Liang Yao, Maeda Osamu, Nishida Kazuki, Chretien Basile, Ando Yuichi
Department of Clinical Oncology and Chemotherapy, Nagoya University Hospital, Nagoya, Japan.
Department of Advanced Medicine, Nagoya University Hospital, Nagoya, Japan.
Cancer Sci. 2025 Apr;116(4):1107-1114. doi: 10.1111/cas.16338. Epub 2025 Jan 29.
The use of immune checkpoint inhibitors (ICIs) for treating melanoma has dramatically improved patient prognosis. The genomic profiles of patients receiving ICI therapy would provide valuable information for disease management and treatment. We investigated the genomic profiles of patients with melanoma who had received ICI therapy and explored associations with clinical features and outcomes via a large-scale nationwide database in Japan (the C-CAT database). We identified 339 patients eligible for this study. The most frequent genetic mutations were found in the BRAF (27%), TERT (24%), and NRAS (19%) genes, and the most common copy number variations (CNVs) were in the CDKN2A (36%), CDKN2B (26%), and MTAP (19%) genes. Associations with high tumor mutational burden (TMB-high) status were significant for TERT (p < 0.001), NF1 (p < 0.001), ROS1 (p = 0.015), POLE (p = 0.045), and POLD1 (p = 0.008) mutations, along with older age (≥65 years, p = 0.036). Patients with multiple metastases (two or more) were more likely to have NOTCH3 mutations (p = 0.017) and be younger than 65 years (p = 0.024). In particular, as well as younger age, patients with brain metastases were more likely to harbor BRAF mutations (p < 0.001), while those with liver metastases were more likely to harbor NOTCH3 mutations (p < 0.001) but not CDKN2B CNVs (p = 0.041). Patients with NRAS mutations were less likely to respond to ICI therapy (p = 0.014) and exhibited shorter overall survival (p = 0.006). In this population, the frequency of BRAF mutations was lower than that in fair-skinned populations, but the associations between genomic profiles, clinical features, and outcomes were similar to those previously reported in fair-skinned populations.
使用免疫检查点抑制剂(ICI)治疗黑色素瘤显著改善了患者的预后。接受ICI治疗患者的基因组图谱将为疾病管理和治疗提供有价值的信息。我们通过日本一个大规模的全国性数据库(C-CAT数据库)研究了接受ICI治疗的黑色素瘤患者的基因组图谱,并探讨了其与临床特征和预后的关联。我们确定了339名符合本研究条件的患者。最常见的基因突变发生在BRAF(27%)、TERT(24%)和NRAS(19%)基因中,最常见的拷贝数变异(CNV)发生在CDKN2A(36%)、CDKN2B(26%)和MTAP(19%)基因中。TERT(p<0.001)、NF1(p<0.001)、ROS1(p = 0.015)、POLE(p = 0.045)和POLD1(p = 0.008)基因突变以及老年(≥65岁,p = 0.036)与高肿瘤突变负荷(TMB高)状态显著相关。有多处转移(两处或更多)的患者更可能有NOTCH3突变(p = 0.017)且年龄小于65岁(p = 0.024)。特别是,除了年龄较小外,有脑转移的患者更可能携带BRAF突变(p<0.001),而有肝转移的患者更可能携带NOTCH3突变(p<0.001)但不是CDKN2B CNV(p = 0.041)。NRAS突变的患者对ICI治疗反应的可能性较小(p = 0.014),且总生存期较短(p = 0.006)。在这一人群中,BRAF突变的频率低于白种人群,但基因组图谱、临床特征和预后之间的关联与先前白种人群中报道的相似。