Abstract 1146P
Background
Retifanlimab, a programmed death receptor-1 (PD-1)–blocking antibody, was recently approved in the United States for treatment of adult patients (pts) with metastatic or recurrent locally advanced MCC based on results from the open-label, single-arm POD1UM-201 study (NCT03599713). In the primary analysis including 65 chemotherapy-naive pts, responses were observed in 52% (95% CI: 40–65) of pts with 62% of responses exceeding 12 months by landmark analysis (ZYNYZTM prescribing information). Safety was as expected for the PD-(L)1 inhibitor class. We present updated results on the full cohort of 101 pts.
Methods
Eligible pts were ≥18 years of age, had metastatic or recurrent unresectable loco-regional MCC, Eastern Cooperative Oncology Group (ECOG) performance status ≤1, measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1, and had not received prior MCC systemic treatment. Retifanlimab 500 mg was administered intravenously every 4 weeks (Q4W) for up to 2 years without premedication prophylaxis. The primary endpoint was overall response rate assessed by independent central review per RECIST v1.1. Secondary endpoints included duration of response, disease control rate, progression-free survival, overall survival, safety, and pharmacokinetics.
Results
The study enrolled 101 pts with chemotherapy-naive advanced/metastatic MCC, with the last pt initiating treatment on 24 June 2021. Pt and disease characteristics were representative of the typical MCC epidemiology. The median age was 71 (range, 38–90) years, 68 (67%) pts were male and predominantly white, 74 (73%) had an ECOG of 0, and one pt was HIV positive. A total of 91 (90%) pts had Stage IV disease, 69 (68%) had prior surgery, and 37 (37%) had prior radiotherapy. In evaluable tumour samples, Merkel cell polyomavirus was detectable in 73/96 (76%) and 83/95 (87%) had PD-L1 expression ≥1%. Efficacy and safety results for the full study population will be presented.
Conclusions
Retifanlimab has shown notable clinical activity with an acceptable safety in advanced/metastatic chemotherapy-naive MCC, and is a promising new treatment option for eligible pts.
Clinical trial identification
NCT03599713, EudraCT 2018-001627-39.
Editorial acknowledgement
Envision Pharma Group (Philadelphia, PA), funded by Incyte Corporation (Wilmington, DE).
Legal entity responsible for the study
Incyte Corporation (Wilmington, DE).
Funding
Incyte Corporation, Wilmington, DE.
Disclosure
G. Grignani: Financial Interests, Institutional, Other, Honoraria: Bayer, Eisai, Eli Lilly and Company, Merck, Novartis, Pfizer, PharmaMar; Financial Interests, Institutional, Advisory Role: Bayer, Eisai, Eli Lilly and Company, Novartis, Pfizer, PharmaMar; Financial Interests, Institutional, Research Grant: Bayer, Novartis, PharmaMar. P. Rutkowski: Financial Interests, Institutional, Advisory Board, Honoraria: AstraZeneca Blueprint Medicines, Bristol Meyers Squibb, Merck Serono, MSD, Novartis, Philogen, Pierre Fabre, Sanofi; Financial Interests, Institutional, Other, Institutional support: Pfizer. C. Lebbe: Financial Interests, Personal, Advisory Board: Bristol Myers Squibb, MSD, Novartis, Amgen, Roche, Merck Serono, Sanofi, Pierre Fabre; Financial Interests, Personal, Funding: Roche, Bristol Myers Squibb; Non-Financial Interests, Advisory Role: Bristol Myers Squibb, MSD, Novartis, Amgen, Roche, Merck Serono, Sanofi, Pierre Fabre; Other, Honoraria, Speaker's Bureau, Research funding: Roche; Other, Honoraria, Speaker's bureau, Travel, Accommodation, Expenses, Research funding, Board: Bristol Myers Squibb; Other, Honoraria, Speaker's bureau, Travel, Accommodations, Expenses, Board: Novartis, MSD; Other, Honoraria, Speaker's bureau: Amgen; Other, Honoraria, Travel, Accommodations, Expenses, Board: Pierre Fabre; Other, Honoraria: Pfizer; Other, Honoraria: Incyte; Other, Travel, accommodations, Expenses, Board: Sanofi; Other, Board: Avantis Medical Systems, Jazz Pharmaceuticals; Other, Participation on a Data Safety Monitoring Board or Advisory Board: InflaRx. M. Guida: Financial Interests, Institutional, Advisory Role: Bristol Myers Squibb, MSD, Novartis, Pierre Fabre. C. Gaudy Marqueste: Financial Interests, Institutional, Advisory Board, Honoraria: Bristol Myers Squibb, MSD, Pierre Fabre; Financial Interests, Institutional, Other, Participated in clinical trials and Travel grants: Bristol Myers Squibb, MSD, Pierre Fabre; Financial Interests, Institutional, Other, Participated