J Am Acad Dermatol. 2022;87(5):989-996.
First-line pembrolizumab versus dabrafenib/trametinib treatment for BRAF V600-mutant advanced melanoma.
제1저자 김창곤, 김미소, 황지언 · 교신저자 신상준, 이지연, 김상겸
소속 (10)
- Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
- Department of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.
- Department of Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea; Songdang Institute for Cancer Research, Yonsei University College of Medicine, Seoul, Republic of Korea.
- Division of Haematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
- Department of Radiation Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
- Department of Dermatology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
- Department of Dermatology, Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
- Department of Pathology, Yonsei University College of Medicine, Seoul, Republic of Korea. Electronic address: nicekyumi@yuhs.ac.
- Division of Haematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea. Electronic address: jyunlee@skku.edu.
- Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea. Electronic address: ssj338@yuhs.ac.
Abstract
BACKGROUND Limited data are available to assist the selection between immune checkpoint inhibitors and BRAF/mitogen-activated protein kinase kinase inhibitors as first-line treatment for patients with BRAF-mutant advanced malignant melanoma.
OBJECTIVE To investigate the outcomes associated with first-line pembrolizumab or dabrafenib/trametinib treatment for advanced melanoma with activating BRAF V600 mutation.
METHODS Data of patients with BRAF V600-mutant melanoma who were treated with first-line pembrolizumab (n = 40) or dabrafenib/trametinib (n = 32) were analyzed. Tumor response, progression-free survival, and overall survival were evaluated. Immune evasion accompanied with emerging resistance to BRAF/mitogen-activated protein kinase kinase inhibitors was assessed.
RESULTS A longer overall survival was observed after first-line pembrolizumab treatment than after first-line dabrafenib/trametinib treatment (hazard ratio = 2.910, 95% CI: 1.552-5.459), although there were no significant differences in progression-free survival (P = .375) and response rate (P = .123). Emergence of resistance to dabrafenib/trametinib co-occurred with immune evasion, enabling melanoma cells to escape recognition and killing by Melan-A-specific CD8+ T cells.
LIMITATIONS Analysis was conducted in a retrospective manner.
CONCLUSION Pembrolizumab may be recommended over BRAF/mitogen-activated protein kinase kinase inhibitors as the first-line treatment in patients with advanced BRAF V600-mutant melanoma.
Copyright © 2022 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.
Keywords
BRAF V600–mutant advanced melanomadabrafenib/trametinibfirst-line treatmentpembrolizumab
Conflict of interest statement
Conflicts of interest None disclosed.
그 밖의 정보
- 출판 형태
- Journal Article, Research Support, Non-U.S. Gov't
- 저널
- Journal of the American Academy of Dermatology · eISSN 1097-6787
- 전자 출판
- 2022-09-06
- MeSH
- Antibodies, Monoclonal, Humanized · Antineoplastic Combined Chemotherapy Protocols / therapeutic use · CD8-Positive T-Lymphocytes / pathology · Humans · Imidazoles · Immune Checkpoint Inhibitors · MART-1 Antigen · Melanoma* / drug therapy / genetics / pathology · Mitogen-Activated Protein Kinase Kinases · Mutation · Oximes / therapeutic use · Protein Kinase Inhibitors / therapeutic use · Proto-Oncogene Proteins B-raf / genetics · Pyridones / adverse effects · Pyrimidinones · Retrospective Studies · Skin Neoplasms* / drug therapy / genetics / pathology
- Substances
- Antibodies, Monoclonal, Humanized · Imidazoles · Immune Checkpoint Inhibitors · MART-1 Antigen · Oximes · Protein Kinase Inhibitors · Pyridones · Pyrimidinones · trametinib · pembrolizumab · BRAF protein, human · Proto-Oncogene Proteins B-raf · Mitogen-Activated Protein Kinase Kinases · dabrafenib