Abstract 1311P
Background
CARMEN-LC05 (NCT04524689), a Phase 2, open-label, non-randomised study, evaluated tusamitamab ravtansine (tusa rav), a CEACAM5-targeting antibody-drug conjugate, in combination with pembrolizumab (pembro) and pembro + platinum-based chemotherapy (pCT) ± pemetrexed in patients (pts) with CEACAM5+ non-squamous non–small-cell lung cancer (NSQ NSCLC). Here, we present updated safety and efficacy data from CARMEN-LC05.
Methods
Tusa rav was assessed in combination with standard-of-care (SoC) therapies via two approaches: with pembro (substitution approach); with pembro + pCT; and with pembro + pCT and pemetrexed (add-on approaches) in advanced NSQ NSCLC with CEACAM5 intensity of ≥ 2+ in ≥ 1% of cells. Tusa rav was given (intravenous, every 3 weeks) at 150 or 170 mg/m2 in each treatment arm. Primary endpoints were dose-limiting toxicity at Cycle 1 and objective response rate (ORR; confirmed partial response or complete response) per RECIST v1.1. For the secondary endpoints of PFS and DOR, median with two-sided 95% CI were estimated using the Kaplan–Meier method.
Results
As of March 21, 2024, 57 pts were treated with tusa rav for a median of 27.3 weeks (range 3.0; 128.9). All pts had treatment-emergent adverse events, of which 21 (36.8%) had any serious adverse events. Corneal events and peripheral neuropathies were reported in 20 (35.1%; Grade ≥ 3: 1 [1.8%]) and 23 (40.4%; Grade ≥ 3: 5 [8.8%]) pts, respectively. Deaths were reported in 16 (28.1%) pts due to disease progression (8 [14.0%]) pts, adverse events (6 [10.5%]) or others (2 [3.5%]). OR was observed in 30 (52.6%) pts with a median PFS of 11.6 months (95% CI 7.7; 15.9) and median DOR of 12.4 months (95% CI 8.4; 24.1) at cut-off date.
Conclusions
Tusa rav in combination with pembro ± chemotherapy demonstrated encouraging antitumor activity across PD-L1 subgroups and was associated with a favourable safety profile.
Table: 1311P
1311P Safety and efficacy
n (%) | Tusa rav + pembro (n=25) | Tusa rav + pembro + pCT (n=7) | Tusa rav + pembro + pCT + pemetrexed (n=25) | All (N=57) | |||
150 mg/m2 (n=23) | 170 mg/m2 (n=2) | 150 mg/m2 (n=6) | 170 mg/m2 (n=1) | 150 mg/m2 (n=22) | 170 mg/m2 (n=3) | ||
TEAEs | |||||||
Any | 23 (100) | 2 (100) | 6 (100) | 1 (100) | 22 (100) | 3 (100) | 57 (100) |
Grade ≥ 3 | 11 (47.8) | 2 (100) | 4 (66.7) | 1 (100) | 17 (77.3) | 2 (66.7) | 37 (64.9) |
Grade 5 | 1 (4.3) | 0 | 0 | 0 | 7 (31.8) | 0 | 8 (14.0) |
ORR | 11 (47.8) | 0 | 4 (66.7) | 0 | 13 (59.1) | 2 (66.7) | 30 (52.6) |
Complete response | 0 | 0 | 0 | 0 | 1 (4.5) | 0 | 1 (1.8) |
Partial response | 11 (47.8) | 0 | 4 (66.7) | 0 | 12 (54.5) | 2 (66.7) | 29 (50.9) |
Stable disease | 8 (34.8) | 2 (100) | 2 (33.3) | 1 (100) | 5 (22.7) | 1 (33.3) | 19 (33.3) |
Progressive disease | 3 (13.0) | 0 | 0 | 0 | 3 (13.6) | 0 | 6 (10.5) |
Not evaluable | 1 (4.3) | 0 | 0 | 0 | 1 (4.5) | 0 | 2 (3.5) |
Clinical trial identification
NCT04524689.
