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.
J Am Acad Dermatol. 2022 Nov;87(5):989-996. doi: 10.1016/j.jaad.2022.07.057. Epub 2022 Sep 6.
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.
To investigate the outcomes associated with first-line pembrolizumab or dabrafenib/trametinib treatment for advanced melanoma with activating BRAF V600 mutation.
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.
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.
Analysis was conducted in a retrospective manner.
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.
目前可用的数据有限,无法协助选择免疫检查点抑制剂和 BRAF/丝裂原活化蛋白激酶激酶抑制剂作为 BRAF 突变型晚期恶性黑色素瘤患者的一线治疗。
探讨一线帕博利珠单抗或达拉非尼/曲美替尼治疗 BRAF V600 突变型晚期黑色素瘤的结局。
分析接受一线帕博利珠单抗(n=40)或达拉非尼/曲美替尼(n=32)治疗的 BRAF V600 突变黑色素瘤患者的数据。评估肿瘤反应、无进展生存期和总生存期。评估伴随 BRAF/丝裂原活化蛋白激酶激酶抑制剂出现的耐药而出现的免疫逃逸。
与一线达拉非尼/曲美替尼治疗相比,一线帕博利珠单抗治疗后患者的总生存期更长(风险比=2.910,95%CI:1.552-5.459),尽管无进展生存期(P=.375)和反应率(P=.123)无显著差异。达拉非尼/曲美替尼耐药的出现伴随着免疫逃逸,使黑色素瘤细胞能够逃避 Melan-A 特异性 CD8 T 细胞的识别和杀伤。
分析是回顾性进行的。
在晚期 BRAF V600 突变黑色素瘤患者中,帕博利珠单抗可能优于 BRAF/丝裂原活化蛋白激酶激酶抑制剂,作为一线治疗药物。