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World Journal of Gastroenterology logoLink to World Journal of Gastroenterology
. 2014 Sep 21;20(35):12615–12620. doi: 10.3748/wjg.v20.i35.12615

Risk factors for combined hepatocellular-cholangiocarcinoma: A hospital-based case-control study

Yan-Ming Zhou 1,2, Xiao-Feng Zhang 1,2, Lu-Peng Wu 1,2, Cheng-Jun Sui 1,2, Jia-Mei Yang 1,2
PMCID: PMC4168099  PMID: 25253966

Abstract

AIM: To identify risk factors contributing to the development of combined hepatocellular-cholangiocarcinoma (CHC) in China.

METHODS: One hundred and twenty-six patients with CHC and 4:1 matched healthy controls were interviewed during the period from February 2000 to October 2012. Logistic regression analysis was used to calculate odds ratios (OR) and 95% confidence intervals (CI) for each risk factor.

RESULTS: Univariate analysis showed that the significant risk factors for CHC development were hepatitis B virus (HBV) infection, heavy alcohol consumption, a family history of liver cancer, and diabetes mellitus. Multivariate stepwise logistic regression analysis showed that HBV infection (OR = 19.245, 95%CI: 13.260-27.931) and heavy alcohol consumption (OR = 2.186, 95%CI: 1.070-4.466) were independent factors contributing to the development of CHC.

CONCLUSION: HBV infection and heavy alcohol consumption may play a role in the development of CHC in China.

Keywords: Risk factors, Combined hepatocellular-cholangiocarcinoma, Hepatitis B virus, Alcohol consumption, Epidemiology


Core tip: Combined hepatocellular-cholangiocarcinoma (CHC) is a rare form of primary liver malignancy that includes intimately mixed elements of both hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinoma (ICC). Although risk factors for the development of HCC and ICC have been studied extensively, the etiology of CHC remains unknown. We carried out a hospital-based case-control study to identify risk factors contributing to the development of CHC in China.

INTRODUCTION

Histologically, primary liver cancer can be grossly classified as either hepatocellular carcinoma (HCC) arising from hepatocytes or intrahepatic cholangiocarcinoma (ICC) arising from the bile duct epithelium. Combined hepatocellular-cholangiocarcinoma (CHC) is a rare form of primary liver malignancy that includes intimately mixed elements of both HCC and ICC[1]. Although risk factors for the development of HCC and ICC have been studied extensively, the etiology of CHC remains unknown. The aim of the present hospital-based case-control study was to identify risk factors for the development of CHC.

MATERIALS AND METHODS

Cases and controls

One hundred and twenty-six patients were treated for CHC between February 2000 and October 2012 in the Eastern Hepatobiliary Surgery Hospital of the Second Military Medical University in Shanghai, China. The pathological specimens were obtained from hepatectomy (n = 123) or needle biopsy (n = 3). The diagnosis of CHC was made based on a combination of histological findings and immunohistochemical staining. The immunoreactivity of HCC component for hepatocyte paraffin 1 (Hep Par 1) but not cytokeratin (CK)7/19, and the reactivity of ICC component for CK7/19 but not Hep Par 1 were confirmed. Patients diagnosed with other cancers within 5 years before the date of CHC diagnosis were excluded. Hospital controls without diagnoses of cancers matched 4:1 with the CHC patients by age (± 2 years) and sex were selected from individuals who underwent routine health examinations in the same hospital. This study was conducted in accordance with the Helsinki Declaration and the guidelines of the ethics committee at our institution.

Data collection

All information was obtained by review of the complete medical histories from the patient archives. The following data were recorded: (1) daily habits including alcohol consumption and smoking; (2) other medical conditions such as primary sclerosing cholangitis (PSC), inflammatory bowel disease (IBD), hepatolithiasis, liver fluke (Clonorchis sinensis or Opisthorchis viverrini) infestation, diabetes mellitus (DM), and hypertension; (3) information concerning hepatitis B virus (HBV) and hepatitis C virus (HCV) infections; and (4) information concerning cancer on the family history in first-degree relatives (parents, siblings, and children).

