CA125, CEA, CA19-9, and Heteroploid Cells in Ascites Fluid May Help Diagnose Peritoneal Carcinomatosis in Patients with Gastrointestinal and Ovarian Malignancies.

BACKGROUND: This study explored the value of ascites and serum CA125, CEA, and CA19-9 levels and ascites DNA ploidy analysis for the diagnosis of peritoneal carcinomatosis (PC) in patients with gastrointestinal and ovarian malignancies, which can cause ascites and may disseminate peritoneally.
METHODS: We measured ascites and serum levels of CA125, CEA, CA19-9 and performed an ascites DNA ploidy analysis in 58 patients with PC and 44 patients without PC.
RESULTS: We found that a high expression level of CA125 in ascites fluid was associated with the occurrence of PC in patients with gastrointestinal and ovarian malignancies (P<0.001), and that high CEA and CA19- 9 levels in ascites fluid were associated with PC in patients with gastrointestinal malignancies (P=0.001, P=0.002). But, these tumor marker expression levels in ascites fluid were not significantly associated with the PC stage (P>0.05). We found similar serum levels of CA125, CEA, and CA19-9 between patients with gastrointestinal and ovarian malignancies and PC and those without PC (P>0.05). We found that the presence of three or more cells with heteroploid in the ascites samples was significantly associated with PC in gastrointestinal and ovarian malignancies (P<0.001). In addition, the best ROC curves and highest AUCs were achieved by combining the CA125 level and heteroploid cell analysis results (AUC for gastrointestinal and ovarian malignancies, 0.815, AUC for gastrointestinal malignancies, 0.873). Moreover, the combined ascites CA125 level and result of heteroploid cell analysis provided the best diagnostic sensitivity and specificity for PC (75.9% and 79.5%, respectively, in gastrointestinal and ovarian malignancies; 85.0% and 86.7%, respectively, in gastrointestinal malignancies).
CONCLUSION: Ascites levels of CA125, CEA, CA19-9, and heteroploid cells can be considered valuable markers for the diagnosis of PC in patients with gastrointestinal and ovarian cancer.

Introduction

Ascites can be caused by a variety of factors such as portal vein tumor thrombosis, malnutrition, peritonitis, vascular or lymphatic vascular invasion, and peritoneal carcinomatosis (PC) in patients with malignant tumors.1 Abdomen pelvic cavity cancer can easily induce the appearance of ascites. Gastrointestinal and ovarian malignancies have the potential to disseminate and grow in the peritoneal cavity, and peritoneal carcinomatosis is often associated with poor prognosis.2,3 Combined therapy mainly composed of surgery should be adopted in patients with gastrointestinal cancer to improve the survival rate, but the occurrence of PC has been shown to signal the failure of surgical therapy.4 Furthermore, this condition is commonly observed in ovarian cancer, and PC of the tumor is the most common cause of death.5 Therefore, early PC diagnosis and treatment in patients with ascites are very important. At present, the gold standard for PC diagnosis is direct peritoneal visualization, either by laparotomy or laparoscopy combined with pathology.6 For patients with massive ascites who are not surgical candidates, imaging techniques (such as Computed Tomography or MRI) and the detection of tumor cells in ascites can be used to help diagnose PC.7,8 However, imaging examinations are limited in their ability to visualize localized PC, due to low sensitivity for small lesions. The detection rate of tumor cells in cases with massive ascites is low. Therefore, new methods to assist in diagnosing PC are needed.

Serum tumor markers are widely used for diagnosis, treatment effect assessment, and disease monitoring.9 However, few studies have explored the diagnostic value of tumor markers for PC in ascites fluid. Some researchers have argued that peritoneal fluid carcinoembryonic antigen (CEA) has predictive value for PC and prognostic value in colorectal cancer.10 The CEA is the most widely used tumor marker. The carbohydrate antigen 125 (CA125) is highly specific for gastrointestinal and ovarian malignancies, and the carbohydrate antigen 199 (CA19-9) is used particularly to diagnose gastrointestinal cancers.11 In this study, we detected the ascites and serum levels of CEA, CA125, and CA19-9 in patients with gastrointestinal and ovarian malignancies, which have the potential to disseminate in the peritoneum, to determine whether these levels are associated with the presence of PC.

