Literature DB >> 30014973

Survival and mortality rates of Wilms tumour in Southern and Eastern European countries: Socioeconomic differentials compared with the United States of America.

Dimitrios Doganis1, Paraskevi Panagopoulou2, Athanasios Tragiannidis3, Theodoros Vichos2, Maria Moschovi4, Sofia Polychronopoulou5, Efthimia Rigatou5, Eugenia Papakonstantinou6, Eftichia Stiakaki7, Helen Dana8, Panagiota Bouka2, Luis Antunes9, Joana Bastos10, Daniela Coza11, Anna Demetriou12, Domenic Agius13, Sultan Eser14, Anton Ryzhov15, Mario Sekerija16, Maciej Trojanowski17, Tina Zagar18, Anna Zborovskaya19, Snezana Zivkovic Perisic20, Katerina Strantzia21, Nick Dessypris2, Theodora Psaltopoulou2, Eleni Th Petridou22.   

Abstract

BACKGROUND: Despite recent therapeutic advancements, Wilms tumour (WT) presents remarkable survival variations. We explored mortality and survival patterns for children (0-14 years) with WT in 12 Southern and Eastern European (SEE) countries in comparison with the United States of America (USA).
METHODS: A total of 3966 WT cases (0-14 years) were registered by a network of SEE childhood cancer registries (N:1723) during available registration periods circa 1990-2016 and surveillance, epidemiology, and end results program (SEER) (N:2243; 1990-2012); mortality data were provided by the respective national statistical services. Kaplan-Meier curves and Cox proportional hazards models were used to assess the role of age, sex, year of diagnosis, urbanisation and Human Development Index (HDI) on overall survival (OS).
RESULTS: Persisting regional variations shape an overall 78% 5-year OS in the participating SEE countries, lagging behind the USA figure (92%, p=0.001) and also reflected by higher SEE mortality rates. Worth mentioning is the gradually escalating OS in SEE (hazard ratio [HR]5-year increment:0.67, 95% confidence interval [CI]:0.60, 0.75) vs. a non-significant 10% improvement in the SEER data, which had a high starting value. OS differentials [two-fold less favourable among children aged 10-14 years, boys and those living in rural SEE areas (HR:1.37; CI:1.10-1.71) or countries with inferior HDI (2-3-fold)] were minimal in the USA.
CONCLUSIONS: Children with WT residing in SEE countries do not equally enjoy the substantial survival gains, especially for those living in rural areas and in lower HDI countries. Noteworthy are steep and sizeable survival gains in SEE along with the newly presented Greek data pointing to achievable survival goals in SEE despite the financial crisis.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Healthcare access; Mortality trends; Sociodemographic differentials; Survival; Urbanisation; Wilms tumour

Mesh:

Year:  2018        PMID: 30014973     DOI: 10.1016/j.ejca.2018.06.012

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  3 in total

1.  Wilms tumour in children: 18 years of experience at Vilnius University Hospital Santaros Klinikos, Lithuania.

Authors:  Milda Rančelytė; Rolanda Nemanienė; Lina Ragelienė; Jelena Rascon
Journal:  Acta Med Litu       Date:  2019

Review 2.  Using big data in pediatric oncology: Current applications and future directions.

Authors:  Ajay Major; Suzanne M Cox; Samuel L Volchenboum
Journal:  Semin Oncol       Date:  2020-02-29       Impact factor: 5.385

Review 3.  Social determinants of health and pediatric cancer survival: A systematic review.

Authors:  Yvette H Tran; Scott L Coven; Seho Park; Eneida A Mendonca
Journal:  Pediatr Blood Cancer       Date:  2022-02-02       Impact factor: 3.838

  3 in total

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