Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
British Columbia Cancer Agency, Vancouver, BC, Canada.
Eur Urol Focus. 2018 Sep;4(5):733-736. doi: 10.1016/j.euf.2016.08.001. Epub 2016 Aug 27.
In men with advanced penile squamous cell carcinoma receiving first-line chemotherapy, visceral metastases (VM) and Eastern Cooperative Oncology Group performance status ≥1 are poor prognostic factors for overall survival (OS). We hypothesized that tumor gene expression profiling may enhance prognostic stratification and identify potential therapeutic targets. In this retrospective study, RNA extracted from macrodissected tumors underwent profiling for the expression of 738 genes using NanoString. Univariate and multivariate analyses assessed the association of genes, VM, and performance status with OS. Tumors were available from 25 men who received first-line cisplatin-based chemotherapy. In univariate analysis, upregulated MAML2 (p=0.004), KITLG (p≤0.0001), and JAK1 (p=0.029) genes were associated with poor OS, and upregulated FANCA was associated with better OS (p=0.024). In stepwise multivariate analyses, VM (hazard ratio=12.75, p=0.0001) and MAML2 (hazard ratio=10.411, p=0.003) were associated with poor OS. The presence of none, one, and both of these poor risk factors was associated with significantly different median OS of 18.4 mo, 7.2 mo, and 2.1 mo, respectively. Unsupervised clustering demonstrated two major molecular subtypes with trend for different survivals (p=0.052). Validation of results is necessary. PATIENT SUMMARY: The expression of the MAML2 gene in penile cancers from men receiving first-line cisplatin-based chemotherapy predicted overall survival independent of clinical factors.
在接受一线化疗的晚期阴茎鳞状细胞癌男性患者中,内脏转移 (VM) 和东部肿瘤协作组体能状态≥1 是总生存期 (OS) 的不良预后因素。我们假设肿瘤基因表达谱可能增强预后分层,并确定潜在的治疗靶点。在这项回顾性研究中,从宏观解剖的肿瘤中提取的 RNA 使用 NanoString 进行了 738 个基因的表达谱分析。单因素和多因素分析评估了基因、VM 和体能状态与 OS 的关联。25 名接受一线顺铂为基础化疗的男性患者的肿瘤标本可用。在单因素分析中,上调的 MAML2(p=0.004)、KITLG(p≤0.0001)和 JAK1(p=0.029)基因与较差的 OS 相关,而上调的 FANCA 与较好的 OS 相关(p=0.024)。在逐步多因素分析中,VM(风险比=12.75,p=0.0001)和 MAML2(风险比=10.411,p=0.003)与较差的 OS 相关。这些不良风险因素中无、一和两者均存在的患者的中位 OS 分别显著不同,为 18.4 个月、7.2 个月和 2.1 个月。无监督聚类显示出两种主要的分子亚型,具有不同生存趋势(p=0.052)。需要进一步验证结果。患者总结:在接受一线顺铂为基础化疗的男性阴茎癌患者中,MAML2 基因的表达独立于临床因素预测总生存期。