Journal List > Lab Med Online > v.6(1) > 1057306

Woo: Human Epididymis Protein 4 as a Diagnostic Marker of Ovarian Cancer and Its Reference Interval in Korean Population

Abstract

Human epididymis protein 4 (HE4), which complements cancer antigen 125 (CA125), has emerged as a new diagnostic biomarker that can discriminate between benign and malignant ovarian tumors. The risk of ovarian malignancy algorithm (ROMA) incorporates CA125, HE4, and menopausal status to classify patients with pelvic masses into those at high or low risk of developing ovarian cancer. The reference interval of HE4 among Korean population was different from those recommended by the manufacturer or evaluated in the Chinese.

Figures and Tables

Table 1

Reference intervals of risk of ovarian malignancy algorithm (ROMA) value for different commercially available diagnostic tests

lmo-6-12-i001
Elecsys HE4+Elecsys CA125 Architect HE4+Architect CA125 HE4 EIA*+ARCHITECT CA125 ARCHITECT HE4+CanAg CA125*
Premenopausal
 High-risk ≥ 11.4 ≥ 7.4 ≥ 13.1 ≥ 12.5
 Low-risk < 11.4 < 7.4 < 13.1 < 12.5
Postmenopausal
 High-risk ≥ 29.9 ≥ 25.3 ≥ 27.7 ≥ 14.4
 Low-risk < 29.9 < 25.3 < 27.7 < 14.4

*Fujirebio Diagnostics.

Table 2

Sensitivity and specificity of HE4 and CA125 for distinguishing between malignant and benign ovarian tumors

lmo-6-12-i002
Group HE4 CA125 ROMA
Sensitivity
(95% CI)
Specificity
(95% CI)
Cutoff* Sensitivity
(95% CI)
Specificity
(95% CI)
Cutoff* Sensitivity
(95% CI)
Specificity
(95% CI)
Cutoff*
Individuals with ovarian cancer (N = 149) 0.57
(0.49-0.66)
0.97
(0.92-0.99)
76 0.74
(0.66-0.81)
0.69
(0.60-0.77)
35 0.61
(0.53-0.69)
0.95
(0.91-0.99)
18.1
Individuals <45 yr (N=44) 0.2
(0.09-0.35)
0.98
(0.92-0.99)
67 0.48
(0.32-0.63)
0.72
(0.61-0.81)
40 0.22
(0.11-0.38)
0.96
(0.90-0.99)
13.7
Individuals ≥ 55 yr (N = 54) 0.78
(0.64-0.88)
0.93
(0.68-1.00)
86 0.89
(0.77-0.96)
0.8
(0.52-0.96)
24 0.94
(0.85-0.99)
0.8
(0.52-0.96)
19.3

*Upper reference values of 97.5%.

Abbreviation: CI, confidence interval.

Table 3

Sensitivity and specificity of HE4 and CA125 for distinguishing between malignant and benign ovarian tumors

lmo-6-12-i003
Group HE4 CA125 ROMA
Sensitivity
(95% CI)
Specificity
(95% CI)
Cutoff* Sensitivity
(95% CI)
Specificity
(95% CI)
Cutoff* Sensitivity
(95% CI)
Specificity
(95% CI)
Cutoff*
Individuals with ovarian cancer (N = 149) 0.7
(0.64-0.73)
0.89
(0.84-0.94)
55 0.68
(0.62-0.72)
0.77
(0.71-0.83)
45 0.67
(0.63-0.70)
0.93
(0.87-0.96)
11.6
Individuals <45 yr (N=44) 0.45
(0.27-0.66)
0.91
(0.84-0.95)
55 0.8
(0.67-0.89)
0.52
(0.44-0.56)
19 0.63
(0.51-0.75)
0.72
(0.64-0.77)
5.9
Individuals ≥ 55 yr (N = 54) 0.83
(0.64-0.88)
0.93
(0.68-1.00)
63 0.96
(0.87-1.00)
0.8
(0.52-0.96)
21 0.98
(0.59-1.00)
0.8
(0.53-0.93)
11.3

*from ROC analysis.

Abbreviation: CI, confidence interval.

