High Levels of Serum IgG for Opisthorchis viverrini and CD44 Expression Predict Worse Prognosis for Cholangiocarcinoma Patients after Curative Resection.

BACKGROUND: Opisthorchis viverrini (OV)-associated cholangiocarcinoma (CCA) has a high immune response with chronic inflammation and oxidative stress. CD44 and Nestin, two cancer stem cell (CSC) markers, play major roles in cancer cell survival. Effects of immune response and expression CSC markers on survival of patients with CCA remain unclear.
OBJECTIVE: To investigate the effects of level of OV IgG together with CSC marker expression and also the combination of these markers on survival of CCA patients after curative resection.
METHODS: All serum specimens from CCA patients who underwent curative surgery from 2005 to 2015 were examined for IgG for OV antigen by ELISA. Tissue specimens were studied for CD44 and Nestin expression. Survival analysis by Cox proportional hazard model was used for estimating hazard ratio (HR) with a 95% confidence interval (CI).
RESULTS: In this study, 122 (69.3%) of 176 were positive for OV IgG, and 35 (19.9%) were considered to have high-positive OV IgG. CD44s positive expression was found in 54 (40%), CD44v6 high expression in 96 (69.6%), CD44v8-10 high expression in 87 (63.5%) and Nestin high expression in 21 (16.1%). Multivariate survival analysis found that high-positive OV IgG and late stage tumor were independent prognostic factors with the adjusted HR of 2.24 (95% CI 1.27-3.93) and 2.78 (95% CI 1.46-5.29), respectively. Subgroup analysis in early and late stage CCA showed that a combined positive OV IgG and CD44s expression with the high expression of CD44v8-10 had the significantly poorest prognosis with HR of 3.75 (95% CI 1.61-8.72) and HR of 1.76 (95% CI 1.02-3.03), respectively.
CONCLUSION: A high level of OV IgG as well as a high level of CSC markers resulted in an aggressive CCA. OV IgG level together with CSC markers can be used as the prognostic markers for CCA patients' survival. The study of the CD44 pathway is promising for adjuvant treatment.

Introduction

Cholangiocarcinoma (CCA) is a cancer of the bile duct epithelial cells arising along the intrahepatic or extrahepatic biliary tract.1 The north-eastern region of Thailand has the highest incidence of CCA in the world. The major risk factor for cholangiocarcinogenesis is chronic biliary tract inflammation caused by liver fluke, Opisthorchis viverrini (OV), infection.2 The mechanisms of inflammation and immunity that are involved in OV associated cholangiocarcinogenesis have been reported.3 Notably, chronic inflammation by OV infection can induce oxidative stress, which leads to abnormal tissue remodelling, DNA damage and an alteration in gene expression, all of which could promote CCA carcinogenesis.3 OV associated CCA is mainly caused by the activation of inflammation, while the cause of non-OV associated CCA is related to the alteration of growth factors.4 Serum IgG against OV antigen is a good marker for OV associated CCA because it can represent past or present infection and is associated with a poor survival outcome.5 The presence of serum IgG for OV is evidence of host immune response induced inflammation and the level of serum IgG may represent the level of oxidative stress that has occurred.

Cancer stem cells (CSC) are known to be a subpopulation of cancer cells with stem-like properties. They are involved in cancer development and progression.6 Cancer stem cell markers are therefore widely used as biomarkers in cancer patients. The cluster of differentiation 44 (CD44) antigen is a cell surface glycoprotein involved in cell-cell interactions, cell adhesion and migration that is important in many types of cancer and CD44 were also reported to be associated with shorter survival in various types of cancer.7–12 CD44 standard form (CD44s) and variant form (CD44v) overexpression was found in hyperplastic bile duct epithelium and cholangiocarcinoma cells in the OV-induced CCA hamster model.13 Several studies have investigated the role of CD44 in CCA. High expression of CD44 in the biliary epithelium indicates an unfavorable patient outcome.14 Another factor, Nestin, is a class VI intermediate filament protein which has been identified as a putative marker of CSC.15 Nestin expression has been observed in many types of human cancers. In some cancers, up-regulated or highly positive Nestin expression has been associated with a poor prognosis and tumor progression such as cell invasion, proliferation and metastasis.16

