Literature DB >> 22811878

The clinical utility of serum CA 19-9 in the diagnosis, prognosis and management of pancreatic adenocarcinoma: An evidence based appraisal.

Umashankar K Ballehaninna, Ronald S Chamberlain.   

Abstract

BACKGROUND: Serum carbohydrate antigen (CA 19-9) is the most common tumor marker assessed in pancreatic cancer patients; nevertheless few articles have comprehensively evaluated the evidence for its utility in pancreatic cancer management.
METHODS: Literature search was performed using Medline with keywords "pancreatic cancer", "tumor markers", "CA 19-9", "diagnosis", "screening", "prognosis", "resectability" and "recurrence". All English language articles pertaining to the role of CA 19-9 in pancreatic cancer were critically analyzed to determine its utility as a biomarker for pancreatic cancer.
RESULTS: Serum CA 19-9 is the most extensively validated pancreatic cancer biomarker with multiple clinical applications. CA 19-9 serum levels have a sensitivity and specificity of 79-81% and 82-90% respectively for the diagnosis of pancreatic cancer in symptomatic patients; but are not useful as a screening marker because of low positive predictive value (0.5-0.9%). Pre-operative CA 19-9 serum levels provide useful prognostic information as patients with normal levels (<37 U/mL) have a prolonged median survival (32-36 months) compared to patients with elevated levels (>37 U/mL) (12-15 months). A CA 19-9 serum level of <100 U/mL implies likely resectable disease whereas levels >100 U/mL suggest unresectablity or metastatic disease. Normalization or a decrease in post-operative CA 19-9 serum levels by ≥20-50% from baseline following surgical resection or chemotherapy is associated with prolonged survival compared to failure of CA 19-9 serum levels to normalize or an increase. Important limitations to CA 19-9 serum level evaluation in pancreatic cancer include poor sensitivity, false negative results in Lewis negative phenotype (5-10%) and increased false positivity in the presence of obstructive jaundice (10-60%).
CONCLUSIONS: CA 19-9 is the most extensively studied and validated serum biomarker for the diagnosis of pancreatic cancer in symptomatic patients. CA 19-9 serum levels can provide important information with regards to prognosis, overall survival, and response to chemotherapy as well as predict post-operative recurrence. However, non-specific expression in several benign and malignant diseases, false negative results in Lewis negative genotype and an increased false positive results in the presence of obstructive jaundice severely limit the universal applicability of serum CA 19-9 levels in pancreatic cancer management.

Entities:  

Keywords:  CA 19-9; Pancreatic cancer; diagnosis; prognosis; recurrence; resectability; screening; tumor markers

Year:  2012        PMID: 22811878      PMCID: PMC3397644          DOI: 10.3978/j.issn.2078-6891.2011.021

Source DB:  PubMed          Journal:  J Gastrointest Oncol        ISSN: 2078-6891


  78 in total

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Authors:  M Ikeda; S Okada; K Tokuuye; H Ueno; T Okusaka
Journal:  Cancer       Date:  2001-02-01       Impact factor: 6.860

2.  Pretreatment CA 19-9 level as a prognostic factor in patients with advanced pancreatic cancer treated with gemcitabine.

Authors:  Everardo D Saad; Marcel C Machado; Dalia Wajsbrot; Roberto Abramoff; Paulo M Hoff; Jacques Tabacof; Artur Katz; Sergio D Simon; René C Gansl
Journal:  Int J Gastrointest Cancer       Date:  2002

3.  Colorectal carcinoma antigens detected by hybridoma antibodies.

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5.  [Does cholestasis change the clinical usefulness of CA 19-9 in pacreatobiliary cancer?].

Authors:  C M Mery; A Duarte-Rojo; F Paz-Pineda; E Gómez; G Robles-Díaz
Journal:  Rev Invest Clin       Date:  2001 Nov-Dec       Impact factor: 1.451

6.  Utility of tumor markers in determining resectability of pancreatic cancer.

Authors:  Michael G Schlieman; Hung S Ho; Richard J Bold
Journal:  Arch Surg       Date:  2003-09

7.  Are serial CA 19-9 kinetics helpful in predicting survival in patients with advanced or metastatic pancreatic cancer treated with gemcitabine and cisplatin?

Authors:  J Stemmler; P Stieber; A M Szymala; A Schalhorn; M M Schermuly; R Wilkowski; T Helmberger; R Lamerz; C Stoffregen; K Niebler; M Garbrecht; V Heinemann
Journal:  Onkologie       Date:  2003-10

8.  CA 19-9 in the therapy monitoring and follow-up of locally advanced cancer of the exocrine pancreas treated with radiochemotherapy.

