At-a-glance – Cancer trends in Canada, 1984 to 2015

Alain A. Demers, PhDAuthor reference 1Author reference 2; Darren R. Brenner, PhDAuthor reference 3; Leah Smith, PhDAuthor reference 4; Amanda Shaw, MScAuthor reference 1

https://doi.org/10.24095/hpcdp.39.11.04

Author references:

Author reference 1

Public Health Agency of Canada, Ottawa, Ontario, Canada

Return to author reference 1 referrer

Author reference 2

Department of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada

Return to author reference 2 referrer

Author reference 3

Departments of Oncology and Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada

Return to author reference 3 referrer

Author reference 4

Canadian Cancer Society, St. John's, Newfoundland and Labrador, Canada

Return to author reference 4 referrer

Correspondence : Alain Demers, Centre for Surveillance and Applied Research, Public Health Agency of Canada, 785 Carling Avenue, room 611B2, Ottawa, ON K1A 0K9; Tel: 613-797-2129; Email: alain.demers@canada.ca

Abstract

Examining incidence trends of all cancers combined in order to understand cancer trends can be misleading, as patterns can vary across individual cancer types. This paper highlights findings on trends over time from Canadian Cancer Statistics 2019, as measured by the annual percent change (APC) of age-standardized incidence rates. Among the results were a recent increase in thyroid cancer in males (APC: 6.4%, 1997–2015), as well as decreases in prostate cancer (APC: −9.1%, 2011–2015) and cervical cancer (APC: −3.3%, 2010–2015).

Keywords: neoplasms, data analysis, trend, cancer

Highlights

  • The incidence of some cancers is changing rapidly in Canada.
  • Recent trends show increasing rates of thyroid cancer in males, drawing attention to the potential impact of overdiagnosis.
  • Prostate cancer incidence is decreasing rapidly, likely reflecting recent changes in screening guidelines.

Introduction

Chronic disease trends are often seen as stable or changing at low rates in populations. For example, the incidence rate of diabetes in Canada went from 6.7 per 1000 population in 2003/04 to 6.3 per 1000 in 2013/14.Footnote 1 Up to 2011, before the incidence rates of prostate cancer started to decline rapidly, this claim of relative stability could also be made for all cancers, if they were presented as an overall group. Canadian Cancer Statistics 2019 (CCS 2019) reports that from 1984 to 2015, cancer incidence rates in Canada increased 0.1% per year on average.Footnote 2 However, this collective picture is misleading, as trends can differ greatly depending on the cancer type and the time period.Footnote 2

Monitoring incidence of individual cancers over time can help identify emerging trends, highlight where progress has been made, and suggest where more work and resources are needed. The purpose of this report is to feature findings from the CCS 2019 report relating to time trends in the incidence of cancers in Canada, with a particular focus on patterns of change for individual cancer types.

Methods

Results are drawn from the incidence chapter of the CCS 2019 report,Footnote 2 covering the period from 1984 to 2015. Quebec was not included because data were available up to 2010 only. The Canadian Cancer Registry (CCR)Footnote 3 was the source of data for 1992 to 2015, and the National Cancer Incidence Reporting System (NCIRS) was utilized prior to 1992.

All analyses were performed by the Public Health Agency of Canada. Age-standardized incidence rates (ASIRs) were calculated through direct standardization using the age structure of the 2011 Canadian population by five-year age group. JoinpointFootnote 4 analysis software (version 4.6.0.0) was used to calculate the annual percent change (APC) using the annual ASIRs for each cancer type from 1984 to 2015, and to determine years in which the APC changed significantly. The minimum time span to report a trend was set at five years. Thus, the most recent trend period possible was 2011 to 2015. Otherwise, default Joinpoint parameters were used. In total, 23 types of cancer were investigated.

Results and discussion

Table 1 shows all trends identified by Joinpoint between 1984 and 2015; Figure 1 pulls out the most recent trend. For both sexes in Figure 1, cancers were divided into those that have decreased or increased significantly (p-value < .05 or p-value < .001) in the most recent trend and those that have been stable (p-value ≥ .05). The following text highlights a few of the results.

