Australian Cancer Database, 2016; Quality Statement
Identifying and definitional attributes
|Metadata item type:||Quality Statement|
|Quality statement summary:|
To avoid excessive repetition in this quality statement, the word ‘cancer’ is used to mean ‘cancer, excluding basal cell carcinomas of the skin and squamous cell carcinomas of the skin’. In most states and territories these two skin cancers are not notifiable diseases and are therefore not collected by cancer registries. Consequently, they are not in the scope of the Australian Cancer Database (ACD).
Summary of Key Points
All states and territories have legislation that makes cancer a notifiable disease. Various institutions such as hospitals, pathology laboratories and registries of births, deaths and marriages must report cancer cases and deaths to their jurisdictional cancer registry.
Each registry supplies incidence data annually to the AIHW under an agreement between the registries and the AIHW. These data are compiled into the ACD, the only repository of national cancer incidence data.
2016 incidence data for NT were not available for inclusion in the 2016 version of the ACD. These data have been estimated by the AIHW. As NT makes up only about 1% of Australia's population, national incidence data for 2016 are unlikely to be much affected if there are any inaccuracies in the estimates for NT.
Australian Institute of Health and Welfare (AIHW) is a major national agency set up by the Australian Government under the Australian Institute of Health and Welfare Act 1987 to provide reliable, regular and relevant information and statistics on Australia's health and welfare. It is an independent Commonwealth entity established in 1987, governed by a management Board, and accountable to the Australian Parliament through the Health Portfolio.
The AIHW aims to improve the health and wellbeing of Australians through better health and welfare information and statistics. It collects and reports information on a wide range of topics and issues, ranging from health and welfare expenditure, hospitals, disease and injury, and mental health, to ageing, homelessness, disability and child protection.
The Institute also plays a role in developing and maintaining national metadata standards. This work contributes to improving the quality and consistency of national health and welfare statistics. The Institute works closely with governments and non-government organisations to achieve greater adherence to these standards in administrative data collections to promote national consistency and comparability of data and reporting.
One of the main functions of the AIHW is to work with the states and territories to improve the quality of administrative data and, where possible, to compile national datasets based on data from each jurisdiction, to analyse these datasets and disseminate information and statistics.
The Australian Institute of Health and Welfare Act 1987, in conjunction with compliance to the Privacy Act 1988, ensures that the data collections managed by the AIHW are kept securely and under the strictest conditions with respect to privacy and confidentiality.
For further information see the AIHW website www.aihw.gov.au.
All states and territories have legislation that makes cancer a notifiable disease. Various institutions such as hospitals, pathology laboratories and registries of births, deaths and marriages must report cancer cases and deaths to their jurisdictional cancer registry. Each registry supplies incidence data annually to the AIHW under an agreement between the registries and the AIHW. These data are checked, standardised and compiled into the ACD, the only repository of national cancer incidence data. The jurisdictions retain ownership of the data and must approve any jurisdiction-level output before it is released. Jurisdictional approval is also required for national-level output if it is sufficiently fine-grained.
The AIHW has been maintaining the ACD since 1986.
This quality statement refers to the 2016 version of the ACD, which contains data on all cancer cases diagnosed between 1982 and 2016.
Each jurisdictional cancer registry supplies data annually to the AIHW. Because each jurisdiction operates on its own data compilation and reporting cycle, the ACD cannot be fully compiled until the final jurisdiction supplies its data.
It generally takes a year or more for the state and territory cancer registries to fully process and release their latest complete year of cancer data to the AIHW. Once the AIHW receives all the data from cancer registries, time is needed to check for data consistency and to de-duplicate the data before the new version of the ACD is available for reporting purposes.
The AIHW website provides cancer incidence and mortality data that can be downloaded without charge. The main online product is Cancer data in Australia. Numerous published reports, including the biennial Cancer in Australia report, are available on the AIHW website where they can also be downloaded without charge.
Users can request data not available online or in reports by lodging a customised data request here, and can ask questions via the Cancer Data and Monitoring Unit of the AIHW on (02) 6244 1000 or via email to [email protected]. Data requests are charged on a cost-recovery basis. General enquiries about AIHW publications can be made to the Website and Publishing Unit on (02) 6244 1000 or via email to [email protected].
Researchers following a cohort of people enrolled in a study of health outcomes can request the AIHW to undertake data linkage of their cohort to the ACD. Such requests must be approved by the AIHW Ethics Committee as well as the ethics committees governing access to the state and territory cancer registries.
