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International trends in primary liver cancer incidence from 1973 to 2007

Abstract

Background

Primary liver cancer (PLC) is a common cancer worldwide, especially in developing countries. Several previous studies using different datasets have summarized PLC incidence rates and trends in different populations. However, with changes in exposure to risk factors and the implementation of preventive measures, the epidemiology of PLC worldwide may have changed.

Methods

We extended the analyses using the latest data from Cancer Incidence in Five Continents over the 35-year period 1973–2007 from 24 populations in Americas, Asia, Europe and Oceania using Joinpoint regression analysis. We examined age-standardized rates (ASRs) of PLC by histologic subtypes for both males and females in 24 populations during the period 2003–2007.

Results

We found that during the period 2003–2007, the highest ASRs for PLC were observed in some Asian populations, ranging from 19.0 to 26.7 per 100,000 in males and 4.8 to 8.7 per 100,000 in females. The international trends between 1973 and 2007 showed that ASRs for PLC were declining in several Asian populations. In contrast, ASRs for PLC were increasing in some European, American and Oceanian populations.

Conclusions

Although the reasons were not fully clear for these trends, public health measures in Asian populations and HCV transmission in European, American and Oceanian populations were likely to have contributed to these patterns. Meanwhile, other possible risk factors such as the consumption of alcohol, obesity, and nonalcoholic fatty liver disease should also be concerned for the burden of PLC.

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Background

It was estimated that for the year 2012, primary liver cancer (PLC) incidence rates ranked fifth in men and ninth in women worldwide [1]. The number of incident cases of PLC was estimated to be 782,000 per year, including 554,000 in men and 228,000 in women [1]. PLC mortality rates ranked the second in both sexes in the world [1]. Five-year relative survival rate for USA tends to be 16.6% based on data from the Surveillance, Epidemiology, and End Results (SEER) (2004–2010) Program of the US National Cancer Institute [2]. In China, the age-standardized 5-year relative survival rate for liver cancer was 10.1% [3]. PLC is the major type of liver cancer, which is composed of several histologic subtypes, including hepatocellular carcinoma (HCC), cholangiocarcinoma (CC), and combined hepatocellular carcinoma and cholangiocarcinoma (cHCC-CC) [4].

Most of the PLC cases (85%) are diagnosed in developing countries. The highest incidence rates have been reported in the regions of Southeast Asia and sub-Saharan Africa [5]. In these high-incidence populations, except for Japan, chronic infection with hepatitis B virus (HBV) and aflatoxin exposure were recognized as major risk factors for PLC. In low-incidence populations, however, PLC was mainly associated to the chronic hepatitis C virus (HCV) infection. It was estimated that most HCC cases (approximately 80%) were associated with HBV and/or HCV infections [6]. Moreover, some recent studies indicated that alcohol-related liver diseases, smoking, immigration, and obesity were also possible risk factors linking to PLC [7-9].

Several previous studies [10-12] using different datasets had reported the international trends in PLC incidence rates, one of which [12] reported the global PLC incidence rates and trends for 1993–2002 (10-year period). However, with changes in exposure to risk factors and the implementation of protective measures, the epidemiology of PLC worldwide may have changed. To give a longer-term and more recent comprehensive picture on the current status of PLC worldwide, we extended the analyses for the 35-year period from 1973 to 2007 from 24 populations in Americas, Asia, Europe and Oceania. This data may provide more useful evidence for evaluating the effect of previous measures of PLC prevention and control, and may facilitate the development of future measures.

Methods

Incidence data

To examine the changing trends in the incidence of PLC over time, age-standardized (by Segi’s world standard population [13]) incidence rates (ASRs) by sex were obtained from Volumes 4–10 of Cancer Incidence in Five Continents (CI5) from the website of the International Agency for Research on Cancer (IARC) [14-20] in which all data is publicly available. Volumes 4–10 of CI5 generally provided data by 5-year periods: 1973–1977, 1978–1982, 1983–1987, 1988–1992, 1993–1997, 1998–2002 and 2003–2007. Incidence data from 2003 to 2007 by histologic subtypes (HCC, CC, other & unspecified carcinoma) were collected from 24 populations in four continents from Vol. 10 of CI5. Classification of PLC from Vols. 4, 5–8 and 9–10 of CI5 was coded according to the International Classification of Diseases (ICD) 8th (155), 9th (155) and 10th (C22) revisions, respectively.