Table 1. Annual percentage change (APC) in age-standardized incidence rates by cancer site and sex, Canada (excluding Quebec), 1984 to 2015
Cancer type Males Females
Year APC p -value Year APC p -value
From To From To
Oral 1984 2004 −2.5 < .001 1984 2003 −1.0 < .001
2004 2011 2.1 .003 2003 2015 0.7 .028
2011 2015 −0.1 .94
Esophagus 1984 2006 0.3 .020 1984 2015 −0.4 < .001
2006 2010 4.3 .068
2010 2015 −2.4 .015
Stomach 1984 2002 −2.5 < .001 1984 1999 −3.0 < .001
2002 2015 −1.1 < .001 1999 2015 −0.8 < .001
Colorectal 1984 1996 −0.7 < .001 1984 1996 −1.5 < .001
1996 2000 0.9 .33 1996 2000 1.2 .23
2000 2011 −0.5 .001 2000 2011 −0.5 < .001
2011 2015 −2.2 < .001 2011 2015 −1.9 .002
Liver 1984 2011 3.8 < .001 1984 2015 2.7 < .001
2011 2015 0.2 .88
Pancreas 1984 2000 −1.5 < .001 1984 2015 0.1 .58
2000 2015 0.8 .009
Larynx 1984 2015 −2.6 < .001 1984 1991 0.7 .64
1991 2015 −3.0 < .001
Lung and bronchus 1984 1990 −0.6 .087 1984 1993 2.9 < .001
1990 2003 −2.2 < .001 1993 2011 0.9 < .001
2003 2011 −0.9 .002
2011 2015 −3.3 < .001 2011 2015 −1.3 .043
Melanoma 1984 2015 2.2 < .001 1984 1994 0.1 .79
1994 2015 2.0 < .001
Breast 1984 2015 0.5 .015 1984 1991 2.1 < .001
1991 2015 −0.2 .010
Cervix N/A 1984 2006 −2.1 < .001
2006 2010 1.5 .41
2010 2015 −3.3 < .001
Uterus N/A 1984 1990 −1.5 .063
1990 2006 0.5 .013
2006 2011 3.7 .002
2011 2015 0.1 .92
Ovary N/A 1984 1994 −1.7 < .001
1994 2015 −0.4 .001
Prostate 1984 1993 6.3 < .001 N/A
1993 1997 −3.0 .38
1997 2001 4.1 .23
2001 2011 −1.6 .006
2011 2015 −9.1 < .001
Testis 1984 2015 1.3 < .001 N/A
Bladder 1984 2009 −1.0 < .001 1984 2009 −0.9 < .001
2010 2015 −1.5 .052 2010 2015 −1.3 .18
Kidney and renal pelvis 1984 1989 4.0 .005 1984 2015 1.0 < .001
1989 2003 0.1 .64
2003 2011 2.8 < .001
2011 2015 −0.3 .76
Brain/CNS 1984 2009 −0.2 .081 1984 2011 −0.3 .002
2009 2015 −1.9 .012 2011 2015 −3.2 .059
Thyroid 1984 1997 2.8 .002 1984 1998 3.8 < .001
1997 2015 6.4 < .001 1998 2002 11.9 < .001
2002 2011 6.5 < .001
2011 2015 0.1 .94
Hodgkin lymphoma 1984 2015 −0.4 < .001 1984 2015 0.0 .74
Non-Hodgkin lymphoma 1984 2015 1.3 < .001 1984 1993 2.2 < .001
1993 2015 0.9 < .001
Multiple myeloma 1984 2007 0.3 .077 1984 2015 0.6 < .001
2007 2015 2.6 < .001
Leukemia 1984 1994 −0.9 .067 1984 2003 −0.2 .18
1994 2015 0.7 < .001 2003 2007 3.7 .071
2007 2015 −0.6 .14

Data source: Canadian Cancer Statistics Advisory Committee. Canadian cancer statistics 2019. Toronto (ON): Canadian Cancer Society; 2019.

Abbreviations: APC, annual percent change; CNS, central nervous system; N/A, not applicable.

