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Vascular endothelial growth factor in relation to the development of hepatocellular carcinoma in hepatitis C virus patients treated by direct-acting antivirals



Hepatocellular carcinoma (HCC) comprises 5.6% of all cancers worldwide representing the sixth most common cancer. It is also the fourth most common cause of cancer-related mortality. Angiogenesis is a main factor in the development of HCC. Vascular endothelial growth factor (VEGF) is considered as the force for physiological and pathological angiogenesis, and overexpression of VEGF is prominent in HCC. We aimed to study the effect of direct-acting antivirals (DAAs) on VEGF considered as the key regulator of angiogenesis in HCC. This cross-sectional study involved fifty patients who were divided into two groups: group I—twenty-five chronic hepatitis C virus (HCV) patients as (cases) subjected to treatment with direct-acting antiviral drugs for 3 months; group II—twenty-five chronic HCV patients developed HCC as (controls). Serum VEGF level was measured in of group I at baseline, at end of treatment, and 3 months after the end of treatment by sofosbuvir 400 mg plus daclatasvir 60 mg for 3 months in the HCV patient group, also VEGF was assessed in group II with HCC.


Serum VEGF was high in both groups, but it was higher in the HCC group with a statistically significant difference (p < 0.001), also serum VEGF in the HCV group decreased after 3 months at the end of DAA treatment from 209.5 ± 137.6 to 44.1 (31.8–55.3) mg/ml, and all patients who received DAAs achieved sustained virologic response (SVR).


We found that change in serum VEGF in HCV patients treated with DAAs in this study cannot explain the risk of HCC after treatment by DAAs.


Liver cancer occupies the sixth rank among common cancers and the fourth among the leading causes of cancer-associated mortalities [1]. Hepatocellular carcinoma (HCC) is considered the commonest liver cancer worldwide [2]. Chronic infection with HCV is considered the most common etiology for HCC [3]. The direct-acting antiviral agents (DAAs) recently improve the standards of therapy that achieve complete cure of hepatitis C virus infection, which in turn leads to a decreased risk of developing HCC and its associated high mortality [4].

Although the novel therapies are effective in treatment, they did not manage to reduce the risk of HCC in those with higher degrees of liver cirrhosis to zero percent [5]. Cirrhosis plays an important role in the occurrence of HCC since the majority of HCV patients who develop HCC are cirrhotic, and patients with advanced cirrhosis are highly prone to develop HCC even after achieving sustained virologic response (SVR) [6]. Many studies have shown the effect of DAA regimens on HCC recurrence and development; however, neither of them could confirm this relation [1, 7,8,9].

AFP has limited sensitivity (41–65%) for the detection hepatocellular carcinoma especially in its early phases. It is not secreted in all cases of HCC, and its serum levels may be within normal ranges in about 40% of patients with HCC. So, detection of serum AFP only is not a reliable indicator in the early phases of HCC [10]. Therefore, the presence of an alternative marker for HCC is important. It was reported that vascular endothelial growth factor (VEGF) is only detected in HCC cells but not in benign liver tissues, and can thus be used as an excellent marker for the diagnosis of early HCC [11].

VEGF signaling is the main regulator of angiogenesis, which is impaired in most solid types of cancer as liver tumors’ growth needs high vascularity through new blood vessel formation to suffice its increased metabolic demands [12]. HCV can affect the process of angiogenesis through triggering of hypoxia-inducible factor 1 alpha (HIF-1α) that turns into increased VEGF expression [13]. Also, HCV activates the signal transducer and activator of transcription 3 (STAT3) which stimulates both the transcriptional activity of androgen receptors and VEGF expression [14].

We aimed to study the impact of DAAs on VEGF expression which is the key regulator of angiogenesis in HCC.