Populations were chosen for inclusion in our study on the basis of the following criteria: (1) incidence for time periods at least as far back as 1983–1987; (2) an absence of changes in population coverage or of warnings regarding data quality reported in CI5 Vols. 4–10; and (3) a sufficiently large number of registered cases in CI5 Vol. 10 to enable analyses of recent rates by histologic subtypes (trends by histologic subtypes were not included in our study). Only one registry from each country was selected; if more than one registry met the basic criteria, the registry with the largest population was included in the analysis (expect for China which included Hong Kong and Shanghai). Twenty four populations were selected: four from the Americas (Canada, British Columbia [BC]; Colombia, Cali; USA, SEER: (9 registries: California: San Francisco; Connecticut; Georgia: Atlanta; Hawaii; Iowa; Michigan: Detroit; New Mexico; Utah; Washington: Seattle) Black/White), six from Asia (China, Hong Kong; China, Shanghai; India, Mumbai; Israel: Jews; Japan, Osaka Prefecture; Singapore: Chinese), five from Northern Europe (Denmark; Finland; Norway; Sweden; UK, England, North Western Region [NWR]), three from Western Europe (France, Bas-Rhin; Germany, Saarland; Switzerland, Geneva), four from elsewhere in Europe [21] (Southern and Central & Eastern Europe including Italy, Varese Province; Poland, Cracow; Slovakia; Spain, Navarra), and two from Oceania (Australia, New South Wales [NSW]; New Zealand). No African populations met all the inclusion criteria. However, four African populations (Algeria, Setif Wilaya; Egypt, Gharbiah; Uganda, Kyadondo; Zimbabwe, Harare: African) were chosen to describe the PLC incidence rates in the last time interval (2003–2007).

Incidence data for white and black populations in US were not included in CI5 vol. four (1973–1977) and vol. five (1978–1982), so we further referred to the US SEER dataset [22]. The SEER program is a population-based cancer registry system covering 18 registries and 28% of the US population. Long-term data from 1973 to 2010 were available from nine registries that included approximately 9.4% of the US population (based on 2010 census).

For New Zealand, we abstracted the data for 1983–1987 and 1988–2002 from CI5plus [23] which was part of CI5 databases and contained annual incidence data for a single registry or a group of populations in one country. The data for the last time period 2003–2007 were obtained from CI5 vol. 10.

Data analysis

Incidence trends in ASRs of PLC were analyzed using Joinpoint regression (Joinpoint regression software, Version 3.5.3-May 2012, available through the Surveillance Research Program of the US National Cancer Institute). The permutation method was used for significance tests. Changes in annual incidence rates from PLC were calculated as annual percentage change (APC) in each segment. In the final model, the Joinpoint analysis provided average annual percentage change (AAPC). The significant test of APC and AAPC to 0 was also conducted.

Age-standardized incidence rates of PLC by histologic subtypes (HCC, CC and other & unspecified carcinoma) and sex for selected populations during the period 2003–2007 were integrated and calculated. Secular trends in ASRs were examined by registry and sex for every five-year period during 1973–2007. PLC trends from New Zealand were described during five-year periods from 1983–1987 to 2003–2007. Figures displaying the incidence trends were prepared using a semi-log scale to facilitate the comparison of temporal trends as well as magnitude. These data were plotted at the midpoint of each five-year interval.

Results

ASRs for PLC in 2003–2007 were highest in some populations of Asia (China, Hong Kong; Japan; China, Shanghai; Singapore: Chinese) and Africa (Egypt and Zimbabwe), and much lower in most populations in Europe, Americas and Oceania (Tables 1 and 2). In Asian populations, ASRs for PLC were ranging from 19.0 to 26.7 per 100,000 in males and 4.8 to 8.7 per 100,000 in females, except for India and Israel (Jews) (5.2 and 3.1 per 100,000 in males, 2.4 and 1.4 per 100,000 in females, respectively). In most populations in Americas, Europe and Oceania, PLC incidence rates varied between 2.2-7.8 per 100,000 for males and 1.0-3.7 per 100,000 for females except for France (13.6 per 100,000 for males and 2.5 per 100,000 for females), Switzerland (13.1 per 100,000 for males and 3.0 per 100,000 for females), Italy (12.6 per 100,000 for males and 3.7 per 100,000 for females), and USA, Black population (11.6 per 100,000 for males and 3.1 per 100,000 for females).

