Analysis of serum HE4 levels in various histologic subtypes of epithelial ovarian cancer and other malignant tumors

Abstract

BACKGROUND:

The measurement of serum HE4 levels has emerged as a sensitive and specific biomarker for epithelial ovarian cancers (EOCs). However, serum levels in women diagnosed with various histologic subtypes of EOC and in women with metastatic non-ovarian primary malignancies have not been widely reported.

OBJECTIVE:

The goal of this study was to identify how serum HE4 levels vary in women diagnosed with different histologic subtypes of EOC and non-ovarian malignancies.

METHODS:

Data from six prospective pelvic mass clinical trials was combined and an evaluation of serum HE4 levels in women diagnosed with a malignancy was performed. For all patients, serum was obtained prior to surgery and final pathology, including primary tumor site, histologic subtype, grade and stage, were recorded. The mean, median, standard deviation, maximum, and minimum HE4 levels were determined for each group.

RESULTS:

A total of 984 patients were included in this study, with the average patient age being 60 years old. There were 230 premenopausal and 754 postmenopausal patients. Serum HE4 levels were elevated (≥70.0 pMol) in 85%of EOCs, 40%of LMP tumors, 21%of non-EOCs (germ cell tumors), 25%of cervical cancers, and 47%of non-gynecologic metastatic cancers. Analysis of histologic subtypes revealed 90%(n = 391) of serous, 85%(n = 73) of endometrioid, 45%(n = 42) of mucinous, 86%(n = 51) of mixed tumors, and 69%(n = 36) of clear cell tumors had elevated serum HE4 levels.

CONCLUSIONS:

Serum HE4 levels are most often elevated in women with high grade serous and endometrioid EOCs, and though serum elevations are seen more often with advanced stage disease, HE4 is also often elevated in early stage disease and lower grade tumors.

Keywords

Serum HE4 biomarker ovarian cancer

1 Introduction

Ovarian cancer is the leading cause of death due to gynecologic malignancies and the fifth leading cause of cancer deaths in women in the United States [1]. World wide it is estamated there are 314,000 new ovarian cancers annually with 207,300 each year [2]. The term Epithelial Ovarian Cancer (EOC) in this report is used to encompass primary epithelial ovarian cancer, fallopian tube cancer and primary peritoneal cancers. The majority of EOCs are high-grade serous cancers (70%) followed by endometrioid (10%), clear cell (10%), mucinous (3%), and low-grade serous tumors (< 5%), with carcinosarcoma and undifferentiated carcinomas being rare. Epithelial ovarian cancers have been placed into two categories based on morphologic, molecular genetic features and prognostic factors [3]. Type 1 EOCs are made up of low grade serous, low grade endometrioid, clear cell, mucinous and transitional cell cancers, while Type 2 EOCs include high grade serous carcinoma, high grade endometrioid, undifferentiated carcinoma and carcinosarcoma. Type 2 serous EOCs typically have TP53 mutations in up to 80%of the tumors, whereas Type 1 low grade serous EOCs harbor KRAS, BRAF and ERBB2 mutations in up to 70%of the tumors. Recent data has called into question the origin of high-grade epithelial ovarian cancers, with the prevailing theory being that the majority are in fact arising from implanted cells of fallopian tube origin. To support this, precursor lesions for serous carcinoma have been identified in the fallopian tube and are labeled as serous tubal intraepithelial carcinomas, or STIC lesions. Additionally, clear cell and endometrioid malignancies have been shown to develop in the background of endometriosis [4, 5].

The WAP Four-Disulfide Core Domain 2 gene (WFDC2) has been identified as a commonly over expressed gene in EOC and encodes the secretory protiein human epididymis protein 4 (HE4). HE4 can be detected in the serum of patients diagnosed with EOC and has been cleared by the US FDA and other countries for the detection and monitoring ovarian cancers [6, 7]. HE4 has emerged as a useful predictive biomarker for EOC, and when combined with CA-125 testing, it improves the sensitivity and specificity for cancer detection amongst women with adnexal masses over that of CA-125 alone [7, 8]. Like CA-125, serum HE4 levels are elevated in approximately 80%of women with EOC, yet HE4 has been demonstrated to have increased specificity, as it is less frequently elevated in benign gynecologic conditions [9, 10]. Serum HE4 levels have also been shown to rise with increasing grade, stage, and aggressiveness of EOC [11, 12]. As a result, HE4 is not only useful for assessing the risk of malignancy in women with adnexal masses, but also for monitoring treatment responses in women with EOC and facilitating the earlier detection of recurrence [13]. Additionally, the overexpression of HE4 in serous ovarian cancer tumors has been associated with tumorogenisis, proliferation, chemoresistance and decreased survival [14].

