Abstract
Objective
A previous Australian study compared the observed numbers of cancer cases and deaths in 2007 with the expected numbers based on 1987 rates. This study examines the impact of cancer rate changes over the 20-year period 1996–2015, for people aged under 75 years.
Results
The overall age-standardised cancer incidence rate increased from 350.7 in 1995 to 364.4 per 100,000 in 2015. Over the period 1996–2015, there were 29,226 (2.0%) more cases (males: 5940, 0.7%; females: 23,286, 3.7%) than expected numbers based on 1995 rates. Smaller numbers of cases were observed compared to those expected for cancers of the lung for males and colorectum, and cancers with unknown primary. Larger numbers of cases were observed compared to those expected for cancers of the prostate, thyroid and female breast. The overall age-standardised cancer mortality rate decreased from 125.6 in 1995 to 84.3 per 100,000 in 2015. During 1996 to 2015 there were 106,903 (− 20.6%) fewer cancer deaths (males: − 69,007, − 22.6%; females: − 37,896, − 17.9%) than expected based on the 1995 mortality rates. Smaller numbers of deaths were observed compared to those expected for cancers of the lung, colorectum and female breast, and more cancer deaths were observed for liver cancer.
Keywords: Australia, Cancer incidence, Cancer mortality, Cancer control
Introduction
Australia has one of the highest cancer incidence rates in the world [1]. A previous Australian study compared numbers of cancer cases and deaths observed in 2007 with expected numbers based on 1987 rates, with much of the difference likely to be due to the impact of cancer control measures [2]. This prior study showed that over the period 1987–2007, for Australians aged under 75, the number of cancer deaths was 61,000 lower than it would have been based on the 1987 rates [2]. The number of cancer cases, however, was greater than would have been expected based on 1987 rates [2]. It was posited that improvements in prevention, early detection and treatments played an integral role in the mortality reduction. Some of the increased incidence was associated with increased use of medical services, such as the widespread uptake from the early 1990s of prostate specific antigen (PSA) testing to assess prostate cancer risk [2].
There have been significant developments in cancer control in Australia over the past few decades [2]. Tobacco control was one of the most successful, which through reduced prevalence of smoking is estimated to have prevented 78,000 deaths from lung cancer alone between 1956 and 2015 [3, 4]. Additionally, organised early detection is provided through national screening programs for cancers of the cervix, breast and colorectum, which have all experienced reductions in mortality [5]. The continued development of cancer control initiatives based on the most recent evidence is vital. To identify areas that warrant further attention this analysis provides more recent summary measures of changes from 1996 to 2015 in cancer incidence and mortality for Australian people aged under 75 years.
Main text
Methods
Population and tabulated data with the numbers of new cancer cases and deaths by sex, 5-year age group and calendar year from 1994 to 2016 for all cancers combined (ICD-10 codes C00–C97, D45, D46, D47.1, D47.3–D47.5) and for 23 individual cancer types were obtained from the Australian Institute of Health and Welfare (AIHW) [6, 7]. The remaining cancer types were grouped as ‘other’. All cancers for children aged 0–14 years were grouped to avoid small numbers. The analyses were restricted to those aged less than 75 years because by default cancer is a more prevalent cause of death for older people who have survived premature mortality from other chronic diseases, data on cause of death and diagnoses are less reliable at older ages, screening programs stop at approximately 74 years of age, and treatment regimens tend to be less aggressive for older patients [2]. Data were smoothed using a three-year moving average to reduce random variation by single year, and 1995 was used as the reference year.
Statistical analysis
The methods have been described previously [2]. In brief, Joinpoint regression analysis was used to test for significant changes in cancer rates and estimate the average annual percentage change (AAPC) over the period from 1995 to 2015 [8]. We also reported the annual percentage change (APC) over the last period identified by Joinpoint. We estimated the change in numbers of cancer cases and deaths due to changes in cancer rates rather than changes in the population size and ageing. To do this, we first estimated the expected numbers of cancer cases and deaths for the 20-year period 1996–2015 if rates had remained at 1995 levels, by multiplying the sex-age-specific rates in 1995 by the estimated populations in 1996–2015 [2]. We then calculated the differences in the expected cumulative numbers of cases and deaths and the corresponding observed numbers [2]. All rates were age-standardised to the Australian 2001 population. Statistical analyses were performed using Joinpoint 4.7.0.0 [8] and STATA [9].
Results
Cancer incidence
The overall age-standardised incidence rate for all cancers combined increased by 3.9% from 350.7 in 1995 to 364.4 per 100,000 in 2015 (Fig. 1a and Table 1A). Different patterns were observed for males and females, with the incidence rate for all cancers combined for males showing fluctuations over the 20-year period (AAPC: − 0.1, 95% CI − 0.4, 0.2), while a significant increase in the incidence rate for all cancers combined was observed for females (AAPC: 0.5, 95% CI 0.4, 0.5). Notably, in the last period identified by Joinpoint there were opposing changes in cancer incidence rates for males and females, with a decrease observed for males (APC: − 1.4, 95% CI − 1.6, − 1.3 in 2008–2015) and an increase observed for females (APC: 0.9, 95% CI 0.7, 1.0 in 2009–2015) (Table 1A). During 1996–2015, a total of 29,226 (2.0%) more cases (males: 5,940, 0.7%; females: 23,286, 3.7%) were observed compared to the expected numbers based on 1995 rates (Table 2A). For males, compared with expected, the largest differences with smaller numbers of cases observed were for lung (− 23,156, − 23.8%) and colorectal (− 9,092 − 8.5%) cancer, while larger numbers of cases were observed for prostate cancer (29,638, 14.8%) and melanoma (7,208, 8.6%). For females, compared with expected, smaller numbers of cases were observed for cervical cancer (− 7,405, − 34.7%) and cancers with unknown primary (CUP) (− 6,123, − 35.8%), while larger numbers of cases were observed for thyroid (10,993, 83.6%%) and breast (9,952, 4.9%) cancers.
Table 1.
