Quality assessment and improvement of nationwide cancer registration system in Taiwan: A review

Chun Ju Chiang, San Lin You, Chien Jen Chen, Ya Wen Yang, Wei Cheng Lo, Mei Shu Lai

Research output: Contribution to journalArticlepeer-review

195 Citations (Scopus)


Cancer registration provides core information for cancer surveillance and control. The populationbased Taiwan Cancer Registry was implemented in 1979. After the Cancer Control Act was promulgated in 2003, the completeness (97%) and data quality of cancer registry database has achieved at an excellent level. Hospitals with 50 or more beds, which provide outpatient and hospitalized cancer care, are recruited to report 20 items of information on all newly diagnosed cancers to the central registry office (called short-form database). The Taiwan Cancer Registry is organized and funded by the Ministry of Health and Welfare. The National Taiwan University has been contracted to operate the registry and organized an advisory board to standardize definitions of terminology, coding and procedures of the registry's reporting system since 1996. To monitor the cancer care patterns and evaluate the cancer treatment outcomes, central cancer registry has been reformed since 2002 to include detail items of the stage at diagnosis and the first course of treatment (called long-form database). There are 80 hospitals, which count for >90% of total cancer cases, involved in the long-form registration. The Taiwan Cancer Registry has run smoothly for >30 years, which provides essential foundation for academic research and cancer control policy in Taiwan.

Original languageEnglish
Article numberhyu211
Pages (from-to)291-296
Number of pages6
JournalJapanese Journal of Clinical Oncology
Issue number3
Publication statusPublished - Mar 1 2015
Externally publishedYes


  • Cancer registry
  • Data quality
  • Population-based system
  • Taiwan

ASJC Scopus subject areas

  • Oncology
  • Radiology Nuclear Medicine and imaging
  • Cancer Research


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