Historically, the treatment of epithelial ovarian cancer has been approached as a homogenous disease, but the evolving understanding of the molecular and histologic differences between subtypes has important implications for the development of more personalized treatment approaches. While cellular and tissue HE4 expression in various histologic subtypes of malignant tissue has been well documented via immunohistochemical staining, western blot and PCR analysis [15, 16], the differential expression of serum HE4 levels has not been thoroughly described in terms of histologic categories of various tumors. The largest study to date by Hertlein et al measured serum HE4 levels from 704 samples from both males and females [17]. However, this study only included 215 ovarian cancers and did not breakdown the tumors by histologic subtypes. Recently, HE4 overproduction has been shown to decrease the cellular immune response in the ovarian cancer tumor microenvironment and may be a targetable protein for treatment [18]. Because of the evolving role of HE4 in ovarian and other gynecologic cancers, it is important to clearly understand which of the various malignancies and histologic subtypes overexpress the WFDC2 gene and can be measured through serum HE4 levels in women with these malignancies. The goal of this study was to determine the differential expression and the measurement of serum HE4 levels in women with various histologic subtypes of EOC and other gynecologic and non-gynecologic malignancies.

2 Methods

This study includes data obtained from six prospective Institutional Review Board (IRB) approved clinical trials. This study was approved by the University of Rochester Medical Center, Wilmot Cancer Institute Institutional Review Board. A database was created by compiling de-identified data from the six clinical trials (BWH pilot study, MD Anderson pilot study, WIH pilot study, FDI-03 pelvic mass trial, FDI-15 pelvic mass trial, WIH-RS study, WIH-Ovarian Biomarker Trial). In each study, serum was obtained from patients within 30 days prior to surgery. Final pathologic diagnoses for each patient were determined by trained gynecologic oncology pathologists, and the primary tumor site, histologic subtype, grade, and stage were recorded for each patient. Demographic factors such as age and menopausal status were also documented. Serum HE4 assays antibodies are manufactured by Fujirebio (Fujirebio Diagnostics, Malvern PA) and are used in the assay kits for the Abbott ARCHITEC i2000 platform (Abbot Diagnostics Inc., Chicago, IL, USA), the Fujirebio (CanAG) HE4 EIA test kit (Fujirebio Diagnostics, Gothenburg, Sweden) and the Lumiplse G-System HE4 assay (Fujirebio Diagnostics, Malvern, PA, USA). The Fujirebio manufactured kits for each platform have been standardized to the Fujirebio HE4 EIA kit, and the measurements are all comparable. Measurement of serum HE4 levels using the Roche and Abbott platforms compared to the Fujirebio HE4 EIA have been verified for harmonization and agreement of the automated methods versus the semi-automatedHE4 EIA method [19]. For each patient, one of the three HE4 assay platforms was used to determine serum HE4 levels prior to surgery, though the exact assay used varied by the clinical trial. An upper limit of normal threshold of < 70.0 pM was chosen for this analysis. This cut point has previously been established and validated in several studies in healthy women and was used for this analysis [20, 21]. The mean, median, standard deviation, maximum, and minimum HE4 levels were determined for each group. The expression levels of HE4 as a biomarker for malignancy was calculated for each category using a threshold of ≥70.0 pM. Student‘s t-testing was used to compare mean HE4 values between groups and Fisher’s Exact test was used to compare proportions of subjects in the different groups with HE4 values below and above the cut point of ≥70.0 pM. One-way ANOVA with a Turnkey multiple comparison post-test was also performed as appropriate. P-values < 0.05 were considered to be statistically significant.

