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J Am Acad Dermatol. 2022;87(5):989-996.

First-line pembrolizumab versus dabrafenib/trametinib treatment for BRAF V600-mutant advanced melanoma.

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제1저자 김창곤, 김미소, 황지언 · 교신저자 신상준, 이지연, 김상겸

PMID 36068115 DOI 10.1016/j.jaad.2022.07.057 IF 12.3 혈액종양내과
소속 (10)
  1. Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
  2. Department of Internal Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.
  3. 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.
  4. Division of Haematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
  5. Department of Radiation Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
  6. Department of Dermatology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
  7. Department of Dermatology, Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
  8. Department of Pathology, Yonsei University College of Medicine, Seoul, Republic of Korea. Electronic address: nicekyumi@yuhs.ac.
  9. Division of Haematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea. Electronic address: jyunlee@skku.edu.
  10. 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