Sato Yusuke, Motoyama Satoru, Nanjo Hiroshi, Wakita Akiyuki, Yoshino Kei, Sasaki Tomohiko, Nagaki Yushi, Liu Jiajia, Imai Kazuhiro, Saito Hajime, Minamiya Yoshihiro
Department of Thoracic Surgery, Akita University Graduate School of Medicine, Akita, Japan.
Department of Pathology, Akita University Graduate School of Medicine, Akita, Japan.
Ann Surg Oncol. 2016 Mar;23(3):936-42. doi: 10.1245/s10434-015-4909-1. Epub 2015 Oct 13.
CXCL10, a member of the CXC chemokine family, is known to mediate chemotaxis, apoptosis, angiogenesis, and cell growth. It is also reportedly involved in tumor development and can affect prognosis in several cancers. However, the precise relationship between CXCL10 and the prognosis of patients with esophageal squamous cell carcinoma (ESCC) is not fully understood.
We used ESCC tissue microarrays containing samples from 177 patients to test whether the CXCL10 expression status, determined using immunohistochemical analysis, is predictive of prognosis. We also tested whether CXCL10 expression status could serve as a clinically useful marker for evaluating the need for adjuvant chemotherapy after surgery.
We found that high CXCL10 expression in clinical samples was an independent prognostic factor and was predictive of a favorable 5-year overall survival and disease-specific survival (p = 0.0102 and 0.0332, respectively). Additionally, no significant difference was detected between patients in the CXCL10-high group treated with surgery alone and those treated with surgery followed by adjuvant chemotherapy. In the CXCL10-low group, on the other hand, patients treated with surgery followed by adjuvant chemotherapy had better 5-year overall survival than those treated with surgery alone.
High CXCL10 expression is an independent prognostic factor and has the potential to serve as a clinically useful marker of the need for adjuvant chemotherapy after surgery in patients with advanced thoracic ESCC.
CXCL10是CXC趋化因子家族的成员,已知其介导趋化作用、细胞凋亡、血管生成和细胞生长。据报道,它还参与肿瘤发展,并可影响多种癌症的预后。然而,CXCL10与食管鳞状细胞癌(ESCC)患者预后的确切关系尚未完全明确。
我们使用包含177例患者样本的ESCC组织微阵列,以检测通过免疫组织化学分析确定的CXCL10表达状态是否可预测预后。我们还检测了CXCL10表达状态是否可作为评估术后辅助化疗必要性的临床有用标志物。
我们发现临床样本中CXCL10高表达是一个独立的预后因素,可预测5年总生存率和疾病特异性生存率良好(分别为p = 0.0102和0.0332)。此外,单纯手术治疗的CXCL10高表达组患者与手术联合辅助化疗的患者之间未检测到显著差异。另一方面,在CXCL10低表达组中,手术联合辅助化疗的患者5年总生存率优于单纯手术治疗的患者。
CXCL10高表达是一个独立的预后因素,有可能作为晚期胸段ESCC患者术后辅助化疗必要性的临床有用标志物。