Third Department of Internal Medicine, University of Toyama, Toyama, Japan; Department of Gastroenterology and Hepatology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.
Third Department of Internal Medicine, University of Toyama, Toyama, Japan.
Gastrointest Endosc. 2023 Jun;97(6):1092-1099. doi: 10.1016/j.gie.2023.01.037. Epub 2023 Jan 24.
A novel EUS-guided fine-needle biopsy sampling (EUS-FNB) needle enabled physicians to obtain sufficient pathologic samples with fewer to-and-fro movements (TAFs) within the lesion. We compared the diagnostic yields of EUS-FNB with 3 and 12 TAFs at each puncture pass.
The primary endpoint of this multicenter, noninferiority, crossover, randomized controlled trial involving 6 centers was diagnostic sensitivity. Secondary endpoints were diagnostic accuracy and quantity and quality evaluation of EUS-FNB specimens. Length of the macroscopically visible core (MVC) and microscopic histologic quantity were used for quantitative evaluation. Macroscopic visual and microscopic histologic evaluations were performed for qualitative evaluation.
Among 110 patients (220 punctures, 110 for 3 TAFs and 12 TAFs each), 105 (210 punctures) had malignant histology. Diagnostic sensitivity for malignancy of 3 TAFs (88.6%) was not inferior to that of 12 TAFs (89.5%; difference, -.9%; 95% confidence interval, -9.81 to 7.86). Diagnostic accuracy for malignancy was 92.7% for 3 TAFs and 94.6% for 12 TAFs. Overall median MVC length was 13.5 mm in both groups. The 3-TAF group had a significantly higher rate of score ≥3 on macroscopic visual quality evaluation than the 12-TAF group (71.8% vs 52.7%, P = .009). No significant intergroup differences existed in microscopic histologic quantity and quality evaluations (quantity evaluation, 88.2% for 3 TAFs vs 83.6% for 12 TAFs; quality evaluation, 90.0% for 3 TAFs vs 89.1% for 12 TAFs).
Diagnostic sensitivity and accuracy of EUS-FNB with 3 TAFs were not inferior to those with 12 TAFs for solid pancreatic lesions. The 3-TAF group showed significantly less blood contamination in sampled tissues than the 12-TAF group. (Clinical trial registration number: UMIN000037309.).
一种新型的超声内镜引导下细针活检采样(EUS-FNB)针能够让医生在病变部位内通过更少的来回穿刺获得足够的病理样本。我们比较了在每个穿刺过程中进行 3 次和 12 次来回穿刺的 EUS-FNB 的诊断效果。
这项涉及 6 个中心的多中心、非劣效性、交叉、随机对照试验的主要终点是诊断敏感性。次要终点是诊断准确性以及 EUS-FNB 标本的数量和质量评估。宏观可见核心(MVC)的长度和微观组织学数量用于定量评估,宏观视觉和微观组织学评估用于定性评估。
在 110 名患者(220 次穿刺,每次穿刺 3 次和 12 次)中,有 105 名(210 次穿刺)患者的组织学表现为恶性。3 次来回穿刺的恶性肿瘤诊断敏感性(88.6%)并不劣于 12 次来回穿刺(89.5%;差值,-0.9%;95%置信区间,-9.81 至 7.86)。恶性肿瘤的诊断准确率在 3 次来回穿刺组为 92.7%,在 12 次来回穿刺组为 94.6%。两组的总体中位数 MVC 长度均为 13.5 毫米。3 次来回穿刺组在宏观视觉质量评估中得分≥3 的比例明显高于 12 次来回穿刺组(71.8%比 52.7%,P=.009)。两组在微观组织学数量和质量评估方面无显著差异(数量评估,3 次来回穿刺组为 88.2%,12 次来回穿刺组为 83.6%;质量评估,3 次来回穿刺组为 90.0%,12 次来回穿刺组为 89.1%)。
对于实性胰腺病变,3 次来回穿刺的 EUS-FNB 诊断敏感性和准确性并不劣于 12 次来回穿刺。3 次来回穿刺组取样组织中的血液污染明显少于 12 次来回穿刺组。(临床试验注册号:UMIN000037309。)