Department of Gastroenterology, Qilu Hospital, Shandong University, Jinan, China.
Department of Gastroenterology, Union Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Endoscopy. 2017 Nov;49(11):1033-1042. doi: 10.1055/s-0043-115382. Epub 2017 Jul 28.
Owing to the indistinctive endoscopic appearance of gastric intestinal metaplasia (GIM), gastric intraepithelial neoplasia (GIN), and early gastric cancer (EGC), a significant number of such lesions may be missed during surveillance endoscopy. The aim of this clinical trial was to assess the value of combined computed virtual chromoendoscopy (flexible spectral imaging color enhancement [FICE]) and probe-based confocal laser endomicroscopy (pCLE) for in vivo detection of GIM, GIN, and EGC. This was a multicenter, randomized controlled trial performed in 238 patients at four tertiary centers. Patients were randomized to FICE-guided pCLE with targeted biopsies (group A) or FICE with standard biopsies (group B). The diagnostic yield of GIM, GIN, or EGC was compared between the two groups. On a per-patient assessment, the diagnostic yield for GIM/GIN/EGC was 73.3 % (88/120) in group A and 63.6 % (75/118) in group B ( = 0.09). On a per-biopsy analysis, FICE-guided pCLE with targeted biopsies significantly increased the diagnostic yield of GIM/GIN/EGC vs. FICE with standard biopsies, from 31.5 % (252/800) to 75.1 % (313/417) ( < 0.001). In addition, pCLE-guided targeted biopsies led to a significant 48.5 % decrease in the number of biopsies per patient vs. FICE with standard biopsies ( < 0.001). Real-time pCLE and targeted biopsies after FICE improved the diagnostic yield for the detection of GIM, GIN, and EGC, and only required about half the number of biopsies vs. FICE with standard biopsies. This may allow a better regimen for endoscopic surveillance and subsequent treatment of patients with premalignant and malignant gastric abnormalities.Trial registered at ClinicalTrials.gov (NCT02515721).
由于胃黏膜肠上皮化生(GIM)、胃上皮内瘤变(GIN)和早期胃癌(EGC)的内镜表现不明显,在监测内镜检查中,大量此类病变可能会被遗漏。本临床试验旨在评估联合计算机虚拟染色内镜(flexible spectral imaging color enhancement [FICE])和探针式共聚焦激光内镜检查(pCLE)在体内检测 GIM、GIN 和 EGC 的价值。这是一项在四个三级中心的 238 例患者中进行的多中心、随机对照试验。患者被随机分为 FICE 引导下靶向活检的 pCLE 组(A 组)或 FICE 标准活检组(B 组)。比较两组 GIM、GIN 或 EGC 的诊断率。在每位患者的评估中,A 组 GIM/GIN/EGC 的诊断率为 73.3%(88/120),B 组为 63.6%(75/118)( = 0.09)。在每次活检分析中,与 FICE 标准活检相比,FICE 引导下靶向活检显著提高了 GIM/GIN/EGC 的诊断率,从 31.5%(252/800)提高到 75.1%(313/417)( < 0.001)。此外,与 FICE 标准活检相比,pCLE 引导下靶向活检使每位患者的活检次数显著减少 48.5%( < 0.001)。实时 pCLE 和 FICE 后靶向活检提高了 GIM、GIN 和 EGC 的诊断率,且与 FICE 标准活检相比,仅需要大约一半的活检次数。这可能为监测和随后治疗有癌前和恶性胃异常的患者提供更好的方案。试验在 ClinicalTrials.gov(NCT02515721)注册。