Information on the content and scope of the ACD is available here.
While numbers of new cancers are easy to interpret, other statistics, such as age-standardised rates, are more complex and their concepts may be confusing to some users. In most cancer publications there is an appendix on statistical methods as well as technical notes. Furthermore, information on interpreting cancer data is available here.
The ACD is highly relevant for monitoring trends in cancer incidence. The data are used for many purposes, such as:
The ACD contains information on all reported cancer cases and deaths in Australia for the period 1982–2016 except for 2016 for NT and approximately 0.9% of 2016 cases for NSW (see ‘Accuracy’ section below). Data can be provided at state and territory level, though this requires approval from the state and territory cancer registries.
The 3rd edition of the International Classification of Diseases for Oncology (ICD-O-3) is used to classify cancer cases. Data can also be classified according to the tenth revision of the International Statistical Classification of Diseases and Related Health Problems (ICD-10).
The ACD contains the name, sex and date of birth of each person diagnosed with cancer. This allows researchers who have enrolled people in a study to link their cohort to the ACD in order to determine which of their study subjects have been diagnosed with cancer, which type of cancer, and when. Such data linkage can only be undertaken after receiving approvals from various ethics committees. This kind of research gives insight into cancer risk factors. Data linkage is also undertaken when a researcher has been contracted to investigate a potential cancer cluster in a workplace or small area.
The book Cancer incidence in five continents is updated about every five years in a collaborative effort between the International Agency for Research on Cancer (IARC) and the worldwide network of cancer registries. The data from each of Australia’s cancer registries are classified by IARC as ‘A’, which is the highest data quality grade in their scale. Details of IARC’s tests can be found in the above-mentioned book and the registries’ annual incidence reports.
Each year, when all the registries’ new data have been compiled into the new ACD, a data linkage process called the national de-duplication is undertaken. This process detects instances where the same person and cancer have been registered in two or more jurisdictions. This could happen, for example, when a person attends hospitals in different jurisdictions. All such instances that are found are provisionally resolved at the AIHW by removing one record while the relevant jurisdictions are notified of the situation so that they can determine in which jurisdiction the person was a usual resident at the time of diagnosis. Their resolution will flow through to the ACD in the following year’s data supply.
While all state and territory cancer registries collect information on Indigenous status, the level of identification of Indigenous Australians is not considered adequate for reporting for all jurisdictions or time periods. The data which are considered suitable for analysis are as follows: WA and NT for 1982 onwards, QLD for 1997 onwards, NSW for 1999 onwards and VIC for 2008 onwards.
2016 incidence data for NT were not available for inclusion in the 2016 version of the ACD. These data were estimated by the AIHW. As NT makes up only about 1% of Australia's population, national incidence data for 2016 are unlikely to be much affected if there are any inaccuracies in the estimates for NT.
2016 incidence data for NSW Death Certificate Only (DCO) cases are only partially complete. DCO cases contribute on average approximately 1.5% of total NSW incident cases. The proportion varies by age group and cancer type. The 2016 data for NSW include 281 DCO cases (approximately 0.6% of NSW cases, excluding DCO cases).
The 2016 ACD contains information on all reported cancer cases and deaths in Australia for the period 1982–2016 except for 2016 for NT (see ‘Accuracy’ section above).
Cancer diagnosis data are classified according to the International Classification of Diseases for Oncology (ICD-O). Sometimes updated codes are issued to align with new understandings of cancer types, and about every ten years an entirely new edition of ICD-O is issued. Updates and new editions can cause trend breaks in time series for particular cancers, but usually only at quite a fine level of detail. These trend-break issues are known to the registries and AIHW and relevant advice is provided to any client who requests data at a fine-enough level of detail for this to be a potential issue.
The data supplied annually by each cancer registry to the AIHW come from a snapshot of their database at a specific point in time. Cancer registry databases change every day, and not just because new records are added.
Existing records are changed if:
As a result of all these factors, for years prior to 2016 the number of cancer cases reported by AIHW based on the 2016 ACD may differ from the corresponding number reported based on previous versions of the ACD. Similarly, the number of cases reported by AIHW for a given jurisdiction may differ from the corresponding number published by that jurisdiction in its own reports if the numbers are derived from different snapshots of the jurisdictional database.
Source and reference attributes
Australian Institute of Health and Welfare
|Steward:||Australian Institute of Health and Welfare|
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