Flow cytometry DNA ploidy analysis can analyze relatively small numbers of cells and provides general chromosomal/ploidy information in many diseases. DNA ploidy analysis can signal gross genomic aberrations and has been used to determine prognoses in pre-cancerous and cancerous lesions.12 According to some authors, DNA flow cytometric parameters have prognostic value in differentiating benign from malignant fluids in the serous membrane cavity.13 In this study, we explored whether DNA ploidy analysis of ascites fluid can assist in the diagnosis of PC.

Patients and Methods

Patients

A total of 102 patients with gastrointestinal and ovarian malignancy with moderate to severe ascites diagnosed and treated at the Tangdu Hospital of the Air Force Military Medical University from January 2016 to January 2020 participated in our study (38 with gastric cancer, 32 with colon cancer, and 32 with ovarian cancer). Among them, 58 patients were diagnosed as having PC, including 22 with gastric cancer, 18 with colon cancer patients, and 18 with ovarian cancer (20 patients diagnosis was confirmed by pathologic results, 38 patients had cancer cells detected in ascites fluid according to pathology results and imaging results); and 44 patients did not have PC, including 16 with gastric cancer, 14 with colon cancer, and 14 with ovarian cancer. All patients had ascites volumes greater than 1500 mL, as evaluated by ultrasound (we found no patients with hemorrhagic or chyliform ascites). To avoid possible effects of chemotherapy on the ascites and serum levels of CEA, CA19-9, and CA125, none of the selected patients had undergone chemotherapy in the month prior to the samplings. We used the Lyon staging system (Gilly PC) descriptions for quantifying PC divided into 5 stages from 0 to 4 and estimated based on imaging techniques (CT, MRI): Stage 0, no macroscopic disease; stage 1, malignant granulations less than 5 mm in diameter in one part of the abdomen; stage 2, malignant granulations less than 5 mm in diameter diffuse throughout the abdomen; stage 3, malignant granulations 5 mm to 2 cm in diameter; and stage 4, large malignant cakes (more than 2 cm in diameter).14 Table 1 presents the detailed characteristics of the patients.

Table 1

Patient Characteristics

Characteristics	CRC (N=32)	GC (N=38)	OC (N=32)
Age (years)
Median	57	59	55
Range	29–79	39–80	37–75
Gender, n(%)
Male	19(59.4)	24(63.2)	0(0)
Female	13(40.6)	14(36.8)	32(100.0)
Performance status
(ECOG), n(%)
1	7(21.8)	13(34.2)	12(37.5)
2	15(46.9)	21(55.3)	16(50.0)
3	10(31.3)	4(10.5)	4(12.5)
Tumor histology, n(%)
Adenocarcinoma	32(100.0)	38(100.0)	－
Serous	－	－	22(81.3)
Mucinous	－	－	10(18.7)
Tumor site, n(%)
Right	17(53.1)	－	－
Left	15(46.9)	－	－
Tumor stage (TNM), n(%)
III	11(34.4)	12(31.6)	16(50.0)
IV	21(65.6)	26(68.4)	16(50.0)
Histologic differentiation
Well	5(15.6)	4(10.6)	4(12.5)
Moderate	17(53.1)	17(44.7)	18(56.3)
Poor	10(31.3)	17(44.7)	10(31.2)
Peritoneal metastasis, n(%)
Positive	18(56.3)	22(57.9)	18(56.3)
Negative	14(43.7)	16(42.1)	14(43.7)
Liver metastasis, n(%)
Positive	16(50.0)	17(44.7)	7(21.9)
Negative	16(50.0)	21(55.3)	25(78.1)
Ascites volume, n(%)
1500–3000mL	13(40.6)	19(50.0)	14(43.8)
over 3000 mL	19(59.4)	19(50.0)	18(56.2)
Diagnosis method of PC(N=58), n(%)
Pathological diagnosis	5(27.8)	8(36.4)	7(38.9)
CT and tumor cell in ascites	9(50.0)	14(63.6)	6(33.3)
MRI and tumor cell in ascites	4(22.2)	0(0)	5(27.8)
Gilly PC (N=58), n(%)
1	6(33.3)	4(18.2)	2(11.1)
2	4(22.2)	4(18.2)	4(22.2)
3	7(38.9)	10(45.4)	7(38.9)
4	1(5.6)	4(18.2)	5(27.8)
Treatment received
Prior chemotherapy, n(%)
Yes	16(50.0)	24(63.2)	11(34.4)
No	16(50.0)	14(36.8)	21(65.6)
Prior surgery, n(%)
Yes	15(46.9)	26(68.4)	12(37.5)
No	17(53.1)	12(31.6)	20(62.5)

