- Original article
- Open Access
Secular trend analysis of lung cancer incidence in Sihui city, China between 1987 and 2011
Chinese Journal of Cancer volume 34, Article number: 33 (2015)
With industrial and econom ic development in recent decades in South China, cancer incidence may have changed due to the changing lifestyle and environment. However, the trends of lung cancer and the roles of smoking and other environmental risk factors in the development of lung cancer in rural areas of South China remain unclear. The purpose of this study was to explore the lung cancer incidence trends and the possible causes of these trends.
Joinpoint regression analysis and the age–period–cohort (APC) model were used to analyze the lung cancer incidence trends in Sihui, Guangdong province, China between 1987 and 2011, and explore the possible causes of these trends.
A total of 2,397 lung cancer patients were involved in this study. A 3-fold increase in the incidence of lung cancer in both sexes was observed over the 25-year period. Joinpoint regression analysis showed that while the incidence continued to increase steadily in females during the entire period, a sharp acceleration was observed in males starting in 2005. The full APC model was selected to describe age, period, and birth cohort effects on lung cancer incidence trends in Sihui. The age cohorts in both sexes showed a continuously significant increase in the relative risk (RR) of lung cancer, with a peak in the eldest age group (80–84 years). The RR of lung cancer showed a fluctuating curve in both sexes. The birth cohorts identified an increased trend in both males and females; however, males had a plateau in the youngest cohorts who were born during 1955–1969.
Increasing trends of the incidence of lung cancer in Sihui were dominated by the effects of age and birth cohorts. Social aging, smoking, and environmental changes may play important roles in such trends.
Lung cancer is the leading cause of cancer-related mortality worldwide, with 1.82 million new cases and 1.2 million deaths per year [1, 2]. The high-risk areas for lung cancer include central-eastern and southern Europe, North America, and eastern Asia . In 1980, it was estimated that 31% of lung cancer cases occurred in developing countries; in 2012, however, the majority of lung cancer cases (55%) occurred in developing countries . Males have a higher incidence of lung cancer than females, with a sex ratio of 2.5:1 [2, 3]. In China, lung cancer is also the most common and deadly cancer in males [4, 5], with an incidence of 70.39/100,000 and a mortality of 56.72/100,000 in 2010 . For females, the incidence and mortality were 39.47/100,000 and 27.04/100,000, respectively, in 2010 .
Sihui city is located in the midwestern Guangdong province, with an area of 1,163 square kilometers. In 2011, the population of Sihui was 418,097 and >75% lived in rural residences. With the development of industry and the growth of the economy in the last 30 years, the lifestyle and living conditions have changed significantly in China. Because lung cancer is mainly caused by cigarette smoking and environmental factors, analysis of the long-term incidence of lung cancer in Sihui will provide valuable information for illustrating the roles of lifestyle and environment in the development of lung cancer in rural areas of South China.
In the current study, we used joinpoint regression and age–period–cohort (APC) analyses with a Poisson regression model to determine the secular trends in the incidence of lung cancer in Sihui between 1987 and 2011.
The data involving all incident lung cancer cases diagnosed between January 1, 1987 and December 31, 2011 (Table 1) were obtained from the Sihui Cancer Registry and analyzed by using year of diagnosis, age at diagnosis, gender, and histologic codes. The International Classification of Diseases (ICD) code corresponding to lung cancer was 162 in the 9th revision (1987–1994), and C33 and C34 in the 10th revision (1995–2004). Populations were estimated on July 1 of each year based on the Chinese population census reports of 1990, 2000, and 2010.
Age-standardized rates (ASRs) of incidence over 25 years were calculated with the direct method according to the Segi’s world standard population in 1962, and the secular trends in lung cancer were compared between both sexes. Long-term trends of ASRs of incidence were analyzed by using a joinpoint regression model, which was developed by the United States National Cancer Institute for the analysis of data from the Surveillance Epidemiology and End Results Program . Joinpoint regression analysis describes changes in data trends by connecting several different line segments on a log scale at joinpoints . The analyses in this study started with the minimum number of joinpoints and tested for model fit with a maximum of four joinpoints. An annual percent change in the ASR of incidence for each line segment and the corresponding 95% confidence interval (CI) was estimated. The Monte Carlo permutation method was used to test for statistical significance [8–10].
