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Oncology Letters logoLink to Oncology Letters
. 2011 Jul 5;2(5):851–854. doi: 10.3892/ol.2011.359

Clinical characteristics of hepatocellular carcinoma in elderly patients

Takuya Honda 1, Hisamitsu Miyaaki 2, Tatsuki Ichikawa 3, Naota Taura 4, Satoshi Miuma 5, Hidetaka Shibata 6, Hajime Isomoto 7, Fuminao Takeshima 8, Kazuhiko Nakao 9
PMCID: PMC3408052  PMID: 22866139

Abstract

The incidence of hepatocellular carcinoma (HCC) in elderly patients in Japan has been on the increase. The aim of the present study was to evaluate the impact of aging on the clinicopathological findings and the survival of HCC patients. A total of 624 patients with HCC were examined in this study. The patients were classified according to their age at the time of diagnosis: one group comprised younger patients (<75 years; n=544) and the second comprised elderly patients [(≥75 years; n=80, (12%)]. Results showed that there were significantly more female patients (younger:elderly, 22:36; p=0.005), normal livers (younger:elderly, 0.3:6%; p=0.0002), non-viral HCC (younger:elderly, 11:31%; p<0.001) and solitary tumors (younger:elderly, 53:76%; p=0.0008) in the elderly group. Five out of seven (71%) non-B non-C (NBNC) HCC patients who developed HCC in the normal liver were elderly patients. Survival between the younger and elderly HCC groups was not significantly different (younger:elderly, 4.38:3.45 years; p=0.665). Additionally, elderly HCC patients had fewer tumors, more mild underlying liver damage, and more frequent NBNC HCC. Their prognosis was not necessarily poorer than that of the younger HCC patients. Additionally, it appears that elderly patients develop HCC even without fibrosis. Therefore, aging may be a factor affecting hepatocarcinogenesis.

Introduction

Hepatocellular carcinoma (HCC) is one of the most common cancers (1,2), with an estimated half a million cases annually, worldwide. Although HCC is generally diagnosed in middle-aged and elderly individuals, the age distribution of HCC varies according to etiology. The differences in age at the time of diagnosis of HCC affect the treatment strategy.

The Japanese population has one of the longest average life spans, and the size of the aged population has been increasing rapidly. As a result, the prevalence of elderly patients with HCC has increased (3-5). There is some controversy regarding whether aging plays a role in the factors and survival of patients with HCC. Previous studies reported that the long-term survival of younger HCC patients is similar to that of elderly patients (6,7). On the other hand, it has been reported that elderly HCC patients tended to have a poorer prognosis (8).

A recent increase in the number of elderly HCC patients in Japan has been reported (4,9,10). However, the impact of aging on the emergence of HCC has yet to be adequately investigated. Therefore, the aim of the present study was to investigate the effect of aging on the clinicopathological findings and the survival of HCC patients.

Patients and methods

Patients. A total of 624 patients presenting with HCC at the Department of Gastroenterology and Hepatology, Nagasaki University School of Medicine, Japan, were recruited for this study, between October 1981 and October 2007. The diagnosis of HCC was based on α-fetoprotein (AFP) levels, des-γ-carboxy prothrombin (DCP) levels, imaging studies including ultrasonography (USG), computerized tomography (CT), magnetic resonance imaging (MRI), hepatic angiography (HAG) and/or liver biopsy. The diagnosis of chronic liver disease and liver cirrhosis was based on the level of platelets and imaging studies and/or liver histology. The patients were classified into two groups according to their age at the time of diagnosis: a younger group (<75 years; n=544) and an elderly group (≥75 years; n=80).

Etiology of HCC. A diagnosis of chronic hepatitis C virus (HCV) infection was based on the presence of HCV antibodies (microparticle enzyme immunoassay; Abbott Laboratories, Tokyo, Japan) and HCV-RNA detected by polymerase chain reaction (PCR), whereas the diagnosis of chronic HBV infection was based on the presence of hepatitis B surface antigen (HBs/Ag) (enzyme-linked immunosorbent assay; Abbot Laboratories). The history of alcohol intake was noted from medical records. Habitual drinking was defined as an average daily consumption of an amount equivalent to 80 g of pure ethanol over a period of >10 years.

Statistical analysis. The SPSS 9.0 for Windows statistical software program was used to assess correlations among multiple variables. When appropriate, clinical and laboratory data were compared with a χ2 analysis, the Student's t-test or the Mann-Whitney test. The survival from time of diagnosis of HCC was analyzed using the Kaplan-Meier method and compared using the log-rank method. P<0.05 was considered to be statistically significant.

Results

Of the 624 patients, 80 (12%) patients were aged 75 years or older. The mean age of these older patients was 78.7±3.6. The clinical characteristics of the patients are shown in Table I. Significantly more patients in the elderly group were female (22:36%; p=0.005). The incidence of patients with liver cirrhosis was significantly higher, and the presence of a normal liver was significantly lower in the younger group than in the elderly group (80:71%; p=0.045; 0.3:6%, p=0.0002). No significant differences were observed in the protrobin time, total bilirubin, albumin or liver function as expressed by the Child-Pugh grade between the two groups (Table II).

Table 1. Patient characteristics.

Table 1

Table 2. Comparison of the patient backgrounds.

Table 2

Regarding viral status, the number of patients positive for HBsAg was significantly lower in the elderly group (24:10%, p=0.004), and the number of patients who were HBsAg and HCV antibody-negative [non-B non-C (NBNC)] was higher in the elderly group than in the younger group (11:31%, p=0.001).