Table 4

Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of ROMA for stratification of patients with pelvic masses, as reported in the literature

lmo-6-12-i004
Author ROMA cut-off point (%) Study population N Diagnostic methods Sensitivity (%) Specificity (%) PPV (%) NPV (%)
All PM M All PM M All PM M All PM M
Moore RG et al. [6] M-27.7 M-283 CA 125-CMIA 88.7 76.5 92.3 74.7 74.8 74.7 60.1 33.8 74.0 93.9 9.5 92.6
PM-13.1 PM-248 HE4-EIA
Molina R et al. [114] M-27.7 AII-495 CA 125-CMIA 90.1 74.1 95.2 87.7 88.9 83.1 74 44.4 88.9 95.8 96.6 92.5
PM-13.1 HE4-CMIA
Moore RG et al. [7] M-27.7 M-217 CA 125-CMIA 88.1 81.3 90.2 74.9 74.2 76 38.1 17.8 56.1 97.3 98.3 95.8
PM-13.1 PM-255 HE4-EIA
Anton C et al. [17] M-39.7 M-73 CA 125-ECLIA 75.9 77.8 63.9 81.8 79.3 97.3 - - - - - -
PM-13.9 PM-47 HE4-EIA
Anton C et al. [17] M-27.7 M-73 CA 125-ECLIA 74.1 77.8 72.2 75.8 69 81.1 - - - - - -
PM-13.1 PM-47 HE4-EIA
Partheen K et al. [114] M-26 M-276 CA 125-CMIA - 75 75 - 81 87.1 - 60.7 62.8 - 90.7 90.7
PM-17 PM-98 HE4-EIA
Van Gorp T et al. [19] M-12.5 AII-374 CA 125-EIA 84.7 66.7 91.0 76.8 87.8 58.8 71 60.5 74.3 88.2 90.4 83.3
PM-14.4 HE4-EIA
Novotny Z et al. [119] M-37.7 M-256 CA 125-CMIA - - 85.7 - - 95 - - 62.06 - - 98.65
HE4-CMIA
Karlsen et al. [116] M-25.3 M-597 CA 125-CMIA 94.8 91.8 92.6 76.5 40.2 75.5 - - - - - -
PM-7.4 PM-621 HE4-CMIA
Ortiz-Munoz et al. [103] M-29.9 M-118 CA 125-ECLIA 93.1 90 94.7 90.7 82.4 94.1 71.1 60 78.3 98.2 96.6 98.8
PM-11.4 PM-61 HE4-ECLIA
Lenhardt et al. [104] M-25.3 M-256 CA 125-CMIA 76.6 66.6 72.1 - - - - - - - - -
PM-7.4 PM-271 HE4-CMIA
Kalapotharacos et al. [105] M-10.4 M-154 CA 125-ECLIA - 82 99 - - - - - - - - -
PM-4.6 PM-123 HE4-EIA
Sandri et al. [116] M-25.3 M-191 CA 125-CMIA 91.2 85.2 91.5 - - - - - - - - -
PM-7.4 PM-158 HE4-CMIA
Montagnana et al. [65] M-14.4 M-53 CA 125-EIA - 53.5 82.5 - 80.6 84.6
PM-12.5 PM-51 HE4-EIA

Imported from Clinica Chimica Acta 2015;440:143-151.

All-PM+M; PM, premenopausal; M, postmenopausal; ECLIA, electro-chemilumines cence immunoassay; ELA, enzyme immunometric assay; CMIA, chemiluminescent micropartide immunoassay.

Table 5

Characteristics of reference individuals

lmo-6-12-i005
Characteristic Number of individuals
Premenopausal 912
Postmenopausal 851
Body mass index (BMI)
 <18.5 (lean) 114
 18.5-22.9 (normal) 923
 23.0-24.9 (overweight) 386
 ≥25.0 (obese) 351
Smoking
 Non-smoker 1,198
 Former smoker 26
 Current Smoker 49
Hormone therapy
 Yes 59
 No 1,704
Table 6

Reference intervals of HE4 and ROMA value according to age groups

lmo-6-12-i006
Age group (n) Upper reference limit (95% CI)
HE4 (pmol/L) < 30 (126) 59.93 (53.59-66.27)
30-49 (751) 64.02 (61.99-66.05)
50-59 (575) 72.06 (65.51-78.61)
≥ 60 (357) 93.84 (66.68-121.00)
Total (1,809) 75.59 (70.90-80.28)
ROMA (%) < 30 (126) 11.4 (8.75- 14.05)
30-49 (726) 12.8 (11.62-13.98)
50-59 (575) 18.5 (15.61- 21.39)
≥ 60 (357) 22.8 (17.70- 27.90)
All (1,809) 17.1 (15.43- 18.77)

Abbreviation: CI, confidence interval.