Table 1 International variation in primary liver cancer incidence rates for males, from 1973–1977 to 2003-2007
Table 2 International variation in primary liver cancer incidence rates for females, from 1973–1977 to 2003-2007

Tables 1 and 2 also showed the results of Joinpoint analysis for ASRs in males and females for all ages, respectively. The secular trends in PLC incidence among 24 populations from 1973 to 2007 were presented in Figure 1. The increasing trends for both males and females in PLC incidence rates were seen in most of the populations in Europe, Americas, and Oceania. UK, England, France, Germany, Switzerland, Italy, Canada, Colombia, USA: Black, USA: White, Australia, and New Zealand (1982–2007) showed a significant increasing trend across all the periods (Tables 1 and 2 and Figure 1).

Figure 1
figure 1

Trends in age-standardized primary liver cancer incidence rates by continent and area for the time period 1973–2007: A. Males B. Females.

In males, ASRs for PLC in Germany, USA, Black, and USA, White increased significantly from the period 1982–1987 (Table 1 and Figure 1A). PLC incidence rates in France, Canada and Australia significantly increased from 1973–1977, leveled off in the 1990s (Table 1 and Figure 1A). ASRs for PLC in Spain significantly increased by 28.9% per year from 1973–1977, significantly decreased by 1.8% per year from 1982–1987, whereas ASRs for PLC in Finland, Norway, Sweden, Poland and Slovakia leveled off in all the period (Table 1 and Figure 1A). In females, the pattern of PLC incidence in each population seemed to be similar except for Denmark, Poland and Spain (Table 2 and Figure 1B). ASRs for PLC in Poland significantly decreased by 3.1% per year from 1973–1977 to 2003–2007, whereas ASRs for PLC in Denmark and Spain showed stable trends from 1973–1977 to 2003–2007.

However, in Asia, ASRs for PLC for both males and females showed significant decreasing trends in two of the six populations (China, Shanghai; Singapore: Chinese) from 1973–1977 to 2003–2007 (Tables 1 and 2 and Figure 1A and B). The stable trends among males and females were seen in two of the six populations (China, Hong Kong and Israel: Jews) from 1973–2007 to 2003–2007. ASRs for PLC in one of the six populations (Japan) significantly increased by 23.0% in males and 23.5% in females from 1973–1977 and reached a plateau in 1990s (Tables 1 and 2 and Figure 1A and B). Whereas ASRs for PLC for females in India significantly increased by 5.3% from 1973–1977 and leveled off in 1980s (Table 2 and Figure 1B).

According to the ASRs of PLC by histologic subtypes from 2003 to 2007, HCC was the leading histologic subtype, followed by CC and other & unspecified carcinoma (Figure 2). The highest incidence rate of HCC was observed in China, Hong Kong (8.5 per 100,000 in males and 1.9 per 100,000 in females), and the lowest one was shown in UK England (0.9 per 100,000 in males and 0.3 per 100,000 in females). The highest incidence of CC was seen in France (2.0 per 100,000 in males and 0.7 per 100,000 in females), followed by other European countries including Spain (1.1 per 100,000 in males and 0.6 per 100,000 in females), Finland (1.0 per 100,000 in males and 0.7 per 100,000 in females), and Italy (1.0 per 100,000 in males and 0.6 per 100,000 in females). China, Hong Kong (0.9 per 100,000 in males and 0.7 per 100,000 in females) and Japan (0.9 per 100,000 in males and 0.5 per 100,000 in females) had relatively higher incidence of CC than other Asian countries.

Figure 2
figure 2

Age-standardized primary liver cancer incidence rates by histologic subtypes for selected populations for the time period 2003–2007.

Discussion

International trends in PLC incidence rates during the period 1973–2007 showed that the PLC incidence rates increased in most European, American and Oceanian populations, although these age-standardized PLC incidence rates in 2003–2007 were much lower than these in Asia. Meanwhile, PLC incidence rates decreased in Asian populations, although their age-standardized PLC incidence rates in 2003–2007 were the highest in the world.

