ArticleFrontiers in oncology2023
Estimating complete cancer prevalence in Europe: validity of alternative vs standard completeness indexes.
Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.
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Who cites it
7 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.
- Evaluation and forecasting methods to estimate number of patients with non-Hodgkin lymphoma: a systematic literature review.Population health metrics · 2025Pooled it
- EndoCompass Project: Research Roadmap for Thyroid Endocrinology.Hormone research in paediatrics · 2025Review
- Low Incidence of Cancer Recorded in the Galapagos Archipelago.Cancer reports (Hoboken, N.J.) · 2024Article
- Patients with cancer who will be cured and projections of complete prevalence in Italy from 2018 to 2030.ESMO open · 2024Article
- Facing further challenges in cancer data quality and harmonisation.Frontiers in oncology · 2024Article
- New Copper Complexes with Antibacterial and Cytotoxic Activity.International journal of molecular sciences · 2023Article
- Complete prevalence and indicators of cancer cure: enhanced methods and validation in Italian population-based cancer registries.Frontiers in oncology · 2023Article
Corrections and comments
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Authors and funding
11 authors at 7 institutions in 3 countries.
Funding
No grant is acknowledged in the PubMed record.
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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