Li Yong-Jiang, Dai Yi-Ling, Zhang Wen-Biao, Li Shuang-Jiang, Tu Chong-Qi
Department of Orthopedics, West China Hospital, Sichuan University, No. 37 Guoxuexiang, Chengdu, 610041, People's Republic of China.
College of Computer Science, Sichuan Normal University, Chengdu, 610068, People's Republic of China.
Clin Exp Med. 2017 Feb;17(1):59-69. doi: 10.1007/s10238-015-0405-y. Epub 2015 Dec 17.
The prognostic significance of CXC chemokine receptor 4 (CXCR4) in patients with bone and soft tissue sarcomas remains controversial. To investigate the impact of its expression on survival and clinicopathological features, we performed a meta-analysis. Comprehensive literature searches were conducted in PubMed, Web of Science, Embase and Cochrane Library for relevant studies. In total, 12 studies with 997 sarcoma patients were included. CXCR4 expression was found to be significantly associated with poor overall survival (HR 2.37, 95 % CI 1.86-3.01; P < 0.001). Further, when the analysis was stratified by histological subtypes (bony sarcoma including osteosarcoma and Ewing sarcoma and soft tissue sarcoma including synovial sarcoma and rhabdomyosarcoma), statistical analysis method (multivariate analysis and univariate analysis) and CXCR4 measuring method (IHC or RT-PCR), the significant correlation to poor overall survival was also observed except for that in Ewing sarcoma and RT-PCR groups. As for clinicopathological features, CXCR4 expression was significantly associated with higher rate of metastasis (OR 6.97, 95 % CI 2.28-21.31; P = 0.001) and higher tumor stage (OR 7.55, 95 % CI 1.25-45.47; P = 0.027), but not associated with gender, age and tumor site. In conclusion, CXCR4 expression may be an effective predictive factor of poor prognosis and clinicopathological features for bone and soft tissue sarcomas. Further studies are needed to validate our findings.
CXC趋化因子受体4(CXCR4)在骨肉瘤和软组织肉瘤患者中的预后意义仍存在争议。为了研究其表达对生存及临床病理特征的影响,我们进行了一项荟萃分析。在PubMed、Web of Science、Embase和Cochrane图书馆中进行了全面的文献检索以查找相关研究。总共纳入了12项研究,涉及997例肉瘤患者。发现CXCR4表达与总体生存率低显著相关(风险比2.37,95%置信区间1.86 - 3.01;P < 0.001)。此外,当按组织学亚型(骨肉瘤包括骨肉瘤和尤因肉瘤,软组织肉瘤包括滑膜肉瘤和横纹肌肉瘤)、统计分析方法(多变量分析和单变量分析)以及CXCR4测量方法(免疫组化或逆转录聚合酶链反应)进行分层分析时,除了在尤因肉瘤组和逆转录聚合酶链反应组外,也观察到与总体生存率低存在显著相关性。至于临床病理特征,CXCR4表达与转移率较高(比值比6.97,95%置信区间2.28 - 21.31;P = 0.001)和肿瘤分期较高(比值比7.55,95%置信区间1.25 - 45.47;P = 0.027)显著相关,但与性别、年龄和肿瘤部位无关。总之,CXCR4表达可能是骨肉瘤和软组织肉瘤预后不良及临床病理特征的有效预测因素。需要进一步研究来验证我们的发现。