharmaceutical Co., LTD. R. Take: Financial Interests, Personal, Full or part-time Employment: Chugai Pharmaceutical Co. Ltd.. K. Yamada: Financial Interests, Personal, Full or part-time Employment: Chugai Pharmaceutical Co. Ltd.. T. Asakawa: Financial Interests, Personal, Full or part-time Employment: Chugai Pharmaceutical Co. Ltd.. Y. Nakagawa: Financial Interests, Personal, Full or part-time Employment: Chugai Pharmaceutical Co. Ltd. M. Ikeda: Financial Interests, Personal, Financially compensated role: Bayer, Chugai Pharmaceutical Co. Ltd, Eisai, Eli Lilly, Takeda; Financial Interests, Personal, Speaker, Consultant, Advisor: Chugai Pharmaceutical Co. Ltd, Eisai; Financial Interests, Personal, Advisory Board: Eli Lilly, Merck Sharp & Dohme, Takeda; Financial Interests, Personal, Research Funding: Bayer, BMS, Chugai Pharmaceutical Co. Ltd, Eisai, Eli Lilly, F. Hoffmann-La Roche Ltd, Merck Sharp & Dohme, Takeda.
Resources from the same session
540P - Phase III study of serplulimab plus chemotherapy as first-line therapy for advanced squamous non-small cell lung cancer: ASTRUM-004 Asian subgroup
Presenter: Caicun Zhou
Session: Poster Display
Resources:
Abstract
541P - Integrated analysis of randomized controlled trials IMpower130 and IMpower132 for advanced non-squamous non-small cell lung cancer (NSCLC)
Presenter: Hibiki Udagawa
Session: Poster Display
Resources:
Abstract
542P - First-line HLX07 plus serplulimab with or without chemotherapy versus serplulimab plus chemotherapy in advanced/recurrent squamous non-small cell lung cancer: A phase II study
Presenter: Zhen Wang
Session: Poster Display
Resources:
Abstract
543P - A multicenter retrospective study to investigate risk factors for immune checkpoint inhibitor-induced pneumonitis in non-small cell lung cancer patients with comorbid interstitial pneumonia
Presenter: Yuriko Ishida
Session: Poster Display
Resources:
Abstract
544P - Single cell level investigation of blood cells representing immune checkpoint inhibitor response in lung adenocarcinoma patients
Presenter: Juyong Seong
Session: Poster Display
Resources:
Abstract
545P - Completion of pembrolizumab in advanced non-small cell lung cancer: Real-world outcomes after two years of therapy (COPILOT)
Presenter: Andrew Fantoni
Session: Poster Display
Resources:
Abstract
546P - Combination therapy with anti-PD-1 antibody plus angiokinase inhibitor exerts synergistic antitumor effect against malignant mesothelioma via tumor microenvironment modulation
Presenter: Akio Tada
Session: Poster Display
Resources:
Abstract
547P - Immunotherapy outcome in advanced/metastatic lung cancer patients in real-world experience: Indian data
Presenter: Naveen K
Session: Poster Display
Resources:
Abstract
548P - B-Myb acts as a mentor instant promoter in non-small cell lung cancer by modifying the PD-1/PD-L1 axis
Presenter: Pan Xu
Session: Poster Display
Resources:
Abstract
549P - Drug-induced interstitial lung disease in patients with non-small cell lung cancer treated with immunotherapy for postoperative recurrence: Evaluation of CT findings and histopathological findings of the background lung
Presenter: shodai fujimoto
Session: Poster Display
Resources:
Abstract