Total alcohol intake was assessed in grams of ethanol consumed per day (g/d) according to the mean ethanol content of wine (12% by volume), beer (5%) and white spirit (40%), based on which an overall measure of lifetime alcohol intake was then calculated. Heavy alcohol consumption was defined as drinking at least 80 g of alcohol per day[2]. A smoker was defined as someone who had smoked one cigarette or more per day for more than 1 year. Heavy smokers were defined as those who had > 20 pack-years of smoking[3].

Blood samples were taken from all patients on the first morning of hospital admission, and tested for HBV surface antigen (HBsAg) and anti-HCV antibody using a commercial ELISA kit (Abbott Laboratories, North Chicago, IL, United States).

Statistical analysis

Univariate analyses were performed using the χ2 or Fisher’s exact test for categorical variables and t test for continuous variables. Multivariate logistic regression was performed to identify independent factors for CHC development. Odds ratios (OR) and 95%CI were calculated for each risk factor. A P-value < 0.05 was considered statistically significant. These analyses were performed using SPSS 11.0 software (SPSS Inc., Chicago, IL, United States).

RESULTS

The CHC patients and healthy controls had a similar mean age (57.7 years vs 58.4 years) and consisted of a similar proportion of men (82.5% vs 82.5%). Univariate analysis showed that HBV infection, heavy alcohol consumption, a family history of liver cancer and DM were possible risk factors contributing to the development of CHC. The prevalence of HCV infection, hypertension, hepatolithiasis and cigarette smoking were not significantly associated with the risk of CHC development (Table 1).

Table 1.

Univariate analysis of risk factors for combined hepatocellular-cholangiocarcinoma n (%)

Risk factor Cases (n = 126) Controls (n = 504) OR (95%CI) P value
HBV < 0.001
HBsAg (-) 38 (30.2) 446 (88.5) 1 (Reference)
HBsAg (+) 88 (69.8) 58 (11.5) 17.808 (11.145-28.452)
HCV 0.563
HCV-Ab (-) 125 (99.2) 502 (99.6) 1 (Reference)
HCV-Ab (+) 1 (0.8) 2 (0.4) 2.008 (0.181-22.322)
Heavy smoking 0.395
No 88 (69.8) 371 (73.6) 1 (Reference)
Yes 38 (30.2) 133 (26.4) 1.205 (0.784-1.850)
Heavy alcohol consumption 0.018
No 105 (83.3) 457 (90.7) 1 (Reference)
Yes 21 (16.7) 47 (9.3) 1.945 (1.115-3.392)
Diabetes mellitus 0.024
No 113 (89.7) 479 (95.0) 1 (Reference)
Yes 13 (10.3) 25 (5.0) 2.204 (1.094-4.443)
Hypertension 0.855
No 110 (87.3) 443 (87.9) 1 (Reference)
Yes 16 (12.7) 61 (12.1) 1.056 (0.586-1.903)
Hepatolithiasis 0.262
No 124 (98.4) 501 (99.4) 1 (Reference)
Yes 2 (1.6) 3 (0.6) 2.694 (0.445-16.294)
Family history of liver cancer < 0.001
No 108 (85.7) 489 (97.0) 1 (Reference)
Yes 18 (14.3) 15 (3.0) 5.433 (2.655-11.120)
Family history of other malignancies 0.636
No 99 (78.6) 386 (76.6) 1 (Reference)
Yes 27 (21.4) 118 (23.4) 0.892 (0.556-1.431)

HBV: Hepatitis B virus; HCV: Hepatitis C virus; HbsAg: Hepatitis B surface antigen; HCV-Ab: Anti-HCV antibody.

