| Literature DB >> 25469245 |
Weilin Wang1, Lufei Zhang1, Linghui Chen1, Jianfeng Wei1, Qiang Sun1, Qingshong Xie1, Xiaohu Zhou1, Dongkai Zhou1, Pengfei Huang1, Qifan Yang1, Haiyang Xie2, Lin Zhou2, Shusen Zheng1.
Abstract
The clinical importance of intraductal papillary mucinous neoplasms (IPMN) of the pancreas has been increasing due to the large number of newly diagnosed cases. A meta-analysis was used to assess the accuracy of serum carcinoembryonic antigen (CEA) and carbohydrate antigen 19-9 (CA19-9) for the identification of malignant and invasive IPMN. A literature search of PubMed and Web of Knowledge was conducted. Studies included in the analysis addressed the diagnostic accuracy of serum CEA and CA19-9 and pooled estimates of sensitivity, specificity, positive- and negative-likelihood ratios (PLR and NLR), diagnostic odds ratio (DOR) and receiver operating characteristic curves were calculated using random-effects models. Predefined subgroup analysis was performed. Fifteen studies (published between 2001 and 2013) were analyzed, including a total of 1,629 patients. Pooled estimates of CEA in malignant and invasive IPNM prediction were: Pooled sensitivity, 18 and 18%; pooled specificity, 93 and 95%; PLR, 2.83 and 3.54; NLR, 0.89 and 0.89; and DOR, 3.35 and 3.6, respectively. Pooled estimates of CA19-9 in malignant and invasive IPMN prediction were: Pooled sensitivity, 40 and 52%; pooled specificity, 89 and 88%; PLR, 2.93 and 3.78; NLR, 0.74 and 0.6; and DOR, 4.34 and 6.33, respectively. In conclusion, serum CEA has low sensitivity and high specificity for malignant and invasive IPMN. Serum CA19-9 is a useful non-invasive preoperative tool for differentiating between invasive and benign IPMN and should be taken into account in the decision to perform surgery.Entities:
Keywords: carbohydrate antigen 19-9; carcinoembryonic antigen; diagnostic odds ratio; intraductal papillary mucinous neoplasms; negative-likelihood ratio; positive-likelihood ratio; sensitivity; specificity
Year: 2014 PMID: 25469245 PMCID: PMC4251113 DOI: 10.3892/br.2014.376
Source DB: PubMed Journal: Biomed Rep ISSN: 2049-9434