A Poisson regression analysis was performed for the effects of age, period, and birth cohort on the incidence of lung cancer for each gender. In this analysis, we used the logarithm of the incidence of lung cancer as the dependent variable, and age, period, and birth cohort as independent variables [11–14]. The periods were arranged in five 5-year periods between 1987 and 2011, the ages were stratified by 5-year age groups from 35–39 years to 80–84 years, and 14 corresponding birth cohorts were included from 1905–1909 to 1970–1974 (Table 2). The 45–49 years age group, the 1997–2001 period group, and the 1915–1919 birth cohort group were used as reference groups, and the results of this model were more reliable than those using the groups of the fewer age-specific rates as the reference groups [15–17]. The deviances of different models and the P value of the Chi square test of the goodness-of-fit were used to check the model fit. The closer the deviance to the degrees of freedom, the better the model fit; the greater the P value of the goodness-of-fit, the better the data fit [15, 16]. Relative risk (RR) of incidences was calculated to summarize the effects of age, period, and birth cohorts from APC models.
A Poisson regression model and other statistical analyses were performed by using the SAS statistical software (version 9.2; SAS Institute, Cary, NC, USA). For all analyses, the significance level was set at P ≤ 0.05.
Between 1987 and 2011, a total of 2,397 lung cancer patients were diagnosed in Sihui city, with a male-to-female ratio of 2.60:1. The average crude incidences of lung cancer in males, females, and the overall population were 35.20/100,000, 14.18/100,000, and 24.93/100,000 and the corresponding ASRs were 37.27/100,000, 11.52/100,000, and 23.05/100,000, respectively (Table 3). The median age at the time of diagnosis for lung cancer in Sihui was 65 years. The ASRs of lung cancer incidence showed upward trends in both males and females, with a 3-fold increase during the entire period (Fig. 1). In females, there was a steady growth of the annual percent change (6.03%; 95% CI, 3.8%–8.3%), and no joinpoint was included in the joinpoint regression model. In males, the increase in trend accelerated between 2005 and 2010 with an annual percent change of 11.9% (95% CI, 3.1%–21.4%) (Fig. 2).
Poisson regression analysis was performed to observe the effects of age, period, and birth cohort on the incidence of lung cancer in both sexes. Five calendar periods (1987–1991, 1992–1996, 1997–2001, 2002–2006, 2007–2011) and 10 age groups (5-year periods from 35–39 years to 80–84 years) were used in all Poisson regression models; thus, 14 corresponding birth cohorts were included from 1905–1909 to 1970–1974. The full APC model fit the data best in both males and females based on the deviance statistic and was chosen as the final model (Table 4).
After adjusting for period and cohort effects, the RR of age on the incidence of lung cancer showed a continuously rising trend until the oldest age cohort (80–84 years) for both sexes (Table 5; Fig. 3a). The RR showed a relatively flat trend, with only a slight increase in the most recent period (2007–2011) in both sexes (Table 5; Fig. 3b). By using the 1915–1919 birth cohort as a reference group, the effects of the birth cohort curve fluctuated, but there was a significant continuous increase in RR during the entire period in females (Table 5; Fig. 3c). The first birth cohort (1905–1909) and the last birth cohort (1970–1974) were not shown because they each contained only one case. The RR continued to increase in males from the 1910–1914 birth cohort to the 1950–1954 birth cohort when it reached its peak; subsequently, there was a plateau in the younger cohort born during 1955–1969.
This study showed that the incidence of lung cancer has been rapidly increasing in Sihui over the last 25 years. Although the overall incidence of lung cancer in Sihui (24.93/100,000) was lower than the average incidence of lung cancer in China (46.08/100,000) , the rate of increase (5.90%) was greater than the average in China (1.64%) . The APC analysis further revealed that the increasing trend in the incidence of lung cancer was mainly due to the effects of aging population and young birth cohort in both sexes. Such temporal patterns may indicate the complex impact of lifestyle and environment changes on the risk of lung cancer in rural areas of South China [5, 19–22].