3 Results

A total of 984 patients with a malignancy were included in this study, of which 230 were premenopausal and 754 were postmenopausal women. The average patient age was 60 years (range 18 to 95). Serum HE4 levels were measured using the Fujirebio HE4 EIA assay in 896 samples, the ARCHITEC i2000 in 25 samples and Lumipulse G-Sytem in 63 samples. The number of patients from each trial included in this cohort as well as the average age and range of ages included in the study population are shown in Table 1. There were 766 patients diagnosed with ovarian malignancies, including 623 invasive EOC, 129 borderline tumors and 14 germ cell or sex cord stromal tumors (SCST). Non-ovarian gynecologic primary malignancies included 143 uterine endometrial cancers, 12 cervical cancers and 10 uterine sarcomas. There were 53 metastatic non-gynecologic cancers, which included 27 colon, 14 small bowel and gastric, 5 pancreatic, 2 mesothelioma, 2 lymphoma and 1 each of kidney, lung, and breast cancers. The distribution of cancer types as a percentage of all pelvic masses in the study cohort are displayed in Fig. 1.

Table 1
Study demographics

Clinical Trial N Average Age (Range) Pre-Menopausal Post-Menopausal

% Average Age (Range) % Average Age (Range)

BWH Pilot Study 166 54 (20–86) 36.1% 44 (20–55) 63.9% 59 (46–86)

MD Anderson Pilot 112 61 (19–88) 20.5% 43 (19–51) 79.5% 65 (52–88)

WIH Pilot Study 227 64 (18–95) 15.0% 42 (18–51) 85.0% 68 (48–95)

FDI-03 National Trial 184 59 (21–87) 25.5% 43 (21–59) 74.5% 65 (42–87)

FDI-15 National Trial 89 58 (25–83) 24.7% 43 (25–55) 75.3% 63 (48–83)

WIH - RS 25 62 (37–84) 12.0% 41 (37–44) 88.0% 65 (51–84)

WIH-OBMT 181 60 (23–91) 22.7% 42 (23–64) 77.3% 65 (45–91)

All Combined 984 60 (18–95) 23.4% 43 (18–64) 76.6% 65 (42–95)

Clinical Trial	N	Average Age (Range)	Pre-Menopausal	Post-Menopausal
BWH Pilot Study	166	54 (20–86)	36.1%	44 (20–55)	63.9%	59 (46–86)
MD Anderson Pilot	112	61 (19–88)	20.5%	43 (19–51)	79.5%	65 (52–88)
WIH Pilot Study	227	64 (18–95)	15.0%	42 (18–51)	85.0%	68 (48–95)
FDI-03 National Trial	184	59 (21–87)	25.5%	43 (21–59)	74.5%	65 (42–87)
FDI-15 National Trial	89	58 (25–83)	24.7%	43 (25–55)	75.3%	63 (48–83)
WIH - RS	25	62 (37–84)	12.0%	41 (37–44)	88.0%	65 (51–84)
WIH-OBMT	181	60 (23–91)	22.7%	42 (23–64)	77.3%	65 (45–91)
All Combined	984	60 (18–95)	23.4%	43 (18–64)	76.6%	65 (42–95)

Fig. 1

Distribution of cancer types as a percentage of all pelvic masses (n = 984).

Evaluation of primary tumors revealed that HE4 was elevated (≥70.0 pM) in 84.9%of all invasive EOC cases, with a lower proportion of the premenopausal women having elevated HE4 at the time of surgery compared to the postmenopausal women (77.4%vs. 86.8%, respectively, p = 0.012). In contrast, the serum levels of HE4 for other primary gynecologic and non-gynecologic malignancies was significantly lower (p < 0.05), indicating an increased expression of HE4 in more of the invasive EOCs compared with other primaries (Table 2, Fig. 2).

Table 2

Summary of HE4 for individual Primary malignancies and All Malignancies by menopausal status

Primary Site	Pre-Menopausal					Post-Menopausal					All
	N	Average±SD	Median	Min	Max	N	Average±SD	Median	Min	Max	N	Average±SD	Median	Min	Max
Invasive EOC	124	434.0±605.2	213.4	17.2	4632.0	499	922.7±1873.0	340.1	4.9	16991.0	623	825.5±1708.6	318.1	4.9	16991.0
Borderline	56	111.3±155.2	62.7	20.1	880.3	73	94.2±109.2	61.9	7.7	820.6	129	101.6±130.9	62.6	7.7	880.3
Germ	9	56.4±18.6	53.5	29.4	85.5	5	63.3±42.9	48.7	28.8	136.7	14	58.9±28.1	51.1	28.8	136.7
Cell &SCST
Uterine	19	178.1±333.9	45.3	25.7	1251.3	124	232.0±492.6	95.2	15.3	4062.7	143	224.8±474.0	84.6	15.3	4062.7
(Endometrial)
Uterine	2	80.1±75.1	80.1	27.0	133.2	8	73.3±28.6	69.6	36.9	114.3	10	74.6±35.6	69.6	27.0	133.2
(Sarcoma)
Cervical	4	48.9±29.3	42.3	23.0	88.1	8	67.4±59.7	41.3	23.3	184.2	12	61.2±50.8	41.3	23.0	184.2
Colon	10	108.5±109.0	53.1	39.4	370.7	17	99.8±59.4	81.7	33.9	214.8	27	103.0±79.4	69.3	33.9	370.7
GI (Upper)	5	48.2±26.6	38.9	25.4	89.6	9	67.1±29.5	57.3	28.9	114.0	14	60.4±29.0	52.8	25.4	114.0
All Metastatic	16	85.8±90.7	50.7	25.4	370.7	37	102.1±79.8	75.4	28.9	393.7	53	97.2±82.7	62.9	25.4	393.7
All Cancers +	230	285.5±488.3	88.4	17.2	4632.0	754	664.9±1579.0	181.4	4.9	16991.0	984	576.2±1411.1	153.2	4.9	16991.0
LMP

Fig. 2

Percentage of elevated HE4 across cancers, ANOVA p-value = <0.0001. ^*Significantly different when compared to All Invasive EOCs, P < 0.05.

Examination of the histologic subtypes of invasive EOC revealed that HE4 was elevated in the majority of serous, endometrioid, and mixed tumors as well as in rare histologic subtypes (undifferentiated, carcinosarcoma and neuroendocrine), with levels ≥70.0 pM in 90.0%, 84.9%, 86.3%and 90.0%, respectively. A significantly smaller proportion of the patients with mucinous and clear cell carcinomas had elevated serum levels of HE4 compared to all other subtypes (Table 3 and Fig. 3, p < 0.05). These findings held true when taking into consideration menopausal status as well. ANOVA analysis demonstrated that serum levels are significantly different between the different histologic subtypes of invasive EOC (p = 0.007).

Table 3

Summary of HE4 for all invasive EOC histologic subtypes

EOC	Pre-Menopausal					Post-Menopausal					All
	N	Average±SD	Median	Min	Max	N	Average±SD	Median	Min	Max	N	Average±SD	Median	Min	Max
Serous	64	585.0±708.9	386.0	39.9	4632.0	327	1021.9±1749.7	447.3	4.9	16991.0	391	950.3±1632.9	412.7	4.9	16991.0
Endometrioid	21	367.0±513.4	167.5	18.6	1976.0	52	916.6±2365.3	283.5	42.6	12800.0	73	758.5±2024.5	269.6	18.6	12800.0
Clear Cell	10	160.4±330.1	58.1	17.2	1095.1	26	261.8±270.0	155.2	30.0	1170.5	36	233.6±286.7	108.7	17.2	1170.5
Mucinous	15	87.4±100.3	50.5	24.4	414.9	27	160.9±204.3	97.0	12.7	1003.6	42	134.6±176.5	63.6	12.7	1003.6
Mixed	10	441.7±551.4	257.7	32.6	1853.8	41	1295.9±3217.3	393.1	33.8	15146.6	51	1128.4±2907.3	336.8	32.6	15146.6
Rare EOC^*	4	333.8±206.4	326.3	90.5	592.0	26	551.9±539.7	451.1	5.3	2095.2	30	522.8±511.0	384.6	5.3	2095.2

^*Undifferentiated, Carcinosarcoma, neuroendocrine.

Fig. 3

Percentage of elevated HE4 across histologic subtypes of invasive EOC. ANOVA p-value = 0.0067. ^*Significantly different when compared to Serous EOCs, P≤0.05. ^**Rare EOC = Undifferentiated, Carcinosarcoma, neuroendocrine.

In addition to differential expression by histologic subtype, HE4 levels were stratified by cancer stage and grade, showing an increasing proportions of patients with elevated serum HE4 levels as both stage and grade increased (Table 4, Fig. 4). Serum HE4 levels increased with increasing FIGO stage in EOC, reflecting a correlation of HE4 expression and tumor burden. Serum HE4 levels were not significantly different between individual stages of EOC but was found to be significantly different between early and late-stage disease, with 65.8%of stage I-II cases (n = 193) having an elevated serum HE4 levels versus 93.6%of stage III-IV cases (n = 424) with elevated serum HE4 levels (p < 0.001). Serum HE4 was elevated in 60.9%, 84.3%, and 88.4%of grade I (n = 69), II (n = 83), and III (n = 465) EOCs respectfully. Of note, the serum HE4 levels were similar for both pre and postmenopausal status across grade and stage (Fig. 4).

Table 4

Summary of HE4 by Stage and Grade of invasive EOC

EOC	Pre-Menopausal					Post-Menopausal					All
	N	Average±SD	Median	Min	Max	N	Average±SD	Median	Min	Max	N	Average±SD	Median	Min	Max
Stage I	38	221.9±429.5	66.4	17.2	1976.0	88	240.9±296.9	109.9	5.3	1628.5	126	235.2±340.6	105.8	5.3	1976.0
Stage II	11	310.0±355.4	243.0	26.1	1253.0	56	288.9±535.6	122.9	18.1	3764.0	67	292.4±508.2	123.4	18.1	3764.0
Stage III	66	515.5±632.3	363.1	39.9	4632.0	315	1263.7±2256.8	576.5	6.7	16991.0	381	1134.1±2087.4	539.7	6.7	16991.0
Stage IV	6	1211.6±976.6	1182.7	71.3	2796.0	37	648.0±752.9	417.1	4.9	3189.0	43	726.6±799.1	515.4	4.9	3189.0
Grade 1	34	241.3±426.9	96.3	17.2	1976.0	35	313.9±465.1	140.2	32.1	2511.9	69	278.1±444.9	115.9	17.2	2511.9
Grade 2	15	330.7±283.4	273.7	49.9	941.0	68	979.1±2063.5	303.7	12.7	13250.0	83	861.9±1885.7	283.0	12.7	13250.0
Grade 3	75	541.9±693.8	349.2	26.0	4632.0	391	975.5±1920.2	395.8	4.9	16991.0	466	905.8±1787.3	387.5	4.9	16991.0

Fig. 4

Percentage of elevated HE4 in relationship to Stage and Grade.

4 Discussion

The purpose of this study was to understand the differential expression of the serum tumor marker HE4 in women diagnosed with EOC and other malignancies. Serum HE4 was stratified across primary site of cancer, histologic subtype, grade, and stage of ovarian cancers. All serum samples were obtained prior to surgery and were correlated with histopathologic diagnosis. When comparing HE4 levels across histologic subtypes of EOC, increased serum HE4 levels were seen in serous, endometrioid and mixed histologic subtypes of EOC. Our findings also demonstrated that increasing serum HE4 levels correlate with advancing stage and grade of EOCs. The biomarker serum CA125 has been shown to be a prognostic indicator when highly elevated in women with EOC, and likewise, serum HE4 levels has also been shown to be an excellent biomarker for prognosis, monitoring response to treatment and detecting recurrent disease [22]. Additionally, both markers have been found to compliment one and another [7].

Serum HE4 measurements employed in the Risk of Malignancy Algorithm (ROMA) is useful as a tool for risk stratification in women with a pelvic mass, and therefore, understanding the expression of HE4 in various cancers is important [7, 8]. HE4 is a relatively new clinical marker for the management of women with EOC and has been shown to be prognostic for stage, grade, disease recurrence, and more recently, chemoresistance [12 , 23–25]. Here, we show that serum HE4 level does vary by cancer subtype, possibly explaining its strong prognostic impact. Additionally, HE4 over-expression has been associated with a more aggressive cancer phenotype, characterized by immune evasion, tumorigenesis, and cancer cell adhesion and motility [14 , 26–28].