Notes

This article is available from http://www.labmedonline.org

References

1. Ferlay J, Soerjomataram I, Ervik E ea, Dikshit R, Eser S, Mathers C, et al. Globocan 2012 v 1.0, Cancer Incidence and Mortality Worldwide: IARC Cancer Base No . 11: International Agency for Research on Cancer, Lyon, France. 2013. cited 2015 Feb 3. Available from: http://globcan.iarc.fr.
2. National Institutes of Health Consensus Development Conference Statement. Ovarian cancer: screening, treatment, and follow-up. Gynecol Oncol. 1994; 55:S4–S14.
3. Kirchhoff C, Habben I, Ivell R, Krull N. A major human epididymis-specific cDNA encodes a protein with sequence homology to extracellular proteinase inhibitors. Biol Reprod. 1991; 45:350–357.
crossref
4. Schummer M, Ng WV, Bumgarner RE, Nelson PS, Schummer B, Bednarski DW, et al. Comparative hybridization of an array of 21,500 ovarian cDNAs for the discovery of genes overexpressed in ovarian carcinomas. Gene. 1999; 238:375–385.
crossref
5. Hellström I, Raycraft J, Hayden-Ledbetter M, Ledbetter JA, Schummer M, McIntosh M, et al. The HE4 (WFDC2) protein is a biomarker for ovarian carcinoma. Cancer Res. 2003; 63:3695–3700.
6. Hallamaa M, Suvitie P, Huhtinen K, Matomäki J, Poutanen M, Perheentupa A. Serum HE4 concentration is not dependent on menstrual cycle or hormonal treatment among endometriosis patients and healthy premenopausal women. Gynecol Oncol. 2012; 125:667–672.
crossref
7. Lin J, Qin J, Sangvatanakul V. Human epididymis protein 4 for differential diagnosis between benign gynecologic disease and ovarian cancer: a systematic review and meta-analysis. Eur J Obstet Gynecol Reprod Biol. 2013; 167:81–85.
crossref
8. Drapkin R, von Horsten HH, Lin Y, Mok SC, Crum CP, Welch WR, et al. Human epididymis protein 4 (HE4) is a secreted glycoprotein that is overexpressed by serous and endometrioid ovarian carcinomas. Cancer Res. 2005; 65:2162–2169.
crossref
9. Iwahori K, Suzuki H, Kishi Y, Fujii Y, Uehara R, Okamoto N, et al. Serum HE4 as a diagnostic and prognostic marker for lung cancer. Tumour Biol. 2012; 33:1141–1149.
crossref
10. Escudero JM, Auge JM, Filella X, Torne A, Pahisa J, Molina R. Comparison of serum human epididymis protein 4 with cancer antigen 125 as a tumor marker in patients with malignant and nonmalignant diseases. Clin Chem. 2011; 57:1534–1544.
crossref
11. Nagy B Jr, Krasznai ZT, Balla H, Csobán M, Antal-Szalmás P, Hernádi Z, et al. Elevated human epididymis protein 4 concentrations in chronic kidney disease. Ann Clin Biochem. 2012; 49:377–380.
crossref
12. Hertlein L, Stieber P, Kirschenhofer A, Krocker K, Nagel D, Lenhard M, et al. Human epididymis protein 4 (HE4) in benign and malignant diseases. Clin Chem Lab Med. 2012; 50:2181–2188.
crossref
13. Moore RG, Miller MC, Eklund EE, Lu KH, Bast RC Jr, Lambert-Messerlian G. Serum levels of the ovarian cancer biomarker HE4 are decreased in pregnancy and increase with age. Am J Obstet Gynecol. 2012; 206:349.
crossref
14. Lowe KA, Shah C, Wallace E, Anderson G, Paley P, McIntosh M, et al. Effects of personal characteristics on serum CA125, mesothelin, and HE4 levels in healthy postmenopausal women at high-risk for ovarian cancer. Cancer Epidemiol, Biomarkers Prev. 2008; 17:2480–2487.
crossref
15. Moore RG, Brown AK, Miller MC, Skates S, Allard WJ, Verch T, et al. The use of multiple novel tumor biomarkers for the detection of ovarian carcinoma in patients with a pelvic mass. Gynecol Oncol. 2008; 108:402–408.
crossref
16. Nolen B, Velikokhatnaya L, Marrangoni A, De Geest K, Lomakin A, Bast RC Jr, et al. Serum biomarker panels for the discrimination of benign from malignant cases in patients with an adnexal mass. Gynecol Oncol. 2010; 117:440–445.
crossref