in clinical trials: GSK, Huyabioscience, Incyte, Merck Serono, Novartis, Regeneron, Replimune, Kartos. F.G.M. De Braud: Financial Interests, Institutional, Advisory Role: Roche, EMD Serono, NMS Nerviano Medical Science, Sanofi, MSD, Incyte, Bristol Myers Squibb, Menarini, AstraZeneca, Pierre Fabre, Mattiolo 1885 , MCCann Health, Taiho; Financial Interests, Institutional, Speaker’s Bureau: Bristol Myers Squibb, Healthcare Research & Pharmacoepidemiology, Merck, MSD, Pfizer, Servier, Sanofi, Roche, Amgen, Incyte, Dephaforum, Seagen, Nadirex, Ambrosetti, Itanet; Financial Interests, Funding, Research: Novartis, Hoffmann LaRoche Ltd., Bristol Myers Squibb, Ignyta Operating INC, Kymab, Pfizer, Tesaro, MSD, MedImmune LCC, Exelixis Inc., Loxo Oncology Incorporated, Daiichi Sankyo Dev. Limited, Basilea Pharmaceutica International AG, Janssen Cilag International NV, Merck KGaA, IQVIA. F. Spagnolo: Financial Interests, Institutional, Advisory Board: Bristol Myers Squibb, Merck, MSD, Novartis, Pierre Fabre, Philogen, Sanofi, Sun Pharma. M. Burgess: Financial Interests, Institutional, Funding, Research: Merck; Financial Interests, Institutional, Advisory Board: EMD Serono, Immune Design, SpringWorks Therapeutics. H. Montaudie: Financial Interests, Institutional, Other, Honoraria: Bristol Myers Squibb, Merck Serono, MSD, Novartis, Pierre Fabre; Financial Interests, Institutional, Other, Institutional support: Bristol Myers Squibb, Leo Pharma; Financial Interests, Institutional, Other, Participated in clinical trials: Bristol Myers Squibb, Checkpoint Therapeutics, Huyabioscience, Incyte, Merck Serono, MSD, Nektar Pharmaceuticals, Novartis, Pierre Fabre, Regeneron, Replimune; Financial Interests, Institutional, Other, Travel grant: Bristol Myers Squibb, Pierre Fabre, Novartis. R. Depenni: Financial Interests, Institutional, Advisory Board: Bristol Myers Squibb, MSD, Novartis, Pierre Fabre, Sanofi. F. Spada: Financial Interests, Institutional, Other, Honoraria for lectures and/or advisory boards and/or manuscript writing: Advanced Accelerator Application, Ipsen, Merck/MSD, Novartis, Pfizer; Financial Interests, Institutional, Invited Speaker, Institutional support: GETNE, Hutchmed, Incyte Corporation. J. Pulini, M. Cornfeld, C. Tian: Financial Interests, Institutional, Full or part-time Employment: Incyte; Financial Interests, Institutional, Stocks/Shares: Incyte. S. Bhatia: Financial Interests, Institutional, Advisory Board: Bristol Myers Squibb, Castle Biosciences, EMD Serono, Exicure, Genentech, Incyte, Sanofi-Genzyme; Financial Interests, Institutional, Research Grant: 4SC, Amphivena Therapeutics, Bristol Myers Squibb, Checkmate, EMD Serono, Immune Design, Incyte Biosciences, Merck, NantKwest, Nektar, Novartis, OncoSec, Regeneron, Xencor; Financial Interests, Institutional, Stocks/Shares: Moderna.
Resources from the same session
1171P - Evaluation of the transcriptomic presence of tumor associated antigens (TAAs) from antibody drug conjugates (ADCs) and PD-L1 in melanoma: Options for new clinical opportunities
Presenter: Jorge Bartolome
Session: Poster session 13
1172P - Analysis of the microbiome of metastatic melanoma patients with complete response to immunotherapy
Presenter: Marin Golcic
Session: Poster session 13
1173P - NRAS mutation as an independent prognostic factor for resectable Chinese acral melanoma
Presenter: Yu Xu
Session: Poster session 13
1174P - Sex differences in advanced melanoma in Spain: Results from the prospective real-world study GEM 1801
Presenter: Eva Muñoz Couselo
Session: Poster session 13
1175P - Return to work after neoadjuvant versus adjuvant immunotherapy in stage III melanoma patients
Presenter: Judith Lijnsvelt
Session: Poster session 13
1176P - Planned drug holidays during immunotherapy in advanced and metastatic melanoma patients: A nation-wide study
Presenter: Anna Czarnecka
Session: Poster session 13
1177P - Assessment of tumour burden reduction per photography vs magnetic resonance imaging in patients with locally advanced basal cell carcinoma receiving sonidegib 200 mg
Presenter: Ralf Gutzmer
Session: Poster session 13
1178P - Melanoma incidence rises for pediatrics: 15-year nationwide retrospective cohort study in Korea (2004-2019)
Presenter: Jisu Oh
Session: Poster session 13
1179P - The underestimated skin cancer risk after liver transplantation: A meta-analysis of 147154 patients
Presenter: Amr Ehab El-Qushayri
Session: Poster session 13