Editorial acknowledgement
Medical writing support for this abstract was provided by Himanshi Bhatia, PhD, of Sanofi.
Legal entity responsible for the study
Sanofi.
Funding
Sanofi.
Disclosure
D. Rodriguez Abreu: Financial Interests, Personal, Advisory Board: BMS, MSD, Roche, AstraZeneca, Boehringer Ingelheim, Novartis, Eli Lilly; Financial Interests, Personal, Other, Honoraria: BMS, MSD, Roche, AstraZeneca, Boehringer Ingelheim, Novartis, Eli Lilly; Financial Interests, Personal, Speaker’s Bureau: BMS, MSD, Roche, Novartis. R. Veillon: Financial Interests, Personal and Institutional, Research Grant: AstraZeneca, Merck-Serono, Bristol Myers Squibb, GSK, Novartis, Janssen, Gilead, Sanofi, Roche, Takeda, AbbVie; Financial Interests, Personal and Institutional, Speaker’s Bureau: MSD, BMS, Takeda, AstraZeneca, Janssen. M. Ravoire: Financial Interests, Personal and Institutional, Research Grant: Roche, AstraZeneca, Merck-Serono, Bristol Myers Squibb, Janssen, Gilead, Sanofi. J.L. Gonzalez-Larriba: Financial Interests, Personal and Institutional, Full or part-time Employment: Ministry of Universities, Spanish National Health System; Financial Interests, Personal and Institutional, Advisory Board: Janssen-Cilag, MSD Oncology, Bristol Myers Squibb, Boehringer Ingelheim; Financial Interests, Personal and Institutional, Research Grant: Miratti Therapeutics, AstraZeneca, Bayer, OncoMed, Astellas Pharma, Janssen-Cilag, Roche, AbbVie, Boehringer Ingelheim, Pfizer, PharmaMar, Bristol-Myers-Squibb, Novartis, Celgene, Ignyta; Financial Interests, Personal and Institutional, Other, Honoraria: MSD Oncology, Pfizer, Astellas Pharma, Roche, Novartis, Janssen-Cilag, Bristol-Myers-Squibb, AstraZeneca; Financial Interests, Personal and Institutional, Speaker’s Bureau: MSD Oncology. F.J. Orlandi: Financial Interests, Institutional, Research Grant: AbbVie, Amgen, Astellas Pharma, AztraZeneca, BMS, Celltrion, Daiichi Sankyo, GSK, MSD, PharmaMar, Pfizer, Sanofi; Financial Interests, Institutional, Advisory Board: AstraZeneca, BMS, MSD, Pfizer, Roche, Takeda; Financial Interests, Institutional, Speaker’s Bureau: AstraZeneca, MSD, Pfizer. L.G. Paz-Ares: Financial Interests, Personal and Institutional, Speaker, Consultant, Advisor: Roche, MSD, BMS, AstraZeneca, Eli Lilly, PharmaMar, BeiGene, Daiichi Sankyo, Medscape, PER; Financial Interests, Personal and Institutional, Advisory Board: Merck Serono, Pfizer, Bayer, Amgen, Janssen, GSK, Novartis, Takeda, Sanofi, Mirati; Financial Interests, Personal and Institutional, Other, Board Member: Genomica, Altum sequencing; Financial Interests, Institutional, Invited Speaker: Daiichi Sankyo, AstraZeneca, Merck Sharp & Dohme Corp, BMS, Janssen-Cilag international NV, Novartis, Roche, Sanofi, Tesaro, Alkermes, Eli Lilly, Takeda, Pfizer, PharmaMar; Financial Interests, Personal, Invited Speaker: Amgen; Financial Interests, Personal, Membership or affiliation: AACR, ASCO, ESMO; Financial Interests, Personal, Other, Foundation Board Member: AECC; Financial Interests, Personal, Other, President: ASEICA; Financial Interests, Personal, Other, Foundation President: ONCOSUR; Financial Interests, Personal, Other, Member: Small Lung Cancer Group. C.H. Huang: Non-Financial