Abstract 1134P
Background
Avelumab, an anti–PD-L1 antibody, was approved worldwide for the treatment of mMCC based on results from the JAVELIN Merkel 200 phase 2 trial (NCT02155647). In patients treated with first-line (1L) avelumab, 1-, 2- and 4-year overall survival (OS) rates were 60%, 49%, and 38%, respectively. In patients treated with second-line or later (2L+) avelumab, 1-, 2- and 5-year OS rates were 50%, 36%, and 26%, respectively. We report the probability of additional OS and safety in patients treated with avelumab for ≥1 or ≥2 years.
Methods
Eligible patients had histologically confirmed stage IV MCC and no prior systemic therapy for metastatic disease (1L cohort; part B) or disease progression following ≥1 prior line of chemotherapy (2L+ cohort; part A). Patients received avelumab every 2 weeks until confirmed disease progression, unacceptable toxicity, or withdrawal of consent.
Results
In 116 and 88 patients who received 1L or 2L+ avelumab, treatment duration was ≥1 year in 40 (34.5%) and 23 (26.1%), and ≥2 years in 22 (19.0%) and 13 (14.8%), respectively. Compared with the overall population, a higher proportion of patients with ≥2 years of treatment had an ECOG performance status of 0 (1L, 72.7% vs 62.1%; 2L+, 69.2% vs 55.7%) or PD-L1+ tumors (1L, 27.3 % vs 18.1%; 2L+, 76.9% vs 64.8%). In patients who received ≥1 year of treatment, the probability of surviving for an additional 1, 2, or 3 years, respectively, was 97.4%, 89.5%, and 75.2% in the 1L cohort, and 87.0%, 78.3%, and 69.6% in the 2L+ cohort. In patients who received ≥2 years of treatment, the probability of surviving for an additional 1 or 2 years, respectively, was 100% and 81.0% in the 1L cohort, and 92.3% and 84.6% in the 2L+ cohort. Among patients in both cohorts who were still receiving treatment, treatment-related adverse events of any grade or grade ≥3 occurred after 1 year in 74.6% and 19.0%, and after 2 years in 45.7% and 5.7%, respectively.
Conclusions
Patients with mMCC who received ≥1 or ≥2 years of avelumab treatment had a high probability of surviving for an additional ≥2 years. Long-term safety was consistent with previous analyses. These results further support avelumab as a standard of care for patients with mMCC.
Clinical trial identification
NCT02155647; June 4, 2014.
Editorial acknowledgement
Medical writing support was provided by Sophie Saunders of Nucleus Global.
Legal entity responsible for the study
Merck.
Funding
This study was sponsored by Merck (CrossRef Funder ID: 10.13039/100009945).
Disclosure
C. Lebbe: Financial Interests, Personal, Other, Honoraria: Amgen; Financial Interests, Personal, Advisory Board, Honoraria: Bristol Myers Squibb, Incyte, MSD, Novartis, Pfizer, Pierre Fabre, Roche; Financial Interests, Personal, Speaker, Consultant, Advisor: Amgen, Bristol Myers Squibb, MSD, Novartis, Roche; Financial Interests, Personal, Speaker’s Bureau: Amgen, Bristol Myers Squibb, Novartis, Roche; Financial Interests, Personal and Institutional, Research Funding: Bristol Myers Squibb, Roche; Financial Interests, Personal, Other, travel and accommodation expenses: Bristol Myers Squibb; Financial Interests, Personal, Other: Avantis Medical Systems. P. Nghiem: Financial Interests, Personal, Speaker, Consultant, Advisor: Almirall, Instil Bio, Merck, Pfizer, Rain Oncology. S. Bhatia: Financial Interests, Personal and Institutional, Research Funding: 4SC, Amphivena, Bristol Myers Squibb, Checkmate, Regeneron, Exicure, Incyte, Merck, MSD, Novartis, Nektar, OncoSec, Agenus; Financial Interests, Personal, Research Funding: Xencor; Financial Interests, Personal, Speaker, Consultant, Advisor: Bristol Myers Squibb, Incyte, Regeneron. L. Mortier: Financial Interests, Personal, Other, travel and accommodation: Bristol Myers Squibb, Novartis, Roche/Genentech. A.S. Brohl: Financial Interests, Personal, Speaker, Consultant, Advisor: Deciphera, Bayer. N. Jacob: Financial Interests, Personal, Full or part-time Employment: Merck. K. Tyroller: Financial Interests, Personal, Full or part-time Employment: EMD Serono Research & Development Institute, Inc, Billerica, MA, USA; Financial Interests, Personal, Stocks or ownership: Merck. J. Hoffman: Financial Interests, Personal, Full or part-time Employment: EMD Serono Research & Development Institute, Inc, Billerica, MA, USA; Financial Interests, Personal, Stocks or ownership: MSD, Pfizer, Merck. S.P. D'Angelo: Financial Interests, Personal, Speaker, Consultant, Advisor: Amgen, Merck, GSK, Immune Design, Incyte, MSD, Nektar; Financial Interests, Personal and Institutional, Research Grant: Amgen, Bristol Myers Squibb, Deciphera, Merck, Incyte, MSD, Nektar; Financial Interests, Personal, Other, travel and accommodation: Adaptimmune, Merck, Nektar.
Resources from the same session
1111P - Genomic and transcriptomic analysis of Japanese melanoma reveals candidate biomarkers for immune checkpoint inhibitor responders
Presenter: Toshihiro Kimura
Session: Poster session 04
1112P - Immunotherapy after progression to double immunotherapy: Pembrolizumab and Lenvatinib versus conventional chemotherapy for patients with metastatic melanoma after failure of PD-1/CTLA-4 inhibition
Presenter: Dimitrios Ziogas
Session: Poster session 04
1113P - A machine learning model based on computed tomography radiomics to predict prognosis in subjects with stage IV melanoma
Presenter: Maria Teresa Maccallini
Session: Poster session 04
1114P - Deciphering unresectable in-transit metastasis in melanoma: Multi-modal and longitudinal insights
Presenter: Giuseppe Tarantino
Session: Poster session 04
1115P - Multiomics clustering of patients with cutaneous melanoma to reveal survival trends based on tumor immune evasion features
Presenter: Adeliya Leleytner
Session: Poster session 04
1116P - Application of the Scottish inflammatory prognostic score to the south-east Scotland cancer network real-world melanoma cohort
Presenter: Karim El-Shakankery
Session: Poster session 04
1117P - Intratumoral microbiota is associated with prognosis in Chinese patients with skin melanoma
Presenter: Hang Jiang
Session: Poster session 04
1118P - Immunological alterations during neoadjuvant BRAF/MEK inhibition in patients with prior unresectable regionally advanced melanoma: Translational analysis from the REDUCTOR trial
Presenter: Femke Burgers
Session: Poster session 04
1119P - Genomic and transcriptomic predictors of resistance to anti-PD1 monotherapy in patients with advanced melanoma
Presenter: Wenya Wang
Session: Poster session 04
1120P - Tumoral and peripheral immunophenotype of patients with stage II/III melanoma undergoing adjuvant immunotherapy following tumor resection
Presenter: Maria Ascierto
Session: Poster session 04