PLC is a common cancer, particularly in Asia countries such as China, Japan and Singapore (Chinese). Among these countries, PLC is closely associated with hepatitis virus infection (HBV infection in China and Singapore, HCV infection in Japan) and exposure to aflatoxin (in China). In our study, the decreasing trends in China and Singapore may be attributed to some public health measures [24-27]. HBV vaccination was incorporated into the national childhood immunization program by China and Singapore from the middle 1980s to the early 1990s. The immunization coverage with three doses of HBV vaccine was 70.7%-95.0% in 1999 [28,29]. Several studies also reported the decreases in PLC incidence rates in China, particularly in Shanghai and in younger age groups [24,30]. Another study in Taiwan showed that the age- and sex- adjusted rate ratios for individuals aged 5 to 29 years decreased by more than 80% for HCC incidence from 1977–1980 to 2001–2004 [25]. In Singapore, Chia et al. [26] suggested that a general declining trend in liver cancer incidence was especially notable in local-born Chinese. Although the measure had no an effect on general population, we expect it will play an important role in the reduction of PLC incidence rates in the coming decades. Moreover, dietary aflatoxin exposure declined in the high-incidence areas of PLC seemed to have contributed to the decrease in PLC incidence in China [31]. A study in Qidong, China [31], where aflatoxin exposures were common, had reported that the decreasing liver cancer incidence in population over 25 years could mainly be attributable to the reduction of exposure to aflatoxin from 1980 to 2008.

In Japan, there were different trends between 1973–1992 and 1988–2007. The increasing trends started in 1973–1977 and reached peak in 1988–1992. This was thought to be in part due to the spread of HCV infection, which began in the 1920s and increase after World War II with an explosion in parenteral amphetamine use and paid blood donation [32,33]. Although APC did not significantly decrease during 1988–2007, the decline in PLC incidence had been continuously seen from 1988–1992 in our analysis. Stiffening of legal penalties against amphetamine use starting in 1954 and conversion from paid to voluntary blood donation in late 1960s might have reduced HCV transmission [34]. After the discovery of HCV RNA, HCV screening tests for first- and second-generation HCV antibodies started in 1989 and 1992, respectively [35]. These tests were adopted by the Red Cross Blood Center for screening blood, which further decreased the risk of post-transfusion hepatitis. The Japanese government has taken urgent comprehensive countermeasures against hepatitis (HBV and HCV) and HCC since 2002 [33]. Therefore, these measures would provide a significant contribution to decrease the number of patients suffering from HCV-related liver diseases including PLC.

In contrast, PLC was not a very common cancer in European, American and Oceanian countries where there were no epidemic regions of HBV infection. However, an increasing trend of PLC incidence rates was seen in most of these populations which were partly due to the widespread HCV infection associated with drug use, exposure to contaminated blood transfusion and/or needles used for medical purposes [36]. The natural history of PLC indicated that the time between exposure to HCV and development of HCC is about 30 years [37]. HCV infections were found in 30-50% of HCC patients in the United States and 44-66% of HCC patients in Italy [38]. Both of these countries had the highest PLC incidence rates in their own continent. The different peak years of HCV infection prevalence for each country were likely responsible for the respective peaks in PLC incidence rates. The increasing trends in PLC incidence rates in the United States could be attributed to increased HCV exposures by contact with contaminated blood and injection drug use during the 1960s and 1970s [39]. In Italy, the upsurge of liver cancer incidence after 1970s was in part attributable to HCV infection caused by the re-use of disposable syringes among intravenous drug users without proper disinfection [40]. Meanwhile, in several studies conducted in Western countries, 30 to 40% of patients with HCC did not have chronic infection with HBV or HCV, suggesting alternative causes [5]. Other factors including alcohol [41,42], obesity [43,44], and non-alcoholic fatty liver disease (NAFLD) [5] might be contributed to the increasing trend. In population-based cohort studies in the United States and Scandinavia [44-46], HCC was 1.5 to 2.0 times as likely to develop in obese persons as in those who were not obese. NAFLD, which is present in up to 90% of all obese persons and up to 70% of persons with type 2 diabetes, has been proposed as a possible risk factor for HCC [47]. Although there were still some difficult problems in the latency period from exposure to these factors and PLC development, more emphasis should be recommended to control these factors.

