Article Data

  • Views 507
  • Dowloads 145

Original Research

Open Access

Evaluation of CA-125, CA72-4, HE-4, and M-CSF as early diagnostic markers for ovarian cancer in Egyptian women

  • Rania Mohamed ElSharkawy1
  • Fady M. Shawky Moiety1,*,

1Department of Chemical Pathology, Medical Research Institute, Alexandria University, Alexandria, Egypt

2Department of Obstetrics and Gynecology, Faculty of Medicine, Alexandria University, Alexandria ,Egypt

DOI: 10.12892/ejgo4145.2018 Vol.39,Issue 3,June 2018 pp.454-457

Published: 10 June 2018

*Corresponding Author(s): Fady M. Shawky Moiety E-mail: fmoiety@gmail.com

Abstract

Objective: To evaluate the diagnostic performance of cancer antigen CA-125, CA72-4, human epididymis protein 4 (HE-4), and macrophage colony stimulating factor (M-CSF), separately or in combination in the diagnosis of early-stage ovarian cancer. Materials and Methods: This was a prospective case control study conducted in a University Gynecology hospital. A total of 127 patients with ovarian cancer, in Stage I (n=40) and Stage II (n=87), and 128 age-matched healthy women (controls) were included. CA-125, CA72- 4, HE-4, and M-CSF serum levels were assessed and compared in patients vs. controls. Results: Seventy-six patients were menopausal (59.8%). A significant difference between cases and controls were detected in terms of each of the serum level of the studied markers.The diagnostic performance for the studied markers in patients in Stage I, namely ; CA 125, CA 72-4, HE-4, and M.CSF, showed sensitivities of 50%, 7%, 68.42%, and 32.14%, respectively. Applying the logistic regression model for all studied markers significantly increased the sensitivity and confirmed a better diagnostic performance in Stage I, when combining the four markers together, with area under the curve (AUC) of 0.978, and a sensitivity of 91.07, at a fixed specificity of 90%. Conclusions: Using non-invasive and simple markers’ panel for early detection of ovarian cancer is the ultimate goal for the best clinical practice. Based on the present results, the authors suggest using the four studied markers in combination for satisfactory and reliable diagnostic performance.


Keywords

Ovarian cancer; Markers; CA-125; CA72-4; HE-4; M-CSF.

Cite and Share

Rania Mohamed ElSharkawy,Fady M. Shawky Moiety. Evaluation of CA-125, CA72-4, HE-4, and M-CSF as early diagnostic markers for ovarian cancer in Egyptian women. European Journal of Gynaecological Oncology. 2018. 39(3);454-457.

References

[1] Wingo P.A., Ries L.A., Rosenberg H.M., Miller D.S., Edwards B.K.: “Cancer incidence and mortality, 1973-1995”. Cancer, 1998, 82, 1197.

[2] van Haaften-Day C., Shen Y., Xu F., Yu Y., Berchuck A., Havrilesky L.J., et al.: “OVX1, macrophage-colony stimulating factor, and CA- 125-II as tumor markers for epithelial ovarian carcinoma”. Cancer, 2001, 92, 2837.

[3] Sinha P., Rastogi M., Agarwal V., Sachan M.: “Protein, methylated DNA and micro RNA: potential candidates towards sustainable ovarian cancer diagnostics”. 2016. Available at: http://www.avidscience.com/wp-content/uploads/2016/07/RAOC-15-02_June-19-2016.pdf

[4] Sarojini S., Tamir A., Lim H., Li S,. Zhang S., Goy A., et al.: “Early detection biomarkers for ovarian cancer”. J. Oncol., 2012, 2012, 709049

[5] Sölétormos G., Duffy M.J., Hassan S.O.A., Verheijen R.H., Tholander B., Bast R.C. Jr., et al.: “Clinical use of cancer biomarkers in epithelial ovarian cancer: updated guidelines from the European Group on Tumor Markers”. Int. J. Gynecol. Cancer, 2016, 26, 43.

[6] Yu S., Yang H.J, Xie S.Q., Bao Y.X.: “Diagnostic value of HE4 for ovarian cancer: a meta-analysis”. Clin. Chem. Lab. Med., 2012, 50, 1439.

[7] Chechlinska M., Kowalska M., Kaminska J.: “Cytokines as potential tumour markers”. Clin. Chem. Lab. Med., 2008, 2, 691.