CCA is reported to have a poor prognosis with 5-year survival rate after resection only 20–30% with high recurrence rate.17–20 Adjuvant treatment after surgery is not well established; many studies and several Phase III clinical trials have failed to address the benefit of adjuvant regimen of treatment. The recent BILCAP study reported that adjuvant treatment after surgery with capecitabine resulted in a significant increase in recurrent free survival compared with observation.21 Although the results from the BILCAP study has changed the standard of care in adjuvant treatment for CCA and there are many ongoing trials focusing on adjuvant treatment for CCA, the use of specific risk factors or gene expression to select patients who may benefit from distinct treatments remain a challenge.22 Even though there are studies demonstrating the prognostic effect of OV IgG level and CSC markers on CCA, the prognostic effect of serum OV IgG in the combination with cancer stem cell markers has not been elucidated. Therefore, in this study, we hypothesized that the combination of OV IgG level with cancer stem cell markers (CD44s, CD44v6, CD44v8-10, Nestin) is associated with poor survival, and that using these combined markers may enhance prognostic efficacy and selection of patients for specific adjuvant treatment.

Materials and Methods

Patients and Serums

CCA patients who were diagnosed at Srinagarind Hospital, Khon Kaen University (January 1, 2005 to December 31, 2017) were included in this study. Informed consent had been obtained from all patients before surgery for usage of excessive tissue and serum samples. Serum specimens were kept in the biobank of the Cholangiocarcinoma Research Institute (CARI), Khon Kaen University. Patients who had undergone palliative surgery or had inadequate serum specimens were excluded. The clinicopathological information was provided by the CARI. The patient’s age, gender, tumor site, histology type, staging, lymph node metastatic status, surgical margin status and adjuvant chemotherapy were recorded. Patient survival was defined as the interval from the day of surgery to the time of death. A patient who was alive at the end of the study on December 31, 2019 were recorded as censor. This research protocol was approved by the Human Research Ethics Committee, Khon Kaen University, based on the Declaration of Helsinki and the ICH Good Clinical Practice Guidelines (HE621147).

Indirect Enzyme Linked Immunosorbent Assay (ELISA)

Immunoglobulin G (IgG) antibodies against OV antigen were investigated in CCA serum using the indirect ELISA method. Briefly, whole adult OV antigen (1500 µg/mL in 1X PBS pH 7.4) was coated into flat bottom microtiter plates that were then incubated at 4°C overnight. Before blocking with 3% skimmed milk in PBS (250 μL/well) at 37°C for 1 h, the plates were washed with 1X PBS with 0.05% Tween 20. After that, patient serum (dilution 1:6000 in 3% skimmed milk) was added into the plate at 100 μL/well in duplicate, then incubated at 4°C overnight. After washing with PBS plus Tween 20 five times, 100 μL of goat anti-human IgG conjugated with horseradish peroxidase (dilution 1:3000 in 3% skimmed milk) was added and incubated at 37°C for 2 h. After washing with PBS plus Tween 20, the signal was developed by adding orthophenylene diamine hydrochloride (OPD) (Zymed, CA, USA) substrate (100 μL/well) and incubated for 30 min. 4N sulfuric acid was used to stop the reaction and the optical density (OD) was measured using an ELISA reader (at 492 nm) (Tecan, Austria). The results were analysed as described in a previous study.23 Patients with positive OV IgG and arbitrary units (AU) above percentile 75 were considered high titer positive.

CCA Tissue Microarray (TMA)

Of the total of 176 CCA cases, there were 163 available sera matched CCA tissue sections observed at selected tumor regions and normal liver tissue for negative controls. A manual tissue microarrayer (2.0 mm diameter needle) was used to prepare the TMA block. This was produced with 70 cores per block. TMA blocks were cut into 4 µm thick sections and mounted on coated glass slides.

Antibodies

Primary antibodies in this study were as follows: mouse anti-Nestin (#ab6320), mouse anti-CD44 (#ab16728), mouse anti-CD44v6 (#ab78960), anti-rat (#ab6734) (Abcam, Cambridge, MA, USA). Rat anti-CD44v8-10 (#LKG-M001, Cosmo Bio, Tokyo, Japan).

