Department of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, 200032, PR China; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, PR China.
Department of Otolaryngology-Head and Neck Surgery, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, 442000, PR China.
Int J Surg. 2018 Dec;60:257-265. doi: 10.1016/j.ijsu.2018.10.035. Epub 2018 Oct 31.
Extensive studies have been carried out to investigate the association between nm23 expression and the prognosis and clinicopathologic significance of various tumors.
Eligible studies were searched from Embase, China National Knowledge Infrastructure (CNKI), PubMed and Web of Science up to May 2017. In this study, we calculated the pooled hazard ratios (HRs) with 95% confidence intervals (95%CIs) to determine the association between nm23 expression and the prognosis of various tumors.
A total of 49 studies were finally included in the meta-analysis. The pooled HRs were 2.00 (95% CIs: 1.44-2.78) for overall survival (OS), 1.23 (95% CIs: 1.04-1.46) for disease-specific survival or progression-free survival (DFS/PFS), and 2.21 (95% CIs: 1.38-3.57) for survival of recurrence-free survival or metastasis-free survival (RFS/MFS). Moreover, the results indicated that low nm23 expression was significantly correlated with the lymph node metastasis (P = 0.002). For the subgroup analysis, the expression of nm23 in patients at N0 stage was obviously higher than the patients with breast carcinoma at N1-N3 stage [Odds ratio (OR) = 2.07, 95%CI (1.31, 3.26), P = 0.002]. Moreover, the expression of nm23 in the patients at N0 stage was remarkably higher than those at N1-N3 stages in the Chinese patients with breast carcinoma and those with nasopharyngeal carcinoma (P < 0.05). Whereas, no statistical difference was noticed in the expression of nm23 in patients of various age, gender, T stage, histological degree, TNM stage, respectively (P > 0.05).
Our study suggests that down-regulation of nm23 is related to poor prognosis in many cancers. The expression of nm23 in cancer tissues may serve as an important factor for evaluating the presence of lymph node metastasis.
大量研究已经探讨了 nm23 表达与各种肿瘤的预后和临床病理意义之间的关系。
从 Embase、中国知网(CNKI)、PubMed 和 Web of Science 中检索到 2017 年 5 月前符合条件的研究。在本研究中,我们计算了合并风险比(HR)及其 95%置信区间(95%CI),以确定 nm23 表达与各种肿瘤预后之间的关系。
共有 49 项研究最终纳入荟萃分析。汇总 HR 为总生存期(OS)2.00(95%CI:1.44-2.78),疾病特异性生存期或无进展生存期(DFS/PFS)为 1.23(95%CI:1.04-1.46),无复发生存期或无转移生存期(RFS/MFS)为 2.21(95%CI:1.38-3.57)。此外,结果表明低 nm23 表达与淋巴结转移显著相关(P=0.002)。亚组分析显示,N0 期患者 nm23 表达明显高于 N1-N3 期乳腺癌患者[优势比(OR)=2.07,95%CI(1.31,3.26),P=0.002]。此外,在中国乳腺癌患者和鼻咽癌患者中,N0 期患者的 nm23 表达明显高于 N1-N3 期患者(P<0.05)。然而,nm23 表达在不同年龄、性别、T 分期、组织学分级、TNM 分期的患者中无统计学差异(P>0.05)。
本研究表明,nm23 下调与许多癌症的不良预后有关。nm23 在肿瘤组织中的表达可能是评估淋巴结转移存在的一个重要因素。