Abbreviations: CRC, colorectal cancer; GC, gastric cancer; OC, ovarian cancer.

Specimen Collection and Tumor Marker Assays

Ascites samples were collected from patients with various conditions during diagnostic or therapeutic paracenteses. The fasting venous blood specimens of all patients for tumor marker detection were obtained through venipuncture. Ascites (approximately 5 mL) and venous blood samples (approximately 3 mL) were centrifuged for 10 min at 3000 rpm. The supernatants were stored in separate tubes at −80 °C for further analysis. CEA levels were investigated using a fluorescence-enzyme immunoassay (FEIA), while CA19-9 and CA125 levels were investigated using a chemiluminescent enzyme immunoassay (CLEIA); these assays were performed at the Department of Clinical Laboratory. Ascites (approximately 200 mL) were taken to the pathology department for cytologic evaluation and DNA ploidy analysis. The peritoneal biopsy, serum collection and paracentesis were done the same week with CT/MRI scans, and there is no change in the tumor stage during this time. The institutional review board (IRB) at Tangdu Hospital, approved this study, and we obtained a prior written informed consent from every patient.

Cell Cycle Analysis and Ploidy Analysis

DNA ploidy analysis was performed using a flow cytometer. After fixing 150 µL ascites samples with 70% alcohol, they were stained with propidium iodide (50 µg/mL, Sigma, St. Louis, Missouri, USA). Nuclear DNA was measured in a flow cytometer. Usually, 10,000 nuclei were counted and DNA ploidy was expressed by the DI. The DI was calculated according to the principles recommended by consensus: DI represents the ratio of the aneuploid G1-G0-DNA peak channel to the diploid G1-G0-DNA peak channel. For this series, we classified populations with 1.0< DI<1.2 as near-diploid cases and separated them from DNA aneuploid tumors. We analyzed DNA ploidy in 102 patient samples. Among them, 18 lacked cells with DNA heteroploidy, 27 had 1 to 2 cells with heteroploidy, and 57 had three or more cells with heteroploidy.

Statistical Analysis

We used the Statistical Package for Social Sciences (SPSS®, IBM) version 20 software for statistical data analyses. All values are expressed as medians (minimum-maximum). After the homogeneity test, we used nonparametric tests (Mann–Whitney U-test, Kruskal–Wallis H-test) for statistical evaluation. We evaluated a difference between positive rates by the Chi-square test. We plotted receiver operating characteristic (ROC) curves and calculated the areas under the curve (AUC). We applied ROC curve and Youden index analyses to calculate the optimal cut-off values for ascites tumor markers. For all analysis, P values <0.05 indicated statistical significance.

Results

Elevated CA125 Levels in Ascites Fluid Were Associated with the Incidence of PC in Patients with Gastrointestinal and Ovarian Cancer

In patients with gastrointestinal and ovarian cancer, the expression level of CA125 in ascites fluid was associated with the presence of PC (P<0.001), but it did not correlate with the tumor stage, histologic differentiation, or liver metastasis (P>0.05). However, we found similar serum levels of CEA, CA19-9, and CA125 between patients with PC and without PC (P=0.88, P=0.82, and P=0.22, respectively) (Table 2). Our results show that ascites fluid CA125 levels may help during PC screening in patients with gastrointestinal and ovarian cancer and ascites. For this study, we calculated the ascites volume of patients by ultrasound and categorized them into 2 groups: 1500 mL to 3000 mL and > 3000 mL. The CA125 level in ascites fluid was associated with the volume of ascites (P=0.04) (Table 2).