Sihui is a county-level city located in the central part of Guangdong province. Before the era of economic reformation and open policy in China, Sihui was a traditional agricultural location with rice paddies and oranges as the main economic crops. Corresponding with the implementation of a policy of openness and reform by Chinese government in 1978, Sihui became one of the earliest economic boom areas in South China. The major industries in Sihui include jade processing, smelting, metallurgic casting, and ceramic manufacturing. As a result of the industrial needs, most of the laborers, especially males, moved from agricultural areas to local factories and therefore a series of life style and environmental changes occurred.
It has been estimated that cigarette smoking causes >75% of all lung cancers . Other known and suspected risk factors for lung cancer include a history of tuberculosis and other inflammatory lung diseases [24, 25], indoor air pollution [26–28], productive dust and fumes in the workplace , and air pollution . Several studies conducted in Guangdong province showed that despite a high prevalence of cigarette smoking, a declining rate of cigarette smoking was observed in males in recent decades . The lower rate of cigarette smoking (1.7%) observed in males accompanied a corresponding increase in the cigarette smoking rate in females [31, 32]. Thus, the rapid growth in the incidence of lung cancer in Sihui cannot be explained fully by cigarette smoking, especially in males.
It has been estimated that nearly half of deaths from lung cancer in China can be attributed to aging in China . Based on the APC analysis, we showed that age cohort had a significantly positive association with the risk of lung cancer after adjusting for the period and birth cohort effects in both sexes, thus implying that increased longevity increases the risk of lung cancer in Sihui . With the economic development in recent decades in Sihui, enhancements in public hygiene, improved nutrition, basic health care availability, and medical progress have brought an increase in life expectancy of its residents. In 2010, the average life expectancy in Sihui (76.6 years) was longer than the average life expectancy in China by 3.1 years .
In addition to the major risk factors (cigarette smoking and longer life expectancy), other known and suspected risk factors of lung cancer have changed considerably. For example, the rapid industrialization and economic development in the 1980s brought air pollution, dust, and fume contaminants to occupational environments, which is especially pertinent to males. After 20–30 years of effects, this may have resulted in the accelerated increase of lung cancer incidence in males from 2005 to 2010, which was demonstrated by joinpoint analysis (Fig. 2).
Birth cohort trends for lung cancer incidence usually suggest that the risk factors exposed to in early life have changed. The incubation time between exposure and cancer occurrence is 20–30 years for lung cancer , and lung cancer has the highest incidence in those ≥60 years of age, so the relevant age of exposure to risk factors would be in the first 4th decade of life. Thus, overexposure to lung carcinogens in Sihui should have occurred prior to the 1940s and 1950s and less frequently after the 1960s. We assume that the combination of a high prevalence of cigarette smoking, advanced age, and exposure to worsening air pollution in the younger generation might be the main reasons underlying the birth cohort effect on the risk of lung cancer in the last 25 years in Sihui.
Variation in the calendar period trend usually indicates the impact of new diagnoses, improved medical interventions, or a change in ascertaining or coding the cause of incidence. In this study, we observed a slight variation over the time periods studied. The slight increase in the calendar period trend coincided with changes in the incidence of lung cancer due to the use of the bronchofiberscopes in the 1990s, computed tomography in the 1990s , and tumor markers in the 2000s .
Our study had some limitations. Specifically, the histologic diagnostic information of patients was incomplete, so we could not analyze the incidence trends in lung cancer of different histologic subtypes. We also did not obtain the data of air quality and cigarette smoking in Sihui to analyze their relationships with the trends in lung cancer incidence.
In summary, a 3.4-fold increase in the incidence of lung cancer was noted in Sihui over the past 25 years. Age, period, and birth cohort effects on the risk of lung cancer in both sexes were observed, which suggests important roles for social aging, cigarette smoking, and environmental risk factors in the risk of lung cancer. Comprehensive measures including decreasing the prevalence of tobacco smoking in males, reducing the occupational exposure, and mitigating the air pollution may be taken to alleviate the burden of lung cancer in rural areas of South China.
Thun MJ, Henley SJ, Burns D, Jemal A, Shanks TG, Calle EE. Lung cancer death rates in lifelong nonsmokers. J Natl Cancer Inst. 2006;98:691–9.
Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, et al. Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015;136:E359–86.
Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 2010;127:2893–917.
