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ARID2 突变可能与不同结局的特定亚组皮肤黑色素瘤患者相关。

ARID2 mutations may relay a distinct subset of cutaneous melanoma patients with different outcomes.

机构信息

Division of Medical Oncology, Department of Medicine, Washington University in Saint Louis, 4921 Parkview Place, Saint Louis, MO, 63110, USA.

Caris Life Sciences, Phoenix, AZ, USA.

出版信息

Sci Rep. 2024 Feb 11;14(1):3444. doi: 10.1038/s41598-024-54136-3.

Abstract

ARID genes encode subunits of SWI/SNF chromatin remodeling complexes and are frequently mutated in human cancers. We investigated the correlation between ARID mutations, molecular features, and clinical outcomes in melanoma patients. Cutaneous melanoma samples (n = 1577) were analyzed by next-generation sequencing. Samples were stratified by pathogenic/likely pathogenic mutation in ARID genes (ARID1A/2/1B/5B). PD-L1 expression was assessed using IHC (SP142; positive (+): ≥ 1%). Tumor mutation burden (TMB)-high was defined as ≥ 10 mutations/Mb. Transcriptomic signatures predictive of response to immune checkpoint inhibitors-interferon gamma and T-cell inflamed score were calculated. Real-world overall survival (OS) information was obtained from insurance claims data, with Kaplan-Meier estimates calculated from time of tissue collection until last date of contact. Mann-Whitney U, Chi-square, and Fisher exact tests were applied where appropriate, with p values adjusted for multiple comparisons. ARID2 mutations were more prevalent in cutaneous melanoma compared to ARID1A (11.0%: n = 451 vs 2.8%: n = 113), with concurrent ARID1A/ARID2 mutation in 1.1% (n = 46) of samples. ARID mutations were associated with a high prevalence of RAS pathway mutations-NF1 (ARID1A, 52.6%; ARID2, 48.5%; ARID1A/2, 63.6%; and ARID-WT, 13.3%; p < 0.0001) and KRAS (ARID1A, 3.5%; ARID2, 3.1%; ARID1A/2, 6.5%; and ARID-WT, 1.0%; p = 0.018)), although BRAF mutations were less common in ARID-mutated cohorts (ARID1A, 31.9%; ARID2, 35.6%; ARID1A/2, 26.1%; and ARID-WT, 50.4%; p < 0.0001). TMB-high was more common in ARID-mutated samples (ARID1A, 80.9%; ARID2, 89.9%; ARID1A/2, 100%; and ARID-WT, 49.4%; p < 0.0001), while PD-L1 positivity was similar across subgroups (ARID1A, 43.8%; ARID2, 51.1%; ARID1A/2, 52.5%; and ARID-WT, 44.9%; p = 0.109). Patients with ARID1A mutations had a higher prevalence of dMMR/MSI-H compared to those with ARID-WT (2.7% vs 0.2%, p = 0.030). Median IFN-γ and T-cell signatures were higher in ARID2-mutated samples compared to ARID-WT (IFN-γ: - 0.15 vs - 0.21, p = 0.0066; T-cell: 23.5 vs - 18.5, p = 0.041). ARID2-mutated patients had improved survival compared to ARID-WT; (HR: 1.22 (95% CI 1.0-1.5), p = 0.022). No additional OS benefit was observed with anti-PD-1 therapy for ARID2 mutation compared to ARID-WT. Melanoma patients with ARID mutations exhibited higher prevalence of markers associated with ICI response, including TMB-H, and immune-related signatures. Our data also suggests improved survival outcome in patients with ARID2 mutations, irrespective of anti-PD1 therapy.

摘要

ARID 基因编码 SWI/SNF 染色质重塑复合物的亚基,并且在人类癌症中经常发生突变。我们研究了 ARID 突变、分子特征与黑色素瘤患者临床结局之间的相关性。通过下一代测序分析了 1577 例皮肤黑色素瘤样本。根据 ARID 基因(ARID1A/2/1B/5B)的致病性/可能致病性突变对样本进行分层。使用 IHC(SP142;阳性(+):≥1%)评估 PD-L1 表达。肿瘤突变负担(TMB)高定义为≥10 个突变/Mb。计算了预测对免疫检查点抑制剂-干扰素 γ和 T 细胞炎症评分反应的转录组学特征。从保险索赔数据中获得了真实世界的总生存(OS)信息,从组织采集时间到最后联系日期计算 Kaplan-Meier 估计值。在适当的情况下应用 Mann-Whitney U、卡方和 Fisher 精确检验,p 值调整了多重比较。与 ARID1A(2.8%:n=113)相比,ARID2 突变在皮肤黑色素瘤中更为常见(11.0%:n=451),同时存在 ARID1A/ARID2 突变的比例为 1.1%(n=46)。ARID 突变与 RAS 通路突变-NF1 的高发生率相关(ARID1A,52.6%;ARID2,48.5%;ARID1A/2,63.6%;和 ARID-WT,13.3%;p<0.0001)和 KRAS(ARID1A,3.5%;ARID2,3.1%;ARID1A/2,6.5%;和 ARID-WT,1.0%;p=0.018),尽管 ARID 突变患者的 BRAF 突变较少(ARID1A,31.9%;ARID2,35.6%;ARID1A/2,26.1%;和 ARID-WT,50.4%;p<0.0001)。TMB 高在 ARID 突变样本中更为常见(ARID1A,80.9%;ARID2,89.9%;ARID1A/2,100%;和 ARID-WT,49.4%;p<0.0001),而 PD-L1 阳性率在亚组间相似(ARID1A,43.8%;ARID2,51.1%;ARID1A/2,52.5%;和 ARID-WT,44.9%;p=0.109)。与 ARID-WT 相比,ARID1A 突变患者的 dMMR/MSI-H 发生率更高(2.7%比 0.2%,p=0.030)。与 ARID-WT 相比,ARID2 突变样本的 IFN-γ和 T 细胞特征中位数更高(IFN-γ:-0.15 比-0.21,p=0.0066;T 细胞:23.5 比-18.5,p=0.041)。与 ARID-WT 相比,ARID2 突变患者的生存时间更长(HR:1.22(95%CI 1.0-1.5),p=0.022)。与 ARID-WT 相比,ARID2 突变患者接受抗 PD-1 治疗并未获得额外的 OS 获益。ARID 突变的黑色素瘤患者表现出更高的与 ICI 反应相关的标志物发生率,包括 TMB-H 和免疫相关特征。我们的数据还表明,无论是否接受抗 PD1 治疗,ARID2 突变患者的生存结局都有所改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08d2/10858967/f4d770e206f9/41598_2024_54136_Fig1_HTML.jpg

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