ISRN Hepatology

Volume 2013 (2013), Article ID 438306, 3 pages

http://dx.doi.org/10.1155/2013/438306

Clinical Study

Predictors of Developing Hepatocellular Carcinoma in Treated HCV-Carriers in Morocco according to University Hospital Experience

Younès Cherradi,¹ Rajaa Afifi,¹ Hanaa Benbrahim,¹ Wafaa Essamri,¹ Imane Benelbarhdadi,¹ Fatima Zahra Ajana,¹ Hadj Omar El Malki,² Mustapha Benazzouz,¹ and Abdellah Essaid¹

¹Department of Hepatogastroenterology (Medicine C), Ibn Sina Hospital, Rabat, Morocco

²Biostatical, Clinical Research and Epidemiological Laboratory (LBRCE), Medical School, University Mohammed Vth Souissi, Rabat, Morocco

Received 29 October 2012; Accepted 22 November 2012

Academic Editors: D. Capone and K. Cheng

Copyright © 2013 Younès Cherradi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Introduction. Hepatitis C is the first major cause for HCC in Morocco. Antiviral treatment reduces the risk of developing HCC but few cases of HCC in HCV-treated patients were reported. We aimed to define this population’s features and to identify predictive factors of developing HCC. Patients and Methods. We included all HCV carriers who developed HCC after antiviral treatment from January 2002 to April 2010. We compare HCV-treated patients with no developed HCC to HCC population using khi-2 and Fisher Exact analysis. Results. 369 HVC-treated patients were considered, and 20 HCC were reported. The risk of HCC was not significant according to gender and genotypes (resp., and ). Advanced age and severe fibrosis were significant risk factors (resp., and ). HCC was reported in 2.6% of sustained virological responders versus 12.5% of nonresponders (). Conclusion. In our series, 5% of previously treated patients developed an HCC. Advanced age and severe fibrosis at HCV diagnosis are predictive factors of HCC occurrence. Sustained virological response reduces considerably the risk of HCC occurrence but screening is indicated even after SVR.

1. Introduction

Hepatocellular carcinoma (HCC) is one of the most common malignant tumors in the world. It is the main type of primary liver cancers and the third most common cause of cancer mortality worldwide [1]. The epidemiology of HCC is variable according to the geographic area because of differences in the repartition of major causative factors. In countries where hepatitis C virus infection is endemic such as Japan and Egypt, high prevalence of HCV infection is reported among people with HCC. In Morocco, according to our department register and the results of a regional study [2], the major risk factor for hepatocellular carcinoma is chronic hepatitis especially hepatitis C virus infection. Hepatocellular carcinoma is closely associated to liver cirrhosis, which is a true precancerous state. Hepatitis viruses B and C contribute to this condition if not treated or diagnosed late [3]. Hepatocarcinogenesis is a long and heterogeneous process and there is still much to understand. The combination of pegylated interferon to ribavirin given for 24 or 48 weeks—according to genotype—has been retained for long years ago as the only consensual and standard treatment of chronic hepatitis C before the development of antiproteasis and antipolymerases for selected patients. It is established too that antiviral treatment limits fibrosis progression and reduces risk of developing HCC but few cases of  HCC in HCV carriers are still reported even after antiviral treatment. The aim of this study is to define this population’s features and to identify predictive factors of developing HCC. The major endpoint is to define patients who must be screened carefully after antiviral therapy in order to early diagnosis and more prognosis involvement.

2. Patients and Methods

It is a monocentric, retroprospective, and analytic study. It concerns our entire patients department with hepatitis C virus infection who developed HCC after antiviral treatment. All participants were treated by pegylated interferon associated to ribavirin. They were all tested for HCC prior to antiviral therapy. At study onset, included patients had no HCC and they were not coinfected by hepatitis B. Diagnosis of HCC was based on histological confirmation when biopsy was performed or on morphological noninvasive criteria (Barcelona criteria) for cirrhotic patients where biopsy was not necessary. Considered parameters were age of HCV diagnosis, gender, baseline viral loads (BVL), genotype, necro-inflammatory activity, and fibrosis degrees at the beginning of antiviral treatment. Fibrosis and histological activity were estimated according to METAVIR score ( was considered as an advanced stage of fibrosis). We compare initially HCV-treated patients who did not develop HCC to patients who developed HCC using khi-2 and Fisher-Exact analysis. In a second step, we were particularly interested to special cases of sustained virological responders who developed HCC. The pretherapeutic parameters previously detailed were collected and analyzed too. We compare sustained virological responders who did not develop HCC to the others using Pearson Chi-square test. Follow-up time was at least 03 years.

3. Results

Three hundred sixty-nine HCV-treated patients were considered from January 2002 to April 2010. Twenty HCC were reported with 12 females (60%) and 8 males (40%), ranging in age between 40 and 72 years; the mean age is 61 years. The mean time of HCC occurrence is years. 53% of patients were HCV-1, 47% were HCV-2, and 94, 6% had severe fibrosis at the beginning of treatment (Table 1). Considered all our treated patients, sustained virological response (SVR) was achieved in 70%. The comparison of HCC occurrence in non-SVR patients and sustained virological responders shows significant results: HCC was reported in 2.6% of sustained virological responders versus 12.5% of non-SVR patients () which demonstrate that SVR reduces significantly the risk of developing HCC. The risk of HCC was not significant according to gender and genotypes (resp., and ). Advanced age and severe fibrosis were significant risk factors (resp., and . 0001) (Table 2).

Table 1: General features of HCV-treated patients with developed HCC.

Gender

    Male
08

    Female
12

Mean age
61 years old.

