Abstract 1136P
Background
Cosibelimab is a high-affinity, fully human monoclonal antibody that directly binds to programmed death ligand-1 (PD-L1) and blocks its interaction with the programmed death receptor-1 (PD-1) and B7.1 receptors to restore an anti-tumor immune response. Cosibelimab also has a functional Fc domain capable of inducing antibody-dependent cell-mediated cytotoxicity (ADCC) as an additional mechanism of anti-tumor immunity. Efficacy and safety data from a pivotal study (NCT03212404) supported a biologics license application for cosibelimab for the treatment of patients (pts) with advanced CSCC (metastatic [mCSCC] or locally advanced [laCSCC]) who are not candidates for curative surgery or radiation. Here, we present new longer-term follow-up data from the pivotal study.
Methods
Pts with mCSCC (Group [Gp] 1) and laCSCC (Gp 2) were treated with cosibelimab 800 mg Q2W. The primary endpoint was objective response rate (ORR; complete response + partial response) by independent central review (ICR) assessed by Gp. The safety analysis included all CSCC pts treated with at least one dose and includes a third Gp of pts with mCSCC treated with cosibelimab 1200 mg Q3W (Gp 3).
Results
As of the 31 March 2023 data cutoff, 192 pts were enrolled and treated (78 in Gp 1, 58 in Gp 2 and 56 in Gp 3), and 109 pts were eligible for long-term efficacy assessment (78 in Gp 1 and 31 in Gp 2). With a median duration of follow-up of 29.3 months (range: 0.4-52.0) for Gp 1 and 24.1 months (range: 2.8-37.3) for Gp 2, ORR per ICR was 50.0% (95% CI: 38.5-61.5) and 54.8% (95% CI: 36.0-72.7), respectively. The complete response rate was 12.8% and 25.8% for Gp 1 and 2, respectively. Median duration of response has not been reached in either Gp, with a probably of maintaining response at 24 months of 72.1% and 80.2% for Gp 1 and 2, respectively. The most common adverse events (AEs) by any grade (Gr) were fatigue (22.9%), anemia (20.3%), constipation (16.1%) and diarrhea (15.1%); Gr ≥ 3 were anemia (5.2%) and lipase increased (3.1%). 3.6% of pts experienced a Gr 3 immune-related AE (no Gr ≥ 4).
Conclusions
Cosibelimab demonstrates robust objective response and complete response rates in advanced CSCC, with manageable safety and notable low rates of overall and severe immune-related AEs.
Clinical trial identification
NCT03212404.
Editorial acknowledgement
Legal entity responsible for the study
Checkpoint Therapeutics, Inc.
Funding
Checkpoint Therapeutics, Inc.
Disclosure
E. Muñoz-Couselo: Financial Interests, Personal, Speaker, Consultant, Advisor: Merck Sharp & Dohme, BMS, Novartis, Pierre Fabre, Sanofi; Financial Interests, Personal, Advisory Role: Immunocore, Regeneron, Menarini, Roche; Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics; Non-Financial Interests, Personal, Leadership Role: Gem, Grupo Español De Melanoma, Seom, Sociedad Española De Oncologia Medica. H. Montaudie: Financial Interests, Personal, Speaker, Consultant, Advisor: Merck Sharp & Dohme, BMS, Pierre Fabre; Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics, Inc. M.A. Berciano Guerrero: Financial Interests, Personal, Speaker, Consultant, Advisor: Merck Sharp & Dohme, BMS, Eisai, Pierre Fabre, Eli Lilly, Novartis, PharmaMar; Financial Interests, Institutional, Research Funding: Novartis; Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics. M.D.C. Alamo De La Gala, J. Charles, H. Shue, A. Tazbirkova, P. Clingan: Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics, Inc. G. Quereux: Financial Interests, Personal, Speaker, Consultant, Advisor: Sanofi; Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics, Inc. C. Nardin: Financial Interests, Personal, Speaker, Consultant, Advisor: Merck Sharp & Dohme; Financial Interests, Personal, Advisory Board: Regeneron; Financial