Immunohistochemistry (IHC)

CCA TMAs were used to investigate the expression of the target proteins using IHC. Briefly, paraffin embedded CCA TMAs were deparaffinized and rehydrated in stepwise xylene followed by 100%, 90%, 80% and 70% ethanol. Antigen retrieval was performed using microwave cooking with 1 mM sodium citrate pH 6.0 plus 0.05% Tween 20 for 10 min. The activity of endogenous peroxide and non-specific binding were blocked using 0.3% (v/v) of hydrogen peroxide and 10% skim milk for 10 minutes for each. Primary antibodies including anti-Nestin (dilution 1:50), anti-CD44 (dilution 1:25), anti-CD44v6 (dilution 1:50) and anti-CD44v8-10 (dilution 1:50) were added and incubated at room temperature for 1 h followed by 4°C overnight. The sections were washed with phosphate buffer saline (PBS) with 0.1% Tween 20 for 5 min (three times) followed by PBS for 5 min. The Envision horseradish peroxidase conjugated secondary antibody (Dako, USA) was added in TMA for 1 h, except for the CD44v8-10 tissue section to which was added anti-rat antibody (dilution 1:100) and left for 3 h. After washing, the signal was developed using a 3,3ʹ diaminobenzidine tetrahydrochloride (DAB) substrate kit (Vector Laboratories, Inc., CA) for 10 min and counterstained with Mayer’s hematoxylin for 5 min. Before mounting, the sections were dehydrated with stepwise 70%, 80%, 90%, 100% ethanol and xylene, for 5 min each. The TMAs were observed under a light microscope.

IHC Scoring System

Protein expression was analysed according to the frequency and intensity scores. The staining frequency score of the target protein was semi-quantitatively scored and classified as 0 if there was no positive staining, 1+ = less than 25% of positive cells, 2+ = 25–50% of positive cells and 3+ = more than 50% of positive cells. The intensity score was defined as 0 if there was no staining, 1+ = weak staining, 2+ = moderate staining and 3+ = strong staining. The final IHC score was calculated by multiplying the intensity score with the frequency score. The IHC scores ranged between 0–9. The IHC score was formed from two independent punctures of each patient which were used to calculate the average IHC score. Finally, the median value, which is calculated from all patients, was used as the cut-off value to classify low and high expression.

Statistical Analysis

The sample size was determined for single or binary covariate cox regression analysis methods proposed by Schmoor et al.24 Setting a power of 80% at a 0.05 significance level, aiming to detect a hazard ratio of 2.0, assuming a prevalence of IgG for OV positive of 0.75 and prevalence of CD44 positive CCA of 0.8, and a correlation coefficient between IgG for OV and CD44 positive of 0, the sample size was 110 cases which allowed for the expected data loss of 10%. Continuous and categorical data were reported as mean ± standard deviation (SD) and percentages, respectively. The Kaplan-Meier survival analysis was used to obtain median survival time with a 95% confidence interval (CI). Cox proportional hazard model was used to estimate the hazard ratio (HR) with a 95% CI as well as p-values. Stata version 14 and SPSS version 17 were used to analyse the data. Significance level was set at 0.05.

Results

Patients’ Characteristics and Histopathology

A total of 221 histologically confirmed CCA patients who underwent surgery are included in this study. The biopsy data of 45 patients who underwent palliative surgery were excluded. Among the 176 patients included, the mean age of patients was 59.6 years (age ranged between 34 and 82 years), and 108 (61.4%) patients were male. Fifty-three (30%) patients were extrahepatic, 97 (55.1%) had papillary carcinoma, 55 (31.2%) had tubular carcinoma and 24 (13.7%) patients had non-specific adenocarcinoma and rare variants. Tumor staging was defined according to the American Joint Committee on Cancer Staging manual, 8th edition. Stage 0, I, II, III and IV were found in 11 (6.3%), 27 (15.3%), 27 (15.3%), 103 (58.5%) and 8 (4.6%) patients, respectively. Lymph node metastasis was found in 92 (52.3%) cases. A negative histological margin was achieved in 96 (54.5%) cases; 80 (45.5%) cases showed a microscopically positive margin (R1). Fifty-three (30%) patients received adjuvant chemotherapy after surgical resection (Table 1).