We included fifty adult patients from Ain Shams University Hospitals; they were divided into two groups:

  • Group I (case group): twenty-five chronic HCV patients as evidenced by positive HCV Ab (at least 6 months duration) and detectable quantitative HCV-RNA were subjected to the treatment of hepatitis C virus by sofosbuvir 400 mg plus daclatasvir 60 mg for 3 months (HCV HCC-free group) and all patients achieved SVR.

  • Group II (control group): twenty-five HCV patients who developed HCC. HCC was confirmed by triphasic abdominal CT with contrast verifying criteria of HCC (HCV related HCC patients).

Any causes of chronic liver disease other than HCV such as hepatitis B virus (HBV) were excluded. We also excluded patients with morbid obesity, dyslipidemia, diabetes mellitus, and patients with any malignancy other than HCC. Also, patients with rheumatoid arthritis, pregnant females, and patients with decompensated liver disease (Child-Pugh C) were excluded from the study.

All patients were subjected to the following:

Full history and clinical examination and the following laboratory tests:

  • Complete blood count (CBC).

  • Serum creatinine.

  • Aspartate aminotransferase (AST), alanine aminotransferase (ALT), and serum albumin.

  • PCR quantitative for HCV.

  • Serum alpha-fetoprotein level (AFP).

  • Serum vascular endothelial growth factor normal range (27–30 ng/ml) was assessed for all patients included in both groups.

    • For group I, VEGF was assessed before starting antiviral treatment (baseline) then at the end of treatment, 1 month after the end of treatment, and 3 months after the end of treatment (SVR).

    • For group II, VEGF was assessed at the beginning of the study.

  • Radiological examination: pelviabdominal ultrasound.

Sample size calculation

After reviewing the literatures [15, 16], we used G*POWER statistical programming version (Franz Faul, University at Kiel, Germany) to calculate the sample size per group. Using a = 0.05, a power of 90%, an effect size of 0.628, and an allocation ration of 1:1 showed that the minimum required sample size to avoid type II error is 58 patients (29 patients in each group) was needed. Four patients were lost to follow-up from each group. So, there were 25 patients in each group.

Statistical analysis

We used SPSS (Statistical Package for Social Sciences) for Windows version 24 (SPSS Inc., Chicago, IL, USA). Numerical data were expressed in terms of mean and standard deviation (mean ± SD) if normally distributed or median and inter-quartile range if not normally distributed. Normality was tested using the Shapiro-Wilk test. Pearson and Spearman correlations were used to test the association between the numerical dependent and independent variables. The Friedman test was used to test the difference between paired numerical data. We conducted a linear regression analysis to test the absolute relations between dependent and independent variables. P value less than 0.05 was sufficient enough to show the statistical significance.


This study was conducted on fifty patients. Both groups were age- and sex-matched. They were subdivided into two groups.

  • Group I (HCV HCC-free group): twenty-five HCV patients were subjected to the treatment of chronic hepatitis C virus by DAAs.

  • Group II (HCV-related HCC group): twenty-five HCV patients who developed HCC.

As regards the demographic data, there were no statistically significant differences in age and sex, although all patients had normal body weight but significantly higher median BMI in the HCC group compared with the other (p < 0.001). Concerning laboratory findings, patients in the HCC group had statistically significantly lower levels of hemoglobin and platelets than others in the HCV group (p < 0.001, p < 0.001, respectively), but serum creatinine levels were significantly higher in the HCC group than in the HCV group (p < 0.001).

Also, AFP was dramatically higher in the HCC group (p < 0.001) than in the HCV group. Concerning liver functions, bilirubin levels were significantly higher in HCC group (p < 0.001), both groups had similar ALT and AST levels (p = 0.15, p = 0.39, respectively). However, albumin levels were significantly higher in the HCV group (p < 0.001) as shown in Table 1.

Table 1 Comparison between the 2 groups regarding demographic and laboratory findings

HCC patients had significantly higher levels of VEGF compared to HCV patients (488.01 ± 194.5 versus 209.5 ± 137.6, respectively).