In the NBNC HCC patients in the elderly group, 6 of 23 patients showed chronic hepatitis and 5 of 25 showed normal livers. No significant differences were found between the younger and elderly HCC groups with regards to alcoholism and diabetes mellitus (Table III).

Table 3. Comparison of risk factors for hepatocellular carcinoma.

Table 3

No significant differences were noted in the tumor diamet­er between the younger and elderly groups. The number of HCC nodules was significantly lower in the elderly group than that in the younger group (4.4±5.2:1.9±2.3, p=0.006). The incidence of solitary cases and TNM stage I or II disease was significantly higher in the elderly group compared to that of the younger group (53:76%, p=0.0008; 62:73%, p=0.043). No significant differences were found between the younger and elderly HCC groups with regards to surgery, ablation therapy and transarterial chemoembolization (TACE) (Table IV).

Table 4. Comparison of tumor characteristics and therapy for hepatocellular carcinoma.

Table 4

The overall survival rate between the younger and elderly HCC groups was not significantly different (p=0.665). The overall median survival for the younger group was 4.38 years, compared with 3.45 years for the elderly group (Fig. 1).

Figure 1. Kaplan-Meier model of the overall survival rate for the younger and elderly groups (younger HCC, 544 cases; elderly HCC, 80 cases). The overall survival between the younger and elderly HCC groups was not significantly different (p=0.665).

Figure 1

Discussion

Age at diagnosis has been shown to have significant prognostic value in certain types of cancer. Although the number of elderly patients with HCC is on the increase in Japan (3,4), the characteristics and prognosis of HCC in elderly patients has yet to be elucidated. In this study, patients with HCC aged 75 years or older were examined, and their clinicopathological characteristics were identified and compared to those of the younger patients.

There were more male patients presenting with HCC in the younger group as compared to the elderly patients; one of the reasons for this being the difference in viral status. In this study, HBV infection, which is more common in males (11,12), was lower in the elderly group than in the younger group. Moreover, males were more likely to be heavy drinkers.

The prevalence of a normal liver was higher, whereas that of liver cirrhosis was lower in the elderly group. Of note is that 5 of 23 (21%) patients with NBNC HCC in the elderly group had normal livers. Additionally, 5 of 7 patients whose HCC developed in a normal liver were in the elderly group.

Chronic inflammation and viral infection are considered to be significant risk factors for HCC, but the elderly patients recruited in this study had neither factor. A previous study reported that the telomere length in the liver is shortened, not only with the progression of fibrosis staging, but also with aging (13). Moreover, the reduction of telomere length has been reported to increase the risk of HCC (14). Thus, elderly patients may have shorter telomeres, predisposing them to develop HCC, even if chronic liver disease was not prevalent. Findings of various studies have suggested that aberrant DNA methylation is a crucial epigenetic alteration in HCC (15-17). Some of the aberrant methylation observed in human cancer may be a consequence of chronic viral inflammation (18,19). On the other hand, aberrant methylation is also observed in the normal aging process (20), and may contribute to the occurrence of HCC in elderly patients with normal livers.

In this study, the HBV infection rate was lower, while the NBNC rate was higher in the elderly group than that in the younger group. Previous reports have shown that the average age of diagnosis of HBV-related HCC is approximately 55 years of age, whereas that of HCV-related HCC is approximately 65 years of age, and that of NBNC HCC is approximately 70 years of age (3,4). In Japan, the predominant time of transmission of the hepatitis B virus is during the prenatal period. The subsequent genomic long interreactions from an early age may lead to hepatocarcinogenesis at a younger age in the infected individuals.

On the other hand, patients with non-alcoholic steato-hepatitis (NASH)-related HCC are older at diagnosis than those with HCC related to HBV and HCV (21,22). These results suggest that some of the NBNC HCC are NASH-related HCC.

The number of HCC nodules was lower, and the prevalence of single nodule HCC was higher in the elderly group than that in the younger group. Two main types of HCC occurrence exist, the first of which occurs at the time of the initial diagnosis with multicenter occurrence, which is associated with the degree of underlying liver damage. In this study, the prevalence of liver cirrhosis in the elderly group was lower than that in the younger group. The mild underlying liver damage in the elderly group may be associated with the smaller number of tumors observed in these patients.

Since elderly patients had fewer tumors and milder underlying liver damage at the time of the initial diagnosis, a more favorable prognosis in the elderly group may be expected. In this study, the overall survival rate was not significantly different between the two HCC groups. Overall, the majority of the elderly patients experienced various comorbidities, including cardiovascular disease, respiratory disease and diabetes mellitus. Taken together, the causes of death unrelated to HCC may have affected the survival rate in the elderly group.

In conclusion, elderly HCC patients had fewer tumors, milder underlying liver damage, and more frequent NBNC HCC. Additionally, it appears that elderly patients develop HCC even without fibrosis. Aging may therefore be a factor affecting hepatocarcinogenesis.

Contributor Information

Takuya Honda, Department of Gastroenterology and Hepatology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8501, Japan.

Hisamitsu Miyaaki, Department of Gastroenterology and Hepatology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8501, Japan.

Tatsuki Ichikawa, Department of Gastroenterology and Hepatology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8501, Japan.

Naota Taura, Department of Gastroenterology and Hepatology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8501, Japan.

Satoshi Miuma, Department of Gastroenterology and Hepatology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8501, Japan.

Hidetaka Shibata, Department of Gastroenterology and Hepatology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8501, Japan.

Hajime Isomoto, Department of Gastroenterology and Hepatology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8501, Japan.

Fuminao Takeshima, Department of Gastroenterology and Hepatology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8501, Japan.

Kazuhiko Nakao, Department of Gastroenterology and Hepatology, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8501, Japan.

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