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. 2022 Jun;7(6):e537-e548.
doi: 10.1016/S2468-2667(22)00090-1.

Cancer incidence and mortality in Australia from 2020 to 2044 and an exploratory analysis of the potential effect of treatment delays during the COVID-19 pandemic: a statistical modelling study

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Cancer incidence and mortality in Australia from 2020 to 2044 and an exploratory analysis of the potential effect of treatment delays during the COVID-19 pandemic: a statistical modelling study

Qingwei Luo et al. Lancet Public Health. 2022 Jun.

Erratum in

Abstract

Background: Long-term projections of cancer incidence and mortality estimate the future burden of cancer in a population, and can be of great use in informing the planning of health services and the management of resources. We aimed to estimate incidence and mortality rates and numbers of new cases and deaths up until 2044 for all cancers combined and for 21 individual cancer types in Australia. We also illustrate the potential effect of treatment delays due to the COVID-19 pandemic on future colorectal cancer mortality rates.

Methods: In this statistical modelling study, cancer incidence and mortality rates in Australia from 2020 to 2044 were projected based on data up to 2017 and 2019, respectively. Cigarette smoking exposure (1945-2019), participation rates in the breast cancer screening programme (1996-2019), and prostate-specific antigen testing rates (1994-2020) were included where relevant. The baseline projection model using an age-period-cohort model or generalised linear model for each cancer type was selected based on model fit statistics and validation with pre-COVID-19 observed data. To assess the impact of treatment delays during the COVID-19 pandemic on colorectal cancer mortality, we obtained data on incidence, survival, prevalence, and cancer treatment for colorectal cancer from different authorities. The relative risks of death due to system-caused treatment delays were derived from a published systematic review. Numbers of excess colorectal cancer deaths were estimated using the relative risk of death per week of treatment delay and different durations of delay under a number of hypothetical scenarios.

Findings: Projections indicate that in the absence of the COVID-19 pandemic effects, the age-standardised incidence rate for all cancers combined for males would decline over 2020-44, and for females the incidence rate would be relatively stable in Australia. The mortality rates for all cancers combined for both males and females are expected to continuously decline during 2020-44. The total number of new cases are projected to increase by 47·4% (95% uncertainty interval [UI] 35·2-61·3) for males, from 380 306 in 2015-19 to 560 744 (95% UI 514 244-613 356) in 2040-44, and by 54·4% (95% UI 40·2-70·5) for females, from 313 263 in 2015-19 to 483 527 (95% UI 439 069-534 090) in 2040-44. The number of cancer deaths are projected to increase by 36·4% (95% UI 15·3-63·9) for males, from 132 440 in 2015-19 to 180 663 (95% UI 152 719-217 126) in 2040-44, and by 36·6% (95% UI 15·8-64·1) for females, from 102 103 in 2015-19 to 139 482 (95% UI 118 186-167 527) in 2040-44, due to population ageing and growth. The example COVID-19 pandemic scenario of a 6-month health-care system disruption with 16-week treatment delays for colorectal cancer patients could result in 460 (95% UI 338-595) additional deaths and 437 (95% UI 314-570) deaths occurring earlier than expected in 2020-44.

Interpretation: These projections can inform health service planning for cancer care and treatment in Australia. Despite the continuous decline in cancer mortality rates, and the decline or plateau in incidence rates, our projections suggest an overall 51% increase in the number of new cancer cases and a 36% increase in the number of cancer deaths over the 25-year projection period. This means that continued efforts to increase screening uptake and to control risk factors, including smoking exposure, obesity, physical inactivity, alcohol use, and infections, must remain public health priorities.

Funding: Partly funded by Cancer Council Australia.

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Conflict of interest statement

Declaration of interests KC is co-principal investigator of an investigator-initiated trial of cervical screening, Compass, run by the Australian Centre for Prevention of Cervical Cancer (ACPCC), which is a government-funded not-for-profit charity; the ACPCC has received equipment and a funding contribution from Roche Molecular Diagnostics, and operational support from the Australian Government. KC is also co-principal investigator on a major investigator-initiated implementation programme Elimination of Cervical Cancer in the Western Pacific (ECCWP) which will receive support from the Minderoo Foundation, the Frazer Family Foundation, and equipment donations from Cepheid. Neither KC nor her institution on her behalf receives direct funding from industry for any project. MC is an investigator on an investigator-initiated trial of cytology and primary human papillomavirus screening in Australia (Compass; ACTRN12613001207707 and NCT02328872), which is conducted and funded by the Australian Centre for the Prevention of Cervical Cancer, a government-funded health promotion charity. The Australian Centre for the Prevention of Cervical Cancer has received equipment and a funding contribution for the Compass trial from Roche Molecular Systems and operational support from the Australian Government. However neither MC nor his institution on his behalf (the Daffodil Centre, a joint venture between Cancer Council NSW and The University of Sydney) receive direct funding from industry for Compass Australia or any other project. All other authors declare no competing interests.

Figures

Figure 1
Figure 1
Observed and predicted overall and age-specific annual incidence and mortality rates for all cancers combined by sex for the baseline scenario, Australia All rates are age-standardised to the Segi World standard population. The points represent the observed rates. The lines with the shaded areas represent the predicted rates with uncertainty intervals from the baseline projection model. Incidence projections were based on data from 1995 onwards because data on prostate-specific antigen testing were only available from 1994 and data on breast cancer screening were only available from 1996. Log scales were used for the y axis.
Figure 2
Figure 2
Observed and predicted age-standardised annual incidence rates for 21 individual cancer types to 2044 for the baseline scenario, Australia All rates are age-standardised to the Segi World standard population. The shaded areas represent the uncertainty intervals from the baseline projection model. Incidence projections for prostate cancer, female breast cancer, and all cancers combined were based on data from 1995 onwards because data on prostate-specific antigen testing were only available from 1994 and data on breast cancer screening were only available from 1996. *Projections for colorectal cancer do not account for the completed roll-out of the Australian National Bowel Cancer Screening Program. Detailed projections for colorectal cancer based on microsimulation modelling have been published elsewhere.
Figure 3
Figure 3
Observed and predicted age-standardised annual mortality rates for 21 individual cancer types to 2044 for the baseline scenario, Australia All rates are age-standardised to the Segi World standard population. The shaded areas represent the uncertainty intervals from the baseline projection model. *Projections for colorectal cancer do not account for the completed roll-out of the Australian National Bowel Cancer Screening Program. Detailed projections for colorectal cancer based on microsimulation modelling have been published elsewhere.

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