Cancer type | Over the study period from 1995 to 2015 | Over the last period identified by Joinpoint | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Males | Females | Total | Males | Females | Total | |||||||
ASR | AAPC (95%CI) | ASR | AAPC (95%CI) | ASR | AAPC (95%CI) | Period | APC (95%CI) | Period | APC (95%CI) | Period | APC (95%CI) | |
(A) Incidence rate (ranked by the total numbers of cases observed in 2015) | ||||||||||||
All cancers aged 0–74 years | 397.8–392.6 | − 0.1 (− 0.4, 0.2)* | 309.9–337.3 | 0.5 (0.4, 0.5) | 350.7–364.4 | 0.2 (0.1, 0.3) | 2008–2015 | − 1.4 (− 1.6, − 1.3) | 2009–2015 | 0.9 (0.7, 1.0) | 2008–2015 | − 0.4 (− 0.5, − 0.3) |
Aged 15–74 years | ||||||||||||
Prostate (C61) | 125.5–137.2 | 0.5 (− 0.9, 1.8)* | 125.5–137.2 | 0.5 (− 0.9, 1.8)* | 2008–2015 | − 4.5 (− 5.2, − 3.7) | 2008–2015 | − 4.5 (− 5.2, − 3.7) | ||||
Breast (C50) | 128.8–144.6 | 0.7 (0.4, 0.9) | 128.8–144.6 | 0.7 (0.4, 0.9) | 2007–2015 | 1.4 (1.1, 1.7) | 2007–2015 | 1.4 (1.1, 1.7) | ||||
Colon and rectum (C18–C20) | 67.4–54.5 | − 1.1 (− 1.4, − 0.8) | 46.2–39.7 | − 0.8 (− 1.4, − 0.2) | 56.5–46.9 | − 1.0 (− 1.2, − 0.8) | 2013–2015 | − 0.6 (− 3.0, 1.7)* | 2007–2015 | − 1.8 (− 2.1, − 1.6) | 2008–2015 | − 2.2 (− 2.6, − 1.8) |
Melanoma (C43) | 53.7–59.9 | 0.4 (0.2, 0.7) | 42.9–45.4 | 0.2 (− 0.1, 0.5)* | 48.2–52.5 | 0.3 (0.1, 0.6) | 2011–2015 | 0.9 (0.0, 1.9) | 2010–2015 | 1.3 (0.6, 1.9) | 2011–2015 | 1.3 (0.4, 2.2) |
Lung (C33–C34) | 61.0–39.7 | − 2.1 (− 2.4, − 1.9) | 24.6–30.8 | 1.1 (0.7, 1.5) | 42.1–35.2 | − 0.9 (− 1.1, − 0.7) | 2010–2015 | − 1.2 (− 1.5, − 1.0) | 2012–2015 | 1.5 (0.3, 2.8) | 2011–2015 | − 0.2 (− 0.5, 0.2)* |
Head and neck (C00–C14, C30–C32) | 32.9–27.4 | − 0.9 (− 1.6, − 0.1) | 9.5–8.8 | − 0.5 (− 0.9, − 0.1) | 21.0–18.0 | − 0.8 (− 1.0, − 0.5) | 2005–2015 | 0.1 (− 0.1, 0.4)* | 2013–2015 | − 2.4 (− 5.8, 1.2)* | 2004–2015 | 0.3 (0.0, 0.6) |
Non-Hodgkin lymphoma (C82–C85) | 18.9–20.2 | 0.4 (− 0.1, 0.9)* | 14.1–14.6 | 0.1 (− 0.3, 0.6)* | 16.5–17.4 | 0.4 (0.3, 0.5) | 2012–2015 | − 1.7 (− 3.2, − 0.2) | 2008–2015 | 0.7 (0.5, 1.0) | 1995–2015 | 0.4 (0.3, 0.5) |
Kidney (C64) | 12.4–18.8 | 2.0 (0.5, 3.6) | 6.2–8.6 | 1.8 (1.2, 2.5) | 9.2–13.6 | 1.9 (1.8, 2.1) | 2010–2015 | 3.8 (2.3, 5.4) | 2013–2015 | − 0.6 (− 4.2, 3.1)* | 1995–2015 | 1.9 (1.8, 2.1) |
Leukaemia (C91–C95) | 13.2–15.1 | 0.8 (0.4, 1.1) | 8.1–9.1 | 0.5 (0.2, 0.8) | 10.6–12.1 | 0.7 (0.4, 1.1) | 2013–2015 | 2.7 (0.6, 5.0) | 2010–2015 | − 0.2 (− 1.1, 0.7)* | 2013–2015 | 2.4 (0.5, 4.2) |
Thyroid (C73) | 2.9–7.6 | 5.1 (4.2, 6.0) | 8.6–21.7 | 4.8 (4.5, 5.1) | 5.7–14.7 | 4.9 (4.6, 5.2) | 2013–2015 | 2.9 (− 1.4, 7.4)* | 2013–2015 | 1.0 (− 0.9, 3.0)* | 2013–2015 | 1.7 (0.2, 3.3) |
Corpus uteri and uterus (C54–C55) | 16.3–20.8 | 1.3 (0.9, 1.7) | 16.3–20.8 | 1.3 (0.9, 1.7) | 2010–2015 | 0.9 (0.5, 1.3) | 2010–2015 | 0.9 (0.5, 1.3) | ||||
Unknown primary (C77–C80, C97) | 14.8–6.4 | − 4.2 (− 4.7, − 3.8) | 10.5–4.1 | − 4.7 (− 5.2, − 4.2) | 12.6–5.2 | − 4.3 (− 4.7, − 4.0) | 2008–2015 | − 3.4 (− 4.0, − 2.9) | 2013–2015 | − 6.9 (− 9.8, − 4.0) | 2008–2015 | − 3.7 (− 4.1, − 3.3) |
Pancreas (C25) | 8.9–10.7 | 1.0 (0.4, 1.6) | 5.8–8.0 | 1.5 (1.2, 1.8) | 7.3–9.3 | 1.1 (0.9, 1.4) | 2012–2015 | 2.2 (0.6, 3.8) | 2007–2015 | 2.2 (1.6, 2.9) | 2001–2015 | 1.5 (1.4, 1.7) |
Stomach (C16) | 12.9–8.8 | − 1.9 (− 2.1, − 1.7) | 5.3–4.0 | − 1.6 (− 1.8, − 1.5) | 9.0–6.4 | − 1.8 (− 2.0, − 1.6) | 2007–2015 | − 0.9 (− 1.3, − 0.5) | 1995–2015 | − 1.6 (− 1.8, − 1.5) | 2007–2015 | − 1.0 (− 1.4, − 0.7) |
Bladder (C67) | 15.2–9.8 | − 2.1 (− 2.4, − 1.9) | 3.8–2.6 | − 1.9 (− 2.9, − 1.0) | 9.3–6.1 | − 2.0 (− 2.5, − 1.5) | 2005–2015 | − 0.8 (− 1.1, − 0.5) | 2005–2015 | − 0.7 (− 1.3, 0.0)* | 2004–2015 | − 0.8 (− 1.0, − 0.6) |
Brain (C71) | 8.4–8.4 | 0.1 (− 0.6, 0.7)* | 5.5–5.1 | − 0.3 (− 1.8, 1.2)* | 6.9–6.7 | − 0.2 (− 0.5, 0.2)* | 2013–2015 | 2.1 (− 1.8, 6.1)* | 2001–2015 | − 0.7 (− 1.1, − 0.3) | 2010–2015 | − 1.3 (− 2.6, − 0.1) |