Zheng T, Holford TR, Boyle P, Chen Y, Ward BA, Flannery J. Time trend and the age–period–cohort effect on the incidence of histologic types of lung cancer in Connecticut, 1960–1989. Cancer. 1994;74:1556–67.
Wen J, Fu JH, Zhang W, Guo M. Lung carcinoma signaling pathways activated by smoking. Chin J Cancer. 2011;30:551–8.
Chen W, Zheng R, Zhang S, Zhao P, Zeng H, Zou X. Report of cancer incidence and mortality in China, 2010. Ann Transl Med. 2014;2:61.
Kim HJ, Fay MP, Feuer EJ, Midthune DN. Permutation tests for joinpoint regression with applications to cancer rates. Stat Med. 2000;19:335–51.
Qiu D, Katanoda K, Marugame T, Sobue T. A joinpoint regression analysis of long-term trends in cancer mortality in Japan (1958–2004). Int J Cancer. 2009;124:443–8.
Tang WR, Fang JY, Wu KS, Shi XJ, Luo JY, Lin K. Epidemiological characteristics and prediction of esophageal cancer mortality in China from 1991 to 2012. Asian Pac J Cancer Prev. 2014;15:6929–34.
Al-Hashimi MM, Wang XJ. Breast cancer in Iraq, incidence trends from 2000–2009. Asian Pac J Cancer Prev. 2014;15:281–6.
Ahacic K, Kennison R, Thorslund M. Trends in smoking in Sweden from 1968 to 2002: age, period, and cohort patterns. Prev Med. 2008;46:558–64.
Utada M, Ohno Y, Shimizu S, Ito Y, Tsukuma H. Cancer incidence and mortality in Osaka, Japan: future trends estimation with an age–period–cohort model. Asian Pac J Cancer Prev. 2012;13:3893–8.
Lee LT, Huang HY, Huang KC, Chen CY, Lee WC. Age–period–cohort analysis of hepatocellular carcinoma mortality in Taiwan, 1976–2005. Ann Epidemiol. 2009;19:323–8.
Mdzinarishvili T, Gleason MX, Sherman S. Estimation of hazard functions in the log-linear age–period–cohort model: application to lung cancer risk associated with geographical area. Cancer Inform. 2010;9:67–78.
Luo J, Chia KS, Chia SE, Reilly M, Tan CS, Ye W. Secular trends of nasopharyngeal carcinoma incidence in Singapore, Hong Kong and Los Angeles Chinese populations, 1973–1997. Eur J Epidemiol. 2007;22:513–21.
Eilstein D, Uhry Z, Lim TA, Bloch J. Lung cancer mortality in france. Trend analysis and projection between 1975 and 2012, using a Bayesian age–period–cohort model. Lung Cancer. 2008;59:282–90.
Cayuela A, Rodriguez-Dominguez S, Lopez-Campos JL, Vigil E. Age–period–cohort analysis of lung cancer mortality rates in Andalusia, 1975–2004. Lung Cancer. 2007;57:261–5.
Chen WQ, Zheng RS, Zhang SW, Zeng HM, Zou XN. The incidences and mortalities of major cancers in China, 2010. Chin J Cancer. 2014;33:402–5.
Al-Hashimi MM, Wang XJ. Trend analysis of lung cancer incidence rates in Ninawa province, Iraq, from 2000 to 2010—decrease and recent stability. Asian Pac J Cancer Prev. 2014;15:385–90.
Mdzinarishvili T, Gleason MX, Sherman S. A novel approach for analysis of the log-linear age–period–cohort model: application to lung cancer incidence. Cancer Inform. 2009;7:271–80.
Yu IT, Chiu YL, Au JS, Wong TW, Tang JL. Dose–response relationship between cooking fumes exposures and lung cancer among Chinese nonsmoking women. Cancer Res. 2006;66:4961–7.
Yang G, Shu XO, Chow WH, Zhang X, Li HL, Ji BT, et al. Soy food intake and risk of lung cancer: evidence from the Shanghai Women’s Health Study and a meta-analysis. Am J Epidemiol. 2012;176:846–55.
Weinberg GB, Kuller LH, Redmond CK. The relationship between the geographic distribution of lung cancer incidence and cigarette smoking in Allegheny county, Pennsylvania. Am J Epidemiol. 1982;115:40–58.
