Childhood cancer survivor cohorts in Europe

Authors

  • Jeanette F. Winther Danish Cancer Society Research Center, Copenhagen, Denmark
  • Line Kenborg Danish Cancer Society Research Center, Copenhagen, Denmark
  • Julianne Byrne Boyne Research Institute, Drogheda, Ireland
  • Lars Hjorth Paediatric Oncology and Haematology, Skåne University Hospital, Lund University, Lund, Sweden
  • Peter Kaatsch German Childhood Cancer Registry (GCCR), Institute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center, Mainz, Germany
  • Leontien C. M. Kremer on behalf of the DCOG LATER group The Netherlands, Emma Children's Hospital/AMC, Amsterdam, VU University Medical Center, Amsterdam, EMC-Sophia Children’s Hospital, Rotterdam, Princess Maxima Center for Paediatric Oncology, Utrecht
  • Claudia E. Kuehni Swiss Childhood Cancer Registry, Institute of Social and Preventive Medicine, University of Bern, Switzerland
  • Pascal Auquier Aix-Marseille University, EA 3279 Research Unit, Department of Public Health, University Hospital, Marseille, France
  • Gérard Michel Departement of Paediatric Onco-haematology, APHM, La Timone Hospital, Marseilles, France
  • Florent de Vathaire Centre for Research in Epidemiology and Population Health (CESP), U1018 Inserm, Radiation Epidemiology Group, Villejuif, France
  • Riccardo Haupt Epidemiology and Biostatistics Unit, G. Gaslini Institute, Genoa, on behalf of the AIEOP-OTR study group, Italy
  • Roderick Skinner Department of Paediatric and Adolescent Haematology and Oncology, Great North Children's Hospital, Royal Victoria Infirmary, Newcastle Upon Tyne, UK
  • Laura M. Madanat-Harjuoja The Finnish Cancer Registry, Helsinki, Finland
  • Laufey Tryggvadottir The Icelandic Cancer Registry, Reykjavik, Iceland; Faculty of Medicine, University of Iceland, Reykjavik, Iceland
  • Finn Wesenberg Department of Paediatrics, Oslo University Hospital, Oslo, Norway; Faculty of Medicine, University of Oslo, Oslo, Norway; Norwegian Cancer Registry, Oslo, Norway
  • Raoul C. Reulen Centre for Childhood Cancer Survivor Studies, School of Health and Population Sciences, University of Birmingham, UK
  • Desiree Grabow German Childhood Cancer Registry (GCCR), Institute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center, Mainz, Germany
  • Cecile M. Ronckers on behalf of the DCOG LATER group The Netherlands, Emma Children's Hospital/AMC, Amsterdam, VU University Medical Center, Amsterdam, EMC-Sophia Children’s Hospital, Rotterdam, Princess Maxima Center for Paediatric Oncology, Utrecht
  • Eline van Dulmen-den Broeder on behalf of the DCOG LATER group The Netherlands, Emma Children's Hospital/AMC, Amsterdam, VU University Medical Center, Amsterdam, EMC-Sophia Children’s Hospital, Rotterdam, Princess Maxima Center for Paediatric Oncology, Utrecht
  • Marry M. van den Heuvel-Eibrink on behalf of the DCOG LATER group The Netherlands, Emma Children's Hospital/AMC, Amsterdam, VU University Medical Center, Amsterdam, EMC-Sophia Children’s Hospital, Rotterdam, Princess Maxima Center for Paediatric Oncology, Utrecht
  • Matthias Schindler Swiss Childhood Cancer Registry, Institute of Social and Preventive Medicine, University of Bern, Switzerland
  • Julie Berbis Aix-Marseille University, EA 3279 Research Unit, Department of Public Health, University Hospital, Marseille, France
  • Anna S. Holmqvist Paediatric Oncology and Haematology, Skåne University Hospital, Lund University, Lund, Sweden
  • Thorgerdur Gudmundsdottir Danish Cancer Society Research Center, Copenhagen, Denmark
  • Sofie de Fine Licht Danish Cancer Society Research Center, Copenhagen, Denmark
  • Trine G. Bonnesen Danish Cancer Society Research Center, Copenhagen, Denmark; Department of Paediatrics, Aarhus University Hospital, Aarhus, Denmark
  • Peter H. Asdahl Danish Cancer Society Research Center, Copenhagen, Denmark; Department of Paediatrics, Aarhus University Hospital, Aarhus, Denmark
  • Andrea Bautz Danish Cancer Society Research Center, Copenhagen, Denmark
  • Anja K. Kristoffersen Danish Cancer Society Research Center, Copenhagen, Denmark
  • Liselotte Himmerslev Danish Cancer Society Research Center, Copenhagen, Denmark
  • Henrik Hasle Department of Paediatrics, Aarhus University Hospital, Aarhus, Denmark
  • Jørgen H. Olsen Danish Cancer Society Research Center, Copenhagen, Denmark
  • Mike M. Hawkins Centre for Childhood Cancer Survivor Studies, School of Health and Population Sciences, University of Birmingham, UK

DOI:

https://doi.org/10.3109/0284186X.2015.1008648

Abstract

With the advent of multimodality therapy, the overall five-year survival rate from childhood cancer has improved considerably now exceeding 80% in developed European countries. This growing cohort of survivors, with many years of life ahead of them, has raised the necessity for knowledge concerning the risks of adverse long-term sequelae of the life-saving treatments in order to provide optimal screening and care and to identify and provide adequate interventions. Childhood cancer survivor cohorts in Europe. Considerable advantages exist to study late effects in individuals treated for childhood cancer in a European context, including the complementary advantages of large population-based cancer registries and the unrivalled opportunities to study lifetime risks, together with rich and detailed hospital-based cohorts which fill many of the gaps left by the large-scale population-based studies, such as sparse treatment information. Several large national cohorts have been established within Europe to study late effects in individuals treated for childhood cancer including the Nordic Adult Life after Childhood Cancer in Scandinavia study (ALiCCS), the British Childhood Cancer Survivor Study (BCCSS), the Dutch Childhood Oncology Group (DCOG) LATER study, and the Swiss Childhood Cancer Survivor Study (SCCSS). Furthermore, there are other large cohorts, which may eventually become national in scope including the French Childhood Cancer Survivor Study (FCCSS), the French Childhood Cancer Survivor Study for Leukaemia (LEA), and the Italian Study on off-therapy Childhood Cancer Survivors (OTR). In recent years significant steps have been taken to extend these national studies into a larger pan-European context through the establishment of two large consortia – PanCareSurFup and PanCareLIFE. The purpose of this paper is to present an overview of the current large, national and pan-European studies of late effects after childhood cancer. This overview will highlight the strong cooperation across Europe, in particular the EU-funded collaborative research projects PanCareSurFup and PanCareLIFE. Overall goal. The overall goal of these large cohort studies is to provide every European childhood cancer survivor with better care and better long-term health so that they reach their full potential, and to the degree possible, enjoy the same quality of life and opportunities as their peers.

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Published

2015-05-28

How to Cite

Winther, J. F., Kenborg, L., Byrne, J., Hjorth, L., Kaatsch, P., Kremer, L. C. M., … Hawkins, M. M. (2015). Childhood cancer survivor cohorts in Europe. Acta Oncologica, 54(5), 655–668. https://doi.org/10.3109/0284186X.2015.1008648