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Estimating complete cancer prevalence in Europe: validity of alternative vs standard completeness indexes.
Demuru, Elena; Rossi, Silvia; Ventura, Leonardo; Dal Maso, Luigino; Guzzinati, Stefano; Katalinic, Alexander; Lamy, Sebastien; Jooste, Valerie; Di Benedetto, Corrado; De Angelis, Roberta.
Afiliação
  • Demuru E; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
  • Rossi S; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
  • Ventura L; Clinical and Descriptive Epidemiology Unit, Istituto per lo Studio, la Prevenzione e la Rete Oncologica (ISPRO), Firenze, Italy.
  • Dal Maso L; Cancer Epidemiology Unit, Centro di Riferimento Oncologico (CRO), Istituto di Ricerca e Cura a Carattere Scientifico (IRCCS), Aviano, Italy.
  • Guzzinati S; Veneto Cancer Registry, Azienda Zero, Padova, Italy.
  • Katalinic A; Cancer Registry of Schleswig-Holstein, Institute for Social Medicine and Epidemiology, University of Lübeck, Lübeck, Germany.
  • Lamy S; Tarn Cancer Registry, Claudius Regaud Institute - Center for Epidemiology and Research in Population Health (CERPOP U1295), University of Toulouse - Inserm, Toulouse, France.
  • Jooste V; Digestive Cancer Registry of Burgundy, Dijon University Hospital, INSERM UMR1231, Dijon, France.
  • Di Benedetto C; IT Service, Istituto Superiore di Sanità, Rome, Italy.
  • De Angelis R; Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
Front Oncol ; 13: 1114701, 2023.
Article em En | MEDLINE | ID: mdl-37168378
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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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prevalence_studies / Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prevalence_studies / Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article