The advent of precise diagnostic tests may increase recognition of the disease, which accounts for a rising incidence, rather than a true increase in its occurrence [48]. Ultrasonography, measurement of serum alpha-fetoprotein, and computed tomography scanning have been routinely used since the early 1980s, which should lead to an increase in the number of hepatic biopsies conducted. However, the percentage of histologically confirmed PLC has not increased significantly during the study period in these countries which had an increasing trend in PLC incidence rates. In addition, females in Poland (from 1973–1977 to 2003–2007) and males in Spain (from 1982–1987 to 2003–2007) also exhibited a decreasing trend of PLC incidence rates. The reasons for this decreasing trend remain unclear.

This study has several strengths. The data were abstracted from large, well-established registries throughout the world. For the first time, data covering 35 years were analyzed to describe the variation of international trends in PLC incidence rates, which may stimulate further etiologic research. In addition, incidence rates for particular histologic subtypes of PLC in different populations were examined separately. One limitation of this study was that trends by histologic subtypes were not examined. The variation of ICD coding might influence the interpretation of our results. In our study, ICD coding contained ICD-8 (Malignant neoplasm of liver and intrahepatic bile ducts, specified as primary), ICD-9 (Malignant neoplasm of liver, specified as primary) and ICD-10 (Malignant neoplasm of liver and intrahepatic bile ducts, specified as primary). CC was not included in ICD-9 (period from 1978–1982 to 1993–1997). Therefore, the changes in PLC rates mainly reflect changes of HCC. Our study was also limited by the lack of nationwide cancer registries in some countries, thus registration data might not accurately reflect the true patterns in the respective countries.

Conclusions

Our analysis on CI5 data suggested that ASRs for PLC were declining in several Asian countries where the highest incidence rates were still seen between 1973 to 1977 and 2003 to 2007. On the contrary, ASRs for PLC were increasing in some American, European and Oceanian countries. HBV vaccination programs and screening tests might play an important role in deceasing trends in Asia. Although the reasons of the increasing trends in American, European and Oceanian populations were not fully clear, the variation was likely to be due to in part the increasing prevalence of HCV infection. While a vaccine for HBV is widely available in most developed and developing countries, there is currently no vaccine available for HCV. Therefore, it is a critical for HCV infection prevention that blood donations are screened, safe injection practices are used at all times, and unnecessary injections are avoided. Additionally, controlling other risk factors such as alcohol consumption, obesity, and NAFLD may help to reduce PLC incidence rates.

Abbreviations

PLC:

Primary liver cancer

SEER:

Surveillance, Epidemiology, and End Results

HCC:

Hepatocellular carcinoma

CC:

Cholangiocarcinoma

cHCC-CC:

Combined hepatocellular carcinoma and cholangiocarcinoma

ASRs:

Age-standardized incidence rates

HBV:

Hepatitis B virus

HCV:

Hepatitis C virus

CI5:

Cancer Incidence in Five Continents

IARC:

International Agency for Research on Cancer

ICD:

International Classification of Diseases

BC:

British Columbia

NWR:

North Western Region

NSW:

New South Wales

APC:

Annual percentage change

AAPC:

Average annual percentage change

HBsAg:

Hepatitis B surface antigen

NAFLD:

Nonalcoholic fatty liver disease

References

  1. Ferlay J, Soerjomataram I, Ervik M, Dikshit R, Eser S, Mathers C, Rebelo M, Parkin DM, Forman D, Bray F. GLOBOCAN 2012 v1.0, Cancer Incidence and Mortality Worldwide: IARC CancerBase No. 11 [Internet]. Lyon, France: International Agency for Research on Cancer; 2013. Available from: http://globocan.iarc.fr, accessed on 20/01/2014.

  2. National Cancer Institute. Surveillance, Epidemiology, and End Results Program http://seer.cancer.gov/statfacts/html/livibd.html (accessed on 28/10/2014).

