Abstract 1102P
Background
Advances in the first-line treatment of metastatic melanoma raised the need for earlier assessment of clinical trials using intermediate endpoints that may reach statistical maturity sooner than overall survival (OS) without being influenced by subsequent treatments.
Methods
We evaluated progression-free survival (PFS), time-to-next-treatment-or-death (TNTD) and objective response rate (ORR) as potential surrogate endpoints (SEs) for OS within the phase II/III RELATIVITY-047 trial (n=714) using patient-level data with ≥21 months of follow-up. Individual-level (IL) correlations with OS were derived from copula functions and measured by Spearman’s (ρ) and Kendall’s (τ) rank correlation coefficients for PFS and TNTD, and by an odds ratio (OR) for ORR. Patients were clustered in 8 non-overlapping regions according to their country of enrolment for trial-level (TL) surrogacy assessment. Within each region treatment effects on PFS, TNTD and OS were calculated by Cox-proportional-hazards models. TL correlations between the SEs and OS were estimated by weighted linear regression and measured by coefficient of determination (R2). Sensitivity of the results were tested with respect to alternative geographic clustering.
Results
At the IL, ORR and TNTD were strongly correlated with OS, whereas PFS showed moderate correlation with OS. At the TL, PFS and ORR showed moderate correlation with OS with wide uncertainty whereas TNTD had strong correlation with OS with narrower margin of uncertainty. Alternative geographic clustering of patients had marginal impact on the IL (≤ 0.02 change in all measures for all SEs) and modest impact on TL correlations (≤ 0.08 change in R2 for all SEs). Table: 1102P
Correlation | IL | TL | |
ρ [95% CI] | τ [95% CI] | R2 [95% CI] | |
PFS - OS | 0.70 [0.68, 0.72] | 0.51 [0.45, 0.58] | 0.71 [0.35, 1.00] |
TNTD - OS | 0.84 [0.81, 0.86] | 0.66 [0.63, 0.69] | 0.95 [0.87, 1.00] |
ORR - OS | OR | ||
10.60 [6.77-14.43] | 0.64 [0.21, 1.00] |
Conclusions
Within the RELATIVITY-047 trial, TNTD-OS surrogacy was stronger and more stable than PFS-OS and ORR-OS surrogacy. The strength of each surrogacy relationship analyzed in this study and their relative order were consistent with those previously reported from other immune-checkpoint inhibitor studies.
Clinical trial identification
Phase II/III study: RELATIVITY-047 (CA224-047), NCT03470922.
Editorial acknowledgement
Writing of the abstract was led by Dr. Murat Kurt (co-author). All other co-authors provided comments on the abstract draft. Final version of the document was shaped by a consensus of all co-authors.
Legal entity responsible for the study
Bristol Myers Squibb.
Funding
Bristol Myers Squibb.
Disclosure
P. Mohr: Financial Interests, Personal, Advisory Board: Bristol Myers Squibb, Merck Sharp & Dohme, Novartis, GSK, Pierre Fabre, Sanofi; Financial Interests, Personal, Invited Speaker: Amgen, Bristol Myers Squibb, Merck Sharp & Dohme, Novartis, Roche, Pierre Fabre, Sanofi, Sun Pharma; Financial Interests, Institutional, Funding: Bristol Myers Squibb, Merck Sharp & Dohme, Novartis; Non-Financial Interests, Principal Investigator: Bristol Myers Squibb, Merck Sharp & Dohme, Regeneron, Sanofi, Novartis, Sun Pharma. P. Squifflet: Financial Interests, Institutional, Speaker, Consultant, Advisor, Pierre Fabre; Squifflet is an employee of IDDI and received consultancy fees from Bristol Myers Squibb through IDDI: Bristol Myers Squibb. E.D. Saad: Financial Interests, Institutional, Speaker, Consultant, Advisor, Everardo Saad is an employee of IDDI and received consultancy fees from Bristol Myers Squibb through IDDI: Bristol Myers Squibb. J. Larkin: Financial Interests, Personal, Invited Speaker: BMS, Pfizer, Roche, Pierre Fabre, AstraZeneca, Novartis, EUSA Pharma, MSD, Merck, GSK, Ipsen, Aptitude, Eisai, Calithera, Ultimovacs, Seagen, Goldman Sachs, eCancer, Inselgruppe, Agence Unik; Financial Interests, Personal, Other, Consultancy: Incyte, iOnctura, Apple Tree, Merck, BMS, Eisai, Debiopharm; Financial Interests, Personal, Other, Honorarium: touchIME, touchEXPERTS, VJOncology, RGCP, Cambridge Healthcare Research, Royal College of Physicians; Financial Interests, Institutional, Funding: BMS, MSD, Novartis, Pfizer, Achilles, Roche, Nektar, Covance, Immunocore, Pharmacyclics, Aveo. M. Kurt, A. Moshyk, F. Ejzykowicz: Financial Interests, Personal, Full or part-time Employment: Bristol Myers Squibb; Financial Interests, Personal, Stocks or ownership: Bristol Myers Squibb. M.E. Buyse: Financial Interests, Institutional, Speaker, Consultant, Advisor, Marc Buyse is an employee of IDDI and received consultancy fees from Bristol Myers Squib through IDDI: Bristol Myers Squibb.
Resources from the same session
1110P - A phase II clinical trial of SHR-1701 combined with temozolomide for advanced melanoma
Presenter: Tu Hu
Session: Poster session 13
1111P - A randomised phase II study of intermittent versus continuous dosing of targeted therapy in patients with BRAFV600 mutant advanced melanoma (INTERIM)
Presenter: Avinash Gupta
Session: Poster session 13
1112P - Five-year survival after intermittent targeted therapy and anti-PD1 in stage IV melanoma: An update of the IMPemBra trial
Presenter: Lotte Hoeijmakers
Session: Poster session 13
1113P - COLUMBUS 7-year update: A randomized, open-label, phase III trial of encorafenib (enco) + binimetinib (bini) vs vemurafenib (vemu) or enco in patients (pts) with BRAF V600–mutant melanoma
Presenter: Dirk Schadendorf
Session: Poster session 13
1114P - Encorafenib (E) plus binimetinib (B) in unresectable advanced or metastatic BRAFV600-mut melanoma, real-world evidence in Spain (GEM 2002 - BECARE)
Presenter: Ainara Soria Rivas
Session: Poster session 13
1115P - Comparison of efficacy and toxicity of dabrafenib/trametinib versus vemurafenib/cobimetinib therapy in routine medical practice: Eight years of BRAF/MEK inhibitor use in routine clinical practice
Presenter: Karolina Piejko
Session: Poster session 13
1116P - Long term outcome of complete responders to immune checkpoint inhibitors (ICI) or target therapy (TT) in advanced melanoma
Presenter: Celine Boutros
Session: Poster session 13
1117P - Overall survival (OS) in patients with metastatic BRAF V600-mutant melanoma treated with encorafenib plus binimetinib (ENCO+BINI): Comparing real-world vs clinical trial data
Presenter: Gino In
Session: Poster session 13
1118P - Real-world treatment patterns and outcomes among patients with BRAF+ metastatic melanoma refractory to first-line immunotherapy
Presenter: Thach-Giao Truong
Session: Poster session 13
1119P - Stage IIIA melanoma with isolated tumor cells in lymph nodes: Time for reviewing the AJCC v8 classification
Presenter: Teresa Amaral
Session: Poster session 13