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

Authors
 Chang Gon Kim  ;  Miso Kim  ;  Jieon Hwang  ;  Seung Tae Kim  ;  Minkyu Jung  ;  Kyoo Hyun Kim  ;  Kyung Hwan Kim  ;  Jee Suk Chang  ;  Woong Sub Koom  ;  Mi Ryung Roh  ;  Kee Yang Chung  ;  Tae Min Kim  ;  Sang Kyum Kim  ;  Jeeyun Lee  ;  Sang Joon Shin 
Citation
 JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, Vol.87(5) : 989-996, 2022-11 
Journal Title
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
ISSN
 0190-9622 
Issue Date
2022-11
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 ; Melanoma* / genetics ; Melanoma* / 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 ; Skin Neoplasms* / genetics ; Skin Neoplasms* / pathology
Keywords
BRAF V600–mutant advanced melanoma ; dabrafenib/trametinib ; first-line treatment ; pembrolizumab
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.
Full Text
https://www.sciencedirect.com/science/article/pii/S0190962222024434?via%3Dihub
DOI
10.1016/j.jaad.2022.07.057
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Dermatology (피부과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers
Yonsei Authors
Koom, Woong Sub(금웅섭) ORCID logo https://orcid.org/0000-0002-9435-7750
Kim, Kyung Hwan(김경환)
Kim, Kyoo Hyun(김규현)
Kim, Sang Kyum(김상겸) ORCID logo https://orcid.org/0000-0003-0768-9923
Roh, Mi Ryung(노미령) ORCID logo https://orcid.org/0000-0002-6285-2490
Shin, Sang Joon(신상준) ORCID logo https://orcid.org/0000-0001-5350-7241
Chang, Jee Suk(장지석) ORCID logo https://orcid.org/0000-0001-7685-3382
Chung, Kee Yang(정기양) ORCID logo https://orcid.org/0000-0003-3257-0297
Jung, Min Kyu(정민규) ORCID logo https://orcid.org/0000-0001-8281-3387
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/192325
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