  3. Zeng H, Zheng R, Guo Y, Zhang S, Zou X, Wang N, et al. Cancer survival in China, 2003–2005: A population-based study. Int J Cancer. 2015;136(8):1921–30.

    Article  CAS  PubMed  Google Scholar 

  4. Tang D, Nagano H, Nakamura M, Wada H, Marubashi S, Miyamoto A, et al. Clinical and pathological features of Allen’s type C classification of resected combined hepatocellular and cholangiocarcinoma: a comparative study with hepatocellular carcinoma and cholangiocellular carcinoma. J Gastrointest Surg. 2006;10(7):987–98.

    Article  PubMed  Google Scholar 

  5. El-Serag HB. Hepatocellular Carcinoma. N Engl J Med. 2011;365:1118–27.

    Article  CAS  PubMed  Google Scholar 

  6. El-Serag HB. Epidemiology of viral hepatitis and hepatocellular carcinoma. Gastroenterology. 2012;142(6):1264–73.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Shih WL, Chang HC, Liaw YF, Lin SM, Lee SD, Chen PJ, et al. Influences of tobacco and alcohol use on hepatocellular carcinoma survival. Int J Cancer. 2012;131(11):2612–21.

    Article  CAS  PubMed  Google Scholar 

  8. Ezzati M, Riboli E. Behavioral and dietary risk factors for noncommunicable diseases. N Engl J Med. 2013;369(10):954–64.

    Article  CAS  PubMed  Google Scholar 

  9. Chuang SC, La Vecchia C, Boffetta P. Liver cancer: descriptive epidemiology and risk factors other than HBV and HCV infection. Cancer Lett. 2009;286(1):9–14.

    Article  CAS  PubMed  Google Scholar 

  10. Nordenstedt H, White DL, El-Serag HB. The changing pattern of epidemiology in hepatocellular carcinoma. Dig Liver Dis. 2010;42:S206–14.

    Article  PubMed  PubMed Central  Google Scholar 

  11. McGlynn KA, Tsao L, Hsing AW, Devesa SS, Fraumeni JFJ. International trends and patterns of primary liver cancer. Int J Cancer. 2001;94(2):290–6.

    Article  CAS  PubMed  Google Scholar 

  12. Center MM, Jemal A. International trends in liver cancer incidence rates. Cancer Epidemiol Biomarkers Prev. 2011;20(11):2362–8.

    Article  PubMed  Google Scholar 

  13. Segi M. Cancer mortality for selected sites in 24 countries (1950–57). Sendai: Tohuku University School of Public Health; 1960.

    Google Scholar 

  14. Waterhouse J, Muir CS, Shanmugaratnam K, Powell J. Cancer Incidence in Five Continents, Vol. IV.IARC Scientific Publications No. 42, Lyon, IARC. 1982.

  15. Muir CS, Waterhouse J, Mack T, Powell J, Whelan SL. Cancer Incidence in Five Continents, Vol. V. IARC Scientific Publications No. 88, Lyon, IARC. 1987.

  16. Parkin DM, Muir CS, Whelan SL, Gao Y-T, Ferlay J, Powell J. Cancer Incidence in Five Continents, Vol. VI. IARC Scientific Publications No. 120, Lyon, IARC. 1992.

  17. Parkin DM, Whelan SL, Ferlay J, Raymond L, Young J. Cancer Incidence in Five Continents, Vol. VII. IARC Scientific Publications No. 143, Lyon, IARC. 1997.

  18. Parkin DM, Whelan SL, Ferlay J, Teppo L, Thomas DB. Cancer Incidence in Five Continents, Vol. VIII. IARC Scientific Publications No. 155, Lyon, IARC. 2002.

  19. Curado MP, Edwards B, Shin HR, Storm H, Ferlay J, Heanue M, et al. Cancer Incidence in Five Continents, Vol. IX. IARC Scientific Publications No. 160, Lyon, IARC. 2007.

  20. Forman D, Bray F, Brewster DH, Gombe Mbalawa C, Kohler B, Piñeros M, et al. Cancer Incidence in Five Continents, Vol. X (electronic version). Lyon, IARC. http://ci5.iarc.fr last accessed on [28/10/2013]. 2013.