Figure 1. Most recentFigure 1 Footnote a annual percent change (APC) in age-standardized incidence rates, by cancer site and sex, Canada (excluding Quebec)
Males
Figure 1a
Text description
Cancer type (time period) Annual percent change p-value
Prostate (2011–2015) −9.1 p < .001
Lung and bronchus (2011–2015) −3.3 p < .001
Larynx (1984–2015) −2.6 p < .001
Esophagus (2010–2015) −2.4 .001 ≤ p < .05
Colorectal (2011–2015) −2.2 p < .001
Brain and CNS (2009–2015) −1.9 .001 ≤ p < .05
Stomach (2002–2015) −1.1 p < .001
Hodgkin lymphoma (1984–2015) −0.4 p < .001
Bladder (2010–2015) −1.5 p ≥ .05
Kidney and renal pelvis (2011–2015) −0.3 p ≥ .05
Oral (2011–2015) −0.1 p ≥ .05
Liver (2011–2015) 0.2 p ≥ .05
Breast (1984–2015) 0.5 .001 ≤ p < .05
Leukemia (1994–2015) 0.7 p < .001
Pancreas (2000–2015) 0.8 .001 ≤ p < .05
Non-Hodgkin lymphoma (1984–2015) 1.3 p < .001
Testis (1984–2015) 1.3 p < .001
Melanoma (1984–2015) 2.2 p < .001
Multiple myeloma (2007–2015) 2.6 p < .001
Thyroid (1997–2015) 6.4 p < .001

Females

Figure 1b

Data source: Canadian Cancer Statistics Advisory Committee. Canadian cancer statistics 2019. Toronto (ON): Canadian Cancer Society; 2019.

Abbreviation: CNS, central nervous system.

Figure 1 Footnote a

The APCs were calculated from 1984 to 2015. If one or more significant change in the trend of rates was detected, the APC reflects the trend from the most recent significant change to 2015. If no significant change was detected, the APC reflects the trend over the entire period.

Return to figure 1 footnote a referrer

Text description
Cancer type (time period) Annual percent change p-value
Cervix (2010–2015) −3.3 p < .001
Larynx (1991–2015) −3.0 p < .001
Colorectal (2011–2015) −1.9 .001 ≤ p < .05
Lung and bronchus (2011–2015) −1.3 .001 ≤ p < .05
Stomach (1999–2015) −0.8 p < .001
Ovary (1994–2015) −0.4 .001 ≤ p < .05
Esophagus (1984–2015) −0.4 p < .001
Breast (1991–2015) −0.2 .001 ≤ p < .05
Brain and CNS (2011–2015) −3.2 p ≥ .05
Bladder (2010–2015) −1.3 p ≥ .05
Leukemia (2007–2015) −0.6 p ≥ .05
Hodgkin lymphoma (1984–2015) 0.0 p ≥ .05
Thyroid (2011–2015) 0.1 p ≥ .05
Uterus (2011–2015) 0.1 p ≥ .05
Pancreas (1984–2015) 0.1 p ≥ .05
Multiple myeloma (1984–2015) 0.6 p < .001
Oral (2003–2015) 0.7 .001 ≤ p < .05
Non-Hodgkin lymphoma (1993–2015) 0.9 p < .001
Kidney and renal pelvis (1984–2015) 1.0 p < .001
Melanoma (1994–2015) 2.0 p < .001
Liver (1984–2015) 2.7 p < .001

Thyroid cancer has stabilized in females after many years of increase; however, it is still increasing rapidly in males. The increase may be due to overdiagnosis resulting from increased use of diagnostic technologies such as ultrasound;Footnote 5 however, recent studies also show an increase in late-stage papillary tumours, suggesting that the overall increase may not be entirely due to overdiagnosis.Footnote 6 The increase in multiple myeloma in males and females could be related to the increased prevalence of obesity.Footnote 7 It may also be due to improved detection and case ascertainment, as the rate of myeloma is relatively stable in countries with high ascertainment.Footnote 8Footnote 9Footnote 10Footnote 11Footnote 12 Melanoma rates are still increasing in males and females. Exposure to ultraviolet radiation through sunlight, tanning beds and sun lamps are well-established risk factors for melanoma.Footnote 13 Increase in ultraviolet light exposure without corresponding increases in sun safety behaviours likely explains these increasing rates.Footnote 14

