Literature DB >> 31132742

The European study on centralisation of childhood cancer treatment.

G Gatta1, L Botta2, H Comber3, N Dimitrova4, M K Leinonen5, K Pritchard-Jones6, S Siesling7, A Trama2, L Van Eycken8, J M van der Zwan7, O Visser7, T Zagar9, R Capocaccia10.   

Abstract

BACKGROUND: It is generally agreed to centralise treatment of childhood cancers (CCs). We analysed (1) the degree of centralisation of CCs in European countries and 2) the relations between centralisation and survival. PATIENTS AND METHODS: The analysis comprised 4415 CCs, diagnosed between 2000 and 2007 and followed up to the end of 2013, from Belgium, Bulgaria, Finland, Ireland, the Netherlands and Slovenia. All these countries had national population-based cancer registries and were able to provide information on diagnosis, treatment, treatment hospitals, and survival. Each case was then classified according to whether the patient was treated in a high- or a low-volume hospital among those providing CC treatment. A Cox proportional hazard model was used to calculate the relation between volume category and five-year survival, adjusting by age, sex and diagnostic group.
RESULTS: The number of hospitals providing treatment for CCs ranged from six (Slovenia) to slightly more than 40 (the Netherlands and Belgium). We identified a single higher volume hospital in Ireland and in Slovenia, treating 80% and 97% of cases, respectively, and three to five major hospitals in the other countries, treating between 65% and 93% of cases. Outcome was significantly better when primary treatment was given in high-volume hospitals compared to low-volume hospitals for central nervous system tumours (relative risk [RR] = 0.71), haematologic tumours (RR = 0.74) and for all CC combined (RR = 0.83).
CONCLUSION: Treatment centralisation is associated with survival benefits and should be further strengthened in these countries. New plans for centralisation should include ongoing evaluation.
Copyright © 2019 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Centralised treatment; Childhood cancers; Hospital; Rare cancers; Survival

Mesh:

Year:  2019        PMID: 31132742     DOI: 10.1016/j.ejca.2019.04.024

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


  2 in total

1.  Variability of Care and Access to Transplantation for Children with Biliary Atresia Who Need a Liver Replacement.

Authors:  Jean de Ville de Goyet; Toni Illhardt; Christophe Chardot; Peace N Dike; Ulrich Baumann; Katherine Brandt; Barbara E Wildhaber; Mikko Pakarinen; Fabrizio di Francesco; Ekkehard Sturm; Marianna Cornet; Caroline Lemoine; Eva Doreen Pfister; Ana M Calinescu; Maria Hukkinen; Sanjiv Harpavat; Fabio Tuzzolino; Riccardo Superina
Journal:  J Clin Med       Date:  2022-04-12       Impact factor: 4.964

2.  The impact of a supranetwork multidisciplinary team (SMDT) on decision-making in testicular cancers: a 10-year overview of the Anglian Germ Cell Cancer Collaborative Group (AGCCCG).

Authors:  Daniel Berney; Anju Sahdev; Jonathan Shamash; Wendy Ansell; Constantine Alifrangis; Benjamin Thomas; Peter Wilson; Sara Stoneham; Danish Mazhar; Anne Warren; Tristan Barrett; Susanna Alexander; Sarah Rudman; Michelle Lockley
Journal:  Br J Cancer       Date:  2020-09-29       Impact factor: 7.640

  2 in total

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