Department of Pathology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Department of Pathology, Qingpu Branch of Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Ann Thorac Surg. 2019 Feb;107(2):436-443. doi: 10.1016/j.athoracsur.2018.07.077. Epub 2018 Sep 28.
We investigated the frequency of c-MYC amplification in esophageal squamous cell carcinoma (ESCC), including both stage I to II and III to IVa disease, and evaluated the correlation of c-MYC amplification with clinicopathologic variables and outcome.
In 259 ESCCs resected at Zhongshan Hospital, Fudan University, from January 2007 to November 2010, c-MYC amplification was analyzed by using tissue microarray, with fluorescence in situ hybridization assay.
c-MYC gene amplification was found in 43.2% (112 of 259) of patients with ESCC. Significant differences were found between c-MYC amplification and patient age (p = 0.009) and lymph node metastasis (p = 0.046). The median follow-up period was 33 months (range: 4 to 102 months). A survival difference was found between patients with different c-MYC status. Among 112 patients with c-MYC amplification, a significantly poorer prognosis was observed, with a median disease-free survival (DFS) and overall survival (OS) of 24.0 and 31.0 months compared with 48.0 and 48.0 months, respectively, for patients without c-MYC amplification (p = 0.011 and 0.018). On univariate and multivariate analysis, site, clinical stage, lymph node metastasis, adjuvant therapy, and c-MYC amplification were associated with DFS and OS. When patients were divided into stage I to II and stage III to IV subgroups, c-MYC amplification tended to associate with poorer survival but without statistical difference (p > 0.05).
c-MYC amplification was associated with age and lymph node metastasis and was an independent poor-prognostic factor for DFS and OS in the full cohort of patients with ESCC.
我们研究了食管鳞状细胞癌(ESCC)中 c-MYC 扩增的频率,包括 I 期至 II 期和 III 期至 IVa 期疾病,并评估了 c-MYC 扩增与临床病理变量和结果的相关性。
在 2007 年 1 月至 2010 年 11 月期间,在复旦大学中山医院切除的 259 例 ESCC 中,使用组织微阵列和荧光原位杂交检测分析 c-MYC 扩增。
在 259 例 ESCC 患者中,发现 43.2%(112 例)的患者存在 c-MYC 基因扩增。c-MYC 扩增与患者年龄(p=0.009)和淋巴结转移(p=0.046)之间存在显著差异。中位随访时间为 33 个月(范围:4 至 102 个月)。不同 c-MYC 状态的患者生存存在差异。在 112 例 c-MYC 扩增患者中,观察到预后明显较差,无 c-MYC 扩增患者的中位无病生存(DFS)和总生存(OS)分别为 24.0 和 48.0 个月,而 c-MYC 扩增患者分别为 31.0 和 48.0 个月(p=0.011 和 0.018)。单因素和多因素分析显示,部位、临床分期、淋巴结转移、辅助治疗和 c-MYC 扩增与 DFS 和 OS 相关。当患者分为 I 期至 II 期和 III 期至 IVa 亚组时,c-MYC 扩增倾向于与较差的生存相关,但无统计学差异(p>0.05)。
c-MYC 扩增与年龄和淋巴结转移相关,是 ESCC 患者全队列 DFS 和 OS 的独立不良预后因素。