Laryngeal cancer is strongly associated with smoking,Footnote 15 and the decreasing trend observed in both males and females likely reflects the decreasing trend in smoking rates in Canada.Footnote 16Footnote 17 The same observations probably explain the recent trend in lung cancer ASIR in males and females. The recent decline in colorectal cancer ASIR is likely due in part to increased screening that identifies treatable precancerous polyps. Since 2007, the majority of provinces and territories have implemented organized colorectal cancer screening programs.Footnote 18 While not evident in this report, increasing rates have been reported in the younger population, likely due in part to the prevalence of obesity.Footnote 19 Esophageal cancer ASIR is decreasing in both males and females. Risk factors for this cancer include obesity, alcohol consumption and tobacco consumption.Footnote 20 Whereas obesityFootnote 7 and sales of alcoholic drinksFootnote 21 have been increasing in Canada, past decreases in tobacco consumptionFootnote 22 may account for the decreasing rates. In males, liver cancer ASIR has stabilized, though it is still increasing in females. Increases in the most common type of liver cancer, hepatocellular carcinoma (HCC), are generally driven by chronic hepatitis B and C infection, as well as increasing rates of excessive alcohol consumption and diabetes.Footnote 23 However, HCC is more prevalent in low-income countries, and the increase in Canada may be partially explained by rising immigration from regions where HCC is common, including parts of Asia and Africa.Footnote 24

Female breast cancer ASIR has decreased slowly since 1991. This pattern is likely due to mammography screening and long-term changes in risk factors.Footnote 25 Cervical cancer is decreasing, largely due to routine screening with Pap tests. Every province in Canada (except Quebec) has an organized cervical cancer screening program. Current guidelines recommend screening every two to three years starting at age 21 or 25 until age 65 or 70.Footnote 26 In the coming years, human papillomavirus vaccination is expected to result in further reductions in cervical cancer incidence.Footnote 27 The ASIR of prostate cancer over time has mirrored the utilization of prostate-specific antigen testing (PSA) in Canada.Footnote 28 In 2014, the Canadian Task Force on Preventive Health Care advised against PSA screening in men of all ages due to a lack of evidence for benefits and the risk of overdiagnosis and harms of unnecessary treatment.Footnote 29 Prostate cancer ASIRs are currently decreasing rapidly.

In 2014, Cancer Care Ontario implemented a new cancer reporting system that brought several enhancements to the identification of cancer cases, including the registration of in situ bladder cancers, which were not previously reported.Footnote 30 The implementation was retrospectively applied to the data from 2010 onward. This change created an apparent increase in incident cases of bladder cancer for the year 2010 and after. Although the decreasing trend for bladder cancer from 2010 to 2015 is comparable to that of 1984 to 2009, this time period is not long enough to be significant. We forced a joinpoint in 2010 to account for the data collection artefact.

Brain and central nervous system (CNS) cancers decreased 3.9% annually in females between 2011 and 2015, although the decrease was not statistically significant (p = .059). The lack of significance is most likely due to the shortness of the trend and the variability in the annual rates. The significant decrease of 1.9% per year in males started in 2009.

Conclusion

Results show that cancer trends in Canada are dynamic and type-specific. The most recent trends show increasing rates of thyroid cancer in males, drawing attention to the potential impact of overdiagnosis on cancer incidence. Conversely, rates of other cancers have recently decreased, most notably prostate and cervical cancers. The decreases for prostate and cervical cancers underscore the potential impact of improving screening guidelines based on the best evidence. Specifically, reductions in overscreening (e.g. prostate cancer) and the implementation of routine screening (e.g. cervical cancer) can both lead to decreased incidence.

Conflicts of interest

The authors have no conflicts of interest to declare.

Authors' contributions and statement

All authors contributed to the design, conceptualization and revision of the work. Drafting, analysis and interpretation of the data were done by the Public Health Agency of Canada.

The content and views expressed in this article are those of the authors and do not necessarily reflect those of the Government of Canada.

