AI Article Synopsis

  • There is a growing need for comparable cancer prevalence indicators in Europe to improve survivorship care planning, as current measures may be biased due to limited registration periods.
  • The study compares standard prevalence estimates with alternative methods, including empirical indices from European cancer registries and pre-calculated indices from US-SEER registries, using data from 62 registries across 27 countries.
  • Results indicate that while empirical methods yield accurate estimates for cancers commonly diagnosed in the elderly, they significantly underestimate prevalence for early-onset cancers, suggesting that SEER estimates may be more reliable for a broader range of cancer types.

Article Abstract

Introduction: Comparable indicators on complete cancer prevalence are increasingly needed in Europe to support survivorship care planning. Direct measures can be biased by limited registration time and estimates are needed to recover long term survivors. The completeness index method, based on incidence and survival modelling, is the standard most validated approach.

Methods: Within this framework, we consider two alternative approaches that do not require any direct modelling activity: i) empirical indices derived from long established European registries; ii) pre-calculated indices derived from US-SEER cancer registries. Relying on the EUROCARE-6 study dataset we compare standard vs alternative complete prevalence estimates using data from 62 registries in 27 countries by sex, cancer type and registration time.

Results: For tumours mostly diagnosed in the elderly the empirical estimates differ little from standard estimates (on average less than 5% after 10-15 years of registration), especially for low prognosis cancers. For early-onset cancers (bone, brain, cervix uteri, testis, Hodgkin disease, soft tissues) the empirical method may produce substantial underestimations of complete prevalence (up to 20%) even when based on 35-year observations. SEER estimates are comparable to the standard ones for most cancers, including many early-onset tumours, even when derived from short time series (10-15 years). Longer observations are however needed when cancer-specific incidence and prognosis differ remarkably between US and European populations (endometrium, thyroid or stomach).

Discussion: These results may facilitate the dissemination of complete prevalence estimates across Europe and help bridge the current information gaps.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166634PMC
http://dx.doi.org/10.3389/fonc.2023.1114701DOI Listing

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