TY - JOUR
T1 - The survival disparity between children and adolescents and young adults (AYAs) with Ewing sarcoma in the Netherlands did not change since the 1990s despite improved survival
T2 - A population-based study
AU - Schulpen, Maya
AU - Haveman, Lianne M
AU - van der Heijden, Lizz
AU - Kaal, Suzanne E J
AU - Bramer, Jos A M
AU - Fajardo, Raquel Dávila
AU - de Haan, Jacco J
AU - Hiemcke-Jiwa, Laura S
AU - Ter Horst, Simone A J
AU - Jutte, Paul C
AU - Schreuder, Hendrik W B
AU - Tromp, Jacqueline M
AU - van der Graaf, Winette T A
AU - van de Sande, Michiel A J
AU - Gelderblom, Hans
AU - Merks, Johannes H M
AU - Karim-Kos, Henrike E
N1 - Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.
PY - 2024/1
Y1 - 2024/1
N2 - BACKGROUND: Adolescents and young adults (AYAs) with Ewing sarcoma have a worse prognosis than children. Population-based survival evaluations stratifying findings by important clinical factors are, however, limited. This Dutch population study comprehensively compared survival of children and AYAs with Ewing sarcoma over three decades considering diagnostic period, tissue of origin, tumor site, and disease stage.METHODS: Data on all children (0-17 years, N = 463) and AYAs (18-39 years, N = 379) diagnosed with Ewing sarcoma in the Netherlands between 1990-2018 were collected from the Netherlands Cancer Registry with follow-up until February 2023. Five-year relative survival was calculated using the cohort method. Multivariable analyses were conducted through Poisson regression.RESULTS: Children with Ewing sarcoma had a significantly higher 5-year relative survival than AYAs (65 % vs. 44 %). An increasing trend in survival was noted reaching 70 % in children and 53 % in AYAs in 2010-2018. Results were similar for Ewing bone sarcoma and extraosseous Ewing sarcoma. AYAs had a poorer prognosis than children for most tumor sites and regardless of disease stage. Survival probabilities were 60 % vs. 78 % for localized disease and 20 % vs. 33 % for metastatic disease. Multivariable-regression analysis, adjusted for follow-up time, diagnostic period, sex, disease stage, and tumor site, confirmed increased excess mortality among AYAs compared with children (excess HR: 1.7, 95 % CI: 1.3-2.1).CONCLUSIONS: Despite survival improvements since the 1990s, AYAs with Ewing sarcoma in the Netherlands continue to fare considerably worse than children. This survival disparity was present irrespective of tissue of origin, tumor site, and disease stage.
AB - BACKGROUND: Adolescents and young adults (AYAs) with Ewing sarcoma have a worse prognosis than children. Population-based survival evaluations stratifying findings by important clinical factors are, however, limited. This Dutch population study comprehensively compared survival of children and AYAs with Ewing sarcoma over three decades considering diagnostic period, tissue of origin, tumor site, and disease stage.METHODS: Data on all children (0-17 years, N = 463) and AYAs (18-39 years, N = 379) diagnosed with Ewing sarcoma in the Netherlands between 1990-2018 were collected from the Netherlands Cancer Registry with follow-up until February 2023. Five-year relative survival was calculated using the cohort method. Multivariable analyses were conducted through Poisson regression.RESULTS: Children with Ewing sarcoma had a significantly higher 5-year relative survival than AYAs (65 % vs. 44 %). An increasing trend in survival was noted reaching 70 % in children and 53 % in AYAs in 2010-2018. Results were similar for Ewing bone sarcoma and extraosseous Ewing sarcoma. AYAs had a poorer prognosis than children for most tumor sites and regardless of disease stage. Survival probabilities were 60 % vs. 78 % for localized disease and 20 % vs. 33 % for metastatic disease. Multivariable-regression analysis, adjusted for follow-up time, diagnostic period, sex, disease stage, and tumor site, confirmed increased excess mortality among AYAs compared with children (excess HR: 1.7, 95 % CI: 1.3-2.1).CONCLUSIONS: Despite survival improvements since the 1990s, AYAs with Ewing sarcoma in the Netherlands continue to fare considerably worse than children. This survival disparity was present irrespective of tissue of origin, tumor site, and disease stage.
KW - Humans
KW - Sarcoma, Ewing/mortality
KW - Adolescent
KW - Netherlands/epidemiology
KW - Male
KW - Female
KW - Child
KW - Young Adult
KW - Adult
KW - Child, Preschool
KW - Infant
KW - Bone Neoplasms/mortality
KW - Infant, Newborn
KW - Registries
KW - Prognosis
KW - Survival Rate
KW - Age Factors
KW - AYAs
KW - Adolescents and young adults
KW - Children
KW - Disease stage
KW - Epidemiology
KW - Ewing sarcoma
KW - Relative survival
UR - https://www.mendeley.com/catalogue/c7f1f214-523a-3083-b6e3-0afb6fa68e9f/
U2 - 10.1016/j.ejca.2024.114209
DO - 10.1016/j.ejca.2024.114209
M3 - Article
C2 - 39018631
SN - 0959-8049
VL - 208
SP - 114209
JO - European journal of cancer (Oxford, England : 1990)
JF - European journal of cancer (Oxford, England : 1990)
ER -