Governing Council GC/52/6
IARC Medium-Term Strategy and Implementation Plan for 2010–2014 Page 4
Core activities
Describing the global cancer burden
17. The Agency aims to be the definitive international point of reference for collection, quality
control, processing and statistical analysis of reliable cancer incidence, mortality, survival and
prevalence information. This is a vital function in order to provide the full range of information
needed at national and regional level to support cancer control programmes. It is recognized
that currently, for many regions and countries, very limited data are available and estimates
involve extrapolation from other geographical locations and/or by basing incidence estimates on
mortality.
18. The Agency will strengthen its efforts to expand the coverage, continuity, and quality of
cancer registration, particularly in regions where data are lacking, through provision of training,
setting standards and quality control. Where population-based cancer registration is not feasible
in the short-term, alternative approaches to exploring cancer occurrence will be developed.
Expected outcomes of this part of the strategy include an increase in the current coverage of
the world population in future volumes of Cancer Incidence in Five Continents (CI5C);
establishment of regional reference centres for cancer registration in Africa, Asia and Latin
America; provision of structured training programmes in cancer registration and new estimates
of the global cancer burden with forward projections. These activities will also provide a
platform for studies of cancer risk factors and a basis for preventive interventions and targeted
screening programmes.
19. It is increasingly recognized that a full understanding of cancer trends within a population
requires information on survival and prevalence alongside incidence and mortality estimates.
Accordingly the Agency will seek to expand its inclusion of these metrics in its publications and
participate in relevant international collaborations (EUROCARE, CONCORD, Cancer Survival in
Developing Countries) and also play a role in methodological development.
20. Improved accessibility to the information generated will be a further priority, including
increasing the use of electronic provision. Specifically the strategy foresees the release on the
IARC website, with a user-friendly interface, of CI5C as well as Childhood Cancer volume 3. The
Agency will continue to provide the focus for the International Association of Cancer Registries
and the European Network of Cancer Registries and seek to integrate its activities with other
regional and multi-national cancer registry networks. The WHO, the Clearing House for a broad
range of international health statistics, is also engaged in estimating the global burden of
disease. IARC and WHO will, therefore, work together to improve the quality and consistency of
their methods for generating disease burden estimates.
21. The
WHO Classification of Tumours
series (WHO “Blue Books”) is vital in terms of
standard-setting for cancer registration and hence the quality and utility of data obtained from
cancer registries. The Blue Books are also of great importance in disease classification in clinical
practice. The series is remarkable for the contribution it has made improving the standardization
of the histological classification of tumours. IARC has been responsible for the “Blue Books”
since the 3rd edition and the Agency will now place priority on providing support to increase the
rate of production of the 4th series.