Hébert-Magee S, Bae S, Varadarajulu S, Ramesh J, Frost A R, Eloubeidi M A, Eltoum I A
Division of Anatomic Pathology, Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35249-6823, USA.
Cytopathology. 2013 Jun;24(3):159-71. doi: 10.1111/cyt.12071.
A meta-analysis has not been previously performed to evaluate critically the diagnostic accuracy of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) of solely pancreatic ductal adenocarcinoma and address factors that have an impact on variability of accuracy. The aim of this study was to determine whether the presence of a cytopathologist, variability of the reference standard and other sources of heterogeneity significantly impacts diagnostic accuracy.
We conducted a comprehensive search to identify studies, in which the pooled sensitivity, specificity, likelihood ratios for a positive or negative test (LR+, LR-) and summary receiver-operating curves (SROC) could be determined for EUS-FNA of the pancreas for ductal adenocarcinoma using clinical follow-up, and/or surgical biopsy or excision as the reference standard.
We included 34 distinct studies (3644 patients) in which EUS-FNA for a solid pancreatic mass was evaluated. The pooled sensitivity and specificity for EUS-FNA for pancreatic ductal adenocarcinoma was 88.6% [95% confidence interval (CI): 87.2-89.9] and 99.3% (95% CI: 98.7-99.7), respectively. The LR+ and LR- were 33.46 (95% CI: 20.76-53.91) and 0.11 (95% CI: 0.08-0.16), respectively. The meta-regression model showed rapid on-site evaluation (ROSE) (P = 0.001) remained a significant determinant of EUS-FNA accuracy after correcting for study population number and reference standard.
EUS-FNA is an effective modality for diagnosing pancreatic ductal adencarcinoma in solid pancreatic lesions, with an increased diagnostic accuracy when using on-site cytopathology evaluation.
此前尚未进行过荟萃分析来严格评估单纯胰腺导管腺癌的内镜超声引导下细针穿刺活检(EUS-FNA)的诊断准确性,并探讨影响准确性变异性的因素。本研究的目的是确定细胞病理学家的在场情况、参考标准的变异性以及其他异质性来源是否会显著影响诊断准确性。
我们进行了全面检索以识别相关研究,在这些研究中,可使用临床随访和/或手术活检或切除作为参考标准,确定胰腺导管腺癌EUS-FNA的合并敏感性、特异性、阳性或阴性试验似然比(LR+、LR-)以及汇总受试者工作特征曲线(SROC)。
我们纳入了34项不同的研究(3644例患者),其中评估了实性胰腺肿块的EUS-FNA。胰腺导管腺癌EUS-FNA的合并敏感性和特异性分别为88.6%[95%置信区间(CI):87.2 - 89.9]和99.3%(95%CI:98.7 - 99.7)。LR+和LR-分别为33.46(95%CI:20.76 - 53.91)和0.11(95%CI:0.08 - 0.16)。荟萃回归模型显示,在校正研究人群数量和参考标准后,快速现场评估(ROSE)(P = 0.001)仍然是EUS-FNA准确性的重要决定因素。
EUS-FNA是诊断实性胰腺病变中胰腺导管腺癌的有效方法,使用现场细胞病理学评估时诊断准确性会提高。