Engels EA. Inflammation in the development of lung cancer: epidemiological evidence. Expert Rev Anticancer Ther. 2008;8:605–15.
Zulueta JJ, Wisnivesky JP, Henschke CI, Yip R, Farooqi AO, McCauley DI, et al. Emphysema scores predict death from COPD and lung cancer. Chest. 2012;141:1216–23.
Straif K, Baan R, Grosse Y, Secretan B, El Ghissassi F, Cogliano V. Carcinogenicity of household solid fuel combustion and of high-temperature frying. Lancet Oncol. 2006;7:977–8.
Seow A, Poh WT, Teh M, Eng P, Wang YT, Tan WC, et al. Fumes from meat cooking and lung cancer risk in Chinese women. Cancer Epidemiol Biomarkers Prev. 2000;9:1215–21.
Ko YC, Cheng LS, Lee CH, Huang JJ, Huang MS, Kao EL, et al. Chinese food cooking and lung cancer in women nonsmokers. Am J Epidemiol. 2000;151:140–7.
Wang L, Lubin JH, Zhang SR, Metayer C, Xia Y, Brenner A, et al. Lung cancer and environmental tobacco smoke in a non-industrial area of China. Int J Cancer. 2000;88:139–45.
Xu ZY, Brown L, Pan GW, Li G, Feng YP, Guan DX, et al. Lifestyle, environmental pollution and lung cancer in cities of Liaoning in northeastern China. Lung Cancer. 1996;14(Suppl 1):S149–60.
Yu W, He LR, Zhao YC, Chan MH, Zhang M, He M. Dynamic protein–protein interaction subnetworks of lung cancer in cases with smoking history. Chin J Cancer. 2013;32:84–90.
Li YG, Gao X. Epidemiologic studies of particulate matter and lung cancer. Chin J Cancer. 2014;33:376–80.
Ershler WB. Cancer: a disease of the elderly. J Support Oncol. 2003;1:5–10.
Ocana-Riola R, Blanco-Reina E, Moreno-Navarro E, Mayoral-Cortés JM. Age–period–cohort effects on mortality from cerebrovascular disease in southern Spain. J Stroke Cerebrovasc Dis. 2014;23:2274–82.
The Fourth National People’s Congress. The Twelfth Five-Year Plan outline of national economic and social development. Beijing: People’s Publishing House; 2011. p. 3–6.
Armenian HK. Incubation periods of cancer: old and new. J Chronic Dis. 1987;40(Suppl 2):9S–15S.
Henschke CI, Yankelevitz DF, Libby DM, Pasmantier MW, Smith JP, Miettinen OS. Survival of patients with stage I lung cancer detected on CT screening. N Engl J Med. 2006;355:1763–71.
Martelli MP, Sozzi G, Hernandez L, Pettirossi V, Navarro A, Conte D, et al. EML4-ALK rearrangement in non-small cell lung cancer and non-tumor lung tissues. Am J Pathol. 2009;174:661–70.
J-LD, XL, S-MC, and Z-EL conceived the study and participated in its design and coordination. Q-HH, XL, Y-HL, S-HX, E-HL, and JG contributed to acquisition of data. J-LD, L-FZ, M-JY, QL, and M-HH performed the statistical analyses and interpretation. J-LD, S-MC, XL, Z-EL, and Q-HH drafted the manuscript. All authors read and approved the final manuscript.
This work was supported by the National High Technology Research and Development Program of China (No. 2012AA02A501) and the Special Fund for Public Health Trade (No. 201202014). We are grateful to the staff at the Sihui Cancer Institute for their efforts in data linkage and follow-up.
Compliance with ethical guidelines
Competing interests The authors declare that they have no competing interests.
Jin-Lin Du and Xiao Lin contributed equally to this work
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
About this article
Cite this article
Du, JL., Lin, X., Zhang, LF. et al. Secular trend analysis of lung cancer incidence in Sihui city, China between 1987 and 2011. Chin J Cancer 34, 33 (2015). https://doi.org/10.1186/s40880-015-0037-3
- Lung cancer
- Secular trend
- Joinpoint regression analysis
- Age–period–cohort model