References

Footnote 1

Government of Canada. Diabetes in Canada [Internet]. Ottawa (ON): Government of Canada; 2017 [modified 2017 Nov 14; cited 2019 Jul 03]. Available from: https://www.canada.ca/en/public-health/services/publications/diseases-conditions/diabetes-canada-highlights-chronic-disease-surveillance-system.html

Return to footnote 1 referrer

Footnote 2

Canadian Cancer Statistics Advisory Committee. Canadian cancer statistics 2019. Toronto (ON): Canadian Cancer Society; 2019. 95 p.

Return to footnote 2 referrer

Footnote 3

Statistics Canada. Canadian Cancer Registry (CCR) [Internet]. Ottawa (ON): Government of Canada; 2019 [modified 2019 Jan 28; cited 2019 Mar 5]. Available from: http://www23.statcan.gc.ca/imdb/p2SV.pl?Function=getSurvey&SDDS=3207

Return to footnote 3 referrer

Footnote 4

National Cancer Institute, Division of Cancer Control & Population Sciences, Surveillance Research Program. Joinpoint trend analysis software, version 4.6.0.0. Bethesda (MD): National Cancer Institute; 2019 Feb 26 [cited 2019 Mar 6]. Available from: https://surveillance.cancer.gov/joinpoint

Return to footnote 4 referrer

Footnote 5

Vaccarella S, Dal Maso L, Laversanne M, et al. The impact of diagnostic changes on the rise in thyroid cancer incidence: a population-based study in selected high-resource countries. Thyroid. 2015;25(10):1127-36.

Return to footnote 5 referrer

Footnote 6

Lim H, Devesa SS, Sosa JA, Check D, Kitahara CM. Trends in thyroid cancer incidence and mortality in the United States, 1974-2013. JAMA. 2017;317(13):1338-48.

Return to footnote 6 referrer

Footnote 7

Twells LK, Gregory DM, Reddigan J, et al. Current and predicted prevalence of obesity in Canada: a trend analysis. CMAJ Open [Internet]. 2014 Mar 3 [cited 2019 May 1];2(1):E18-E26. Available from: http://cmajopen.ca/content/2/1/E18.long

Return to footnote 7 referrer

Footnote 8

Velez R, Turesson I, Landgren O, Kristinsson SY, Cuzick J. Incidence of multiple myeloma in Great Britain, Sweden, and Malmo, Sweden: the impact of differences in case ascertainment on observed incidence trends. BMJ Open [Internet]. 2016 Jan 21 [cited 2019 May 1];6(1):e009584.

Return to footnote 8 referrer

Footnote 9

Andres M, Feller A, Arndt V, NICER Working Group. Trends of incidence, mortality, and survival of multiple myeloma in Switzerland between 1994 and 2013. Cancer Epidemiol. 2018;53:105-10.

Return to footnote 9 referrer

Footnote 10

Kyle RA, Therneau TM, Rajkumar SV, Larson DR, Plevak MF, Melton LJ 3rd. Incidence of multiple myeloma in Olmsted County, Minnesota: trend over 6 decades. Cancer. 2004;101(11):2667-74.

Return to footnote 10 referrer

Footnote 11

Renshaw C, Ketley N, Moller H, Davies EA. Trends in the incidence and survival of multiple myeloma in South East England 1985-2004. BMC Cancer. 2010;10:74.

Return to footnote 11 referrer

Footnote 12

Soutar RL, Dawson AA, Wilson BJ. Multiple myeloma in north east Scotland: a review of incidence and survival over three decades. Health Bull. 1996;54(3):232-40.

Return to footnote 12 referrer

Footnote 13

International Agency for Research on Cancer. Exposure to artificial UV radiation and skin cancer. Geneva (CH): World Health Organization; 2006. 76 p.

Return to footnote 13 referrer

Footnote 14

National Skin Cancer Prevention Committee. Exposure to and protection from the sun in Canada: a report based on the 2006 Second National Sun Survey. Toronto (ON): Canadian Partnership Against Cancer; 2010.

