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Suboptimal accuracy of carcinoembryonic antigen in differentiation of mucinous and nonmucinous pancreatic cysts: results of a large multicenter study.
Gaddam, Srinivas; Ge, Phillip S; Keach, Joseph W; Mullady, Daniel; Fukami, Norio; Edmundowicz, Steven A; Azar, Riad R; Shah, Raj J; Murad, Faris M; Kushnir, Vladimir M; Watson, Rabindra R; Ghassemi, Kourosh F; Sedarat, Alireza; Komanduri, Srinadh; Jaiyeola, Diana-Marie; Brauer, Brian C; Yen, Roy D; Amateau, Stuart K; Hosford, Lindsay; Hollander, Thomas; Donahue, Timothy R; Schulick, Richard D; Edil, Barish H; McCarter, Martin; Gajdos, Csaba; Attwell, Augustin; Muthusamy, V Raman; Early, Dayna S; Wani, Sachin.
Afiliação
  • Gaddam S; Division of Gastroenterology and Hepatology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Ge PS; Division of Digestive Diseases, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
  • Keach JW; Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Centennial, Colorado, USA.
  • Mullady D; Division of Gastroenterology and Hepatology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Fukami N; Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Centennial, Colorado, USA.
  • Edmundowicz SA; Division of Gastroenterology and Hepatology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Azar RR; Division of Gastroenterology and Hepatology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Shah RJ; Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Centennial, Colorado, USA.
  • Murad FM; Division of Gastroenterology and Hepatology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Kushnir VM; Division of Gastroenterology and Hepatology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Watson RR; Division of Digestive Diseases, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
  • Ghassemi KF; Division of Digestive Diseases, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
  • Sedarat A; Division of Digestive Diseases, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
  • Komanduri S; Division of Gastroenterology, Feinberg School of Medicine Northwestern University, Chicago, Illinois, USA.
  • Jaiyeola DM; Division of Gastroenterology, Feinberg School of Medicine Northwestern University, Chicago, Illinois, USA.
  • Brauer BC; Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Centennial, Colorado, USA.
  • Yen RD; Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Centennial, Colorado, USA.
  • Amateau SK; Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Centennial, Colorado, USA.
  • Hosford L; Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Centennial, Colorado, USA.
  • Hollander T; Division of Gastroenterology and Hepatology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Donahue TR; Department of Surgery, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
  • Schulick RD; Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Centennial, Colorado, USA.
  • Edil BH; Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Centennial, Colorado, USA.
  • McCarter M; Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Centennial, Colorado, USA.
  • Gajdos C; Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Centennial, Colorado, USA.
  • Attwell A; Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Centennial, Colorado, USA.
  • Muthusamy VR; Division of Digestive Diseases, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
  • Early DS; Division of Gastroenterology and Hepatology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Wani S; Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Centennial, Colorado, USA; Division of Gastroenterology and Hepatology, Veterans Affairs Medical Center, Denver, Colorado, USA.
Gastrointest Endosc ; 82(6): 1060-9, 2015 Dec.
Article em En | MEDLINE | ID: mdl-26077458
ABSTRACT
BACKGROUND AND

AIMS:

The exact cutoff value at which pancreatic cyst fluid carcinoembryonic antigen (CEA) level distinguishes pancreatic mucinous cystic neoplasms (MCNs) from pancreatic nonmucinous cystic neoplasms (NMCNs) is unclear. The aim of this multicenter retrospective study was to evaluate the diagnostic accuracy of cyst fluid CEA levels in differentiating between MCNs and NMCNs.

METHODS:

Consecutive patients who underwent EUS with FNA at 3 tertiary care centers were identified. Patients with histologic confirmation of cyst type based on surgical specimens served as the criterion standard for this analysis. Demographic characteristics, EUS morphology, FNA fluid, and cytology results were recorded. Multivariate logistic regression analysis to identify predictors of MCNs was performed. Receiver-operating characteristic (ROC) curves were generated for CEA levels.

RESULTS:

A total of 226 patients underwent surgery (mean age, 61 years, 96% white patients, 39% female patients) of whom 88% underwent Whipple's procedure or distal pancreatectomy. Based on surgical histopathology, there were 150 MCNs and 76 NMCNs cases. The median CEA level was 165 ng/mL. The area under the ROC curve for CEA levels in differentiating between MCNs and NMCNs was 0.77 (95% confidence interval, 0.71-0.84, P < .01) with a cutoff of 105 ng/mL, demonstrating a sensitivity and specificity of 70% and 63%, respectively. The cutoff value of 192 ng/mL yielded a sensitivity of 61% and a specificity of 77% and would misdiagnose 39% of MCN cases.

CONCLUSIONS:

Cyst fluid CEA levels have a clinically suboptimal accuracy level in differentiating MCNs from NMCNs. Future studies should focus on novel cyst fluid markers to improve risk stratification of pancreatic cystic neoplasms.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Antígeno Carcinoembrionário / Cistadenoma Mucinoso / Cistadenocarcinoma Mucinoso Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Antígeno Carcinoembrionário / Cistadenoma Mucinoso / Cistadenocarcinoma Mucinoso Idioma: En Ano de publicação: 2015 Tipo de documento: Article