Project Description

Oral Abstract Presentation
Selected by the 2020 Annual Meeting Scientific Program Committee
Type: Oral Abstract Presentation
Presenter: Axel Hauschild
Presented: May 29, 2020
Abstract ref: 10001
Subtitles/Captions:

Authors: Axel Hauschild, Reinhard Dummer, Mario Santinami, Victoria Atkinson, Mario Mandalà, John M. Kirkwood, Vanna Chiarion Sileni, James M. G. Larkin, Marta Nyakas, Caroline Dutriaux, Andrew Mark Haydon, Caroline Robert, Laurent Mortier, Jacob Schachter, Kohinoor Dasgupta, Eduard Gasal, Monique Tan, Georgina V. Long, Dirk Schadendorf; University Hospital Schleswig-Holstein, Kiel, Germany; University Hospital Zürich Skin Cancer Center, Zürich, Switzerland; Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy; Princess Alexandra Hospital, Gallipoli Medical Research Foundation, University of Queensland, Greenslopes, QLD, Australia; Papa Giovanni XXIII Cancer Center Hospital, Bergamo, Italy; Melanoma Program, UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA; Melanoma Oncology Unit, Veneto Oncology Institute-IRCCS, Padua, Italy; Royal Marsden NHS Foundation Trust, London, United Kingdom; Oslo University Hospital, The Norwegian Radium Hospital, Oslo, Norway; Centre Hospitalier Universitaire de Bordeaux, Hôpital Saint-André, Bordeaux, France; The Alfred Hospital, Melbourne, VIC, Australia; Gustave Roussy and Paris-Sud-Paris-Saclay University, Villejuif, France; Université de Lille, INSERM U 1189, Lille, France; Ella Lemelbaum Institute for Immuno-Oncology and Melanoma, Sheba Medical Center, Tel Hashomer, and Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel; Novartis Healthcare Pvt Ltd, Hyderabad, India; Novartis Pharmaceuticals Corporation, East Hanover, NJ; Melanoma Institute Australia, The University of Sydney, and Royal North Shore and Mater Hospitals, Sydney, NSW, Australia; University Hospital Essen, Essen, and German Cancer Consortium, Heidelberg, Germany

Abstract Disclosures

Research Funding: Novartis Pharmaceuticals Corporation

Background: Previous results of the COMBI-AD trial (NCT01682083) showed a significant relapse-free survival (RFS) benefit with 12 mo of adjuvant D+T vs placebo (PBO) in pts with high-risk resected stage III BRAF V600E/K–mutant melanoma. In the primary analysis, 3-year RFS rates with D+T vs PBO were 58% vs 39% (hazard ratio [HR], 0.47 [95% CI, 0.39-0.58]; P< .001). An interim analysis of overall survival (OS) yielded 3-year OS rates of 86% with D+T vs 77% with PBO (HR, 0.57 [95% CI, 0.42-0.79]). Here we report data from 5-year analyses including long-term RFS and an updated cure rate model.

Methods: COMBI-AD is a randomized, Phase III trial evaluating 12 mo of adjuvant D 150 mg twice daily + T 2 mg once daily vs 2 matched PBOs in pts with resected stage III BRAF V600E/K–mutant melanoma. Pts were stratified by BRAF status and disease stage (per AJCC 7 criteria). The primary endpoint is RFS; secondary endpoints include OS and distant metastasis–free survival (DMFS). A Weibull mixture cure rate model was applied to estimate the fraction of pts who will remain relapse free in the long term. As all patients had completed treatment by the time of the primary analysis, updated safety analyses were not performed.

Results: This analysis represents a median follow-up of 60 mo for the D+T arm and 59 mo for the PBO arm. As of the data cutoff (Nov 8, 2019), 190 of 438 pts in the D+T arm and 262 of 432 pts in the PBO arm had an RFS event. Median RFS was not reached (NR; 95% CI, 47.9 mo-NR) with D+T vs 16.6 mo (95% CI, 12.7-22.1 mo) with PBO (HR, 0.51 [95% CI, 0.42-0.61]). The 4- and 5-year RFS rates were 55% (95% CI, 50%-60%) and 52% (95% CI, 48%-58%) with D+T vs 38% (95% CI, 34%-43%) and 36% (95% CI, 32%-41%) with PBO. These findings match those estimated by the cure rate model. The RFS benefit with D+T was evident across all AJCC 7 substages (HR [95% CI]: IIIA, 0.61 [0.35-1.07]; IIIB, 0.50 [0.37-0.67]; IIIC, 0.48 [0.36-0.64]). Median DMFS was NR in either arm but favored D+T (HR, 0.55 [95% CI, 0.44-0.70]). OS was not updated at this data cutoff as the prespecified number of events for the final OS analysis had not yet occurred.

Conclusions: This 5-year analysis confirms the long-term benefit of adjuvant D+T in pts with resected stage III BRAF V600E/K–mutant melanoma. Clinical trial information: NCT01682083

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Oral Abstract Presentation
Selected by the 2020 Annual Meeting Scientific Program Committee
Type: Oral Abstract Presentation
Presenter: Axel Hauschild
Presented: May 29, 2020
Abstract ref: 10001
Subtitles/Captions: