- Open Access
The use of HE4, CA125 and CA72-4 biomarkers for differential diagnosis between ovarian endometrioma and epithelial ovarian cancer
Journal of Ovarian Research volume 6, Article number: 44 (2013)
Endometriosis is frequently associated with high levels of CA125. This marker is therefore not useful for discriminating ovarian endometrioma from ovarian malignancy. The aim of this study was to establish a panel of complementary biomarkers that could be helpful in the differential diagnosis between ovarian endometriosis or other ovarian benign masses and ovarian cancer.
Blood samples from 50 healthy women, 17 patients with benign ovarian tumors, 57 patients with ovarian endometrioma and 39 patients with ovarian cancer were analyzed and serum values were measured for the following biomarkers: CA125, HE4 and CA72-4.
Serum CA125 concentration was elevated in both patients with ovarian endometriosis and ovarian cancer but not in patients with other benign ovarian masses. HE4 was never increased in patients with endometriosis or benign masses whereas it was significantly higher in all patients with ovarian cancer (p < 0.05). A marked difference in CA72-4 values was observed between women with ovarian cancer (67%) and those with endometriosis (p < 0.05).
The results of the study suggest that HE4 and CA72-4 determination is the best approach to confirm the benign nature of ovarian endometrioma in women with high CA125 levels.
Endometriosis is a common chronic disease, present in 5-10% of women in reproductive age . The disease, characterized by the presence and growth of endometrial tissue outside the uterine cavity, is often associated with infertility and pelvic pain and it tends to recur [2, 5]. Endometriosis can be diagnosed by clinical and ultrasound examinations (US) but the most accurate procedure to confirm the diagnosis is laparoscopy that allows visualization of lesions and histological confirmation  .
Endometriosis is a benign disease but it shares several characteristics with invasive cancer. Cancer antigen 125 (CA125) measurement is an important component in the work-up of a woman with an adnexal mass . However, CA125 is characterized by a low diagnostic specificity, as abnormally high concentrations can be found in malignancies of different origin including non-ovarian gynecological cancer, such as endometrial, pancreatic, lung, breast and colorectal cancer . In patients with endometriosis CA125 levels can be high. In fact, CA125 is the most extensively investigated and used peripheral biomarker of endometriosis . In addition, elevated serum levels of CA125 are associated with non-gynecological diseases such as tuberculosis, liver cirrhosis and also in physiological conditions such as pregnancy or different phases of the menstrual cycle [10, 11]. Thus, CA125 has a limited role in the differential diagnosis between endometriosis and ovarian cancer due to the lack of specificity . Recently, the role of surgery for the treatment of ovarian endometriosis in women with pregnancy desire has been criticized because of the fear of ovarian health tissue damage [6, 13, 14]. In selected cases, particularly in women undergoing assisted reproductive techniques, it is mandatory rule out an ovarian malignancy before ovarian stimulation and embryo-transfer . Misdiagnosed ovarian cancer has been found in women with suspected ovarian endometriosis [16, 17].
Therefore identification of non-invasive and accessible markers of epithelial ovarian carcinoma (EOC) is valuable. For this reason serum tumor markers are being increasingly used for the differential diagnosis of adnexal masses.
Recently, the human epididymis protein 4 (HE4) has proved to be a promising marker for epithelial ovarian cancer with higher specificity and sensitivity than CA125 in distinguishing malignant from benign pelvic masses [18, 19]. Particularly, measuring both HE4 and CA125 serum concentrations increases the accuracy of ovarian cancer diagnosis and provides valuable information for discriminating ovarian tumors from ovarian endometriotic cysts [20, 21] or other gynecologic conditions . However, an increased HE4 levels have been observed also in other types of cancer, i.e. lung adenocarcinoma  and in patients with impaired renal function .
Other biomarkers have been studied for clinical application in EOC. Among these, cancer antigen 72–4 (CA72-4), a glycoprotein, which increases in gastric, colon, breast and ovarian adenocarcinomas, may be employed alone or in combination with CA125 and HE4. CA72-4 is less sensitive than CA125 for EOC, but it is not influenced by pregnancy or the phase of menstrual cycle [24, 25].
The aim of this study was to evaluate the role of those biomarkers, which are usually elevated in patients with EOC, that could be useful to confirm the nature of ovarian cystic endometriosis or other benign ovarian masses.
From June 2012 to February 2013, 115 consecutive Italian women (mean age: 35 years, range: 22–82) referred to the Department of Gynecology, Obstetrics and Urology at the University of Rome ”Sapienza” for the presence of an adnexal mass detected at clinical and ultrasound examinations were enrolled in the study. Control group consisted of 50 healthy women (mean age: 30 years, range: 21–57) with clinical and US outcome negative for ovarian masses.
Exclusion criteria included current hormonal therapy, pregnancy, chronic diseases or other types of cancer. Two patients were excluded from the study because they were at the beginning of pregnancy. The study was part of a study protocol approved by local Ethics Committees. All patients signed written informed consent to the study. At enrolment, medical history was collected and peripheral blood samples were drawn from all women and immediately sent to the laboratory for analysis of tumor markers. All groups underwent complete physical and gynecological examination and transvaginal ultrasound (TVUS) with color Doppler imaging.
Women diagnosed with a pelvic mass subsequently underwent surgery. Disease was confirmed by histopathological examination. The women were divided into the following 4 Groups:
Group 1: 50 healthy women (mean age: 30 years, range: 21–57) with clinical and US examinations negative for ovarian masses.
Group 2: 17 patients with benign ovarian tumors (mean age: 40 years, range: 20–74) with clinical and instrumental diagnosis of benign adnexal disease. Mean diameter of cysts was 57 ± 30.6 mm (range 20–110). Histopathology confirmed mature teratoma in 6 patients (35%) and simple serous cyst in 11 patients (65%).
Group 3: 57 patients with ovarian endometrioma (mean age: 36 years, range: 23–48). Diagnosis of endometriosis was achieved on the basis of medical history, clinical and pelvic transabdominal and/or transvaginal US examinations. Patients with indeterminate findings underwent pelvic magnetic resonance imaging (MRI) to confirm suspected endometriosis using the previously described technique [26, 27]. At laparoscopy, the disease was staged according to the rASRM classification . Mean diameter of endometriomas was 33 ± 18.9 mm (range 10–80). One patient had both endometriosis and an ovarian dermoid cyst.
Group 4: 39 patients with ovarian carcinoma (mean age: 64 years, range: 28–91). Histology confirmed the diagnosis and staging was made according to the International Federation of Gynecology and Obstetrics (FIGO).
Population characteristics are summarized in Table 1.
All sera were acquired following a standard collection protocol. Briefly, samples were collected in a Red Top Vacutainer, clotted 60–90 min and centrifuged for 10 min at 1300 × g. The serum fractions were aliquoted and stored at −80°C until analysis.
Lumipulse® G1200 CA125II is an assay system for the quantitative measurement of CA125 in specimens based on chemiluminescent enzyme immunoassay technology (CLEIA) by a two-step sandwich method (Innogenetics-Fujirebio, Belgium-Japan). This assay makes use of solid phase and ALP-labeled monoclonal antibodies (OC125 and M11 respectively).
CA125 in specimens specifically binds to anti-CA125 monoclonal antibody immobilized on the particles forming antigen-antibody immunocomplexes. The particles are then washed and rinsed in order to remove unbound materials. Alkaline phosphatase (ALP)-labeled anti-CA125 monoclonal antibody specifically binds to CA125 of the immunocomplexes. After a second wash, substrate solution is added. AMPPD contained in the substrate solution is dephosporylated by the catalysis of ALP indirectly conjugated to the particles. A luminescent signal is generated by the cleavage reaction of dephosphorylated 3-(2′-spiroadamantyl)-4-methoxy-4-(3″-phosphoryloxy)-phenyl-1,2-dioxetane (AMPPD) and reflects the amount of CA125 in the sample. Normal levels of CA125 were considered less than 35 U/mL.
HE4 levels were determined using the HE4 enzymatic immunoassay (EIA)(Fujirebio Diagnostics). The HE4 EIA is a solid phase, non competitive immunoassay based upon the direct ”sandwich” technique using two monoclonal antibodies, 2H5 and 3D8, directed against two epitopes in the C-WFDC domain of HE4. Controls or patient serum samples and standards were incubated with biotinylated anti-HE4 monoclonal antibody 2H5 aliquots in streptavidin coatedmicrostrips. HE4 present in standards or serum samples was adsorbed to the streptavidin coatedmicrostrips by the biotinylated anti-HE4 monoclonal antibody during the incubation period. The strips were then washed and incubated with horseradish peroxidase (HRP) labeled anti-HE4 monoclonal antibody 3D8. After washing, buffered substrate/chromogen reagent was added to each well and the enzyme reaction was allowed to proceed. During the enzyme reaction a blue color developed if the antigen was present. The intensity of the color was directly proportional to the amount of HE4 present in the samples. According to the manufacturer’s indications, normal values of HE4 were considered less than 150 pmol/L.
CA72-4 was detected utilizing a solid phase two-site immunoradiometric ELSA- CA72-4 assay (Cisbio Bioassays, France). Two monoclonal antibodies were prepared against sterically remote antigenic sites on the TAG 72 molecule: the first was coated on the ELSA solid phase, the second, radiolabeled with iodine 125, was used as tracer. TAG 72 molecules present in the standards or the samples to be tested were “sandwiched” between the two antibodies. Following the formation of the coated antibody/antigen/ antibody sandwich, the unbound tracer was easily removed by a washing step. The radioactivity bound to the Elsa was proportional to the concentration of TAG 72 present in the sample. Normal levels of CA72-4 were considered to be less than 3.8 U/mL.
Women were stratified by disease in four groups. In each group, the median, range, mean, SD for serum CA125, HE4and CA72-4 levels were determined. Mann–Whitney test was used to assess difference in distributions of tumor markers between different patient populations. Log base 10–transformed whisker-box plots were generated for each marker by disease group. The diagnostic performance of the markers was also expressed as sensitivity, specificity, positive predictive values (PPV) and negative predictive values (NPV) using the following cut-off values: 35 U/mL for CA125, 150 pmol/L for HE4, 3.8 U/mL for CA72-4. Receiver operator characteristic (ROC) curves were constructed and the areas under the curve (AUC) with binomial exact 95% confidence intervals (95% CI) were calculated. The method described by DeLong et al. was used to calculate the difference between two AUCs . For all statistical comparisons, a level of P < 0.05 was accepted as statistically significant. All statistical analyses were performed using MedCalc v.126.96.36.199.
CA125, HE4 and CA72-4 serum marker levels were evaluated in all groups (163 women). Results expressed as mean, median and ranges are shown in Table 2.
All markers showed significant difference between Group 1 and Group 2 and Group 4 (p < 0.05). HE4 and CA72-4 were significantly higher in Group 4 than in all the other groups (p < 0.05). CA125 was significantly higher in Group 3 and Group 4 than in Group 1 and Group 2 (p < 0.05). The distribution of marker levels for each studied group is shown in Figure 1.
Tumor marker sensitivity and specificity in malignant and benign disease
In Group 4, HE4 was increased in 89.7% (35/39) of cases, in this group CA72-4 was elevated in 67% (26/39) of cases, while CA125 was positive in 92% (36/39) of patients.
In Group 3, CA125 was elevated in 56.1% (32/57) of cases and a slight but not statistically significant increase of CA72-4 was observed in 7% (4/57) of patients.
HE4 correctly discriminated malignant from benign disease (Group 2 and Group 3 vs Group 4) with a sensitivity and specificity of 87% and 100%, respectively. PPV and NPV of HE4 were 100% and 96% respectively.
In patients with malignancy, CA125 showed a significantly higher sensitivity than CA72-4 (90% vs 67%, p < 0.001), but a lower specificity than CA72-4 (70% vs 96%, p < 0.001). PPV was 51% and 84%, and NPV was 95% and 89% for CA125 and CA72-4, respectively (Table 3).
Diagnostic performance of the markers in discriminating malignant from benign gynecologic conditions was verified using ROC analysis. The resultant accuracy (ROC Area) values for HE4, CA125 and CA72-4 and their corresponding ROC curves are shown in Figure 2A. All the three markers showed good performance, with AUCs of 0.985, 0.921 and 0.843 for HE4, CA125 and CA72-4 respectively. When the ROC analysis was performed for endometriosis, AUCs were 0.986 for HE4, 0.883 for CA125 and 0.845 for CA72-4 (Figure 2B).
Endometriosis is a known cause of CA125 elevation and represents a common gynecologic disorder in women of reproductive age . Generally the diagnosis of ovarian endometriosis is made by clinical and imaging technique examinations  and confirmed by surgery with histological examination . Recently surgical treatment of ovarian endometriosis in women desiring pregnancy has been criticized because of the risk of ovarian healthy tissue damage [13, 14]. Therefore, in selected cases with ovarian endometrioma treated by medical therapy or undergoing assisted reproductive techniques (ART) without prior surgery, a correct diagnosis is mandatory. In these cases, the use of tumor markers with high sensitivity and specificity could help to reduce the risk, even small, of undetected ovarian cancer. In fact, there is a recognized association between endometriosis and clear cell, low-grade serous and endometrioid ovarian cancer . So far, very little is known about the underlying factors involved in the malignant progression of endometriosis. For more than two decades CA125 has been the only marker employed in the diagnosis of EOC, but, although overexpressed in more than 80% of ovarian cancers, it lacks of specificity .
In the present study, we investigated the role of serum CA125, HE4 and CA72-4 in the diagnostic evaluation of ovarian endometrioma and adnexal mass. In agreement with data reported in literature , more than 50% of women with endometriosis expressed high levels of CA125, confirming the low specificity of this marker.
It was recently observed that HE4 rarely increases in benign gynecologic conditions suggesting its complementary role to CA125 [18, 19, 25, 34, 35]. In women with endometriosis, Moore et al. observed a marked difference between HE4 levels, which was increased only in 3% of cases, compared to CA125, which was elevated in 67% of cases . Hamed et al. showed that serum HE4 and CA125 concentrations were significantly higher in patients with ovarian cancer compared with levels observed in patients with benign disease or healthy controls. In their study CA125 and HE4 had high sensitivity (90% vs 83.3%) and combining the two markers EOC were correctly detected in 97% of cases . Moreover HE4 measurement, in healthy premenopausal women as well as in women with endometriosis, can be carried out at any phase of the menstrual cycle, and irrespective of hormonal therapy, extending the benefits of HE4 use in clinical practice [37, 38]. However, HE4 overexpression has been also observed in non-oncologic conditions such as chronic kidney disease, which represents the most important known source of false-positive HE4 results . In addition, recent studies have reported high HE4 levels also in some benign gynecological conditions such as uterine fibroma and pelvic inflammatory disease [8, 19]. Moreover, HE4 levels in healthy women are affected by age, BMI and smoking .
In our study CA125 and HE4 yielded a sensitivity of 90% and 87% and a specificity of 70% and 100% respectively in the diagnosis of epithelial ovarian cancer. HE4 never increased in women with endometriosis and it was able to correctly discriminate malignant from all benign ovarian masses. Therefore we agree with previous reports that HE4 is the most useful marker for the differential diagnosis between EOC and ovarian endometriosis . However, since some benign conditions can be associated with high HE4 levels, in selected cases CA72-4 may be useful for the differential diagnosis. Nevertheless the role of CA72-4 in the differential diagnosis between benign form malignant ovarian mass is still controversial .
In our study a slight and not statistically significant increase of CA72-4 was found in a small number of patients with endometriosis, with the highest observed value of 6.2 U/mL, which is indeed a borderline value, found only in one woman. Our data confirm the results reported by Lenhard et al. who showed that CA125 but not CA72-4 tends to be increased in the presence of endometriosis . A multimarker approach, consisting of HE4, CA125 and CA72-4, can provide a more accurate tool for a differential diagnosis of patients with ovarian endometriotic cysts, other benign ovarian masses and ovarian cancer.
In conclusion our results suggest that the use of serum HE4, CA125 and CA72-4 may be a valuable approach for distinguishing patients with ovarian endometrioma or other benign adnexal masses from those with ovarian malignancy. This approach could reduce medical costs related to more expensive diagnostic procedures and it may have a reassuring effect on the patient. Further studies are needed to confirm these results.
Cancer antigen 125
Epithelial ovarian carcinoma
Human epididymis protein 4
Cancer antigen 72–4
Magnetic resonance imaging
revised American Society of Reproductive Medicine
International Federation of Gynecology and Obstetrics
Chemiluminescent enzyme immunoassay
3-(2IGO: International Fedthoxy-4- (3(3zyme immunoassay
Positive predictive values
Negative predictive values
Receiver operator characteristic
Areas under the curve
Assisted reproductive techniques.
Eskenazi B, Warner ML: Epidemiology of endometriosis. Obstet Gynecol Clin North Am 1997,24(2):235–258. 10.1016/S0889-8545(05)70302-8
Giudice LC: Clinical practice. Endometriosis. N Engl J Med 2010,362(25):2389–2398. 10.1056/NEJMcp1000274
Porpora MG, Koninckx PR, Piazze J, Natili M, Colagrande S, Cosmi EV: Correlation between endometriosis and pelvic pain. J Am Assoc Gynecol Laparosc 1999,6(4):429–434. 10.1016/S1074-3804(99)80006-1
Porpora MG, Pallante D, Ferro A, Crisafi B, Bellati F, Benedetti Panici P: Pain and ovarian endometrioma recurrence after laparoscopic treatment of endometriosis: a long-term prospective study. Fertil Steril 2010,93(3):716–721. 10.1016/j.fertnstert.2008.10.018
Coccia ME, Rizzello F, Palagiano A, Scarselli G: Long-term follow-up after laparoscopic treatment for endometriosis: multivariate analysis of predictive factors for recurrence of endometriotic lesions and pain. Eur J Obstet Gynecol Reprod Biol 2011,157(1):78–83. 10.1016/j.ejogrb.2011.02.008
Kennedy S, Bergqvist A, Chapron C, D’Hooghe T, Dunselman G, Greb R, Hummelshoj L, Prentice A, Saridogan E: On behalf of the ESHRE special interest group for endometriosis endometrium guideline development group. ESHRE guideline for the diagnosis and treatment of endometriosis. Hum Reprod 2005, 20: 2698–2704. 10.1093/humrep/dei135
Bordin L, Fiore C, Donà G, Andrisani A, Ambrosini G, Faggian D, Plebani M, Clari G, Armanini D: Evaluation of erythrocyte band 3 phosphotyrosine level, glutathione content, CA-125, and human epididymal secretory protein E4 as combined parameters in endometriosis. Fertil Steril 2010,94(5):1616–1621. 10.1016/j.fertnstert.2009.10.038
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(11):1534–1544. 10.1373/clinchem.2010.157073
Gupta S, Agarwal A, Sekhon L, Krajcir N, Cocuzza M, Falcone T: Serum and peritoneal abnormalities in endometriosis: potential use as diagnostic markers. Minerva Ginecol 2006, 58: 527–551.