  21. Lortet-Tieulent J, Renteria E, Sharp L, Weiderpass E, Comber H, Baas P, et al. Convergence of decreasing male and increasing female incidence rates in major tobacco-related cancers in Europe in 1988–2010. Eur J Cancer. 2013; http://dx.doi.org/10.1016/j.ejca.2013.10.014.

  22. Surveillance, Epidemilology, and End Results (SEER) Program (November 2012 submission). Public use database (1973–1982). Surveillance Research Program, National Cancer Institute SEER*Stat software (seer.cancer.gov/seerstat) version < Version 8.0.4>, Released April 15, 2013.

  23. Ferlay J, Parkin DM, Curado MP, Bray F, Edwards B, Shin HR, et al. Cancer Incidence in Five Continents, Volumes I to IX: IARC CancerBase No. 9 [Internet]. International Agency for Research on Cancer: Lyon, France; 2010. Available from: http://ci5.iarc.fr.

    Google Scholar 

  24. Jin F, Devesa SS, Chow WH, Zheng W, Ji BT, Fraumeni JF, et al. Cancer incidence trends in urban Shanghai, 1972–1994: an update. Int J Cancer. 1999;83(4):435–40.

    Article  CAS  PubMed  Google Scholar 

  25. Chiang CJ, Yang YW, You SL, Lai MS, Chen CJ. Thirty-Year Outcomes of the National Hepatitis B Immunization Program in Taiwan. JAMA. 2013;310(9):974–6.

    Article  CAS  PubMed  Google Scholar 

  26. Chia KS, Lee HP, Lee J. Incidence of primary liver cancer in Singapore, 1968–1982. Ann Acad Med Singapore. 1989;18(3):313–6.

    CAS  PubMed  Google Scholar 

  27. Lu W, Zheng Y. Prevalence and prevention measure of cancer in Shanghai. China Cancer. 2009;18:90–1.

    Google Scholar 

  28. Liang X, Bi S, Yang W, Wang L, Cui G, Cui F, et al. Epidemiological serosurvey of hepatitis B in China–declining HBV prevalence due to hepatitis B vaccination. Vaccine. 2009;27(47):6550–7.

    Article  PubMed  Google Scholar 

  29. Ang LW, Cutter J, James L, Goh KT. Seroepidemiology of hepatitis B virus infection among adults in Singapore: a 12-year review. Vaccine. 2013;32(1):103–10.

    Article  PubMed  Google Scholar 

  30. Gao S, Yang WS, Bray F, Va P, Zhang W, Gao J, et al. Declining rates of hepatocellular carcinoma in urban Shanghai: incidence trends in 1976–2005. Eur J Epidemiol. 2012;27(1):39–46.

    Article  PubMed  Google Scholar 

  31. Sun Z, Chen T, Thorgeirsson SS, Zhan Q, Chen J, Park JH, et al. Dramatic reduction of liver cancer incidence in young adults: 28 year follow-up of etiological interventions in an endemic area of China. Carcinogenesis. 2013;34(8):1800–5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Yoshizawa H. Hepatocellular carcinoma associated with hepatitis C virus infection in Japan: projection to other countries in the foreseeable future. Oncology. 2002;62 Suppl 1:8–17.

    Article  PubMed  Google Scholar 

  33. Tsukuma H. Liver cancer and its prevention. Asian Pac J Cancer Prev. 2005;6:244–50.

    PubMed  Google Scholar 

  34. Hideo T, Yasuharu I, Naoki H, Yuri I, Kazuho I, Masahide O, et al. Declining Incidence of Hepatocellular Carcinoma in Osaka, Japan, from 1990 to 2003. Ann Intern Med. 2008;148:820–6.

    Article  Google Scholar 

  35. Chung H, Ueda T, Kudo M. Changing trends in hepatitis C infection over the past 50 years in Japan. Intervirology. 2010;53(1):39–43.

    Article  PubMed  Google Scholar 

  36. Jemal A, Center MM, DeSantis C, Ward EM. Global patterns of cancer incidence and mortality rates and trends. Cancer Epidemiol Biomarkers Prev. 2010;19(8):1893–907.