In the cancers evaluated in this analysis, mean levels of serum HE4 differed between histologic subtypes of EOC, with higher levels being more suggestive of serous or mixed EOC and lower levels more likely to be mucinous or clear cell on histologic examination. As our understanding of EOC has progressed, the heterogeneity of the disease has become more apparent. It is now widely known that EOC subtypes behave very differently. This difference in behavior is reflective of the varying genetic mutations that are found to be hallmarks for a particular subtype. As mentioned in the introduction, type 2 tumors, such as high-grade serous carcinoma, are more likely to harbor p53 mutations and carry a worse prognosis. In our study, patients with these types of tumors were more likely to exhibit higher serum levels of HE4. In 2013, Kristjansdottir and colleagues reported similar findings in a smaller cohort of 373 patients [29].

HE4 itself may prove to be a useful therapeutic target. Recent work focusing on HE4’s function in cellular pathways has shown that its over-expression promotes proliferation, invasion, and metastases of cancer cells. HE4 has been implicated in diverse processes, from the EGFR-MAPK signaling pathway to steroid biosynthesis [30]. HE4 over-expression has also been shown to promote cisplatin resistance in ovarian cancer cells. In a 2014 study looking at ovarian cancer tumor cells and tumor growth in a mouse model, nuclear translocation of HE4 was linked with activity of VEGF and antisense targeting of HE4 suppressed tumor growth [14]. HE4 has also been shown in the tumor microenvironment to increase PD-L1 expression, inhibit CD8+ T cell infiltration, and decrease Natural Killer cell recruitment and differentiation of macrophages to the inactive M2 type, resulting in a decrease immune response in the tumor microenvironment [18]. Further investigation of the potential regulatory role of HE4 in these pathways may provide insight into why certain EOC subtypes respond poorly to standard therapies and provide new potential therapeutic targets to improve outcomes for patients. This study also highlighted an association between HE4 expression and more advanced grades and stages of EOC. This may be explained by recent studies that suggest a role for HE4 in cell adhesion and motility, which are essential to metastatic spread and the epithelial-to-mesenchymal transition [31]. Additionally, HE4 has been implicated in immune system evasion, and it is possible that targeting HE4 in this setting may restore the natural immune response and prevent or delay disease progression [27].

This is the largest study to date analyzing serum from 984 women to compare serum levels of HE4 amongst histologic subtypes of EOC as well as other gynecologic and non-gynecologic malignancies. Our data demonstrate that mean levels of serum HE4 differ across EOC subtypes, grade, and stage. Serum HE4 was elevated in a greater percentage of patients with serous, endometrioid and mixed subtypes. These findings provide further insight to the expression of HE4 in ovarian cancer tumors. The large number of cases included in the study is a major strength, and it is to our knowledge the largest study examining serum HE4 expression across pelvic tumors to date. Limitations of the study include the small number of other ovarian, gynecologic, and non-gynecologic malignancies, resulting in the inability to make a broader statement on malignancies. However, typically at least 10 cases are needed to determine expression in various tumors, and these numbers were reached in most instances of non-EOC tumors.

In summary, serum HE4 is elevated and over expressed for EOCs, particularly in patients facing advanced stage or high-grade disease. HE4 is not often expressed in non-EOCs or non-gynecologic metastatic pelvic tumors. HE4 expression shows variation among different histologic subtypes, with higher levels being found in serous, endometrioid and mixed subtypes.

5 Author contributions

CONCEPTION: RGM

DATA CURATION: RS, KKK, EK, RCB, GM, MCM and RGM

ANALYSIS OF DATA: AB, JM, SS, GM, MCM and RGM

PREPARATION OF THE MANUSCRIPT: All authors

REVISION FOR IMPORTANT INTELLECTUAL CONTENT: All authors

SUPERVISION: RGM

Footnotes

Acknowledgments

The authors have no acknowledgments.

Conflict of interest

Alexandra Blackman: no conflicts of interest.

Jesica Mitchel: no conflicts of interest.

Rakesh Singh: no conflicts of interest.

Kyu Kwang Kim: no conflicts of interest.

Steven Skates: Consulting for LUNGevity Foundation; Scientific Advisory Board for SISCAPA Assay Technologies and Mercy BioAnalytics.

Robert Bast: Royalties from Fujirebio Diagnostics Inc.

Geralyn Lambert-Messerlian: Research grants Fujirebio Diagnostics Inc.

M. Craig Miller: Consultant Fujirebio Diagnostics Inc.

Richard Moore: Consulting for Fujirebio Diagnostics Inc and Abcodia; Research grants Angle plc.

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