University of California, Los Angeles, Los Angeles, California; Liver and Pancreatobiliary Disease Research Center, Digestive Disease Research Institute, Tehran University of Medical Science, Tehran, Iran.
Washington University School of Medicine, St. Louis, Missouri.
Clin Gastroenterol Hepatol. 2017 Jul;15(7):1071-1078.e2. doi: 10.1016/j.cgh.2016.12.018. Epub 2016 Dec 23.
BACKGROUND & AIMS: It is not clear exactly how many passes are required to determine whether pancreatic masses are malignant using endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA). We aimed to define the per-pass diagnostic yield of EUS-FNA for establishing the malignancy of a pancreatic mass, and identify factors associated with detection of malignancies.
In a prospective study, 239 patients with solid pancreatic masses were randomly assigned to groups that underwent EUS-FNA, with the number of passes determined by an on-site cytopathology evaluation or set at 7 passes, at 3 tertiary referral centers. A final diagnosis of pancreatic malignancy was made based on findings from cytology, surgery, or a follow-up evaluation at least 1 year after EUS-FNA. The cumulative sensitivity of detection of malignancy by EUS-FNA was calculated after each pass; in the primary analysis, lesions categorized as malignant or suspicious were considered as positive findings.
Pancreatic malignancies were found in 202 patients (84.5% of the study population). EUS-FNA detected malignancies with 96% sensitivity (95% confidence interval [CI], 92%-98%); 4 passes of EUS-FNA detected malignancies with 92% sensitivity (95% CI, 87%-95%). Tumor size greater than 2 cm was the only variable associated with positive results from cytology analysis (odds ratio, 7.8; 95% CI, 1.9-31.6). In masses larger than 2 cm, 4 passes of EUS-FNA detected malignancies with 93% sensitivity (95% CI, 89%-96%) and in masses ≤2 cm, 6 passes was associated with 82% sensitivity (95% CI, 61%-93%). Sensitivity of detection did not increase with increasing number of passes.
In a prospective study, we found 4 passes of EUS-FNA to be sufficient to detect malignant pancreatic masses; increasing the number of passes did not increase the sensitivity of detection. Tumor size greater than 2 cm was associated with malignancy, and a greater number of passes may be required to evaluate masses 2 cm or less. ClinicalTrials.gov number, NCT01386931.
目前尚不清楚使用内镜超声引导下细针抽吸术(EUS-FNA)确定胰腺肿块是否为恶性时需要进行多少次穿刺。本研究旨在明确 EUS-FNA 单次穿刺的诊断效能,以确定胰腺肿块的恶性程度,并确定与恶性肿瘤检出相关的因素。
在一项前瞻性研究中,239 例胰腺实性肿块患者被随机分为两组,分别在 3 家三级转诊中心接受 EUS-FNA,其中一组的穿刺次数由现场细胞病理学评估决定,另一组则设定为 7 次。根据细胞学、手术或 EUS-FNA 后至少 1 年的随访评估结果,确定胰腺恶性肿瘤的最终诊断。在每次穿刺后计算 EUS-FNA 检测恶性肿瘤的累积敏感性;在主要分析中,将归类为恶性或可疑的病变视为阳性结果。
202 例患者(研究人群的 84.5%)中发现了胰腺恶性肿瘤。EUS-FNA 检测恶性肿瘤的敏感性为 96%(95%CI,92%-98%);4 次 EUS-FNA 穿刺检测恶性肿瘤的敏感性为 92%(95%CI,87%-95%)。肿瘤直径大于 2cm 是与细胞学分析阳性结果相关的唯一变量(比值比,7.8;95%CI,1.9-31.6)。在直径大于 2cm 的肿块中,4 次 EUS-FNA 穿刺检测恶性肿瘤的敏感性为 93%(95%CI,89%-96%),而在直径≤2cm 的肿块中,6 次穿刺的敏感性为 82%(95%CI,61%-93%)。检测敏感性并未随穿刺次数的增加而提高。
在一项前瞻性研究中,我们发现 4 次 EUS-FNA 足以检测胰腺恶性肿块;增加穿刺次数并不能提高检测的敏感性。肿瘤直径大于 2cm 与恶性肿瘤相关,对于直径 2cm 或更小的肿块可能需要更多的穿刺次数来评估。临床试验注册号:NCT01386931。