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Year : 2008  |  Volume : 45  |  Issue : 4  |  Page : 167--172

Evaluation of serum squamous cell carcinoma antigen as a novel biomarker for diagnosis of hepatocellular carcinoma in Egyptian patients

MM Hussein1, AA Ibrahim1, HM Abdella1, IF Montasser1, MI Hassan2,  
1 Department of Tropical Medicine, Ain Shams University Cairo, Egypt
2 Department of Diagnostic Oncology, Ain Shams University Cairo, Egypt

Correspondence Address:
H M Abdella
Department of Tropical Medicine, Ain Shams University Cairo
Egypt

Abstract

Background: Hepatocellular carcinoma (HCC) is the fifth most common malignancy in the world. In Egypt, HCC was reported to account for about 4.7% of chronic liver disease (CLD) patients. Squamous cell carcinoma antigen (SCCA) has been reported to be strongly expressed in HCC tissue hampering its extensive use in clinical practice. Aim: To evaluate the clinical usefulness of serum SCCA levels as a serological marker for early detection of HCC among high-risk patients compared to AFP. Materials and Methods: The study comprised of three groups. Group A included 30 patients with CLD diagnosed based on clinical, laboratory, and ultrasonographical investigations; group B included 49 patients with HCC diagnostically confirmed by spiral CT, elevated alfafetoprotein (AFP), and/or liver biopsy; and group C, the control group, included 15 healthy subjects matched for age and sex. All groups were subjected to thorough history taking, full clinical examination, and laboratory investigations including liver functions, viral markers, and AFP and SCCA estimation using ELISA technique. Results: This study revealed a highly significant difference between patients with HCC, CLD, and controls regarding serum SCCA levels (5.138 7.689, 1.133 0.516, and 0.787 0.432 ng/ml, respectively). SCCA level was persistently elevated in patients with HCC with normal AFP levels representing its useful role in early detection and follow-up of patients treated for HCC. The area under the curve (AUC) of SCCA was 0.869 (95% CI 0.783-0.929), the cut-off value was established at 1.5 ng/ml with sensitivity of 77.6% and specificity of 84.4%). The difference between AUC of SCCA and that of AFP was 0.09 which mounted statistical significance. Conclusions: SCCA could represent a useful tool as a marker for detection of HCC.



How to cite this article:
Hussein M M, Ibrahim A A, Abdella H M, Montasser I F, Hassan M I. Evaluation of serum squamous cell carcinoma antigen as a novel biomarker for diagnosis of hepatocellular carcinoma in Egyptian patients.Indian J Cancer 2008;45:167-172


How to cite this URL:
Hussein M M, Ibrahim A A, Abdella H M, Montasser I F, Hassan M I. Evaluation of serum squamous cell carcinoma antigen as a novel biomarker for diagnosis of hepatocellular carcinoma in Egyptian patients. Indian J Cancer [serial online] 2008 [cited 2020 Nov 30 ];45:167-172
Available from: https://www.indianjcancer.com/text.asp?2008/45/4/167/44666


Full Text

 Introduction



Hepatocellular carcinoma (HCC) is the fifth most common cause of cancer deaths worldwide. The incidence is rising, and is expected to increase by another 81% by 2020 primarily due to HCV epidemic. [1]

Egypt, like the Western countries, has an overall frequency of 2.3% among other types of cancer. [2] There is an apparent increase in the number of HCC patients attending the various oncology centers in Egypt and all over the world. [3] In 2001, HCC in Egypt was reported to account for about 4.7% of chronic liver disease (CLD) patients. [4] In another study, in 2005, a remarkable increase from 4-7.2% was reported over a decade. [5] Patients with advanced liver disease, particularly cirrhosis, are those at risk for HCC and should be screened every six months for its development. [6]

Currently, standard surveillance includes a combination of six monthly abdominal ultrasound scans and serum alpha fetoprotein (AFP) measurement, but this strategy does not reliably detect early disease. AFP may be elevated in CLD, especially in viral hepatitis, in the absence of HCC. The differential diagnosis of elevated AFP levels also includes gastric, biliary, and pancreatic cancers and germ cell tumors. [7]