Interests, Personal, Advisory Board: Jazz Pharmaceuticals; Financial Interests, Personal, Other, Self/Spouse: Vanguard Health Care Mutual Fund; Financial Interests, Institutional, Research Grant: Sanofi, Amgen, Novartis, Pfizer, Incyte, Genentech, Exelixis, Nektar, EpicentrRx. N. Isambert: Financial Interests, Personal, Advisory Board: Eisai; Financial Interests, Personal, Other, Honoraria: BMS, Amgen, Daiichi Sankyo; Financial Interests, Personal, Other: Pfizer, Roche, PharmaMar, Novartis. M.R. García Campelo: Financial Interests, Personal, Speaker, Consultant, Advisor: Roche/Genentech, MSD Oncology, AstraZeneca, Bristol Myers Squibb, Pfizer, Novartis, Takeda, Boehringer Ingelheim, Janssen Oncology; Financial Interests, Personal, Speaker’s Bureau: Roche, AstraZeneca, Bristol Myers Squibb, Pfizer, Novartis, Takeda, Boehringer Ingelheim, MSD Oncology, Sanofi/Aventis, Janssen Oncology, Amgen; Financial Interests, Personal, Other, Travel, Accommodations, Expenses: Roche/Genentech, MSD Oncology, Pfizer. A. Onn: Financial Interests, Personal, Speaker, Consultant, Advisor: Roche Israel, MSD Israel, Boehringer Ingelheim, and AstraZeneca. L. Charbonnier, C. Soufflet: Financial Interests, Personal, Full or part-time Employment: Sanofi. All other authors have declared no conflicts of interest.
Resources from the same session
1270P - Lazertinib for patients with NSCLC harboring uncommon EGFR mutations: A single-arm, phase II multi-center trial
Presenter: Sehhoon Park
Session: Poster session 05
1271P - Integrating machine learning prediction and causal inference analysis to unravel determinants of progression in EGFR-mutant, advanced NSCLC
Presenter: Hakan Bozcuk
Session: Poster session 05
1272P - Updated results from a first-in-human, phase I/II study of GB263T, a novel EGFR/cMET/cMET tri-specific antibody, in patients with advanced EGFR-mutated (EGFRm) non-small cell lung cancer (NSCLC)
Presenter: Jin-Ji Yang
Session: Poster session 05
Resources:
Abstract
1274P - Osimertinib versus first/second generation tyrosine kinase inhibitors as first-line therapy for metastatic EGFR-mutated non-small cell lung carcinoma: Overall survival using real-world data from TriNetX platform
Presenter: Lisardo Ugidos De La Varga
Session: Poster session 05
1276P - EXcellenT (exercise in extended oncogene addicted lung cancer in active treatment) trial: Preliminary results on impact of physical activity (PA) on emotional, metabolic and immune status
Presenter: Chiara Bennati
Session: Poster session 05
1277P - Optimising targeted therapy in NSCLC: A comprehensive analysis of oncogenic fusion mutations and co-mutation landscapes
Presenter: Li Dongge
Session: Poster session 05
1278P - Update of the INSPIRE study: Iruplinalkib versus crizotinib in ALK TKI-naïve locally advanced or metastatic ALK+ non-small cell lung cancer (NSCLC)
Presenter: Yuan-Kai Shi
Session: Poster session 05
1279P - First-line lorlatinib vs crizotinib in Asian patients with ALK+ non-small cell lung cancer (NSCLC): 5-year outcomes from the CROWN study
Presenter: Yi-Long Wu
Session: Poster session 05
1280P - Effects of semaglutide on the exposure of alectinib in patients with NSCLC
Presenter: Daan Lanser
Session: Poster session 05