Ovary (C56) | 13.0–9.5 | − 1.5 (− 2.0, − 0.9) | 13.0–9.5 | − 1.5 (− 2.0, − 0.9) | 2013–2015 | − 4.5 (− 7.9, − 1.1) | 2013–2015 | − 4.5 (− 7.9, − 1.1) | ||||
Liver (C22) | 4.9–11.6 | 4.5 (4.3, 4.7) | 1.4–3.2 | 4.5 (4.0, 5.1) | 3.1–7.3 | 4.6 (4.5, 4.7) | 2003–2015 | 5.1 (4.8, 5.3) | 2004–2015 | 3.8 (3.1, 4.4) | 1995–2015 | 4.6 (4.5, 4.7) |
Oesophagus (C15) | 7.0–6.9 | 0.2 (− 0.2, 0.5)* | 2.7–2.0 | − 1.7 (− 2.8, − 0.5) | 4.8–4.4 | − 0.4 (− 0.9, 0.2)* | 2011–2015 | − 1.8 (− 3.2, − 0.4) | 2009–2015 | − 1.2 (− 2.1, − 0.2) | 2009–2015 | − 1.4 (− 2.0, − 0.9) |
Cervix (C53) | 13.8–8.8 | − 1.9 (− 2.2, − 1.7) | 13.8–8.8 | − 1.9 (− 2.2, − 1.7) | 2002–2015 | 0.5 (0.3, 0.8) | 2002–2015 | 0.5 (0.3, 0.8) | ||||
Testis (C62) | 7.6–9.8 | 1.3 (1.0, 1.6) | 7.6–9.8 | 1.3 (1.0, 1.6) | 2012–2015 | 2.0 (0.4, 3.7) | 2012–2015 | 2.0 (0.4, 3.7) | ||||
Gallbladder and bile duct (C23–C24) | 2.6–2.5 | − 0.3 (− 1.0, 0.5)* | 2.7–2.4 | − 0.7 (− 1.5, 0.0)* | 2.7–2.5 | − 0.5 (− 1.3, 0.2)* | 2013–2015 | 5.3 (− 0.7, 11.8)* | 2008–2015 | 1.6 (0.9, 2.3) | 2009–2015 | 2.2 (1.4, 3.0) |
Other cancers | 33.9–41.9 | 1.2 (0.9, 1.4) | 22.8–33.2 | 1.8 (1.3, 2.4) | 28.3–37.5 | 1.4 (1.0, 1.8) | 2009–2015 | 1.1 (0.7, 1.5) | 2009–2015 | 1.8 (1.3, 2.2) | 2013–2015 | 0.5 (− 1.4, 2.4)* |
All cancers aged 0–14 years | 16.0–16.7 | 0.2 (− 0.5, 0.9)* | 13.1–15.6 | 0.9 (0.6, 1.2) | 14.6–16.1 | 0.6 (− 0.1, 1.2)* | 2012–2015 | − 2.5 (− 4.4, − 0.5) | 2009–2015 | 2.1 (1.5, 2.7) | 2012–2015 | − 0.5 (− 2.6, 1.5)* |
(B) Mortality rate (ranked by the total numbers of deaths observed in 2015) | ||||||||||||
All cancers aged 0–74 years | 151.1–96.3 | − 2.2 (− 2.3, − 2.2) | 102.6–72.6 | − 1.7 (− 1.8, − 1.7) | 125.6–84.3 | − 2.0 (− 2.0, − 1.9) | 2001–2015 | − 2.1 (− 2.2, − 2.1) | 1999–2015 | − 1.6 (− 1.7, − 1.6) | 2000–2015 | − 1.9 (− 1.9, − 1.9) |
Aged 15–74 years | ||||||||||||
Lung (C33–C34) | 51.5–26.3 | − 3.2 (− 3.3, − 3.2) | 19.4–18.0 | − 0.3 (− 0.6, − 0.1) | 34.8–22.1 | − 2.2 (− 2.4, − 2.1) | 2002–2015 | − 2.9 (− 3.0, − 2.8) | 2011–2015 | − 1.4 (− 2.8, 0.0)* | 2011–2015 | − 2.3 (− 2.9, − 1.8) |
Colon and rectum (C18–C20, C26.0) | 26.8–14.0 | − 3.2 (− 3.5, − 3.0) | 17.1–9.3 | − 3.2 (− 3.4, − 3.0) | 21.8–11.6 | − 3.2 (− 3.3, − 3.1) | 2006–2015 | − 3.5 (− 3.7, − 3.3) | 1995–2015 | − 3.2 (− 3.4, − 3.0) | 1995–2015 | − 3.2 (− 3.3, − 3.1) |
Breast (C50) | 28.6–17.2 | − 2.5 (− 2.9, − 2.1) | 28.6–17.2 | − 2.5 (− 2.9, − 2.1) | 2003–2015 | − 2.4 (− 2.6, − 2.2) | 2003–2015 | − 2.4 (− 2.6, − 2.2) | ||||
Unknown primary (C77–C80, C97) | 10.9–5.9 | − 3.2 (− 4.2, − 2.3) | 7.4–4.0 | − 3.3 (− 3.9, − 2.6) | 9.1–4.9 | − 3.2 (− 3.9, − 2.5) | 2005–2015 | − 5.9 (− 6.4, − 5.4) | 2006–2015 | − 5.9 (− 6.4, − 5.5) | 2005–2015 | − 5.7 (− 6.1, − 5.3) |
Pancreas (C25) | 8.1–7.9 | − 0.2 (− 0.5, 0.2)* | 5.2–5.5 | 0.3 (− 0.9, 1.5)* | 6.6–6.7 | 0.1 (0.0, 0.3)* | 2007–2015 | − 0.8 (− 1.2, − 0.4) | 2004–2015 | − 0.3 (− 0.7, 0.1)* | 2006–2015 | − 0.4 (− 0.7, − 0.2) |
Brain (C71) | 7.2–6.5 | − 0.6 (− 1.3, 0.1)* | 4.7–3.9 | − 0.9 (− 1.5, − 0.2) | 5.9–5.2 | − 0.7 (− 1.1, − 0.3) | 2005–2015 | 0.1 (− 0.3, 0.4)* | 2006–2015 | 0.3 (− 0.1, 0.8)* | 2006–2015 | 0.3 (0.0, 0.5)* |
Prostate (C61) | 15.3–7.9 | − 3.4 (− 3.7, − 3.1) | 15.3–7.9 | − 3.4 (− 3.7, − 3.1) | 2004–2015 | − 3.8 (− 4.1, − 3.5) | 2004–2015 | − 3.8 (− 4.1, − 3.5) | ||||
Melanoma (C43) | 6.6–5.0 | − 1.1 (− 1.7, − 0.6) | 3.2–2.5 | − 1.1 (− 2.1, − 0.2) | 4.9–3.7 | − 1.1 (− 1.5, − 0.7) | 2012–2015 | − 8.0 (− 11.2, − 4.7) | 2008–2015 | − 2.6 (− 4.0, − 1.1) | 2012–2015 | − 6.9 (− 9.6, − 4.0) |
Non-Hodgkin lymphoma (C82–C85) | 7.7–4.0 | − 3.3 (− 3.7, − 2.9) | 5.4–2.1 | − 4.6 (− 5.0, − 4.1) | 6.5–3.0 | − 3.8 (− 4.1, − 3.5) | 2007–2015 | − 2.6 (− 3.2, − 2.0) | 2008–2015 | − 2.2 (− 3.0, − 1.4) | 2008–2015 | − 2.3 (− 2.8, − 1.9) |