Table 1

Patient Characteristics by Level of OV IgG

Variables	Overall	Level of OV IgG			p-value
		Negative	Low-Positive	High-Positive
Overall	176	54 (30.7%)	87 (49.4%)	35 (19.9%)
Age (mean, year)	59.6	59.1	60.1	59.4
Gender					0.10
Female	68 (38.6%)	23 (42.6%)	37 (42.5%)	8 (22.8%)
Male	108 (61.4%)	31 (57.4%)	50 (57.5%)	27 (77.2%)
Tumor site					0.57
Intrahepatic	123 (70%)	36 (66.7%)	64 (73.6%)	23 (65.7%)
Extrahepatic	53 (30%)	18 (33.3)	23 (26.4%)	12 (34.3%)
Histology					0.35
Papillary	97 (55.1%)	33 (61.1%)	45 (51.7%)	19 (54.3%)
Non-papillary	79 (44.9%)	21 (38.9%)	42 (48.3%)	10 (45.7%)
Stage					0.39
0	11 (6.3%)	7 (13%)	4 (4.6%)	0
I	27 (15.3%)	7 (13%)	15 (17.2%)	5 (14.3%)
II	27 (15.3%)	9 (16.6%)	14 (16.1%)	4 (11.4%)
III	103 (58.5%)	29 (53.7%)	50 (57.5%)	24 (68.5%)
IV	8 (4.6%)	2 (3.7%)	4 (4.6%)	2 (5.7%)
Lymph node metastasis					0.10
No	84 (47.7%)	31 (57.4%)	41 (47.1%)	12 (34.3%)
Yes	92 (52.3%)	23 (42.6%)	46 (52.9%)	23 (65.7%)
Surgical margin					0.48
Negative	96 (54.5%)	12 (48%)	22 (40%)	9 (56.3%)
Positive	80 (45.5%)	13 (52%)	33 (60%)	7 (43.7%)
Adjuvant chemotherapy					0.07
Yes	53 (30%)	13 (24%)	33 (37.9%)	7 (20%)
No	123 (70%)	41 (76%)	54 (62.1%)	28 (80%)

The 176 CCA patients who received curative surgery were studied for serum OV IgG antibody. Of these, 54 (30.7%) cases were negative for OV IgG, while 122 (69.3%) cases were positive. Among these 122 patients, 35 (19.9%) were considered to have a high level of OV IgG. In addition, the expression of CD44s, CD44v6, CD44v8-10 and Nestin were investigated in 176 CCA tissues. IHC staining in CCA tissue was demonstrated (Figure 1). For CD44s, 54 (40%) cases were classified as positive. For CD44 variant, CD44v6 showed high expression in 96 (69.6%) cases and CD44v8-10 in 87 (63.5%) cases. A high expression of Nestin was found in 21 (16.1%) cases. The association between histopathology factors and IHC results was explored according to OV IgG levels. There was no difference in the histopathology factors and IHC results between OV IgG negative, positive and high-positive groups (Table 2).

Figure 1

Representative IHC staining of CD44s, CD44v6, CD44v8-10 and Nestin in human CCA tissues (magnification 20X).

Table 2

The Expression of CD44s, CD44v6, CD44v8-10 and Nestin by Level of OV IgG

Variables	Overall	Level of OV IgG			p-value
		Negative	Low-Positive	High-Positive
Overall	176	54 (30.7%)	87 (49.4%)	35 (19.9%)
CD44	135	41	67	27	0.98
Negative	81 (60%)	25 (61%)	40 (59.7%)	16 (59.3%)
Positive	54 (40%)	16 (39%)	27 (40.3%)	11 (40.7%)
CD44v6	138	43	68	27	0.59
Low	42 (30.4%)	11 (25.6%)	21 (30.9%)	10 (37%)
High	96 (69.6%)	32 (74.4%)	47 (69.1%)	17 (63%)
CD44v8	137	43	67	27	0.37
Low	50 (36.5%)	12 (27.9%)	27 (40.3%)	11 (40.7%)
High	87 (63.5%)	31 (72.1%)	40 (59.7%)	16 (59.3%)
Nestin	130	40	64	26	0.65
Low	109 (83.9%)	32 (80%)	54 (84.4%)	23 (88.5%)
High	21 (16.1%)	8 (20%)	10 (15.6%)	3 (11.5%)

Survival Analysis by Level of Serum OV IgG, Histopathological Factors and IHC Results (CD44s, CD44v6, CD44v8-10, Nestin)

The overall median survival time (MST) after curative resection was 18.6 months and 1-year, 3-year and 5-year survival rates were 67.0% (95% CI 59.6–73.4), 30.3% (95% CI 23.6–37.2) and 21.2% (95% CI 15.3–27.7), respectively.