None of the 126 CHC patients had PSC, IBD, or liver fluke infestation. Histopathologic examination showed that 81 (64.3%) patients had liver cirrhosis, 69 of whom were serologically positive for HBV. As no information about liver cirrhosis of the controls was available, we were unable to estimate the magnitude of CHC risk associated with the factor.

Multivariate stepwise logistic regression analysis showed that HBV infection (OR = 19.245, 95%CI: 13.260-27.931) and heavy alcohol consumption (OR = 2.186, 95%CI: 1.070-4.466) were independent.

DISCUSSION

CHC is a rare entity that represents 1.0%-4.7% of primary liver malignancies[1]. Although the clinicopathologic features and radiological presentations of CHC have been studied extensively[4-14], little is known about risk factors for its development.

To the best of our knowledge, this is the first hospital-based case-control study in China to examine risk factors for CHC. Our results suggest that HBV infection is a strong risk factor for the development of CHC, which is similar to what is noted in HCC and ICC[15]. We did not observe any significant association between HCV infection and CHC. HBV infection is more common than HCV infection in China. Previous studies indicated that prevalence of HCV infection in CHC patients ranged from 0% to 70% and that of HBV infection from 7.6% to 92.8% (Table 2)[4-14,16-36]. The disparities between these series may be mainly attributed to the geographic and ethnic differences in the prevalence of viral hepatitis.

Table 2.

Rates of cirrhosis, hepatitis B virus and hepatitis C virus infection in studies with more than 10 cases of combined hepatocellular-cholangiocarcinoma

Author Country Year No. of Male/Female Age Cirrhosis HBsAg HCV-Ab
patients year1 n (%) n (%) n (%)
Aoki et al[4] Japan 1993 20 18/2 55.8 12 (60) 5 (25) NA
Haratake et al[5] Japan 1995 13 10/3 64.8 11 (84.6) 1 (7.6) 3/5 (60)
Maeda et al[6] Japan 1995 29 27/2 59.8 10 (34.5) 6 (22.2) 10/16 (62.5)
Taguchi et al[7] Japan 1996 23 15/8 64.0 9 (39) 4 (17) 14/20 (70)
Sasaki et al[8] Japan 1999 21 NA NA 17 (80.9) 7 (33.3) 5/16 (31.3)
Yano et al[9] Japan 2003 26 23/3 57.0 14 (54) 7 (27) 10 (38)
Sanada et al[10] Japan 2005 11 7/4 66.4 5 (46) 5 (46) 6 (55)
Aishima et al[11] Japan 2006 40 36/4 58.1 11 (27.5) 17/37 (45.9) 12/32 (37.5)
Wakasa et al[12] Japan 2007 18 14/4 56.7 5 (27.7) 4 (22.2) 7/16 (43.8)
Ariizumi et al[13] Japan 2011 44 31/11 65.0 23 (52) 11 (25) 24 (55)
Akiba et al[14] Japan 2013 54 45/9 66.0 14 (25.9) 14 (25.9) 21 (38.8)
Koh et al[16] Korea 2005 24 16/8 55.0 13 (54.2) 13 (54.2) 3 (12.5)
Lee et al[17] Korea 2006 33 22/11 52.0 16 (48.5) 16 (48.5) 4 (12.1)
Shin et al[18] Korea 2007 12 11/1 48.1 8 (66.6) 9 (75) 1 (8.3)
Kim et al[19] Korea 2009 29 23/6 53.0 17 (58.6) 22 (75.9) 1 (3.4)
Kim et al[20] Korea 2010 50 41/9 56.3 27 (54) 40 (80) 2 (4)
Lee et al[21] Korea 2011 30 26/4 61.1 22 (73.3) 19 (63.3) 1 (3.3)
Park et al[22] Korea 2011 21 15/6 59.0 13 (62) 17 (81) 0
Zuo et al[23] China 2007 15 11/4 49.0 11 (73.3) 11 (73.3) 3 (20)
Zhang et al[24] China 2008 12 8/4 48.0 7 (58.3) 7 (58.3) 0
Yu et al[25] China 2011 14 12/2 53.6 10 (71.4) 13 (92.8) 0
Yin et al[26] China 2012 103 83/20 50.0 69 (66.9) 76 (73.4) 1 (0.97)
Zhan et al[27] China 2012 27 24/3 58.3 10 (37) 8 (29.6) 4 (14.8)
Yap et al[28] Taiwan 2012 11 8/3 61.0 8 (72) 6 (54) 2 (18)
Lee et al[29] Taiwan 2013 65 48/17 55.7 27/47 (57.4) 32 (49.2) 11 (16.9)
Ng et al[30] Hong Kong 1998 21 18/3 49.7 10 (47.6) 12/16 (75) NA
Chantajitr et al[31] Thailand 2006 25 18/7 53.4 11 (50.0) 12 (66.7) 2 (13.3)
Phongkitkarun et al[32] Thailand 2007 10 7/3 53.5 5 (50) 4 (40) 1 (10)
Jarnagin et al[33] USA 2002 27 14/13 61.0 0 4 (15)2 NA
Panjala et al[34] USA 2010 12 8/4 61.0 10 (83.3) 2 (16.6) 5 (41.6)
Cazals-hatem et al[35] France 2004 15 14/1 59.8 4 (27) NA 4 (27)
Portolani et al[36] Italy 2008 18 NA NA 14 (77.7) 3 (16.6) 11 (61.1)
1