Leukaemia (C91–C95) | 6.8–4.3 | − 2.2 (− 2.5, − 1.9) | 3.9–2.8 | − 1.5 (− 1.7, − 1.2) | 5.3–3.6 | − 1.9 (− 2.4, − 1.5) | 2001–2015 | − 2.6 (− 2.9, − 2.3) | 2008–2015 | − 0.6 (− 1.0, − 0.1) | 2005–2015 | − 2.1 (− 2.4, − 1.8) |
Liver (C22) | 4.3–7.7 | 2.6 (2.2, 3.0) | 1.7–2.9 | 3.3 (2.9, 3.6) | 3.0–5.3 | 2.9 (2.6, 3.1) | 2010–2015 | 2.7 (1.9, 3.5) | 1995–2015 | 3.3 (2.9, 3.6) | 2003–2015 | 3.5 (3.3, 3.7) |
Head and neck (C00–C14, C30–C32) | 9.0–5.2 | − 2.7 (− 3.0, − 2.3) | 2.0–1.4 | − 1.7 (− 3.0, − 0.4) | 5.4–3.3 | − 2.5 (− 3.1, − 1.9) | 2007–2015 | − 1.1 (− 1.8, − 0.4) | 2006–2015 | 0.2 (− 0.7, 1.1)* | 2006–2015 | − 0.9 (− 1.4, − 0.5) |
Oesophagus (C15) | 6.5–5.6 | − 0.8 (− 1.4, − 0.2) | 2.0–1.3 | − 2.1 (− 2.4, − 1.8) | 4.2–3.4 | − 1.1 (− 1.6, − 0.6) | 2004–2015 | − 1.5 (− 1.8, − 1.2) | 1995–2015 | − 2.1 (− 2.4, − 1.8) | 2004–2015 | − 1.7 (− 2.0, − 1.3) |
Stomach (C16) | 7.7–3.8 | − 3.5 (− 4.1, − 2.9) | 3.3–2.0 | − 2.8 (− 3.1, − 2.4) | 5.4–2.8 | − 3.2 (− 3.9, − 2.5) | 2013–2015 | − 6.9 (− 11.8, − 1.7) | 1995–2015 | − 2.8 (− 3.1, − 2.4) | 2013–2015 | − 5.2 (− 10.6, 0.6)* |
Ovary (C56) | 7.7–5.0 | − 2.1 (− 2.8, − 1.3) | 7.7–5.0 | − 2.1 (− 2.8, − 1.3) | 2013–2015 | − 5.0 (− 9.7, − 0.1) | 2013–2015 | − 5.0 (− 9.7, − 0.1) | ||||
Kidney (C64) | 4.7–3.3 | − 1.7 (− 1.9, − 1.5) | 2.5–1.3 | − 3.2 (− 4.1, − 2.3) | 3.6–2.3 | − 2.1 (− 2.2, − 2.0) | 1995–2015 | − 1.7 (− 1.9, − 1.5) | 2001–2015 | − 3.5 (− 3.8, − 3.1) | 1995–2015 | − 2.1 (− 2.2, − 2.0) |
Bladder (C67) | 3.8–2.1 | − 3.2 (− 3.9, − 2.5) | 1.2–0.7 | − 2.7 (− 3.1, − 2.3) | 2.5–1.4 | − 3.0 (− 3.7, − 2.4) | 2011–2015 | − 6.5 (− 9.7, − 3.1) | 1995–2015 | − 2.7 (− 3.1, − 2.3) | 2011–2015 | − 5.8 (− 8.9, − 2.7) |
Corpus uteri and uterus (C54–C55) | 2.2–2.5 | 0.6 (− 0.4, 1.7)* | 2.2–2.5 | 0.6 (− 0.4, 1.7)* | 2010–2015 | 4.0 (2.6, 5.4) | 2010–2015 | 4.0 (2.6, 5.4) | ||||
Cervix (C53) | 3.8–1.9 | − 3.5 (− 4.5, − 2.4) | 3.8–1.9 | − 3.5 (− 4.5, − 2.4) | 2004–2015 | − 0.3 (− 0.7, 0.2)* | 2004–2015 | − 0.3 (− 0.7, 0.2)* | ||||
Gallbladder and bile duct (C23–C24) | 1.0–0.5 | − 4.0 (− 5.9, − 2.1) | 1.5–0.6 | − 5.6 (− 6.2, − 5.1) | 1.3–0.5 | − 4.8 (− 7.1, − 2.5) | 2005–2015 | − 1.0 (− 2.4, 0.4)* | 1995–2015 | − 5.6 (− 6.2, − 5.1) | 2005–2015 | − 3.4 (− 5.0, − 1.7) |
Thyroid (C73) | 0.3–0.3 | 1.0 (− 1.2, 3.4)* | 0.3–0.4 | 0.4 (− 3.8, 4.9)* | 0.3–0.3 | 0.8 (− 1.2, 2.8)* | 1997–2015 | − 0.5 (− 1.1, 0.1)* | 2004–2015 | 1.3 (− 0.3, 2.8)* | 2004–2015 | 0.5 (− 0.2, 1.1)* |
Testis (C62) | 0.4–0.2 | − 3.4 (− 4.3, − 2.4) | 0.4–0.2 | − 3.4 (− 4.3, − 2.4) | 2002–2015 | − 0.9 (− 2.1, 0.3)* | 2002–2015 | − 0.9 (− 2.1, 0.3)* | ||||
Other cancers | 13.2–12.1 | − 0.4 (− 0.8, 0.0)* | 7.3–7.0 | − 0.2 (− 0.8, 0.4)* | 10.1–9.5 | − 0.3 (− 0.7, 0.1)* | 2005–2015 | − 0.3 (− 0.5, 0.0) | 2007–2015 | − 0.8 (− 1.1, − 0.5) | 2004–2015 | − 0.2 (− 0.4, − 0.1) |
All cancers aged 0–14 years | 4.5–2.3 | − 3.6 (− 4.5, − 2.7) | 3.1–1.6 | − 2.9 (− 3.4, − 2.5) | 3.8–2.0 | − 3.2 (− 3.9, − 2.5) | 2007–2015 | − 1.0 (− 3.2, 1.2)* | 1995–2015 | − 2.9 (− 3.4, − 2.5) | 2008–2015 | − 1.1 (− 3.1, 0.9)* |
All cancers combined: ICD-10 codes C00–C97, D45, D46, D47.1, D47.3–D47.5. C26.0 (“malignant neoplasms of the intestinal tract unspecified”) was included in colorectal cancer mortality, as it has been reported that deaths certified as ‘bowel cancer’ tended to be coded to C26.0 [7]
ASR age-standardised rate. All rates were age-standardised to the Australian 2001 population, AAPC average annual percent change over the whole study period from 1995 to 2015, APC annual percent change, CI confidence interval
*Change not statistically significant (p value ≥ 0.05) for the Joinpoint analysis of changes in rates
Table 2.
Cancer type | Observed in 1996–2015 (O) | Expected in 1996–2015 (E)a | Difference (O − E) | % change [100 × (O − E)/E] | ||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Male | Female | Total | Male | Female | Male | Total | Female | Total | Male | Female | Total | |