Bivariable analysis showed that CCA patients with a low-positive OV IgG had a poor prognosis with an MST of 18.6 months (95% CI 9.2–16.0) and an HR of 1.45 (95% CI 0.98–2.15, p = 0.06). Patients with high-positive OV IgG had a significantly shorter survival with an MST of 10.5 months (95% CI 4.8–17.4) and an HR of 1.99 (95% CI 1.24–3.19) compared with OV IgG negative patients (Figure 2A). Other factors that had a significant influence on survival were positive resection margin (HR 2.28, 95% CI 1.63–3.19, p < 0.01), papillary type (HR 0.56, 95% CI 0.40–0.68, p< 0.01), lymph node metastasis (HR 3.73,95% CI 2.58–5.39, p < 0.01) and late stage tumor (HR 4.21, 95% CI 2.85–6.23, p<0.01). For IHC results, the positive expression of CD44s had a significant influence on survival (HR 1.52, 95% CI 1.04–2.23, p = 0.03) (Figure 2B) (Table 3). Multivariate analysis showed that only high-positive OV IgG and late stage tumor were independent prognostic factors with an adjusted HR of 2.24 (95% CI 1.27–3.93, p < 0.01) and 2.78 (95% CI 1.46–5.29, p < 0.01), respectively (Table 3).

Figure 2

Kaplan–Meier analysis of serum IgG for OV and CD44s expression in 176 CCA patients. (A) Survival by different levels of serum IgG for OV. (B) Survival by different levels of CD44s.

Table 3

Median Survival Time and Multivariate Analyses of Clinicopathological Data and CSC Markers

Variables	N	IR/100	MST, Months (95% CI)	Crude HR (95% CI)	Adjusted HR (95% CI)	p-value
Overall	176	2.7	18.6 (15.8–28.9)
Level of OV IgG
Negative	54	1.9	29.2 (15.9–42.1)	1	1
Low-positive	87	2.9	18.6 (15.6–24.2)	1.45 (0.98–2.15)	1.50 (0.95–2.37)	0.08
High-positive	35	4.0	10.5 (4.8–17.4)	1.99 (1.24–3.19)	2.24 (1.27–3.93)	<0.01*
Gender
Female	68	2.8	16.3 (12.8–28.8)	1	–	–
Male	108	2.6	18.9 (15.6–24.2)	0.97 (0.69–1.36)
Tumor site
Intrahepatic	123	2.7	17.4 (13.1–23.6)	1	–	–
Extrahepatic	53	2.7	20.8 (15.3–29.5)	0.97 (0.68–1.39)
Histology
Non-papillary	79	4.1	13.0 (8.9–16.3)	1	1
Papillary	97	2.0	26.9 (19.7–33.8)	0.56 (0.40–0.68)	0.72 (0.49–1.06)	0.10
Stage
0, I, II	65	1.1	51.8 (35.7–123.9)	1	1
III, IV	111	5.5	12.7 (9.2–15.9)	4.21 (2.85–6.23)	2.78 (1.46–5.29)	<0.01*
Lymph node metastasis
No	84	1.4	41.5 (28.1–63.0)	1	1
Yes	92	6.2	12.5 (8.5–15.9)	3.73 (2.58–5.39)	1.53 (0.86–2.71)	0.14
Resection margin
Negative	96	1.9	30.2 (21.8–41.5)	1	1
Positive	80	4.5	12.7 (8.9–16.3)	2.28 (1.63–3.19)	1.15 (0.76–1.72)	0.50
Adjuvant chemotherapy
Yes	53	2.8	19.2 (13.7–25.9)	1	–	–
No	123	2.6	18.1 (10.1–24.2)	1.06 (0.75–1.5)
CD44
Negative	81	2.4	22.8 (15.6–29.5)	1	1
Positive	54	4.2	15.8 (8.9–18)	1.52 (1.04–2.23)	1.43 (0.97–2.11)	0.07
CD44v6
Low	42	3.1	19.7 (11.1–24)	1	–	–
High	96	2.7	17.0 (13.2–24.9)	0.95 (0.64–1.42)
CD44v8-10
Low	50	3.0	17.4 (12.5–24.9)	1	–	–
High	87	2.7	18.6 (13.2–24)	0.90 (0.62–1.32)
Nestin
Low	109	2.9	16.8 (12.9–21.8)	1	–	–
High	21	2.2	26.2 (9.2–35.9)	0.78 (0.46–1.33)

Note: *P value equal to or less than 0.05 was considered statistically significant.

Abbreviations: N, number of patients; HR, hazard ratio; IR/100, incidence rate per 100 persons-month; MST, median survival time.

