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
1120P - Development and external validation of a clinical prediction model to predict recurrence-free survival and melanoma-specific survival in patients with melanoma after sentinel lymph node biopsy
Presenter: Robert Stassen
Session: Poster session 13
1121P - Interferon-gamma (IFNy) gene signature as a predictive biomarker for response in lactate dehydrogenase (LDH) low advanced melanoma patients
Presenter: Lotte Hoeijmakers
Session: Poster session 13
1122P - Neutrophil/lymphocyte ratio and systemic inflammatory index as prognostic biomarkers in metastatic melanoma patients under immune checkpoint inhibitors: Could any of them be used?
Presenter: Maria Menezes
Session: Poster session 13
1123P - Baseline tumor-infiltrating lymphocytes and response to immune checkpoint inhibition in advanced melanoma
Presenter: Mark Schuiveling
Session: Poster session 13
1124P - IL-6 as prognostic factor in adjuvant or metastatic skin cancer patients treated with immunotherapy: A deep biomarker analysis
Presenter: Domenico Mallardo
Session: Poster session 13
1125P - Identification of a subset of metastatic melanoma patients demonstrating germline determined insensitivity to immunotherapy
Presenter: Benjamin Fairfax
Session: Poster session 13
1126P - REtrospective Study of definitive therapy for head and neck mUcosal MElanoma: The RESUME study
Presenter: Motoo Nomura
Session: Poster session 13
1127P - Efficacy of immune checkpoint inhibitors (ICIs) in advanced mucosal melanoma (MM): A systematic review and meta-analysis
Presenter: James Pham
Session: Poster session 13
1128P - A phase I dose escalation and expansion study of FHD-286, a novel BRG1/BRM (SMARCA4/SMARCA2) inhibitor, for the treatment of metastatic uveal melanoma
Presenter: Sapna Patel
Session: Poster session 13
1129P - Effect of subsequent therapies including checkpoint inhibitors on overall survival in a phase III randomized trial of tebentafusp in first-line metastatic uveal melanoma: Long-term follow-up
Presenter: Marlana Orloff
Session: Poster session 13