Yao Kenshi, Doyama Hisashi, Gotoda Takuji, Ishikawa Hideki, Nagahama Takashi, Yokoi Chizu, Oda Ichiro, Machida Hirohisa, Uchita Kunihisa, Tabuchi Masahiko
Department of Endoscopy, Central Research Institute for Endoscopy, Fukuoka University Chikushi Hospital, Fukuoka University, 1-1-1 Zokumyoin, Chikushino, Fukuoka, 818-8502, Japan,
Gastric Cancer. 2014 Oct;17(4):669-79. doi: 10.1007/s10120-013-0332-0. Epub 2014 Jan 10.
Curative treatment of patients with gastric cancer requires reliable detection of early gastric cancer. Magnifying endoscopy with narrow-band imaging (M-NBI) is useful for the accurate preoperative diagnosis of early gastric cancer. However, the role of M-NBI in screening endoscopy has not been established. The aims of this study were to determine the feasibility and limitations of M-NBI in screening endoscopy.
We conducted a multicenter prospective uncontrolled trial of patients undergoing routine screening endoscopy patients. We determined the diagnostic accuracy, sensitivity and specificity of M-NBI according to the degree of certainty and need for biopsy, as assessed using the VS (vessel plus surface) classification system. We analyzed the endoscopic and histopathological characteristics of both false negative and false positive high confidence M-NBI diagnoses. We then developed a provisional diagnostic strategy based on the diagnostic performance and limitations identified in this study.
A total of 1097 patients were enrolled in the study. We analyzed 371 detected lesions (20 cancers and 351 non-cancers). The accuracy, sensitivity and specificity of high confidence M-NBI diagnoses were 98.1, 85.7 and 99.4 %, respectively. The false negative case was a pale mucosal lesion with tissue diagnosis of signet-ring cell carcinoma. Exclusion of pale mucosal lesions increased the accuracy, sensitivity and specificity of high confidence M-NBI diagnoses to 99.4, 100 and 99.4 %, respectively. We therefore propose a practical strategy targeting non-pale mucosal lesions.
With a refined strategy considering its limitations, M-NBI can act as an "optical biopsy" in screening endoscopies.
胃癌患者的根治性治疗需要可靠地检测早期胃癌。窄带成像放大内镜检查(M-NBI)有助于早期胃癌的准确术前诊断。然而,M-NBI在筛查内镜检查中的作用尚未确立。本研究的目的是确定M-NBI在筛查内镜检查中的可行性和局限性。
我们对接受常规筛查内镜检查的患者进行了一项多中心前瞻性非对照试验。我们根据使用VS(血管加表面)分类系统评估的确定性程度和活检需求,确定了M-NBI的诊断准确性、敏感性和特异性。我们分析了M-NBI高置信度诊断的假阴性和假阳性病例的内镜和组织病理学特征。然后,我们根据本研究中确定的诊断性能和局限性制定了一种临时诊断策略。
共有1097例患者纳入本研究。我们分析了371个检测到的病变(20例癌症和351例非癌症)。M-NBI高置信度诊断的准确性、敏感性和特异性分别为98.1%、85.7%和99.4%。假阴性病例是一例苍白黏膜病变,组织诊断为印戒细胞癌。排除苍白黏膜病变后,M-NBI高置信度诊断的准确性、敏感性和特异性分别提高到99.4%、100%和99.4%。因此,我们提出了一种针对非苍白黏膜病变的实用策略。
通过考虑其局限性的优化策略,M-NBI可在筛查内镜检查中充当“光学活检”。