(A) Number of new cases (ranked by the total numbers of cases observed in 2015) | ||||||||||||
All cancers aged 0–74 years | 811,377 | 655,832 | 1,467,209 | 805,437 | 632,546 | 1,437,983 | 5940 | 23,286 | 29,226 | 0.7 | 3.7 | 2.0 |
Aged 15–74 years | ||||||||||||
Prostate (C61) | 230,348 | 230,348 | 200,710 | 200,710 | 29,638 | 29,638 | 14.8 | 14.8 | ||||
Breast (C50) | 214,545 | 214,545 | 204,593 | 204,593 | 9952 | 9952 | 4.9 | 4.9 | ||||
Colon and rectum (C18–C20) | 98,326 | 70,456 | 168,782 | 107,418 | 75,022 | 182,440 | − 9092 | − 4567 | − 13,658 | − 8.5 | − 6.1 | − 7.5 |
Melanoma (C43) | 91,016 | 69,800 | 160,816 | 83,808 | 67,162 | 150,970 | 7208 | 2638 | 9846 | 8.6 | 3.9 | 6.5 |
Lung (C33–C34) | 74,067 | 45,530 | 119,597 | 97,223 | 40,198 | 137,422 | − 23,156 | 5331 | − 17,825 | − 23.8 | 13.3 | − 13.0 |
Head and neck (C00–C14, C30–C32) | 44,829 | 14,176 | 59,006 | 52,087 | 15,269 | 67,356 | − 7257 | − 1093 | − 8350 | − 13.9 | − 7.2 | − 12.4 |
Non-Hodgkin lymphoma (C82–C85) | 31,421 | 22,760 | 54,181 | 29,527 | 22,698 | 52,226 | 1894 | 62 | 1956 | 6.4 | 0.3 | 3.7 |
Kidney (C64) | 24,477 | 12,162 | 36,639 | 19,579 | 9,894 | 29,473 | 4897 | 2268 | 7166 | 25.0 | 22.9 | 24.3 |
Leukaemia (C91–C95) | 22,572 | 13,812 | 36,384 | 20,747 | 12,966 | 33,713 | 1825 | 846 | 2671 | 8.8 | 6.5 | 7.9 |
Thyroid (C73) | 8092 | 24,150 | 32,241 | 4434 | 13,157 | 17,590 | 3658 | 10,993 | 14,651 | 82.5 | 83.6 | 83.3 |
Corpus uteri and uterus (C54–C55) | 30,178 | 30,178 | 26,353 | 26,353 | 3825 | 3825 | 14.5 | 14.5 | ||||
Unknown primary (C77–C80, C97) | 15,491 | 10,956 | 26,447 | 23,574 | 17,079 | 40,652 | − 8083 | − 6123 | − 14,205 | − 34.3 | − 35.8 | − 34.9 |
Pancreas (C25) | 15,207 | 11,178 | 26,385 | 14,170 | 9461 | 23,632 | 1037 | 1717 | 2753 | 7.3 | 18.1 | 11.7 |
Stomach (C16) | 16,156 | 7365 | 23,520 | 20,448 | 8617 | 29,065 | − 4292 | − 1253 | − 5545 | − 21.0 | − 14.5 | − 19.1 |
Bladder (C67) | 17,543 | 4921 | 22,465 | 24,066 | 6296 | 30,362 | − 6523 | − 1375 | − 7897 | − 27.1 | − 21.8 | − 26.0 |
Brain (C71) | 13,115 | 8604 | 21,719 | 13,193 | 8782 | 21,976 | − 78 | − 179 | − 257 | − 0.6 | − 2.0 | − 1.2 |
Ovary (C56) | 17,894 | 17,894 | 20,716 | 20,716 | − 2822 | − 2822 | − 13.6 | − 13.6 | ||||
Liver (C22) | 12,813 | 3808 | 16,621 | 7703 | 2282 | 9985 | 5110 | 1526 | 6636 | 66.3 | 66.8 | 66.5 |
Oesophagus (C15) | 11,232 | 3534 | 14,766 | 11,163 | 4398 | 15,561 | 69 | − 863 | − 795 | 0.6 | − 19.6 | − 5.1 |
Cervix (C53) | 13,959 | 13,959 | 21,364 | 21,364 | − 7405 | − 7405 | − 34.7 | − 34.7 | ||||
Testis (C62) | 13,314 | 13,314 | 11,516 | 11,516 | 1799 | 1799 | 15.6 | 15.6 | ||||
Gallbladder and bile duct (C23-C24) | 3607 | 3785 | 7392 | 4191 | 4474 | 8665 | − 584 | − 689 | − 1273 | − 13.9 | − 15.4 | − 14.7 |
Other | 60,980 | 46,568 | 107,548 | 53,126 | 36,493 | 89,619 | 7854 | 10,075 | 17,928 | 14.8 | 27.6 | 20.0 |
All cancers aged 0–14 years | 6768 | 5693 | 12,461 | 6754 | 5270 | 12,024 | 15 | 423 | 437 | 0.2 | 8.0 | 3.6 |
(B) Number of deaths (ranked by the total numbers of deaths observed in 2015) | ||||||||||||
All cancers aged 0–74 years | 236,831 | 174,406 | 411,236 | 305,838 | 212,302 | 518,140 | − 69,007 | − 37,896 | − 106,903 | − 22.6 | − 17.9 | − 20.6 |
Aged 15–74 years | ||||||||||||
Lung (C33–C34) | 55,411 | 30,826 | 86,237 | 81,911 | 31,698 | 113,610 | − 26,500 | − 872 | − 27,373 | − 32.4 | − 2.8 | − 24.1 |
Colon and rectum (C18–C20, C26.0) | 30,069 | 19,822 | 49,892 | 42,666 | 27,939 | 70,604 | − 12,596 | − 8116 | − 20,713 | − 29.5 | − 29.1 | − 29.3 |
Breast (C50) | 34,542 | 34,542 | 45,804 | 45,804 | − 11,262 | − 11,262 | − 24.6 | − 24.6 | ||||
Unknown primary (C77–C80, C97) | 13,234 | 9531 | 22,765 | 17,317 | 12,133 | 29,450 | − 4083 | − 2602 | − 6685 | − 23.6 | − 21.4 | − 22.7 |
Pancreas (C25) | 12,716 | 8991 | 21,707 | 12,899 | 8448 | 21,348 | − 183 | 542 | 359 | − 1.4 | 6.4 | 1.7 |