Table 2

The Ascites and Serum Tumor Marker Levels in Gastrointestinal and Ovarian Cancer Patients

Characteristics (N=102)	Ascites CEA	P-value	Serum CEA	P-value	Ascites CA19-9	P-value	Serum CA19-9	P-value	Ascites CA125	P-value	Serum CA125	P-value
Peritoneal metastasis
Positive	137.90(0.24–1000.00)	0.15a	20.40(0.25–1000.00)	0.88a	180.91(0.60–10,000.00)	0.06a	53.91(0.60–10,000.00)	0.82a	638.73 (72.98–5000.00)	<0.001a	258.92(28.45–5000.00)	0.22a
Negative	79.72(0.20–497.54)		17.70(0.50–290.80)		55.25(0.60–917.50)		32.34(0.60–1396.00)		372.01(35.89–1850.00)		161.82(48.02–855.62)
Tumor stage(TNM)
III	17.98 (0.20–871.56)	0.13a	10.29 (0.25–290.80)	0.48a	31.25 (0.60–917.50)	0.06a	27.03(0.60–1396.00)	0.35a	490.79 (35.89–5000.00)	0.20a	158.90 (48.02–2501.00)	1.00a
IV	127.58 (0.24–1000.00)		25.78 (0.28–1000.00)		202.21 (0.60–10,000.00)		68.07(0.60–10,000.00)		589.00 (72.98–5000.00)		233.20 (28.45–5000.00)
Histologic differentiation
Well	80.89 (0.35–871.56)	0.57b	23.47(0.25–290.80)	0.97b	50.66 (0.60–917.50)	0.54b	43.79 (0.60–1396.00)	0.96b	440.50 (69.85–3547.50)	0.78b	143.60 (89.20–579.86)	0.52b
Moderate	91.00 (0.20–1000.00)		17.70(0.28–877.20)		119.31 (0.60–10,000.00)		32.34 (0.60–9903.00)		519.54 (35.89–5000.00)		189.37 (28.45–1007.00)
Poor	127.58 (0.33–1000.00)		15.02(0.33–1000.00)		161.48 (2.12–10,000.00)		41.25 (1.64–10,000.00)		593.50 (74.58–5000.00)		270.56 (32.56–5000.00)
Liver metastasis
Positive	135.51 (0.33–1000.00)	0.07a	32.44 (0.28–1000.00)	0.21a	202.86 (1.20–10,000.00)	0.05a	64.86 (1.29–9903.00)	0.38a	591.25 (89.66–5000.00)	0.27a	195.03 (28.45–5000.00)	0.18a
Negative	19.93 (0.20–1000.00)		12.13 (0.25–290.80)		31.68 (0.60–10,000.00)		30.18 (0.60–10,000.00)		484.85 (35.89–5000.00)		250.73 (48.02–2501.00)
Ascites volume
1500–3000mL	84.21 (0.20–1000.00)	0.76a	11.30 (0.50–877.20)	0.56a	138.73 (0.60–6213.00)	0.45a	41.27 (0.60–5371.00)	0.64a	445.87 (69.85–5000.00)	0.04a	158.90 (28.45–1622.00)	0.13a
Over 3000mL	104.20 (0.24–1000.00)		23.69 (0.25–1000.00)		116.11 (1.00–10,000.00)		32.71 (0.60–10,000.00)		597.38 (35.89–5000.00)		267.08 (32.56–5000.00)

Notes: aMann–Whitney U-test; bKruskal–Wallis H-test. P<0.05.

Elevated CEA and CA19-9 Levels in Ascites Fluid Were Associated with the Incidence of PC in Patients with Gastrointestinal Cancer

CEA and CA19-9 are more specific tumor markers for gastrointestinal cancer than for ovarian cancer. Through our clinical data analysis, we found that increased ascites CEA and CA19-9 levels in patients with gastrointestinal cancer and PC may be meaningful (P=0.001, P=0.002, respectively). But, ascites CEA and CA19-9 levels were not correlated with tumor stage, histologic differentiation, ascites volume, or liver metastasis (P>0.05). We found similar serum levels of CEA and CA19-9 between patients with PC and without PC (P=0.19, P=0.08, respectively) (Table 3).