17. Montagnana M, Danese E, Ruzzenente O, Bresciani V, Nuzzo T, Gelati M, et al. The ROMA (Risk of Ovarian Malignancy Algorithm) for estimating the risk of epithelial ovarian cancer in women presenting with pelvic mass: is it really useful? Clin Chem Lab Med. 2011; 49:521–525.
crossref
18. Kalapotharakos G, Asciutto C, Henic E, Casslén B, Borgfeldt C. High preoperative blood levels of HE4 predicts poor prognosis in patients with ovarian cancer. J Ovarian Res. 2012; 5:20.
crossref
19. Steffensen KD, Waldstrøm M, Brandslund I, Jakobsen A. Prognostic impact of prechemotherapy serum levels of HER2, CA125, and HE4 in ovarian cancer patients. Int J Gynecol Cancer. 2011; 21:1040–1047.
crossref
20. Trudel D, Têtu B, Grégoire J, Plante M, Renaud MC, Bachvarov D, et al. Human epididymis protein 4 (HE4) and ovarian cancer prognosis. Gynecol Oncol. 2012; 127:511–515.
crossref
21. Schummer M, Drescher C, Forrest R, Gough S, Thorpe J, Hellström I, et al. Evaluation of ovarian cancer remission markers HE4, MMP7 and Mesothelin by comparison to the established marker CA125. Gynecol Oncol. 2012; 125:65–69.
crossref
22. Moore RG, Miller MC, Disilvestro P, Landrum LM, Gajewski W, Ball JJ, et al. Evaluation of the diagnostic accuracy of the risk of ovarian malignancy algorithm in women with a pelvic mass. Obstet Gynecol. 2011; 118:280–288.
crossref
23. Moore RG, McMeekin DS, Brown AK, DiSilvestro P, Miller MC, Allard WJ, et al. A novel multiple marker bioassay utilizing HE4 and CA125 for the prediction of ovarian cancer in patients with a pelvic mass. Gynecol Oncol. 2009; 112:40–46.
crossref
24. Chan KK, Chen CA, Nam JH, Ochiai K, Wilailak S, Choon AT, et al. The use of HE4 in the prediction of ovarian cancer in Asian women with a pelvic mass. Gynecol Oncol. 2013; 128:239–244.
crossref
25. Ruggeri G, Bandiera E, Zanotti L, Belloli S, Ravaggi A, Romani C, et al. HE4 and epithelial ovarian cancer: comparison and clinical evaluation of two immunoassays and a combination algorithm. Clin Chim Acta. 2011; 412:1447–1453.
crossref
26. Van Gorp T, Cadron I, Despierre E, Daemen A, Leunen K, Amant F, et al. HE4 and CA125 as a diagnostic test in ovarian cancer: prospective validation of the Risk of Ovarian Malignancy Algorithm. Br J Cancer. 2011; 104:863–870.
crossref
27. Chudecka-Glaz AM. ROMA, an algorithm for ovarian cancer. Clin Chim Acta. 2015; 440:143–151.
crossref
28. Paulsen T, Kjaerheim K, Kaern J, Tretli S, Trope C. Improved short-term survival for advanced ovarian, tubal, and peritoneal cancer patients operated at teaching hospitals. Int J Gynecol Cancer. 2006; 16:Suppl 1. 11–17.
crossref
29. Jacobs I, Oram D, Fairbanks J, Turner J, Frost C, Grudzinskas JG. A risk of malignancy index incorporating CA 125, ultrasound and menopausal status for the accurate preoperative diagnosis of ovarian cancer. Br J Obstet Gynaecol. 1990; 97:922–929.
crossref
30. Bast RC Jr, Skates S, Lokshin A, Moore RG. Differential diagnosis of a pelvic mass: improved algorithms and novel biomarkers. Int J Gynecol Cancer. 2012; 22:Suppl 1. S5–S8.
31. Jacob F, Meier M, Caduff R, Goldstein D, Pochechueva T, Hacker N, et al. No benefit from combining HE4 and CA125 as ovarian tumor markers in a clinical setting. Gynecol Oncol. 2011; 121:487–491.
crossref
32. Kaijser J, Van Gorp T, Van Hoorde K, Van Holsbeke C, Sayasneh A, Vergote I, et al. A comparison between an ultrasound based prediction model (LR2) and the risk of ovarian malignancy algorithm (ROMA) to assess the risk of malignancy in women with an adnexal mass. Gynecol Oncol. 2013; 129:377–383.
crossref
33. Yang J, Sa M, Huang M, Yang J, Xiang Z, Liu B, et al. The reference intervals for HE4, CA125 and ROMA in healthy female with electrochemiluminescence immunoassay. Clin Biochem. 2013; 46:1705–1708.
crossref
TOOLS
Similar articles