Brain (C71) | 10,302 | 6538 | 16,841 | 11,293 | 7518 | 18,811 | − 990 | − 980 | − 1970 | − 8.8 | − 13.0 | − 10.5 |
Prostate (C61) | 16,596 | 16,596 | 23,916 | 23,916 | − 7320 | − 7320 | − 30.6 | − 30.6 | ||||
Melanoma (C43) | 9985 | 4801 | 14,786 | 10,389 | 5116 | 15,505 | − 404 | − 315 | − 719 | − 3.9 | − 6.2 | − 4.6 |
Non–Hodgkin lymphoma (C82–C85) | 8468 | 5518 | 13,987 | 12,111 | 8775 | 20,886 | − 3643 | − 3256 | − 6899 | − 30.1 | − 37.1 | − 33.0 |
Leukaemia (C91–C95) | 8449 | 5252 | 13,701 | 10,586 | 6243 | 16,830 | − 2137 | − 991 | − 3129 | − 20.2 | − 15.9 | − 18.6 |
Liver (C22) | 9402 | 3614 | 13,015 | 6886 | 2699 | 9585 | 2516 | 915 | 3431 | 36.5 | 33.9 | 35.8 |
Head and neck (C00–C14, C30–C32) | 10,001 | 2505 | 12,507 | 14,439 | 3180 | 17,619 | − 4438 | − 674 | − 5112 | − 30.7 | − 21.2 | − 29.0 |
Oesophagus (C15) | 9799 | 2542 | 12,340 | 10,301 | 3299 | 13,600 | − 502 | − 757 | − 1260 | − 4.9 | − 23.0 | − 9.3 |
Stomach (C16) | 8093 | 3924 | 12,016 | 12,189 | 5323 | 17,511 | − 4096 | − 1399 | − 5495 | − 33.6 | − 26.3 | − 31.4 |
Ovary (C56) | 9899 | 9899 | 12,361 | 12,361 | − 2462 | − 2462 | − 19.9 | − 19.9 | ||||
Kidney (C64) | 6202 | 2846 | 9048 | 7478 | 4045 | 11,523 | − 1276 | − 1199 | − 2475 | − 17.1 | − 29.6 | − 21.5 |
Bladder (C67) | 4668 | 1545 | 6213 | 6016 | 1993 | 8009 | − 1348 | − 448 | − 1796 | − 22.4 | − 22.5 | − 22.4 |
Corpus uteri and uterus (C54–C55) | 3659 | 3659 | 3635 | 3635 | 24 | 24 | 0.7 | 0.7 | ||||
Cervix (C53) | 3365 | 3365 | 5975 | 5975 | − 2610 | − 2610 | − 43.7 | − 43.7 | ||||
Gallbladder and bile duct (C23–C24) | 1058 | 1535 | 2593 | 1659 | 2528 | 4187 | − 600 | − 993 | − 1594 | − 36.2 | − 39.3 | − 38.1 |
Thyroid (C73) | 527 | 523 | 1051 | 406 | 516 | 922 | 121 | 8 | 129 | 29.9 | 1.5 | 14.0 |
Testis (C62) | 384 | 384 | 642 | 642 | − 258 | − 258 | − 40.2 | − 40.2 | ||||
Other | 20,275 | 11,702 | 31,978 | 20,832 | 11,838 | 32,670 | − 557 | − 135 | − 693 | − 2.7 | − 1.1 | − 2.1 |
All cancers aged 0–14 years | 1190 | 926 | 2116 | 1901 | 1237 | 3138 | − 711 | − 311 | − 1022 | − 37.4 | − 25.1 | − 32.6 |
All cancers combined: ICD-10 codes C00–C97, D45, D46, D47.1, D47.3–D47.5, C26.0 (“malignant neoplasms of the intestinal tract unspecified”) was included in colorectal cancer mortality, as it has been reported that deaths certified as ‘bowel cancer’ tended to be coded to C26.0 [7]
aThe expected total number of new cases or deaths in 1996–2015 was calculated by multiplying the smoothed sex-age-specific incidence or mortality rate in 1995 by the estimated populations for 1996–2015
Cancer mortality
The age-standardised mortality rate for all cancers combined decreased by 32.9% from 125.6 in 1995 to 84.3 per 100,000 in 2015 (Fig. 1b and Table 1B). Significant decreases in mortality rates were observed for both males (AAPC: − 2.2, 95% CI − 2.3, − 2.2) and females (AAPC: − 1.7, 95% CI − 1.8, − 1.7). Mortality rates for most cancer types, except liver cancer, decreased throughout the 20-year period. There were only negligible changes in mortality rates for cancers of the pancreas, thyroid, corpus uteri and uterus over the whole study period 1995–2015. However, a significant increase in mortality rates for cancer of corpus uteri and uterus in the last period from 2010 to 2015 was identified by Joinpoint (Table 1B). During 1996–2015 there were 106,903 fewer cancer deaths (males: − 69,007, − 22.6%; females: − 37,896, − 17.9%) than expected based on the 1995 mortality rates (Table 2B). For males, compared with expected, the largest differences were for lung (− 26,500, − 32.4%) and colorectal (− 12,596, − 29.5%) cancers. For females compared with expected, the largest differences were for breast (− 11,262, − 24.6%) and colorectal (− 8,116, − 29.1%) cancers. Liver cancer was the only cancer with a significantly larger number of deaths compared to that expected (3.431, 35.8%) (Table 2B).
