TY - JOUR
T1 - Estimating complete cancer prevalence in Europe: validity of alternative vs standard completeness indexes
AU - Demuru, Elena
AU - the EUROCARE-6 Working Group
AU - Rossi, Silvia
AU - Ventura, Leonardo
AU - Dal Maso, Luigino
AU - Guzzinati, Stefano
AU - Katalinic, Alexander
AU - Lamy, Sebastian
AU - Jooste, Valerie
AU - Di Benedetto, Corrado
AU - De Angelis, Roberta
N1 - Publisher Copyright:
Copyright © 2023 Demuru, Rossi, Ventura, Dal Maso, Guzzinati, Katalinic, Lamy, Jooste, Di Benedetto, De Angelis and the EUROCARE-6 Working Group.
PY - 2023
Y1 - 2023
N2 - IntroductionComparable 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.MethodsWithin 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.ResultsFor 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).DiscussionThese results may facilitate the dissemination of complete prevalence estimates across Europe and help bridge the current information gaps.
AB - IntroductionComparable 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.MethodsWithin 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.ResultsFor 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).DiscussionThese results may facilitate the dissemination of complete prevalence estimates across Europe and help bridge the current information gaps.
UR - http://www.scopus.com/inward/record.url?scp=85159002485&partnerID=8YFLogxK
UR - http://www.ncbi.nlm.nih.gov/pubmed/37168378
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=PMC10166634
UR - https://www.mendeley.com/catalogue/f313fa28-87b6-3eee-a466-3e0854844436/
U2 - 10.3389/fonc.2023.1114701
DO - 10.3389/fonc.2023.1114701
M3 - Journal articles
C2 - 37168378
SN - 2234-943X
VL - 13
SP - 1114701
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 1114701
ER -