Abstract 1504TiP
Background
For patients (pts) with EGFR-mutant NSCLC, upfront treatment with tyrosine kinase inhibitors is standard. Drug resistance remains a challenge and an effective therapy after progression is needed. Ivonescimab (SMT112/AK112) is a novel bispecific antibody that provides dual blockade of PD-1 and VEGF activity. And coengagement of these 2 targets increases affinity to PD-1 by more than 10 fold. Given the correlation between VEGF-A and PD-1 expression in the tumor microenvironment, simultaneous blockade of these 2 targets by ivonescimab may produce enhanced antitumor activity, with an improved safety profile, compared to co-administration of individual anti-PD-(L)1 and an anti-VEGF agents. Phase 2 trial data reported that in 19 pts with EGFR mutated NSCLC who progressed following TKI therapy, the response rate to ivonescimab plus pemetrexed and carboplatin was of 68.4% (13/19) and a tolerable safety profile in the total population (N=83) treated with ivonescimab plus chemotherapy.
Trial design
HARMONi is a randomized, double-blind, multiregional phase 3 trial of ivonescimab or placebo in combination with pemetrexed and carboplatin in pts with locally advanced or metastatic EGFR-mutant NSCLC. 470 pts will be randomized 1:1 and to receive ivonescimab/placebo plus pemetrexed and carboplatin (Q3W, 4 cycles, 21 days per cycle) followed by ivonescimab/placebo plus pemetrexed for maintenance therapy for up to 2 yrs until progression or unacceptable toxicity. The co-primary endpoints are overall survival and progression-free survival assessed by IRC per RECIST v1.1. Secondary endpoints include overall response rate, incidence/severity of adverse events and immunogenicity of ivonescimab. Key eligibility criteria include advanced or metastatic NSq- NSCLC with an activating EGFR mutation, Eastern Cooperative Oncology Group Performance Status 0 or 1 and progression on/following third generation EGFR-TKI. The study will be a multi-national study including United States, Cana, Euroadpe and China.
Clinical trial identification
NCT05184712.
Editorial acknowledgement
Legal entity responsible for the study
Summit Therapeutics and Akeso Biopharma.
Funding
Summit Therapeutics and Akeso Biopharma.
Disclosure
F. Cappuzzo: Financial Interests, Personal, Invited Speaker: Roche, AstraZeneca, BMS, Pfizer, Takeda, Lilly, Bayer, Amgen, Sanofi, PharmaMar, Mirati, Novocure, Ose, and MSD; Financial Interests, Personal, Advisory Board: Roche, AstraZeneca, BMS, Pfizer, Takeda, Lilly, Bayer, Amgen, Sanofi, Mirati, PharmaMar, Novocure, Ose, Galecto and MSD. J.W. Goldman: Financial Interests, Personal, Invited Speaker: AstraZeneca; Financial Interests, Personal, Advisory Board: Genentech, Eli Lilly, Janssen, AbbVie, Gritstone; Financial Interests, Institutional, Coordinating PI: AstraZeneca, Eli Lilly; Financial Interests, Institutional, Local PI: Genentech, Janssen, BMS, AbbVie. J. Remon Masip: Financial Interests, Personal, Invited Speaker: Roche, MSD, Boehringer Ingelheim; Financial Interests, Personal, Writing Engagement: Pfizer; Financial Interests, Personal, Advisory Board: AstraZeneca, Ose Immunotherapeutics, BMS, Janssen, Takeda, Sanofi; Financial Interests, Institutional, Invited Speaker: Merck Portugal; Non-Financial Interests, Principal Investigator, PI of PECATI trial in Thymic malignancies endorsed by a grant by MSD: MSD; Non-Financial Interests, Other, Co-PI of APPLE trial (EORTC-1525): AstraZeneca; Non-Financial Interests, Member, Secretary of the Lung Cancer Group at the EORTC: EORTC. W. Li, M. Xia: Financial Interests, Personal, Full or part-time Employment: Akeso. J. Li, D. James, L. Styles: Financial Interests, Personal, Full or part-time Employment: Summit Therapeutics; Financial Interests, Personal, Stocks/Shares: Summit Therapeutics. H.L. West: Financial Interests, Personal, Advisory Role: Summit Therapeutics. L. Zhang: Financial Interests, Institutional, Research Grant, research grant & Trial Chair: AZ; Financial Interests, Institutional, Research Grant: BMS, Roche; Financial Interests, Institutional, Trial Chair: QiLu pharm, Henrui Pharm, Novartis, Hansoh Pharma, China Shiyao Pharma, Kelun Pharm. All other authors have declared no conflicts of interest.
Resources from the same session
1468P - Patients’ perspective on tolerability of dostarlimab in NSCLC: Patient-reported outcomes from the phase II PERLA trial
Presenter: Martin Reck
Session: Poster session 21
1469P - The role of the CXCL12/CXCR4 pathway in the immunotherapy of non-small cell lung cancer
Presenter: Jacobo Rogado
Session: Poster session 21
1470P - Statin use and overall mortality in patients with advanced non-small cell lung cancer receiving anti-PD(L)1 immunotherapy: A SEER Medicare database analysis
Presenter: Joshua Reuss
Session: Poster session 21
1471P - Immunotherapy prolongs long-term real-world survival compared to chemotherapy for metastatic non-small cell lung cancer: A propensity score-matched analysis
Presenter: Kun Kim
Session: Poster session 21
1472P - Radiotherapy affects immunotherapy efficacy based on tumor mutation status in patients with metastatic NSCLC
Presenter: Shenduo Li
Session: Poster session 21
1473P - Efficacy of anti-PD1/PDL1 antibody monotherapy in patients with advanced non-small cell lung cancer with increased hepcidin expression
Presenter: Masaki Yamamoto
Session: Poster session 21
1474P - Outcome of nivolumab and ipilimumab-based therapy for advanced non-small cell lung cancer with low or negative PD-L1 expression
Presenter: Takafumi Fukui
Session: Poster session 21
1475P - Torque teno virus DNA load as biomarker for tumor response to mono immune checkpoint inhibition in non-small cell lung cancer
Presenter: Benthe Muntinghe
Session: Poster session 21
1476P - Outcomes to first-line pembrolizumab in patients with advanced NSCLC and high PD-L1 expression: A Spanish multicentric study
Presenter: Aida Piedra
Session: Poster session 21
1477P - STK11 mutations predict poor prognosis for advanced NSCLC treated with first-line immunotherapy or chemo-immunotherapy according to KRAS, TP53, KEAP1, and SMARCA4 status
Presenter: Andrea De Giglio
Session: Poster session 21