Buamah P: Benign conditions associated with raised serum CA-125 concentration. J Surg Oncol 2000,75(4):264–265. 10.1002/1096-9098(200012)75:4<264::AID-JSO7>3.0.CO;2-Q
McLemore MR, Aouizerat BE, Lee KA, Chen LM, Cooper B, Tozzi M, Miaskowski C: A comparison of the cyclic variation in serum levels of CA125 across the menstrual cycle using two commercial assays. Biol Res Nurs 2012,14(3):250–256. 10.1177/1099800411412766
Bast RC Jr, Klug TL, St John E, Jenison E, Niloff JM, Lazarus H, Berkowitz RS, Leavitt T, Griffiths CT, Parker L, Zurawski VR Jr, Knapp RC: A radioimmunoassay using a monoclonal antibody to monitor the course of epithelial ovarian cancer. N Engl J Med 1983,309(15):883–887. 10.1056/NEJM198310133091503
Tsoumpou I, Kyrgiou M, Gelbaya TA, Nardo LG: The effect of surgical treatment for endometrioma on in vitro fertilization outcomes: a systematic review and meta-analysis. Fertil Steril 2009, 92: 75–87. 10.1016/j.fertnstert.2008.05.049
Raffi F, Metwally M, Amer S: The impact of excision of ovarian endometrioma on ovarian reserve: a systematic review and meta-analysis. J Clin Endocrinol Metab 2012,97(9):3146–3154. 10.1210/jc.2012-1558
Vlahos NF, Economopoulos KP, Fotiou S: Endometriosis, in vitro fertilisation and the risk of gynaecological malignancies, including ovarian and breast cancer. Best Pract Res Clin Obstet Gynaecol 2010, 24: 39–50. 10.1016/j.bpobgyn.2009.08.004
Zygouris D, Leontara V, Makris GM, Chrelias C, Trakakis E, Christodoulaki C, Panagopoulos P: Endometrioid ovarian cancer arising from an endometriotic cyst in a young patient. Eur J Gynaecol Oncol 2012,33(3):324–325.
Vasilakaki T, Skafida E, Arkoumani E, Grammatoglou X, Firfiris N, Manoloudaki K: Borderline clear cell adenofibroma of the ovary associated with ovarian endometriosis: a case report. Eur J GynaecolOncol 2012,33(2):230–232.
Moore RG, Brown AK, Miller MC, Skates S, Allard WJ, Verch T, Steinhoff M, Messerlian G, Di Silvestro P, Granai CO, Bast RC Jr: The use of multiple novel tumor biomarkers for the detection of ovarian carcinoma in patients with a pelvic mass. Gynecol Oncol 2008,108(2):402–408. 10.1016/j.ygyno.2007.10.017
Moore RG, Miller MC, Steinhoff MM, Skates SJ, Lu KH, Lambert-Messerlian G, Bast RC Jr: Serum HE4 levels are less frequently elevated than CA125 in women with benign gynecologic disorders. Am J Obstet Gynecol 2012,206(4):351.
Huhtinen K, Suvitie P, Hiissa J, Junnila J, Huvila J, Kujari H, Setälä M, Härkki P, Jalkanen J, Fraser J, Mäkinen J, Auranen A, Poutanen M, Perheentupa A: Serum HE4 concentration differentiates malignant ovarian tumours from ovarian endometriotic cysts. Br J Cancer 2009,100(8):1315–1319. 10.1038/sj.bjc.6605011
Nolen B, Velikokhatnaya L, Marrangoni A, De Geest K, Lomakin A, Bast RC Jr, Lokshin A: Serum biomarker panels for the discrimination of benign from malignant cases in patients with an adnexal mass. Gynecol Oncol 2010,117(3):440–445. 10.1016/j.ygyno.2010.02.005
Galgano MT, Hampton GM, Frierson HF Jr: Comprehensive analysis of HE4 expression in normal and malignant human tissues. Mod Pathol 2006,19(6):847–853.
Nagy B Jr, Krasznai ZT, Balla H, Csobán M, Antal-Szalmás P, Hernádi Z, Kappelmayer J: Elevated human epididymis protein 4 concentrations in chronic kidney disease. Ann Clin Biochem 2012,49(4):377–380. 10.1258/acb.2011.011258
Lenhard MS, Nehring S, Nagel D, Mayr D, Kirschenhofer A, Hertlein L, Friese K, Stieber P, Burges A: Predictive value of CA125 and Ca72–4 in borderline ovarian tumors. Clin Chem Lab Med 2009,47(5):537–542.