Discussion
Our results indicated that the overall incidence rate for all cancers for Australians aged under 75 years was relatively stable from 1995 to 2015, while the mortality rate for all cancers declined by 32.9% over the same period. Over the period 1996–2015, the number of cancer cases was 2% higher and the number of cancer deaths was 20.6% lower compared to those expected based on 1995 rates. The patterns observed in the current study were somewhat consistent with those reported for 1987–2007 [2]. However, there was a greater decrease in the cancer mortality rate and a much smaller increase in the cancer incidence rate [2]. These differences are likely to be attributable to multiple factors including risk factor control, changes in diagnostic practices and cancer screening activities, as well as improvements in cancer treatments, which were highlighted in the previous study [2]. Broadly, Australia has seen a variety of improvements in cancer treatment and the development of tailored and targeted therapies which have led to improvements in cancer outcomes [10]. We identified different patterns in cancer incidence for males and females, with the incidence rate for males being relatively stable while the rate for females showed an increase. These were largely driven by lung cancer incidence due to differences in sex-specific smoking behaviours in the population [3, 11].
For several cancer types that have an established association with tobacco smoking, including cancers of the lung for males, colorectum, head and neck, stomach, bladder, ovary, oesophagus for females and cervix [12], significant decreases in both cancer incidence and mortality rates have resulted in smaller numbers of new cancer cases and cancer deaths being observed compared to those expected based on rates 20 years ago are likely attributable to Australia’s successful tobacco control interventions [3, 4]. However, an increase in the incidence of lung cancer was observed for females, and for lung cancer alone the observed numbers of cases and deaths in 2015 were still substantial, highlighting that continued efforts in tobacco control and the development of effective lung cancer screening and treatments remain significant public health priorities [3]. The first enquiry into the possibility of a national lung cancer screening program is currently progressing in Australia [13].
In the case of colorectal and cervical cancers, organised screening has played a major role in reducing the incidence and mortality rates. Australia’s National Cervical Screening Program (NCSP) was implemented in 1991, the reductions in cervical cancer incidence and mortality rates observed in this study can be mainly attributed to the NCSP. However, a previous study reported that the cervical cancer incidence rate appears to have plateaued during the late 2000s following the levelling off of screening participation rates, and a new screening technology and revised protocol were introduced in 2017 [14]. In addition, the national human papillomavirus (HPV) vaccination program was introduced in April 2007 [15], and over time this will be expected to further reduce the incidence rate of cervical cancer [16]. While the National Bowel Cancer Screening Program (NBCSP) has been phased in from 2006, reaching full implementation from 2020 [5], opportunistic screening occurred prior to its launch and continues, so decreases in colorectal cancer incidence and mortality rates are likely to be attributable to both organised and opportunistic screening [17, 18]. However, in contrast to the overall decrease in the incidence and mortality rates for colorectal cancer, a previous study reported increases in the incidence rates for people aged under 50 years [19]. Further research focusing on the increase in the colorectal cancer incidence rate for young people is warranted.