Table 3

The Ascites and Serum Tumor Marker Levels in Gastrointestinal Cancer Patients

Characteristics (N=70)	Ascites CEA	P-value	Serum CEA	P-value	Ascites CA19-9	P-value	Serum CA19-9	P-value	Ascites CA125	P-value	Serum CA125	P-value
Peritoneal metastasis
Positive	278.50(0.63–1000.00)	0.001a	45.76(0.77–1000.00)	0.19a	310.86(0.60–10,000.00)	0.002a	142.40(0.60–10,000.00)	0.08a	563.95(72.98–2954.00)	0.001a	190.05 (28.45–847.10)	0.22a
Negative	118.50 (0.20–497.54)		29.90(0.94–290.80)		155.91(0.60–917.50)		74.50(0.60–1396.00)		272.85(35.89–843.20)		131.78 (48.02–584.20)
Tumor stage(TNM)
III	145.69 (0.20–871.56)	0.17a	37.15 (1.36–290.80)	0.66a	150.33 (0.60–917.50)	0.13a	49.47 (0.60–1396.00)	0.36a	314.89 (35.89–698.20)	0.06a	135.00 (48.02–584.20)	0.48a
IV	223.63 (0.63–1000.00)		41.13 (0.77–1000.00)		289.15 (0.60–10,000.00)		134.12 (0.60–10,000.00)		515.52 (72.98–2954.00)		189.54 (28.45–847.10)
Histologic differentiation
Well	90.54 (0.35–871.56)	0.32b	48.78 (1.43–290.80)	0.59b	159.60 (0.60–917.50)	0.39b	108.90 (0.60–1396.00)	1.00b	402.65 (69.85–1217.00)	0.47b	135.00 (89.20–391.40)	0.38b
Moderate	172.26 (0.20–1000.00)		39.83 (0.77–877.20)		227.92 (0.60–10,000.00)		122.64 (0.60–9903.00)		449.41 (35.89–1841.00)		140.32 (28.45–584.20)
Poor	221.23 (0.63–1000.00)		34.98 (0.94–1000.00)		297.89 (2.12–10,000.00)		127.46 (1.64–10,000.00)		497.47 (74.58–2954.00)		199.50 (41.95–847.10)
Liver metastasis
Positive	221.23 (0.63–1000.00)	0.62a	48.88 (0.77–1000.00)	0.72a	289.15 (2.12–10,000.00)	0.24a	134.12 (1.64–9903.00)	0.72a	341.36 (35.89–2954.00)	0.05a	165.90 (28.45–382.10)	0.61a
Negative	169.32 (0.20–1000.00)		37.15 (1.36–290.80)		202.21 (0.60–10,000.00)		119.64 (0.60–10,000.00)		541.98 (89.66–1841.00)		154.24 (48.02–847.10)
Ascites volume
1500–3000mL	144.05 (0.20–1000.00)	0.20a	29.90 (0.77–877.20)	0.11a	288.03 (0.60–6213.00)	0.42a	122.64 (0.60–5371.00)	0.93a	388.94 (69.85–1764.00)	0.16a	133.35 (28.45–501.32)	0.07a
Over 3000mL	227.42 (0.63–1000.00)		48.78 (0.94–1000.00)		214.43 (1.34–10,000.00)		118.18 (1.64–10,000.00)		504.01 (35.89–2954.00)		200.38 (44.48–847.10)

Notes: aMann–Whitney U-test; bKruskal–Wallis H-test. P<0.05.

Association Between Ascites CEA, CA19-9, and CA125 Levels and PC Stage in Patients with Gastrointestinal and Ovarian Cancer

In our previous research, we considered that the expression levels of CEA, CA19-9, and CA125 in ascites were associated with the occurrence of PC. We used the Lyon staging system (Gilly PC) descriptions for quantifying PC into 5 grades from 0 to 4 as estimated using imaging techniques (CT, MRI). However, we found no correlation between ascites tumor marker levels and the Gilly PC stage (P>0.05) (Table 4).