Survival Analysis by Level of Serum OV IgG, Histopathological Factors and IHC Results (CD44s, CD44v6, CD44v8-10, Nestin) According to Tumor Stage

It is possible that the strong effect of tumor stage on patient survival may obscure the effect of other factors on survival outcome, therefore, survival based on OV IgG level, CD44, CD44v6, CD44v8-10 and Nestin expression was analysed according to tumor stage grouping at an early and late stage.

In early stage CCA (stages 0, I, II), a positive expression of CD44s showed a poorer prognosis, with an HR of 2.31 (95% CI 1.25–4.26, p= 0.008) compared with negative expression (Table 4) (). On the other hand, there was no difference in prognosis found based on OV IgG level (), CD44v6, CD44v8-10 and Nestin expression (). Survival analysis based on the combination of OV IgG level and protein expression was also explored. The results with significant outcomes for survival were CD44s positive expression with OV IgG positive (HR 2.45, 95% CI 1.22–4.95, p = 0.012), CD44v8-10 high expression with OV IgG positive (HR 2.10, 95% CI 1.14–3.87, p= 0.018), CD44s positive expression with CD44v8-10 high expression (HR 3.27, 95% CI 1.68–6.36, p < 0.001) and OV IgG positive together with CD44s positive expression and CD44v8-10 high expression (HR 4.39, 95% CI 1.90–10.14, p = 0.001) (Table 4) (Figure 3). Interestingly, multivariate analysis showed that a combination of OV IgG level and protein expression were independent prognostic factors for patient survival. The worst prognostic value was found with the combination of OV IgG positive and positive CD44s and high CD44v8-10 expression with an adjusted HR of 3.75 (95% CI 1.61–8.72, p = 0.002) (Table 5).

Table 4

Survival Analysis by Level of Serum OV IgG, Clinicopathological Factors and IHC Results (CD44s, CD44v6, CD44v8-10, Nestin) According to Tumor Stage

Variables		Early Stage			Late Stage
	N	Crude HR (95% CI)	p-value	N	Crude HR (95% CI)	p-value
Gender (Ref: Female)	65			111
Male		0.82 (0.49–1.38)	0.447		1.03 (0.70–1.50)	0.901
Tumor site (Ref: Intrahepatic)	65			111
Extrahepatic		1.05 (0.59–1.56)	0.866		0.78 (0.52–1.16)	0.211
Histology (Ref: Non-papillary)	65			111
Papillary		0.55 (0.32–0.92)	0.024*		0.70 (0.48–1.03)	0.069
Resection margin (Ref: Negative)	65			111
Positive		0.97 (0.54–1.75)	0.929		1.59 (1.08–2.35)	0.018*
Adjuvant chemotherapy (Ref: Yes)	65			111
No		1.25 (0.69–2.26)	0.455		1.50 (1.00–2.24)	0.048*
Level of OV IgG (Ref: Negative)	65			111
Low-positive		1.41 (0.82–2.44)	0.212		1.12 (0.72–1.75)	0.607
High-positive		2.01 (0.91–4.46)	0.085		1.36 (0.79–2.32)	0.269
CD44s (Ref: Negative)	47			88
Positive		2.31 (1.25–4.26)	0.008*		1.20 (0.78–1.84)	0.416
CD44v6 (Ref: Low)	49			89
High		0.83 (0.45–1.54)	0.557		0.86 (0.55–1.36)	0.524
CD44v8-10 (Ref: Low)	49			88
High		1.41 (0.74–2.68)	0.292		1.00 (0.65–1.54)	0.989
Nestin (Ref: Low)	46			83
High		0.79 (0.76–2.29)	0.669		0.58 (0.32–1.04)	0.066
CD44s and OV IgG	47			88
Positive		2.45 (1.22–4.95)	0.012*		1.53 (0.96–2.46)	0.077
CD44v8-10 and OV IgG	49			88
High and Positive		2.10 (1.14–3.87)	0.018*		1.41 (0.91–2.19)	0.120
CD44s and CD44v8-10	47			88
Positive and High		3.27 (1.68–6.36)	<0.001*		1.27 (0.78–2.05)	0.336
OV IgG and CD44s and CD44v8-10	47			88
Positive and Positive and High		4.39 (1.90–10.14)	0.001*		1.74 (1.01–2.98)	0.044*

Notes: *P value equal to or less than 0.05 was considered statistically significant. Early stage, tumor stage 0–II; late stage, tumor stage III–IV.