For HCV patients, there was a positive correlation between baseline VEGF levels and BMI, bilirubin, AST, PCR, and AFP levels. VEGF was negatively correlated with age, Hb levels, platelet count, albumin level, ALT level, and creatinine levels. However, none of those correlations was statistically significant as shown in Table 2.

Table 2 Correlation between baseline VEGF and laboratory findings in both groups

For HCC patients, there was a positive correlation with age, bilirubin levels, ALT levels, AST levels, and AFP levels. There was a negative correlation between baseline VEGF levels and BMI of patients, Hb levels, platelets count, Alp levels, and creatinine levels. Only AST levels showed a significant correlation with baseline VEGF in HCC patients (p < 0.001) as shown in Table 2.

On follow-up of HCV patients, treatment with DAAs could significantly decrease VEGF values at the end of the treatment period, 1 month after treatment (p < 0.001), and even 3 months post-treatment (Table 3).

Table 3 VEGF through the study period

There was a positive correlation between VEGF values and age of patients, platelets count, bilirubin levels Alp levels, and PCR values. Age of patients and PCR values were significant determinants of SVR VEGF values (p = 0.04, p = 0.03, respectively) as shown in Table 4.

Table 4 Correlation between 3 months VEGF values and laboratory findings in HCV HCC-free patients

After adjustment of the co-founding factors through linear regression analysis, we found that neither age of patients nor PCR values were significant predictors of the VEGF value 3 months post-treatment by DAAs (p = 0.064, p = 0.219, respectively) as shown in Table 5.

Table 5 Linear regression analysis to predict SVR VEGF values in HCV patients


The modern use of direct-acting antiviral drugs (DAAs) in the treatment of HCV has a major advantage in achieving more than 90% SVR despite the degree of liver cirrhosis. This allowed the treatment of many more patients, some of them with more advanced liver function impairment and more susceptibility for HCC [17]. However, the impact of DAA-based treatment on HCC occurrence in patients with cirrhosis is still controversial.

In this study, we found high statistically significant higher VEGF serum level in HCC patients than in HCV patients reflecting the pro-inflammatory and pro-angiogenic state that continued from benign to malignant liver disease and the impact of VEGF in addition to other angiogenic and growth factors on the growth, propagation, and spread of HCC as previously reported by Villani et al. [16], Debes et al. [18], and Faillaci et al. [19].

In spite of the great advancement in the HCV treatment after DAA introduction and achievement of more than 90% SVR in respective of fibrosis stage, which will improve the HCV natural history of infection, however, several recent reports have raised concerns about DAA treatment because of higher rates of HCC recurrence observed after DAA therapy [16, 20] and even early occurrence of HCC after treatment by DAAs [21].

We addressed in this study the possibility that serum VEGF after successful viral eradication by DAAs may be one of the molecular mechanisms responsible for early occurrence and recurrence of HCC as reported by Villani et al. [16]; however, we found that serum VEGF in our studied patients dropped after 1 month and 3 months after DAA treatment in controversy to the finding of Villani et al. who reported that although DAAs reduce the inflammation, they increase serum VEGF level and they considered this as a rationale for HCC occurrence risk during anti-HCV treatment; however, due to different finding in the present study in our patients, this reflects the different population number and characteristics included in different studies and reflect the multi-factorial explanation for HCC occurrence after DAA therapy.

It is known that platelets can produce many growth factors for HCC including VEGF [22]. We found statistically significant thrombocytopenia (p < 0.001) in the HCC group in contrast to the HCV group; this comes in agreement with the study by Carr et al. who demonstrated that non-cirrhotic HCC patients have lower levels of thrombocytopenia than cirrhotic HCC patients specially in those patients who had larger tumors [23]. In the current study, there was statistically significant anemia (p < 0.001) in the HCC group, and this reflect the impact of developing HCC on the deterioration of liver function reserve and deterioration of portal hypertension with increased anemia whether related to malignancy or portal hypertension related to blood loss and reduced platelet count expected in cirrhotic patients with or without malignancy.