Mean or median;

2

Hepatitis B or C. NA: Not available; HBsAg: Hepatitis B surface antigen; HCV: Hepatitis C virus; HCV-Ab: Anti-HCV antibody.

The mechanism underlying the more likelihood of CHC development in patients infected with HBV remains unclear. Hepatic progenitor cells (HPCs), also known as oval cells, which are located in the ductules and/or canal of Hering and are thought to differentiate into either hepatocytes or cholangiocytes, can give rise to hepatic malignancies. Theise et al[37] found that the tumors contained undifferentiated cells that merged with both HCC and ICC components as well as with mature appearing hepatocytes. The morphological and immunohistochemical features of these cells are strikingly similar to those of HPCs. In addition, tumor cells of transition zone in CHC have been shown to frequently express HPC markers such as CK7, CK19 and c-kit[24]. Furthermore, Suzuki et al[38] demonstrated that HPCs isolated from the 3,5-diethoxycarbonyl-1,4-dihydrocollidine-treated p53-null mouse liver could form tumors with some characteristics of both HCC and ICC in NOD/SCID mice. Therefore, it could be postulated that CHC may derive from HPCs undergoing a malignant transformation. Hepatitis B virus X (HBX) protein, a small 17-kDa soluble protein, functions as a transcriptional activator that is implicated in HBV-associated hepatocarcinogenesis. There is evidence that HBX treatment resulted in an increase in the S phase cell cycle fraction and a decrease in apoptosis of HPCs[39].

Cirrhosis was identified in 64.3% CHC cases in our series. Indeed, most CHC patients have underlying cirrhosis in a world context (Table 2). It is possible that cirrhosis is a premalignant condition that predisposes to CHC, as is the case with HCC and ICC.

In addition to the association with HBV infection, our study also revealed an association between CHC and heavy alcohol consumption. It is possible that this association is related to alcoholic liver disease including cirrhosis.

Many studies have examined the association between DM and HCC or ICC and yielded inconsistent findings[40,41]. DM is suggested as a risk factor for nonalcoholic fatty liver disease and more severe nonalcoholic steatohepatitis, which can lead to liver fibrosis, cirrhosis, and subsequently to liver cancer[40]. HCV, a well-known risk factor for HCC and ICC, was also reported to be associated with DM[42]. A case-control study from the United States reported that DM increased the risk of HCC (OR = 1.57) only in the presence of HCV, HBV, or alcoholic cirrhosis but not in cases without these risk factors (OR = 1.08)[43]. Similarly, another case-control study from the United States reported that DM was not a significant risk factor for ICC after controlling for race, age, gender, HCV, HBV, and heavy drinking[44]. Univariate analysis of the present study showed that DM was a significant risk for CHC, but multivariate analysis failed to confirm this association. It is possible that that DM might be a confounding factor associated with other risk factors rather than a true risk factor per se.

