Jiao Xiaolong, Eslami Afshin, Ioffe Olga, Kwong King F, Henry Michael, Zeng Qingling, Refaely Yael, Burrows Whitney, Gamliel Ziv, Krasna Mark J
Division of Thoracic Surgery, Department of Pathology, University of Maryland School of Medicine, Maryland, Baltimore 21201, USA.
Ann Thorac Surg. 2003 Oct;76(4):996-9; discussion 999-1000. doi: 10.1016/s0003-4975(03)00658-1.
With recent advances in neoadjuvant therapy in esophageal cancer, pretreatment lymph node staging has become increasingly important in stratifying patients to appropriate treatment regimens and for prognostication. Immunohistochemical analysis (IHC) using epithelial markers has been shown to identify micrometastases in histologically negative lymph nodes. We performed this study to evaluate if IHC analysis in thoracoscopic/laparoscopic (Ts/Ls) pretreatment staging lymph nodes can reveal additional diagnostic information to routine histopathology.
Specimens of 106 patients with esophageal cancer who had pretreatment Ts/Ls staging were retrospectively studied. Lymph node biopsies were obtained for IHC staining using cytokeratin (CK) of AE1/AE3. IHC staining for p53, an apoptosis protein associated with poor prognosis in esophageal cancer, was also performed.
331 Ts/Ls staging lymph node biopsies were collected from 106 patients. A total of 15.4% (51/331) of the lymph nodes or 34.9% (37/106) of patients were found to have metastatic deposits by routine histology. All the histologically positive lymph nodes were CK positive. Among the remaining 280 histologically negative lymph nodes, 11(3.9%) were found to have micrometastasis by CK staining. Three patients (4.3%, 3/69) were upstaged from N0 to N1. They died of early recurrences after treatment. A total of 67.6% (25/37) of the patients with histologically positive lymph node were p53 positive. No histologically negative lymph node was found to be p53 positive in this series.
Immunohistochemical analysis for CK can detect micrometastatic involvement of lymph nodes that are missed on routine pathologic examination, and, therefore, can improve lymph node staging. Its clinical significance in esophageal cancer warrants further study.
随着食管癌新辅助治疗的近期进展,治疗前淋巴结分期在将患者分层至合适的治疗方案以及预后判断方面变得越来越重要。使用上皮标志物的免疫组织化学分析(IHC)已被证明可识别组织学阴性淋巴结中的微转移。我们进行本研究以评估在胸腔镜/腹腔镜(Ts/Ls)治疗前分期淋巴结中进行IHC分析是否能揭示比常规组织病理学更多的诊断信息。
对106例接受治疗前Ts/Ls分期的食管癌患者的标本进行回顾性研究。获取淋巴结活检组织,使用AE1/AE3细胞角蛋白(CK)进行IHC染色。还对与食管癌预后不良相关的凋亡蛋白p53进行IHC染色。
从106例患者中收集了331份Ts/Ls分期淋巴结活检组织。通过常规组织学发现,共有15.4%(51/331)的淋巴结或34.9%(37/106)的患者有转移灶。所有组织学阳性的淋巴结CK均为阳性。在其余280个组织学阴性的淋巴结中,通过CK染色发现11个(3.9%)有微转移。3例患者(4.3%,3/69)从N0期上调至N1期。他们在治疗后死于早期复发。组织学阳性淋巴结的患者中共有67.6%(25/37)p53阳性。在本系列中未发现组织学阴性的淋巴结p53阳性。
CK免疫组织化学分析可检测到常规病理检查遗漏的淋巴结微转移累及情况,因此可改善淋巴结分期。其在食管癌中的临床意义值得进一步研究。