The decreases in the incidence and mortality rates for CUP could potentially be explained by continuous improvements in diagnostic techniques which may have resulted in these cases being correctly classified as a known primary cancer type [20]. Consequently, this could be a potential factor contributing to the increases in the numbers of new diagnoses of other cancer types compared with expected. Reductions in mortality for cancer types commonly thought to be responsible for CUP, including lung cancer, are likely to have also contributed to the smaller than expected number of deaths from CUP [21].
Increasing or relatively stable incidence rates but decreasing mortality rates were observed for some cancer types, including cancers of the prostate, breast, kidney and melanoma. Although prostate cancer and melanoma are often detected early and treated successfully as a result, currently there is no organised population screening for either as the potential harms are considered to outweigh the benefits [22–25]. The decrease in the prostate cancer incidence rate after 2008 [6] is likely to be attributable to clinical guidelines recommending against PSA testing for prostate cancer since 2008 [22, 23]. For breast cancer, despite debate around mammographic screening [26, 27], assessments of different methods of screening for breast cancer estimated a reduction in mortality of 21–28% for women invited to screening [28, 29].
As found in the previous study which considered a time period starting a decade earlier than the current study, there were statistically significant increases in both incidence and mortality rates for liver cancer, resulting in significantly larger numbers of liver cancer cases and deaths occurring compared to those expected based on 1995 rates [2]. Multiple factors may be the cause of these increases. The prevalence of hepatitis B and C has remained high in some migrant communities, and among Aboriginal and Torres Strait Islander Australians, and there is a substantial burden of undiagnosed chronic hepatitis infections in high risk groups [30]. Other risk factors such as obesity, diabetes and alcohol consumption may also be a factor [2]. In addition, the misclassification of other cancers which have metastasised to the liver could be a factor [31]. Future research focusing on the increase in incidence and mortality rates for liver cancer is a major priority. This study also found that the mortality rate for cancer of corpus uteri and uterus increased in the recent period from 2010 to 2015, which was likely caused by increases in obesity, diabetes, insufficient physical activity, and decreasing use of estrogen plus progestin menopausal hormone therapy [32, 33].
In the context of the Covid-19 pandemic, health services have been severely disrupted in a number of countries and in Australia cancer services have been disrupted to some extent [34], including a pause of BreastScreen Australia services in April–May 2020. Furthermore, population-level health-seeking may be impacted. It will be important to ensure that these disruptions are minimised and that appropriate recovery strategies are in place; one means by which this is occurring is the establishment of the Covid-19 and Cancer Global Modelling Consortium, which aims to help countries minimise the impact of disruptions [35].
Conclusion
We found that the cancer mortality rate in Australia in 2015 was about a third lower than the rate in 1995, with a total of almost 107,000 fewer deaths over the 20-year period 1996–2015 than would have been expected had the mortality rate remained at the 1995 level. This is likely to in part reflect the success of past cancer control efforts, especially tobacco control, cancer screening, and improvements in treatment. Despite the improvements observed, an increase in cancer incidence remains a concern, with the number of new cancer diagnoses being greater than that expected based on 1995 rates. Although a proportion of these are likely to be due to increased detection, these findings imply that continuing commitment to further research and the implementation of evidence-based cancer control measures must remain public health priorities.
Limitations
The main limitation of this analysis is that the estimated changes in incidence and mortality are likely to be sensitive to the reference year selected for comparison. To reduce the impact of this and account for random variations in cancer rates for a single year, the 1995 rates were estimated using a three-year moving average.
Acknowledgements
We would like to acknowledge the Australian Institute of Health and Welfare who provided the national tabulated data on cancer incidence and mortality. However, they bear no responsibility for the analyses presented within this publication or the interpretation of them. We would like to thank Clare Kahn for editorial assistance.
Abbreviations
- APC
Annual percent change
- AAPC
Average annual percentage change
- AIHW
Australian Institute of Health and Welfare
- CDA
Cancer Data in Australia
- CI
Confidence interval
- CUP
Cancers with unknown primary
- HPV
Human papilloma virus
- ICD
International Classification of Diseases
- NBCSP
National Bowel Cancer Screening Program
- NCSP
National Cervical Cancer Screening Program
- NHL
Non-Hodgkin lymphoma
- PSA
Prostate specific antigen
Authors’ contributions
EF: conceived a similar earlier study. KC: suggested updating the analysis. QL conducted the statistical analysis, interpreted the results and drafted the manuscript. JS contributed to the statistical analysis and methods used. DO’C, KC and EF contributed to the methods. KC, JS, EF, PG and DO’C contributed to the interpretation of the results and drafting of the manuscript. All authors read and approved the final manuscript.
Funding
Not applicable.
Availability of data and materials
The datasets generated and/or analysed for the current study are available from Cancer Data in Australia via: https://www.aihw.gov.au/reports/cancer/cancer-data-in-australia/contents/summary.
Ethics approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Competing interests
KC is co-PI of an unrelated investigator-initiated trial of cytology and primary HPV screening in Australia ('Compass’), which is conducted and funded by the Victorian Cytology Service (VCS), a government-funded health promotion charity. The VCS has received equipment and a funding contribution for the Compass trial from Roche Molecular Systems and Ventana Inc USA. However, neither KC nor her institution (Cancer Council NSW) receives direct funding from industry for this trial or any other project.
Footnotes
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Contributor Information
Qingwei Luo, Email: qingweil@nswcc.org.au.
Julia Steinberg, Email: julia.steinberg@nswcc.org.au.
Dianne L. O’Connell, Email: dianneo@nswcc.org.au
Paul B. Grogan, Email: paul.grogan@nswcc.org.au
Karen Canfell, Email: karen.canfell@nswcc.org.au.
Eleonora Feletto, Email: eleonoraf@nswcc.org.au.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The datasets generated and/or analysed for the current study are available from Cancer Data in Australia via: https://www.aihw.gov.au/reports/cancer/cancer-data-in-australia/contents/summary.