Table 4

Association of Ascites Tumor Marker Levels with Gilly PC Stage in Gastrointestinal and Ovarian Cancer Patients

Category	Gilly PC Stage		P-valuea
	Stage 0–2	Stage 3–4
In gastrointestinal and ovarian cancer patients (N=58)
CA125	556.78(87.65–5000.00)	850.65(72.98–5000.00)	0.08
In gastrointestinal cancer patients (N=40)
CEA	278.50(0.63–1000.00)	231.40(0.71–1000.00)	0.74
CA19-9	289.15(2.12–10,000.00)	378.35(0.60–10,000.00)	0.70

Notes: aMann–Whitney U-test. P<0.05.

Significance of Ascites DNA Ploidy Analysis in Diagnosis of PC

We analyzed DNA ploidy in 102 patients. We defined ascites samples with three or more heteroploid cells as positive, and those without DNA heteroploidy or with only 1 to 2 heteroploid cells as negative. We found that the heteroploid positivity was significantly associated with the presence of PC in patients with gastrointestinal and ovarian cancer (P<0.001) (Table 5).

Table 5

Comparison of Positive Rates of Heteroploid Cells in the Two Groups

Category	Peritoneal Metastasis		x2	P-valuea
	Positive (n, %)	Negative (n, %)
In gastrointestinal and ovarian cancer patients (N=102)
Positive	43(42.2)	14(13.7)	18.18	<0.001
Negative	15(14.7)	30(29.4)
In gastrointestinal cancer patients (N=70)
Positive	31(44.3)	7(10.0)	20.27	<0.001
Negative	9(12.9)	23(32.8)

Notes: aChi-square test. P<0.05.

Receiver Operating Characteristic (ROC) Curve Analysis and Evaluation of the Sensitivity and Specificity of Each of the Tumor Markers for PC Diagnosis

To better assess the diagnostic value of tumor makers and DNA ploidy analysis to detect PC, we plotted ROC curves and calculated AUCs. The results of DNA ploidy analysis were divided into three grades: absence of cells with DNA heteroploidy; 1 to 2 cells with heteroploidy; and 3 or more cells with heteroploidy.

In patients with gastrointestinal and ovarian cancer, the best ROC curves and highest AUC were achieved using a combination of the CA125 level and the heteroploid cell analysis results (AUC, 0.815), followed by using the CA125 level alone (AUC, 0.732). The lowest AUC was achieved using the heteroploid cell analysis results (AUC, 0.703). The cutoff for CA125 was 549.4 U/mL (Figure 1, Table 6). When using two indicators for PC diagnosis, the best sensitivity (75.9%) and specificity (79.5%) were shown when combining the CA125 level and the heteroploid cell analysis result. The highest Youden’s index also was obtained with the CA125 level and heteroploid cell analysis result combination at 55.4% (Table 7).

Figure 1

ROC of tumor markers and heteroploid cells in the diagnosis of PC in gastrointestinal and ovarian cancer patients.

Table 6

The Area of ROC of Ascites Tumor Markers and Heteroploid Cells in Gastrointestinal and Ovarian Cancer Patients

Category	Area	P	95% CI
CA125	0.732	<0.001	0.637–0.828
Heteroploid cells	0.703	<0.001	0.598–0.807
CA125+Heteroploid cells	0.815	<0.001	0.730–0.899

Table 7

Tumor Markers and Heteroploid Cells in the Diagnosis of PC in Gastrointestinal and Ovarian Cancer Patients

Category	Sensitivity (%)	Specificity (%)	Youden’s Index (%)
CA125	63.8	72.7	36.5
Heteroploid cells	74.1	68.2	42.3
CA125+Heteroploid cells	75.9	79.5	55.4