The relatively poor sensitivity of conventional AFP as a marker has led to a search for more sensitive and specific markers. Other tumor markers include serum Des-gamma-carboxy prothrombin (DCP) that has been used for screening of HCC. The failure of hepatoma cells to express prothrombin carboxylase leads to a higher DCP serum levels. The sensitivity of DCP is better than that of AFP only in larger tumors and hence is of limited benefit in clinical practice. [8]

It has been reported that squamous cell carcinoma antigen (SCCA), a member of the high molecular weight family of serine protease inhibitors, is strongly expressed in a number of different epithelial cancers such as those of the cervix, lung, and head and neck, and so can be used as a clinical marker of these malignancies. [9]

Overexpression of SCCA variants (SCCA1, SCCA2) has been reported in all surgically resected HCC specimens but in none of the normal control livers as detected by immunohistochemistry. [10]

The aim of this work was to evaluate the clinical usefulness of serum SCCA levels as a marker for early detection of HCC among high-risk patients compared to AFP as a known biomarker for diagnosis of HCC.

 Materials and Methods



Patients attending the Tropical Medicine Department, Ain Shams University, as well as the outpatient clinic for early detection of hepatic tumors (clinic of Ain Shams Hepatoma Group), during May 2005 to March 2007 were evaluated. Apart from obtaining a detailed clinical history, general and abdominal examinations were done for all the selected patients. The patients underwent laboratory investigations that included complete blood count and ESR, liver function tests, viral markers (HBsAg, HBcAbs, and HCVAbs), and determination of AFP levels by an ELISA technique. [11] Abdominal ultrasonography to determine the liver size, echogenicity, presence of focal lesions (size, number, echogenicity), and portal vein (patency, diameter) was also done. Spiral triphasic abdominal CT scan was used to confirm the findings of abdominal ultrasonography and for studying of suggestive criteria for HCC (early enhancement in arterial phase, rapid washout in subsequent phases - portovenous and delayed phases). If needed, liver biopsy and histopathological examination were done for patients with hepatic focal lesion detected by the ultrasound and missing the HCC criteria in spiral CT or with normal AFP.

Then the selected patients were set into two groups: group A consisting of 30 patients with chronic liver disease (CLD) diagnosed based on clinical, laboratory, and/or ultrasonographic examinations; and group B consisting of 49 patients with HCC confirmed by spiral triphasic CT scan, elevated AFP levels > 200, and/or liver biopsy. [12]

Fifteen age and sex matched healthy subjects were included in the control group, designated as group C. Their age ranged between 25-65 years (mean 48 12.3). There were seven men and eight women. All their laboratory data were within normal range. SCCA level [13] by ELISA according to the recommendations of the manufacturer was measured in the sera of the subjects in all three groups.

Exclusion criteria included patients with other suspected epithelial malignancies of cervix, lung, head and neck, metastatic liver tumors, and other types of CLD such as autoimmune hepatitis and primary biliary cirrhosis.

Statistical Methods

Analysis of the data was done using statistical program for social science (SPSS). The quantitative variables are described in the form of mean and standard deviation, while the qualitative variables are described in the form of frequency and percentages. Unpaired t test ( t value) was used to compare a quantitative variable between two independent groups in parametric data. Mann Whitney test ( Z value) was used instead of the t test to compare a quantitative variable between two independent groups when data were nonparametric (SD > 25% of mean). Chi square test (X 2 value) was used to compare a qualitative variable between two independent groups. Spearman correlation test (rho value) was used to rank different nonparametric variables against each other, either positively or inversely. P value (which is either nonsignificant (NS) if > 0.05, significant (S) if P P r = 0.06, P > 0.05.

[Table 7] shows that no statistical significant difference of SCCA level in both groups among different Child classes which reflect the severity of the liver disease. Pearson correlation: r = 0.17, P > 0.05.

 Discussion



HCC is the fifth most common malignancy in the world. Its incidence is increasing worldwide ranging between 3-9%. [14] The estimated annual number of cases exceeds 500,000. [15]

In Egypt, HCC was reported to account for about 4.7% of CLD patients. [4] Over a decade, there were nearly two-fold increases in proportion of HCC among CLD patients in Egypt with a significant decline in HBV infection and a slight increase of HCV infection as a risk factor. [5]

Unfortunately, surveillance programs are hindered by the poor performance of the commonly used serum markers, namely, AFP, [15] even in combination with abdominal ultrasound. A tremendous amount of effort has been and continues to be applied to the search for improved HCC biomarkers.