    Article  PubMed  Google Scholar 

  37. Kiyosawa K, Sodeyama T, Tanaka E, Gibo Y, Yoshizawa K, Nakano Y, et al. Interrelationship of blood transfusion, non-A, non-B hepatitis and hepatocellular carcinoma: analysis by detection of antibody to hepatitis C virus. Hepatology. 1990;12:671–5.

    Article  CAS  PubMed  Google Scholar 

  38. El-Serag HB, Rudolph KL. Hepatocellular carcinoma: epidemiology and molecular carcinogenesis. Gastroenterology. 2007;132(7):2557–76.

    Article  CAS  PubMed  Google Scholar 

  39. Bosch FX, Ribes J, Díaz M, Cléries R. Primary liver cancer: Worldwide incidence and trends. Gastroenterology. 2004;127(5):S5–16.

    Article  PubMed  Google Scholar 

  40. Maso LD, Lise M, Zambon P, Crocetti E, Serraino D, Ricceri F, et al. Incidence of primary liver cancer in Italy between 1988 and 2002: an age-period-cohort analysis. Eur J Cancer. 2008;44(2):285–92.

    Article  Google Scholar 

  41. Donato F, Tagger A, Gelatti U, Parrinello G, Boffetta P, Albertini A, et al. Alcohol and hepatocellular carcinoma: the effect of lifetime intake and hepatitis virus infections in men and women. Am J Epidemiol. 2002;155(4):323–31.

    Article  CAS  PubMed  Google Scholar 

  42. Carlo LV. Alcohol and liver cancer. Eur J Cancer Prev. 2007;16(6):495–7.

    Article  Google Scholar 

  43. Larsson SC, Wolk A. Overweight, obesity and risk of liver cancer: a meta-analysis of cohort studies. Brit J Cancer. 2007;97(7):1005–8.

    CAS  PubMed  PubMed Central  Google Scholar 

  44. Calle EE, Rodriguez C, Walker-Thurmond K, Thun MJ. Overweight, obesity, and mortality from cancer in a prospectively studied cohort of U.S. adults. N Engl J Med. 2003;348(17):1625–38.

    Article  PubMed  Google Scholar 

  45. Wolk A, Gridley G, Svensson M, Nyren O, McLaughlin JK, Fraumeni JF, et al. A prospective study of obesity and cancer risk (Sweden). Cancer Causes Control. 2001;12(1):13–21.

    Article  CAS  PubMed  Google Scholar 

  46. Møller H, Mellemgaard A, Lindvig K, Olsen JH. Obesity and cancer risk: a Danish record-linkage study. Eur J Cancer. 1994;30A:344–50.

    Article  PubMed  Google Scholar 

  47. Neuschwander-Tetri BA, Caldwell SH. Nonalcoholic steatohepatitis: Summary of an AASLD Single Topic Conference. Hepatology. 2003;37(5):1202–19.

    Article  PubMed  Google Scholar 

  48. El-Serag HB, Mason AC. Rising incidence of hepatocellular carcinoma in the United States. N Engl J Med. 1999;340:745–50.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

We are very grateful to Rong-Shou Zheng and Si-Wei Zhang from National Office for Cancer Prevention and Control, Cancer Institute & Hospital, Chinese Academy of Medical Sciences for providing us with valuable opinions and suggestions for data collection. We sincerely thank Ms. Catherine Lerro (Yale School of Public Health) for language proof reading. This study was funded by the State Key Projects Specialized for Infectious Diseases (No. 2008ZX10002008-001) and the Research Special Fund for Public Welfare Industry of Health (No. 201402003). The grant sponsors had no role in the study design, data collection, data analysis, data interpretation, or the writing of the manuscript.

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Correspondence to Min Dai.

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The authors declare that they have no competing interests.

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YZ participated in acquisition of data, analysis and interpretation of data and drafted the manuscript. JSR participated in acquisition of data, analysis and interpretation of data and revised the manuscript. MD participated in the design of study, acquisition of data, analysis and interpretation of data and revised the manuscript. JFS, NL, YTW, CFQ and YWZ gave some substantial comments to draft the manuscript. All authors read and approved the final manuscript.

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Zhang, Y., Ren, JS., Shi, JF. et al. International trends in primary liver cancer incidence from 1973 to 2007. BMC Cancer 15, 94 (2015). https://doi.org/10.1186/s12885-015-1113-4

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