In patients with gastrointestinal cancer, the best ROC curves and highest AUC were achieved using the heteroploid cell analysis results (AUC, 0.760), followed by the CA125 level (AUC, 0.742), and the CEA level (AUC, 0.723). The lowest AUC was achieved using the CA19-9 level (AUC, 0.718). The cutoff levels of CA125, CEA, and CA19-9 were 528.8 U/mL, 211.9 ng/mL, and 283.0 U/mL, respectively. When two indicators were combined, the largest AUC was obtained using the CA125 level and the heteroploid cell analysis result (AUC, 0.873), while the smallest AUC was obtained using the CEA and CA19-9 levels (AUC, 0.788) (Figure 2, Table 8). When using one indicator for PC diagnosis, the best sensitivity was shown by the heteroploid cell analysis result at 77.5%, and the best specificity by the CA125 level at 86.6%. We obtained the highest Youden’s index using the heteroploid cell analysis result (54.2%) and the lowest using the CA125 level (41.7%). The combined use of the CA125 level and the heteroploid cell analysis result led to the highest sensitivity (85.0%) and specificity (86.7%) for two PC indicators. We also obtained the highest Youden’s index (71.7%) after using the same PC indicators’ combination, and we obtained the lowest Youden’s index (52.5%) after using the combination between the CA125 and CEA levels (Table 9).

Figure 2

ROC of tumor markers and heteroploid cells in the diagnosis of PC in gastrointestinal cancer patients.

Table 8

The Area of ROC of Ascites Tumor Markers and Heteroploid Cells in Gastrointestinal Cancer Patients

Category	Area	P	95% CI
CA125	0.742	0.001	0.626–0.857
CEA	0.723	0.001	0.604–0.843
CA19-9	0.718	0.002	0.597–0.839
Heteroploid cells	0.760	<0.001	0.643–0.878
CA125+Heteroploid cells	0.873	<0.001	0.787–0.960
CA125+CEA	0.813	<0.001	0.713–0.912
CA125+CA19-9	0.792	<0.001	0.686–0.897
CEA+Heteroploid cells	0.813	<0.001	0.711–0.915
CEA+CA19-9	0.788	<0.001	0.681–0.896
CA19-9+Heteroploid cells	0.819	<0.001	0.717–0.921

Table 9

Tumor Markers and Heteroploid Cells in the Diagnosis of PC in Gastrointestinal Cancer Patients

Category	Sensitivity (%)	Specificity (%)	Youden’s Index (%)
CA125	55.0	86.6	41.7
CEA	65.0	80.0	45.0
CA19-9	62.5	80.0	42.5
Heteroploid cells	77.5	76.7	54.2
CA125+Heteroploid cells	85.0	86.7	71.7
CA125+CEA	72.5	80.0	52.5
CA125+CA19-9	72.5	83.3	55.8
CEA+Heteroploid cells	82.5	73.3	55.8
CEA+CA19-9	80.0	73.3	53.3
CA19-9+Heteroploid cells	70.0	86.6	56.7

Discussion

Abdomen pelvic cavity cancers, such as gastrointestinal and ovarian cancers, can easily induce the appearance of ascites, and they also can disseminate and grow in the peritoneal cavity.15 Ascites is a common complication of advanced stage cancers with PC.16 Therefore, the appearance of ascites in patients with advanced tumors is associated with an increased risk of PC. Moreover, the appearance of PC is often associated with a poor prognosis. Early PC diagnosis and prompt treatment can prolong the survival of patients. Although the gold standard for PC diagnosis is a pathology result, collecting biopsy tissues from the peritoneum of patients with massive ascites is difficult. Imaging techniques (such as CT or MRI) and the detection of tumor cells in ascites can be used to help diagnose PC, but imaging examinations are limited by their low sensitivity for small lesions, and the detection rate of tumor cells in cases with massive ascites is low. Therefore, new methods to assist in diagnosing PC are needed.

Recently, Kim showed that the ascites CEA level is a risk factor for PC in patients with colorectal cancer.10 This suggests that ascites tumor markers may be clinically useful markers for PC diagnoses. Clinical experience indicates that the presence of malignant cells in ascites fluid is associated with an increase in the risk of PC. Some researchers have argued that the prognosis of patients with gastric cancer and malignant ascites is associated with the presence of PC.17,18 Although cytomorphology remains the foremost diagnostic modality to detect malignant cells in effusions, DNA flow cytometry can detect heteroploid cells and has a complementary value.19 A previous report stated that ascites tumor markers and heteroploid cell analysis results exhibit an excellent diagnostic performance for diagnosing malignant ascites.20–23 In this study, we explored whether ascites tumor markers and heteroploid cell analysis results can assist in diagnosing PC.