In this study, we found highly statistically significantly higher serum AFP in the HCC group in comparison with the HCV infection group; this comes in agreement with Zhang et al. who estimated the performance of AFP in diagnosing HCC and they found that AFP serum level is a good sensitive biomarker to diagnose HCC whether used alone or combined with ultrasound, they found that 400 ng/mL was better than 200 ng/mL as a cutoff value for diagnosis of HCC [24].

Also, we found that BMI was significantly higher in HCC patients than in HCV group (p < 0.001); this comes in agreement with study by Divella et al. who explores the risk of obesity in the development of HCC whether due to the post-viral cirrhosis or in NAFLD [25].

As regards the serum creatinine level, it was significantly higher in the HCC group (p < 0.001). Shariff et al. suggested that this increase may be due to the increased metabolic activity that resulted in the increased rate of cellular turnover causing overproduction of carnitine to be sufficient for beta-oxidation and excessive needs of energy [26]. However, reduced serum creatinine in case of chronic liver disease can be due to a 50% decline in hepatic production of creatine; it can be also attributed not only to accumulation of extracellular fluid in the form of edema and ascites which increases the volume of distribution but also to malnutrition and decrease in muscular mass related to recurrent attacks of sepsis affecting satiety of patients [20].

Regarding serum albumin, it was significantly lower in the HCC group also (p < 0.001); this result agrees fully with Carr and Guerra who studied the association between serum albumin levels and HCC severity [27]. Albumin production is a marker for hepatocyte function differentiation; low serum albumin level may denote poorly differentiated and more aggressive HCC; on the other hand, normal serum albumin level can be a good indicator for well-differentiated, slowly growing HCCs [28]. However, low albumin level reflects also poor nutrition and could be an indicator of bad prognosis [29]

In this study, we found significantly higher bilirubin in HCC patients compared to the HCV patients’ group, and this comes in contact with the study by Carr et al. who also stated that abnormal levels of bilirubin in HCC patients reflect a poor prognosis in contrast to those with normal levels [30].

In our Egyptian cohort of cirrhotic HCV-related and HCC patients, the number is relatively small and genotype 4 is different from other genotypes in other studies, and in addition, other molecular mechanisms may be more involved in our Egyptian patients as alteration of immune system function and inflammatory cytokines.


After successful viral eradication by DAAs, VEGF, the one responsible for both physiological and pathological angiogenesis in HCC, significantly decrease at end of treatment, after 1 month and 3 months of treatment. So, we can conclude that VEGF is not incriminated in the debate of increased incidence of HCC after treatment by DAAs.

Availability of data and materials

The authors confirm that the data supporting the finding of this study are available within the article.



Hepatocellular carcinoma


Vascular endothelial growth factor


Direct-acting antivirals


Hepatitis C virus


Sustained virologic response




Hypoxia-inducible factor 1 alpha


Signal transducer and activator of transcription 3


Hepatitis B virus


Complete blood count


Aspartate aminotransferase


Alanine aminotransferase


Polymerase chain reaction


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The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Author information




MMS, AME, and ABS analyzed and interpreted the patient data. EMB, WAI, and MMS put the study design. NMT and AME were the major contributors in writing the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Nahla Mohamed Teama.

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This study was approved according to the ethical standards of Ain Shams University Research Committee (committees reference number 387/2017) and the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

A written informed consent was obtained from all patients in the study.

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Informed consent to publish patient’s data was signed by all participants prior to the beginning of the research.

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ElGhandour, A.M., Bayoumy, E.M., Ibrahim, W.A. et al. Vascular endothelial growth factor in relation to the development of hepatocellular carcinoma in hepatitis C virus patients treated by direct-acting antivirals. Egypt Liver Journal 11, 5 (2021).

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  • Vascular endothelial growth factor A
  • HCV
  • DAAs
  • HCC