Interests, Personal, Speaker, Consultant, Advisor, Board, consulting: BMS; Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics, Inc. R. Yaya Tur: Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics, Inc. S. Dalle: Financial Interests, Institutional, Advisory Board: MSD, BMS; Financial Interests, Personal, Stocks/Shares, Spouse Sanofi employee and stock owner: Sanofi; Financial Interests, Institutional, Research Grant: BMS, MSD, AstraZeneca. M. Beylot-Barry: Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics, Inc. R. Ladwa: Financial Interests, Personal, Advisory Role, Speaker fees, advisory role/ consultancy: Merck Sharp & Dohme; Financial Interests, Personal, Advisory Role, Speaker fees, advisory role: Sanofi; Financial Interests, Personal, Advisory Role: AstraZeneca; Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics, Inc; Financial Interests, Institutional, Other, Investigator initiated research: Merck Sharp & Dohme. M. McGrath: Financial Interests, Personal, Advisory Role, Speaker fee, advisory role: Merck Sharp & Dohme; Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics, Inc. D. Brungs: Financial Interests, Personal, Advisory Board, Honoraria: Merck Sharp & Dohme; Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics, Inc. D. Harris: Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics, Inc; Non-Financial Interests, Personal, Member: ASCO, AGITG, NZSO. S.J. Fourie: Financial Interests, Personal, Speaker, Consultant, Advisor, Speaker Honoraria: Merck Sharp & Dohme, Roche, Sanofi, MundiPharma; Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics; Financial Interests, Personal, Member of Board of Directors: ICON Oncology Holdings Pty(Ltd), Gamma Knife South Africa; Financial Interests, Personal, Member of Board of Directors, Board member and equity interest: Drs Alberts Bouwer Jordaan Inc. D.R. Malan: Financial Interests, Personal, Member of Board of Directors: Phoenix Pharma; Financial Interests, Institutional, Principal Investigator: Checkpoint Therapeutics, Inc. J. Oliviero: Financial Interests, Personal, Officer, Officer and ownership interest: Checkpoint Therapeutics, Inc.
Resources from the same session
1121P - Artificial Intelligence to predict BRAF mutational status from whole slide images in melanoma
Presenter: Céline Bossard
Session: Poster session 04
1122P - The role of imaging during follow-up after radical surgery of stage IIb-c and III cutaneous malignant melanoma: Survival results from an interim analysis of a randomized prospective multicenter study (TRIM)
Presenter: Cecilia Ladjevardi
Session: Poster session 04
1123P - Melanoma incidence and mortality decline in younger adults in Sweden: Start of a shift in the upgoing trend?
Presenter: Hildur Helgadottir
Session: Poster session 04
1124P - Adjuvant treatment of patients with stage III melanoma: 4-year follow-up time of multicenter real-world study
Presenter: Elisabeth Livingstone
Session: Poster session 04
1125P - Accuracy of PET-CT to assess extent of nodal disease in clinical stage III melanoma
Presenter: Ronen Stoff
Session: Poster session 04
1126P - A phase II study of nivolumab/relatlimab in metastatic uveal melanoma
Presenter: Jose Lutzky
Session: Poster session 04
1127P - Subgroup analysis of FOCUS phase III trial efficacy results
Presenter: Matthew Wheater
Session: Poster session 04
1128P - Preliminary results of first-in-human study of 225-Actinium MTI-201 (225Ac-MTI-201) in metastatic uveal melanoma
Presenter: Nikhil Khushalani
Session: Poster session 04
1129P - Clinical outcomes from a tebentafusp UK expanded access program in patients with metastatic uveal melanoma (mUM)
Presenter: Paul Nathan
Session: Poster session 04
1130P - Phase II trial on nivolumab plus radiotherapy in patients with metastatic mucosal melanoma: PORTER-M3 trial
Presenter: Motoo Nomura
Session: Poster session 04