This study was conducted to evaluate the clinical usefulness of serum SCCA as a serologic marker for early detection of HCC among high-risk patients and to compare it with AFP as a known biomarker for diagnosis of HCC.

In the present study, the age of patients with CLD ranged from 25-70 years with a mean of 49.7 11.3, while that of patients with HCC was 40-77 years with a mean of 56 8.15 and a high statistical difference in between ( P et al , [5] who found slight shift of age of patients with HCC to the younger age group (40-59 years).

Our demographic data showed that there were 13 males (43.3%) and 17 (56.7%) females among patients with CLD, while there was male predominance in patients with HCC (39 patients representing 79.6%, with high statistical difference in between, P et al , [5] in a series of 1328 HCC cases; they found that HCC is significantly higher in males than females (77.7% and 23.3%), respectively.

AFP was discovered in 1963 by Abelev, and since then, its measurement is the only marker used in clinical practice for serological diagnosis of HCC, although it has questionable reliability. [16] AFP levels could be normal during the early assessment of HCC growth and even with persistent tumor growth; there may be a spontaneous AFP fall. It also seems that determination of only the serum AFP level is an unreliable indicator in the early detection of HCC. [17]

Regarding AFP, this study showed a significant difference ( P P [15] In the present study, at AFP level of 200 ng/ml, the sensitivity was 40.8%, while the specificity was 100%.

Regarding SCCA, our study detected a highly significant difference ( P P et al , [18] who also recommended the combined use of AFP, SCCA, and immunocomplexed forms of AFP and SCCA increases the accuracy of HCC diagnosis.

In HCC patients, there were 29 patients with AFP 200 ng/ml. The SCCA level was persistently elevated in both groups (5.3 and 4.9 ng/ml, respectively), representing its useful role as a serological marker for diagnosis of HCC patients with normal level of AFP.

Pontisso et al , [10] performed a case control study on 65 patients with HCC and 20 normal livers. SCCA was detected by immunohistochemistry in 55 out of 65 patients' (85%) tumor specimens, but none in the 20 controls. There was no significant correlation between SCCA and other clinical and biochemical parameters including age, sex, and transaminases levels and this agrees with the results obtained in this study.

In our study, the AUC of SCCA was 0.869 (95% CI 0.783-0.929), the cut-off value was established at 1.5 ng/ml with sensitivity of 77.6% and specificity of 84.4%). In the study performed by Giannelli et al , [19] on SCCA combined with AFP on 120 patients with HCC, 90 patients with CLD, and 41 healthy subjects, AFP values in HCC patients and CLD patients were 23.06 IU/ml and 5.05 IU/ml, respectively, with statistically significant difference in between, while mean levels of SCCA were 0.678 g/L and 0.376 g/L, respectively, which mounted a statistically significant difference, this agrees with our results. The AUC of SCCA was 0.705 (95% CI 0.638-0.766), the cut-off point was established at 0.368 with sensitivity of 84.2% and specificity of 48.9%. The AUC of AFP was 0.717 (95% CI 0.651-0.777), the cut-off value was established at 13.7 IU/ml with sensitivity of 45% and specificity of 86.7%. The difference between AUC of SCCA and that of AFP was 0.009 with no statistical difference in between. This may be attributed to larger size of their sample.

It is worth mentioning that Beale et al , [20] found that SCCA1 was not elevated in patients with HCC arising on top of nonalcoholic and alcoholic fatty liver disease which suggests that this HCC marker may be etiology related and so results are different in Egyptian patients as most HCC here arise on top of HCV and/or HBV liver disease. Also, the choice of optimal biomarkers for HCC surveillance may be determined by the etiology of underlying liver disease.

Data in our study pointed to absence of correlation between the SCCA level, size and burden of the tumor, and severity of CLD, but further studies on larger number of patients are needed to clarify this finding.

 Conclusions



The results of our study suggest that SCCA could represent a useful tool as a marker for detection of HCC and for differential diagnosis between HCC and cirrhosis as we found that the levels of SCCA are significantly higher in patients with HCC than in CLD patients and controls.

Recommendations: More studies on a large scale are needed to assess the diagnostic as well as the prognostic value of SCCA in patients with HCC with different etiologies of liver disease. Also, multivariate analytical studies are needed to evaluate various clinical, laboratory, and radiological parameters to improve the diagnostic accuracy for early detection of HCC.

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