Return to footnote 14 referrer

Footnote 15

IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. Tobacco smoke and involuntary smoking. IARC Monogr Eval Carcinog Risks Hum. 2004;83:1-1438.

Return to footnote 15 referrer

Footnote 16

Statistics Canada. Canadian Tobacco, Alcohol and Drugs Survey (CTADS): 2013 summary [Internet]. Ottawa (ON): Health Canada; 2015 [modified 2015 Feb 03; cited 2019 Mar 30]. Available from: https://www.canada.ca/en/health-canada/services/canadian-tobacco-alcohol-drugs-survey/2013-summary.html

Return to footnote 16 referrer

Footnote 17

Health Canada. Canadian Alcohol and Drug Use Monitoring Survey (CADUMS) [Internet]. 2014 [modified 2014 Apr 08; cited 2019 Mar 30]. Available from: https://www.canada.ca/en/health-canada/services/health-concerns/drug-prevention-treatment/canadian-alcohol-drug-use-monitoring-survey.html

Return to footnote 17 referrer

Footnote 18

Major D, Bryant H, Delaney M, et al. Colorectal cancer screening in Canada: results from the first round of screening for five provincial programs. Curr Oncol. 2013;20(5):252-7.

Return to footnote 18 referrer

Footnote 19

Cancer Care Ontario. Cancer fact - Colorectal cancer incidence increasing in younger adults [Internet]. 2016 [cited 2019 Mar 30]; Available from: https://www.cancercareontario.ca/en/cancer-facts/colorectal-cancer-increasing-younger-adults

Return to footnote 19 referrer

Footnote 20

Otterstatter MC, Brierley JD, De P, et al. Esophageal cancer in Canada: trends according to morphology and anatomical location. Can J Gastroenterol. 2012;26(10):723-7.

Return to footnote 20 referrer

Footnote 21

Agriculture and Agri-Food Canada. Consumer trends: wine, beer and spirits in Canada. Ottawa (ON): Government of Canada; 2013. 21 p.

Return to footnote 21 referrer

Footnote 22

Organisation for Economic Co-operation Development (OECD). Daily smokers. 2018 [cited 2019 Mar 30]. Available from: https://data.oecd.org/healthrisk/daily-smokers.htm

Return to footnote 22 referrer

Footnote 23

Trad D, Bibani N, Sabbah M, et al. Known, new and emerging risk factors of hepatocellular carcinoma (review). Presse Med. 2017;46(11):1000-7.

Return to footnote 23 referrer

Footnote 24

Bosetti C, Turati F, La Vecchia C. Hepatocellular carcinoma epidemiology. Best Pract Res Clin Gastroenterol. 2014;28(5):753-70.

Return to footnote 24 referrer

Footnote 25

Holford TR, Cronin KA, Mariotto AB, et al. Changing patterns in breast cancer incidence trends. J Natl Cancer Inst Monogr. 2006;(36):19-25.

Return to footnote 25 referrer

Footnote 26

Canadian Partnership Against Cancer. Cervical cancer screening in Canada: environmental scan (2018). Toronto (ON): Canadian Partnership Against Cancer; 2018 [cited 2019 Mar 30]. Available from: https://www.partnershipagainstcancer.ca/topics/cervical-cancer-screening-environmental-scan-2018

Return to footnote 26 referrer

Footnote 27

Canadian Cancer Society's Advisory Committee on Cancer Statistics. Canadian cancer statistics 2016. Toronto (ON): Canadian Cancer Society; 2016. 142 p.

Return to footnote 27 referrer

Footnote 28

LeBlanc AG, Demers A, Shaw A. Recent trends in prostate cancer in Canada. Health Rep. 2019;30(4):12-17.

Return to footnote 28 referrer

Footnote 29

Bell N, Connor Gorber S, Shane A, et al. Recommendations on screening for prostate cancer with the prostate-specific antigen test. CMAJ. 2014;186(16):1225-34.

Return to footnote 29 referrer

Footnote 30

Cancer Care Ontario. Ontario cancer statistics 2018. Toronto (ON): Cancer Care Ontario; 2018. 172 p.

Return to footnote 30 referrer

Page details

Date modified: