Long-Term Follow-Up of Real-World Adjuvant Anti–PD-1 Checkpoint Inhibition and Targeted Therapy in Patients With Stage III Melanoma
Abstract
PURPOSE Adjuvant treatment with immune checkpoint inhibition (PD-1) and targeted therapy (TT) with BRAF + MEK inhibitors significantly improved recurrence-free survival (RFS) of patients with stage III melanoma. We investigated efficacy of adjuvant therapy with PD-1 or TT under real-world conditions. MATERIALS AND METHODS A total of 589 patients with stage III melanoma who started adjuvant PD-1 or TT between June 2018 and September 2019 from 11 major German Dermatologic Cooperative Oncology Group skin cancer centers were followed for 4 years. End points were RFS, overall survival (OS), and melanoma-specific survival. Survival analyses and adjusted hazard ratios (HRs) were estimated with Kaplan-Meier and Cox proportional hazards model, inverse probability treatment weighting, and propensity score matching. RESULTS RFS at 48 months was 42.9% (95% CI, 38.5 to 47.8) for all PD-1 patients and 52.6% (95% CI, 43.6 to 63.3) for TT patients. Among patients with BRAF mutation, rate of recurrence was higher for PD-1 compared with TT (HR, 1.57 [95% CI, 1.09 to 2.26]). OS at 4 years was 80.8% (95% CI, 73.6 to 88.7) for PD-1–treated patients with BRAF mutation and 87.3% (95% CI, 81.0 to 94.0) for TT patients. Patients starting adjuvant PD-1 after resection of macroscopic lymph node metastases had a higher risk of rapid recurrence (1-year RFS all PD-1 58%) compared with 87% in TT patients. Rate of recurrence after premature discontinuation (≤6 v >6 months treatment) was higher in TT patients (HR, 1.47 [95% CI, 0.67 to 3.23]), but not in PD-1 patients (HR, 1.07 [95% CI, 0.73 to 1.55]). CONCLUSION PD-1–treated patients with BRAF mutation had a markedly higher rate of relapse compared with TT patients. Rapid recurrences occurred particularly in PD-1–treated patients with previous macroscopic lymph node metastasis. Treatment duration shorter than 6 months did not negatively affect RFS in PD-1, but in TT patients.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (27)
Georg C. Lodde
Department of Dermatology, Venereology and Allergology, University Hospital Essen, Essen, Germany
Jessica C. Hassel
Imke von Wasielewski
Department of Dermatology and Allergy, Skin Cancer Center Hannover, Hannover Medical School, Hannover, Germany
Friedegund Meier
Peter Mohr
Elbe Klinikum Buxtehude, Buxtehude, Germany
Katharina Kähler
Department of Dermatology, Venereology and Allergology, University Hospital Kiel, Kiel, Germany
Axel Hauschild
Department of Dermatology, University Hospital, Kiel, Germany
Valerie Glutsch
Department of Dermatology, Venereology and Allergology, University Hospital Wuerzburg, Wuerzburg, Germany
Henner Stege
Carola Berking
Svea Hüning
Department of Dermatology, Klinikum Dortmund gGmbH, Dortmund, Germany
Julia Huynh
Department of Dermatology, University Hospital Tuebingen, Tuebingen, Germany
Ralf Gutzmer
Department of Dermatology, Johannes Wesling Medical Center, Ruhr University, Minden, Germany
Lydia Reinhardt
Skin Cancer Center at the University Cancer Centre Dresden and National Center for Tumor Diseases, Dresden, Germany
Bastian Schilling
Carmen Loquai
Department of Dermatology, University Hospital Mainz, Mainz, Germany
Michael Erdmann
Department of Dermatology, Uniklinikum Erlangen, Friedrich Alexander University
Andreas Stang
Bernd Kowall
Wolfgang Galetzka
Institute for Medical Informatics, Biometry and Epidemiology, University Hospital Essen, Essen, Germany
Alexander Roesch
Department of Dermatology, Venereology and Allergology, University Hospital Essen, Essen, Germany
Daniel Tilkorn
Department of Dermatology, Venereology and Allergology, University Hospital Essen, Essen, Germany
Selma Ugurel
Lisa Zimmer
Dirk Schadendorf
Andrea Forschner
Elisabeth Livingstone
Department of Dermatology, Venereology and Allergology, University Hospital Essen, Essen, Germany