Mean time of HCC occurrence
5 ± 2 years

HCV genotypes

    HCV-1
53%

    HCV-2
47%

Fibrosis (METAVIR score)

    Severe
94.6%

    Reduced
5.4%

Response to antiviral treatment

    Sustained virological responders
06

    Non-SVR patients
14

Table 2: Predictors of developing HCC in treated HVC carriers.

Gender

Age of diagnosis > 60 y.o

Genotype

Initial fibrosis

Non-SVR

Of the 20 patients who developed HCC, six were previously sustained virological responders. They were 3 males and 3 females, ranging in age between 51 and 70 years. Mean age is 60 years. Five patients were HCV-2 and one patient was HCV-1. All patients were in severe fibrosis (F3-F4). Time of follow-up ranges between 3 and 9 years with a median of 6 years. The risk of HCC occurrence in sustained virological responders seems not to be significant according to gender, genotypes, and initial high viral loads (resp., and ). High necroinflammatory activity did not influence hepatocarcinogenesis. Severe fibrosis was the only significant risk factor () in our real life experience (Table 3).

Table 3: Fibrosis is significantly associated to HCC occurrence in sustained virological responders ****.

Patients with developed HCC

Patients with no HCC

Gender

    Male
3.3%
Versus
96.7%

    Female

3.4%
Versus
96.6%

Age of diagnosis

    Age ≤ 55
1%
Versus
99%

    Age > 55
5.7%
Versus
94.3%

HCV Genotypes

    1
1.3%
Versus
98.7%

    2
4.7%
Versus
95.3%

Baseline viral loads (BVL)

    High BVL
3%
Versus
97%

    Low BVL
1.1%
Versus
98.9%

Necroinflammatory activity

3.2%
Versus
96.8%

6.3%
Versus
93.7%

Fibrosis****

0%
Versus
100%

8.8%
Versus
91.2%

4. Comment

Hepatitis C is a real public health trough the world. There are more than 170 million people infected worldwide [4]. Approximately, 80% of HCV carriers develop chronic hepatitis C [4]. About 20% of these patients will develop severe chronic hepatitis C and cirrhosis which is considered as a precancerous condition predisposing to development of hepatocellularcarcinoma.

Treatment of hepatitis C virus infection has been developed rapidly and, in twenty years, SVR rates increased from 6% to 60% [5]. Actually, and in expectation of protease and polymerase inhibitors for particular situations, the association of pegylated interferon and ribavirin is retained as standard of care in HCV-chronically-infected patients. Effectiveness of antiviral treatment is proved and in our department patients, where genotypes 1 and 2 are more prevalent, SVR is achieved in 70% of all patients which is very interesting result. Actually, there is strong evidence that eradicate HCV infection improves the prognosis of patients and limits fibrosis progression which reduces—but does not abolish—the risk of developing hepatocellular carcinoma [6]. It means that possibility of HCC development is still present in treated patients and screening is still indicated even after SVR especially when HCV was diagnosed late (>50 years old in our study) with severe fibrosis (F3-F4). In another sense, SVR is certainly a significant protector factor. It was demonstrated that in patients with chronic hepatitis B or C, antiviral treatment in a noncirrhotic stage is protective for HCC occurrence in responders, probably by prevention of cirrhosis development [7]. When cirrhosis is already present, the protective effect is less clear. For cirrhosis due to hepatitis C, some studies—especially in Japan—showed a protective role of interferon-alfa [7, 8]. Virological response, but also merely biochemical response, seems to be associated with a lower risk of development of HCC [7], but screening is indicated even after SVR. In our study, predictors of HCC occurrence in all treated HCV carriers are advanced age (>50 years old), severe fibrosis, and non-SVR; the protective role of SVR was established. In the special case of sustained virological responders, severe fibrosis is the only significant predictor of developing HCV. we conclude that patients with advanced fibrosis must be considered carefully with necessity of continuous screening even after SVR.

5. Conclusion

Considering our real life experience, significant predictors of HCC occurrence in treated HCV carriers are advanced age, severe fibrosis, and non-SVR. In other side, this study confirms the fact that SVR reduces significantly the risk of HCC development; so, screening is indicated even after SVR especially in patients with severe fibrosis.

References

E. Maillard, “Epidemiology, natural history and pathogenesis of hepatocellular carcinoma,” Cancer/Radiotherapie, vol. 15, no. 1, pp. 3–6, 2011.

O. Bahri, S. Ezzikouri, N. B. Alaya-Bouafif, et al., “First multicenter study for risk factors for hepatocellular carcinoma development in North Africa,” World Journal of Hepatology, vol. 3, no. 1, pp. 24–30, 2011.

S. Bühler and R. Bartenschlager, “Promotion of hepatocellular carcinoma by hepatitis C virus,” Digestive Diseases, vol. 30, no. 5, pp. 445–452, 2012.

P. P. Michielsen, S. M. Francque, and J. L. van Dongen, “Viral hepatitis and hepatocellular carcinoma,” World Journal of Surgical Oncology, vol. 3, article 27, 2005.

P. Marcellin, “Hepatitis C: the recovery,” Gastroentérologie Clinique et Biologique, vol. 33, no. 8-9, pp. 819–829, 2009.

G. Farrell, “Prevention of hepatocellular carcinoma in the Asia-Pacific region: consensus statements,” Journal of Gastroenterology and Hepatology, vol. 25, no. 4, pp. 657–663, 2010.

S. G. Lim, R. Mohammed, M. F. Yuen, and J. H. Kao, “Prevention of hepatocellular carcinoma in hepatitis B virus infection,” Journal of Gastroenterology and Hepatology, vol. 24, no. 8, pp. 1352–1357, 2009.

Y. Du, T. Su, Y. Ding, and G. Cao, “Effects of antiviral therapy on the recurrence of hepatocellular carcinoma after curative resection or liver transplantation,” Hepatitis Monthly, vol. 12, no. 10, Article ID e6031, 2012.