[8] Lenhard M.S., Nehring S., Nagel D., Mayr D., Kirschenhofer A., Hertlein L., et al.: “Predictive value of CA 125 and CA 72-4 in ovarian borderline tumors”. Clin. Chem. Lab. Med., 2009, 47, 537.

[9] Buys S.S., Partridge E., Black A., Johnson C.C., Lamerato L., Isaacs C., et al.: “Effect of screening on ovarian cancer mortality: the Prostate, Lung, Colorectal and Ovarian (PLCO) cancer screening randomized controlled trial”. JAMA, 2011, 305, 2295.

[10] Shadfan B.H., Simmons A.R., Simmons G.W., Ho A., Wong J., Lu K.H., et al.: “A multiplexable, microfluidic platform for the rapid quantitation of a biomarker panel for early ovarian cancer detection at the point-of-care”. Cancer Prev. Res. (Phila.), 2015, 8, 37.

[11] Barakat R.R., Markman M., Randall M.: “Principles and practice of gynecologic oncology”. Philadelphia: Lippincott Williams & Wilkins, 2009.

[12] Badgwell D., Bast R.C. Jr.: “Early detection of ovarian cancer”. Dis. Markers, 2007, 23, 397.

[13] Skates S.J., Horick N., Yu Y., Xu F.J., Berchuck A., Havrilesky L.J., et al.: “Preoperative sensitivity and specificity for early-stage ovarian cancer when combining cancer antigen CA-125II, CA 15-3, CA 72-4, and macrophage colony-stimulating factor using mixtures of multivariate normal distributions”. J. Clin, Oncol., 2004, 22, 4059.

[14] Wu L., Dai Z.Y., Qian Y.H., Shi Y., Liu F.J., Yang C.: “Diagnostic value of serum human epididymis protein 4 (HE4) in ovarian carcinoma: a systematic review and meta-analysis”. Int. J. Gynecol. Cancer, 2012, 22, 1106.

[15] Anastasi E., Manganaro L., Granato T., Benedetti Panici P., Frati L., Porpora M.G.: “Is CA72-4 a useful biomarker in differential diagnosis between ovarian endometrioma and epithelial ovarian cancer?” Dis. Markers, 2013, 35, 331.

[16] Będkowska G.E., Ławicki S., Gacuta E., Pawłowski P., Szmitkowski M.: “M-CSF in a new biomarker panel with HE4 and CA 125 in the diagnostics of epithelial ovarian cancer patients”. J. Ovarian Res., 2015, 8, 1.

[17] Bian J., Li B., Kou X.J., Liu T.Z., Ming L.: “Clinical significance of combined detection of serum tumor markers in diagnosis of patients with ovarian cancer”. Asian Pac J Cancer Prev., 2013, 14, 6241.

Abstracted / indexed in

Science Citation Index Expanded (SciSearch) Created as SCI in 1964, Science Citation Index Expanded now indexes over 9,500 of the world’s most impactful journals across 178 scientific disciplines. More than 53 million records and 1.18 billion cited references date back from 1900 to present.

Biological Abstracts Easily discover critical journal coverage of the life sciences with Biological Abstracts, produced by the Web of Science Group, with topics ranging from botany to microbiology to pharmacology. Including BIOSIS indexing and MeSH terms, specialized indexing in Biological Abstracts helps you to discover more accurate, context-sensitive results.

Google Scholar Google Scholar is a freely accessible web search engine that indexes the full text or metadata of scholarly literature across an array of publishing formats and disciplines.

JournalSeek Genamics JournalSeek is the largest completely categorized database of freely available journal information available on the internet. The database presently contains 39226 titles. Journal information includes the description (aims and scope), journal abbreviation, journal homepage link, subject category and ISSN.

Current Contents - Clinical Medicine Current Contents - Clinical Medicine provides easy access to complete tables of contents, abstracts, bibliographic information and all other significant items in recently published issues from over 1,000 leading journals in clinical medicine.

BIOSIS Previews BIOSIS Previews is an English-language, bibliographic database service, with abstracts and citation indexing. It is part of Clarivate Analytics Web of Science suite. BIOSIS Previews indexes data from 1926 to the present.

Journal Citation Reports/Science Edition Journal Citation Reports/Science Edition aims to evaluate a journal’s value from multiple perspectives including the journal impact factor, descriptive data about a journal’s open access content as well as contributing authors, and provide readers a transparent and publisher-neutral data & statistics information about the journal.

Submission Turnaround Time

Conferences

Top