Granato T, Midulla C, Longo F, Colaprisca B, Frati L, Anastasi E: Role of HE4, CA72–4, and CA125 in monitoring ovarian cancer. Tumor Biol 2012,33(5):1335–1339. 10.1007/s13277-012-0381-8
Manganaro L, Vittori G, Vinci V, Fierro F, Tomei A, Lodise P, Sollazzo P, Sergi ME, Bernardo S, Ballesio L, Marini M, Porpora MG: Beyond laparoscopy: 3-T magnetic resonance imaging in the evaluation of posteriorcul-de-sac obliteration. Magn Reson Imaging 2012,30(10):1432–1438. 10.1016/j.mri.2012.05.006
Manganaro L, Fierro F, Tomei A, Irimia D, Lodise P, Sergi ME, Vinci V, Sollazzo P, Porpora MG, Delfini R, Vittori G, Marini M: Feasibility of 3.0T pelvic MR imaging in the evaluation of endometriosis. Eur J Radiol 2012,81(6):1381–1387. 10.1016/j.ejrad.2011.03.049
American Society for Reproductive Medicine: Revised American society for reproductive medicine classification of endometriosis: 1996. Fertil Steril 1997,67(5):817–821. 10.1016/S0015-0282(97)81391-X
Heintz AP, Odicino F, Maisonneuve P, Quinn MA, Benedet JL, Creasman WT, Ngan HY, Pecorelli S, Beller U: Carcinoma of the ovary. FIGO 26th Annual Report on the Results of Treatment in Gynecological Cancer. Int J Gynaecol Obstet 2006,95(Suppl 1):S161–92.
DeLong ER, DeLong DM, Clarke-Pearson DL: Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach. Biometrics 1988,44(3):837–845. 10.2307/2531595
Van Holsbeke C, Van Calster B, Guerriero S, Savelli L, Paladini D, Lissoni AA, Czekierdowski A, Fischerova D, Zhang J, Mestdagh G, Testa AC, Bourne T, Valentin L, Timmerman D: Endometriomas: their ultrasound characteristics. Ultrasound Obstet Gynecol 2010,35(6):730–740.
Pearce CL, Templeman C, Rossing MA, Lee A, Near AM, Webb PM, Nagle CM, Doherty JA, Cushing-Haugen KL, Wicklund KG, et al.: Association between endometriosis and risk of histological subtypes of ovarian cancer: a pooled analysis of case–control studies. Lancet Oncol 2012, 13: 385–394. 10.1016/S1470-2045(11)70404-1
Bast RC Jr, Xu FJ, Yu YH, Barnhill S, Zhang Z, Mills GB: CA 125: the past and the future. Int J Biol Markers 1998,13(4):179–187.
Anastasi E, Granato T, Coppa A, Manganaro L, Giannini G, Comploj S, Frati L, Midulla C: HE4 in the differential diagnosis of a pelvic mass: a case report. Int J Mol Sci 2011,12(1):627–632.
Yamashita S, Tokuishi K, Hashimoto T, Moroga T, Kamei M, Ono K, Miyawaki M, Takeno S, Chujo M, Yamamoto S, Kawahara K: Prognostic significance of HE4 expression in pulmonary adenocarcinoma. Tumour Biol 2011,32(2):265–271. 10.1007/s13277-010-0118-5
Hamed EO, Ahmed H, Sedeek OB, Mohammed AM, Abd-Alla AA, Abdel Ghaffar HM: Significance of HE4 estimation in comparison with CA125 in diagnosis of ovarian cancer and assessment of treatment response. Diagn Pathol 2013, 8: 11. 10.1186/1746-1596-8-11
Anastasi E, Granato T, Marchei G, Viggiani V, Colaprisca B, Comploj S, Reale M, Frati L, Midulla C: Ovarian tumor marker HE4 is differently expressed during the phases of the menstrual cycle in healthy young women. Tumour Biol 2010,31(5):411. 10.1007/s13277-010-0049-1
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. 10.1016/j.ygyno.2012.03.011
Bolstad N, Øijordsbakken M, Nustad K, Bjerne J: Human epididymis protein reference limits and natural variation in a Nordic reference population. Tumor Biol 2012, 33: 141–148. 10.1007/s13277-011-0256-4
We are thankful Barbara Colaprisca and Valentina Viggiani for their technical assistance.
All authors declare that they have no competing interest.
EA and MGP conceived and design the experiments. EA, MGP, RF, PS and AT performed the experiments. EA, MGP, TG, LF and PBP analyzed the data. TG contributed reagents/material/analysis tools. EA, MGP, RF, PS and AT wrote the paper. All authors read and approved the final manuscript.