We also observed a relationship between a family history of liver cancer and the risk of CHC, but this effect was not confirmed by multivariate analysis. HBV infection is thought to be one of the main environmental factors responsible for familial aggregations of liver cancer. In the current study, the proportion of HBsAg positivity was higher in CHC patients with a family history of liver cancer than those without a family history of liver cancer (88.9% vs 66.7%; P = 0.057). It is possible that in the absence of environmental factors, a familial tendency for CHC is not expressed.

A study from a United States reported that two of their 27 CHC patients had documented intrahepatic infection with Clonorchiasis sinensis and Schistosoma mansoni[33]. Hong et al[45] reported a case of CHC from the Philippines with underlying Schistosoma mansoni, maintaining that the HCC and ICC each developed coincidentally or subsequently from fibrosis after recurrent inflammation at the site of Schistosoma mansoni infection. However, no patient in our series showed evidence of liver fluke infestation. Further research on the etiological relationship between liver fluke infestation and CHC is needed.

The present study has some limitations. (1) it is a hospital-based rather population-based study in a single medical institution, which may lead to selection bias; (2) the number of CHC cases in our study was small because of the relatively low incidence of this disease, resulting in a wide confidence interval in the estimated OR; and (3) virological factors, including positive HBeAg, genotype C compared to B, pre-S deletion, precore mutations and basal core promoter mutations, have been identified to be associated with an increased risk of HCC[46]. Given the absence of adequate information concerned in this study, further studies are needed to investigate the role of these virological factors in the development of CHC.

In conclusion, our results suggest that HBV infection and heavy alcohol consumption may be risk factors for CHC in China. Vaccination plays a central role in HBV prevention strategies worldwide, and a decline in the incidence of HCC following the introduction of neonatal HBV vaccination has been observed in China. Compared with 1980-1983, liver cancer incidence during 1990-1993 significantly decreased 3.4-fold at ages 20-24, and 1.9-fold at ages 25-29 when the first vaccinees were < 11 years old[47]. On the other hand, nucleoside analogue therapy use was found to be associated with reduced risk of HBV related HCC[48]. Accordingly, vaccination against and treatment of HBV might have the potential benefits in prevention of CHC. Additional studies regarding this issue are warranted.

ACKNOWLEDGMENTS

We thank Doctor Yan-Fang Zhao (Department of Health Statistics, Second Military Medical University, Shanghai 200438, China) for her critical revision of the statistical analysis section.

COMMENTS

Background

Histologically, primary liver cancer can be grossly classified as either hepatocellular carcinoma (HCC) arising from hepatocytes or intrahepatic cholangiocarcinoma (ICC) arising from the bile duct epithelium. Combined hepatocellular-cholangiocarcinoma (CHC) is a rare form of primary liver malignancy that includes intimately mixed elements of both HCC and ICC. Although risk factors for the development of HCC and ICC have been studied extensively, the etiology of CHC remains unknown.

Research frontiers

The present hospital-based case-control study was to identify risk factors for the development of CHC.

Innovations and breakthroughs

This is the first hospital-based case-control study in China to examine risk factors for CHC. The authors found that hepatitis B virus (HBV) infection is a strong risk factor for the development of CHC, which is similar to what is noted in HCC and ICC.

Applications

Vaccination against and treatment of HBV might have the potential benefits in prevention of CHC.

Peer review

The paper deals with an important clinical problem, i.e., the risk factors for hepatocellular-cholangiocarcinoma.

Footnotes

P- Reviewer: Festi D, Nakano H S- Editor: Nan J L- Editor: Wang TQ E- Editor: Du P

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