Abbreviations: HR, hazard ratio.

Figure 3

Kaplan–Meier analysis of overall survival with a combination of serum IgG for OV and IHC results in early stage CCA. (A) Survival with a combination of CD44s and IgG for OV. (B) Survival with a combination of CD44v8-10 and IgG for OV. (C) Survival with a combination of CD44s and CD44v8-10. (D) Survival with a combination of CD44s, CD44v8-10 and IgG for OV.

Table 5

Multivariable Analysis of IHC Results in Early Stage CCA

Early Stage (0, I, II)
Variables	N	Adjusted HR (95% CI)	p-value
Model A
Histology	65
Papillary		0.51 (0.27–0.97)	0.040*
CD44s	47
Positive		2.13 (1.14–3.96)	0.017*
Model B
Histology	65
Papillary		0.47 (0.25–0.89)	0.021*
CD44s and OV IgG	47
Positive		2.38 (1.17–4.81)	0.016*
Model C
Histology	65
Papillary		0.42 (0.22–0.80)	0.008*
CD44v8-10 and OV IgG	49
High and Positive		2.37 (1.26–4.45)	0.007*
Model D
Histology	65
Papillary		0.44 (0.23–0.85)	0.014*
CD44s and CD44v8-10	47
Positive and High		3.34 (171–6.52)	<0.001*
Model E
Histology	65
Papillary		0.53 (0.28–1.03)	0.060
OV IgG and CD44s and CD44v8-10	47
Positive and Positive and High		3.75 (1.61–8.72)	0.002*

Note: *P value equal to or less than 0.05 was considered statistically significant.

Abbreviation: HR, hazard ratio.

In late stage (stages III, IV) CCA, bivariate analysis showed that a positive resection margin and no adjuvant chemotherapy led to a poor prognosis with a crude HR of 1.59 (95% CI 1.08–2.35) and 1.50 (95% CI 1.00–2.24), respectively. For IHC factors, only the combination of OV IgG positive together with CD44s positive expression and CD44v8-10 high expression showed a significantly poor prognosis with a crude HR of 1.74 (95% CI 1.01–2.98, p= 0.044), while there was no effect on survival outcome by using one factor alone or the combination of two factors (Table 4) (, Figure 4). Multivariable analysis showed no adjuvant chemotherapy and the combination of OV IgG positive together with CD44s positive expression and CD44v8-10 high expression led to a significantly poorer survival with an adjusted HR of 1.72 (95% CI 1.08–2.76, p= 0.023) and 1.76 (95% CI 1.02–3.03, p = 0.041), respectively (Table 6).

Figure 4

Kaplan–Meier analysis of overall survival with a combination of serum IgG for OV and IHC results in late stage CCA. (A) Survival with a combination of CD44s and IgG for OV. (B) Survival with a combination of CD44v8-10 and IgG for OV. (C) Survival with a combination of CD44s and CD44v8-10. (D) Survival with a combination of CD44s, CD44v8-10 and IgG for OV.

Table 6

Multivariate Analyses of IHC Results in Late Stage CCA

Late Stage (III, IV)
Variables	N	Adjusted HR (95% CI)	p-value
Resection margin	111
Positive		1.54 (0.99–2.39)	0.056
Adjuvant chemotherapy	111
No		1.72 (1.08–2.76)	0.023*
OV IgG and CD44s and CD44v8-10	88
Positive and Positive and High		1.76 (1.02–3.03)	0.041*

Note: *P value equal to or less than 0.05 was considered statistically significant.

Abbreviation: HR, hazard ratio.

Discussion

Thailand has the highest incidence of CCA in the world25 and the major risk factor is OV infection. A previous study in 1994 reported that up to 89% of CCA patients were positive for serum OV IgG.26 The current study had a lower prevalence of CCA patients with positive serum OV IgG at 70%. As the current study included only patients who underwent curative resection, this may not reflect the true prevalence of OV associated CCA. Another reason could be the reduction of OV infection incidence. Over the past 30 years there have been many campaigns to eliminate OV infection which have resulted in a decline in the prevalence of OV infection from 89.5% in 198427 to 15.7% in 2009,28 and and to 10% in 2019 from population-based studies.29

OV associated CCA has a grave prognosis as a previous study from Thailand reported 5-year survival after curative resection of only 20%,17 while 5-year survival after resection from countries with non-OV associated CCA was 30–42%.18,30 A prospective study in 2016 reported that most CCA patients present at an advanced, unresectable stage, 65% of walk-in patients received only symptomatic care and the resectable cases were only 10%.31 In our study more than 60% of patients who underwent surgery were in stages III or IV and had a poor survival outcome, while in non-OV associated CCA countries resectable cases with stages III or IV only accounted for 6–20% of the total.19,32,33 The aggressiveness of CCA in OV IgG positive cases may be explained by immune response inflammatory processes that induce cellular adaptation to oxidative stress, immune evasion and cellular proliferation. This concept is supported by our report of a high level of antibody mediated response resulting in significantly poorer survival.