Authors:  Oliver Micke; Frank Bruns; Ulrich Schäfer; Rene Kurowski; Eckehard Horst; Norman Willich
Journal:  Anticancer Res       Date:  2003 Mar-Apr       Impact factor: 2.480

9.  Decrease of CA 19-9 during chemotherapy with gemcitabine predicts survival time in patients with advanced pancreatic cancer.

Authors:  U Halm; T Schumann; I Schiefke; H Witzigmann; J Mössner; V Keim
Journal:  Br J Cancer       Date:  2000-03       Impact factor: 7.640

10.  Prognostic value of CA 19-9 levels in patients with inoperable adenocarcinoma of the pancreas treated with gemcitabine.

Authors:  C Ziske; C Schlie; M Gorschlüter; A Glasmacher; U Mey; J Strehl; T Sauerbruch; I G H Schmidt-Wolf
Journal:  Br J Cancer       Date:  2003-10-20       Impact factor: 7.640

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  247 in total

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Authors:  Yì-Xiáng J Wáng; Jing-Shan Gong; Romaric Loffroy
Journal:  Chin J Cancer Res       Date:  2015-08       Impact factor: 5.087

2.  Pancreatic Cancer: a Challenge to Cure.

Authors:  M Tewari
Journal:  Indian J Surg       Date:  2015-10-19       Impact factor: 0.656

3.  The Association of Serum Carcinoembryonic Antigen, Carbohydrate Antigen 19-9, Thymidine Kinase, and Tissue Polypeptide Specific Antigen with Outcomes of Patients with Metastatic Colorectal Cancer Treated with Bevacizumab: a Retrospective Study.

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Authors:  Nerissa Therese Viola-Villegas; Samuel L Rice; Sean Carlin; Xiaohong Wu; Michael J Evans; Kuntal K Sevak; Marija Drobjnak; Govind Ragupathi; Ritsuko Sawada; Wolfgang W Scholz; Philip O Livingston; Jason S Lewis
Journal:  J Nucl Med       Date:  2013-09-12       Impact factor: 10.057

5.  Quantitation of circulating satellite RNAs in pancreatic cancer patients.

Authors:  Takahiro Kishikawa; Motoyuki Otsuka; Takeshi Yoshikawa; Motoko Ohno; Keisuke Yamamoto; Natsuyo Yamamoto; Ai Kotani; Kazuhiko Koike
Journal:  JCI Insight       Date:  2016-06-02

Review 6.  Intensity of follow-up after pancreatic cancer resection.

Authors:  Jason A Castellanos; Nipun B Merchant
Journal:  Ann Surg Oncol       Date:  2013-10-04       Impact factor: 5.344

7.  Distinguishing pancreatic cancer and autoimmune pancreatitis with in vivo tomoelastography.

Authors:  Liang Zhu; Jing Guo; Zhengyu Jin; Huadan Xue; Menghua Dai; Wen Zhang; Zhaoyong Sun; Jia Xu; Stephan R Marticorena Garcia; Patrick Asbach; Bernd Hamm; Ingolf Sack
Journal:  Eur Radiol       Date:  2020-10-30       Impact factor: 5.315

8.  Leveraging Bioorthogonal Click Chemistry to Improve 225Ac-Radioimmunotherapy of Pancreatic Ductal Adenocarcinoma.

Authors:  Sophie Poty; Lukas M Carter; Komal Mandleywala; Rosemery Membreno; Dalya Abdel-Atti; Ashwin Ragupathi; Wolfgang W Scholz; Brian M Zeglis; Jason S Lewis
Journal:  Clin Cancer Res       Date:  2018-10-23       Impact factor: 12.531

9.  Dual-phase CT findings of groove pancreatitis.

Authors:  Atif Zaheer; Maera Haider; Satomi Kawamoto; Ralph H Hruban; Elliot K Fishman
Journal:  Eur J Radiol       Date:  2014-05-27       Impact factor: 3.528

10.  Important CT and histopathological findings for recurrence and overall survival in patients with pancreatic ductal adenocarcinoma who underwent surgery after neoadjuvant FOLFIRINOX.

Authors:  Sae-Jin Park; Jung Hoon Kim; Ijin Joo; Kyoung Bun Lee; Joon Koo Han
Journal:  Eur Radiol       Date:  2020-11-17       Impact factor: 5.315

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