We analyzed the diagnostic value of ascites and serum tumor marker levels and heteroploid cell analysis results in ascites fluid for PC in 102 patients with gastrointestinal and ovarian cancer and moderate to severe ascites; we found 58 patients with PC and 44 without it. Our results indicate that an elevated ascites CA125 level was associated with the incidence of PC in patients with gastrointestinal and ovarian cancer (P<0.001). The CA125 level in ascites fluid was significantly associated with the volume of ascites (P<0.05). In addition, elevated ascites CEA and CA19-9 levels were associated with peritoneal dissemination in gastrointestinal cancers (P<0.05). However, we found similar serum levels of CEA, CA19-9, and CA125 between patients with PC and those without PC (P>0.05). Further, we found no correlation between ascites tumor marker levels and Gilly PC stages (P>0.05). Furthermore, we found that the presence of 3 or more cells with heteroploidy in ascites samples was significantly associated with the presence of PC in patients with gastrointestinal and ovarian cancer (P<0.001).

Our data suggest that ascites CEA, CA19-9, and CA125 levels and the quantity of heteroploid cells may be helpful for diagnosing PC in patients with gastrointestinal and ovarian cancer with ascites. However, the sensitivity was low when using a single indicator to diagnosis PC, making it impractical during clinical diagnoses. However, we found that using a combination of two indicators for PC detection (the CA125 level and the number of heteroploid cells) yields a high diagnostic sensitivity and specificity in patients with gastrointestinal and ovarian cancer (75.9% and 79.5%, respectively) and in those with gastrointestinal cancer (85.0% and 86.7%, respectively). Moreover, the highest Youden’s index were also found with the combination of the same indicators in patients with gastrointestinal and ovarian cancer patients at 55.4%, and in those with gastrointestinal cancer at 71.7%.

Based on the above results, ascites tumor markers and heteroploid cells may become valuable markers for the diagnosis of PC. We found that the ascites CA125, CEA, and CA19-9 levels are useful markers for the diagnosis of PC in patients with gastrointestinal and ovarian cancer. But, the serum CEA, CA19-9, and CA125 levels may not be associated with the occurrence of PC, although several articles have argued that serum tumor marker levels are clinically useful markers predicting the prognosis of patients with peritoneal dissemination.24,25 We suspect that enlarging the sample size of this study might produce similar results. Because ascites fluid is in direct contact with primary tumors and large amounts of tumor cells are present in ascites fluid, the detection of tumor marker levels in ascites more may directly and effectively reflect tumor changes than the serum marker levels.26 Furthermore, the heteroploid cells in ascites fluid may help diagnose PC. The presence of 3 or more heteroploid cells in the ascites samples could predict the occurrence of PC. In addition, a combination of ascites CA125 level and heteroploid cell presence can increase the sensitivity and specificity of the PC diagnoses.

Compared to peritoneal biopsy and laparoscopy, paracentesis is much easier to carry out in clinical settings to obtain samples for detection with minimum invasion. Furthermore, the cost of paracentesis is far less than the cost of the peritoneal biopsy and laparoscopy. In addition, flow cytometer has much higher detection rate of heteroploid cells in ascites than that of by cytology. In all, our proposed method has such advantages as simple, safe, cost low, easy to operate, and with higher detection rate. Although tumor markers and DNA ploidy analysis in ascites fluid cannot replace pathological and imaging diagnoses, they can help make the PC diagnoses more accurate.

In summary, the ascites levels of CEA, CA125, CA19-9 and the heteroploid cell analysis results can be considered valuable markers for the diagnosis of PC in patients with gastrointestinal and ovarian cancer. Moreover, a combination of the ascites CA125 level and the result of the heteroploid cell analysis had the best diagnostic sensitivity and specificity for PC.