Because cancer stem cells are believed to be key regulators of tumor aggressiveness,34 the levels of cancer stem cell markers may also be used as prognostic markers for patient outcome. The expression of CD44s in CCA from previous studies was 49% associated with poor survival.14,35 Our study showed a similar result with 40% of cases with CD44s expression having significantly poorer survival in early stage CCA. Moreover, our result also supports a previous study that found a high expression of cancer stem cell markers, CD44s, CD44v6 and CD44v8-10, associated with poor prognosis in early stage CCA patients.36 CD44v8-10 is a variant isoform of CD44 that plays a role in the regulation of oxidative stress in tumors by stabilizing the cystine–glutamate transporter and promoting glutathione synthesis.37 In OV induced hamster CCA tissues, the expression of CD44v8-10 was induced during bile duct transformation, and it was associated with a poor prognosis.13 In addition, CD44v8-10 showed a higher level in OV associated CCA compared with non-OV associated CCA, and it has been suggested as a marker related to inflammation associated cancer development.38 In our result, we found that patients positive for OV IgG and CD44s with a high expression of CD44v8-10 showed the poorest prognosis compared with other patients in both early and late stages of CCA. This result may be explained by the high level of oxidative stress, which may induce tumor aggressiveness and lead to a poor prognosis.

Survival of CCA patients not only depends on tumor aggressiveness, but also depends on treatment options provided. Surgical resection is the only main treatment which had a chance to achieve long-term survival, but the 5-year survival rate after resection was unsatisfactory. Adjuvant treatment should be a beneficial option in selected patients by data from a previous retrospective study.39 A meta-analysis published in 2019, that included 30 retrospective studies and 5 randomized trials, reported significantly better overall survival in CCA patients who received any adjuvant chemotherapy compared with surgery alone and reported benefits in the lymph node positive and surgical margin positive groups.40 Our study shows the same result, that patients with stages III and IV with adjuvant chemotherapy had better survival. Given this information, we advocate the use of adjuvant chemotherapy for stages III and IV patients. The randomized trial addressed the benefit of adjuvant capecitabine in improving recurrence free survival compared with surgery alone, but overall survival was not different by intention to treat analysis.21 However, because of discrepancies of study methods and heterogenicity of patients, the role of adjuvant treatment remains controversial. The distinctive risk factors and effective biomarkers not only guided prognosis, but also apply for selection of patients for adjuvant treatment in a personalized treatment strategy.22 Our study found positive OV IgG and expression of CD44 were significant prognostic factors for poor survival either in early or late stage CCA therefore CD44 pathway targeting is promising for adjuvant treatment. Many advanced preclinical CCA model have recently been rapidly developed, including cell line culture, 3D spheroid model, 3D organoid model and patient’s derived xenograft; these model are fundamental tools for initiating personalized treatment.41 A recent study reported that sulfasalazine (a CD44 targeting agent) enhanced cytotoxicity of cisplatin in CCA cell line and combined sulfasalazine with cisplatin treatment had significant tumor growth inhibition, increased apoptosis and decreased cell proliferation in high CD44v9 expressed CCA cell implanted xenograft model.42 Clinical study of sulfasalazine combined with chemotherapy is promising in OV associated CCA or CD44 expressed CCA both in adjuvant and advanced settings.

The limitation of this study was the reliance on retrospective data, therefore some parameters may be imbalanced between groups.

Conclusion

In summary, OV-associated CCA is an inflammatory induced cancer with a preventable cause. High levels of antibody mediated immune response to the parasite had consequences for the aggressiveness of CCA. Moreover, a combination of OV IgG level with CD44s and CD44v8-10 was associated with tumor aggressiveness and showed the poorest prognosis in patients after resection. Therefore, these markers may be used as prognostic markers for CCA patients: targeting and blocking the CD44 pathway is a promising study for adjuvant treatment.