Cover Page Contents Foreword Chapter 1. Introduction Chapter 2. History of cancer registration Chapter 3. Purposes and uses of cancer registration Chapter 4. Planning a cancer registry Chapter 5. Data sources and reporting Chapter 6. Items of patient information which may be collected by registries Chapter 7. Classification and coding of neoplasms Chapter 8. Manual and computerized cancer registries Chapter 9. Quality and quality control Chapter 10. Reporting of results Chapter 11. Statistical methods for registries Chapter 12. Analysis of survival Chapter 13. The hospital-based cancer registry Chapter 14. Cancer registration in developing countries Chapter 15. Cancer registration: legal aspects and confidentiality Appendix 1. United Nations Standard Country Codes Appendix 2. Editing for consistency of data items
Appendix 3. 3A - The Danish Cancer Registry, a self-reporting national cancer registration system with elements of active data collection 3B - The Thames Cancer Registry 3C - Cancer registration in Ontario 3D - The Department of Health-Rizal Cancer Registry Appendix 4. CANREG: Cancer registration software for microcomputers References Index
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