Health-Related Quality of Life in European Childhood Cancer Survivors: Protocol for a Study Within PanCareLIFE.

Europe adolescents children epidemiology health status neoplasms quality of life survivors of childhood cancer

Journal

JMIR research protocols
ISSN: 1929-0748
Titre abrégé: JMIR Res Protoc
Pays: Canada
ID NLM: 101599504

Informations de publication

Date de publication:
25 Jan 2021
Historique:
received: 28 06 2020
accepted: 03 11 2020
revised: 13 10 2020
entrez: 25 1 2021
pubmed: 26 1 2021
medline: 26 1 2021
Statut: epublish

Résumé

Survival after childhood cancer has improved to more than 80% during the last few years, leading to an increased number of childhood cancer survivors. Cancer itself, or its treatment, may cause chronic health conditions, including somatic and mental sequelae, which may affect survivors' health-related quality of life (HRQoL). The project PanCareLIFE aims to establish a large database with comprehensive data on childhood cancer survivors from different European countries, including data on HRQoL. Within PanCareLIFE, this study aims to describe HRQoL in survivors, investigate predictors of HRQoL, and describe the association of HRQoL with hearing and female fertility impairment. This paper describes the design of the HRQoL study, the origin of data, strategies for data collection, and sampling characteristics of survivors from each contributing country. A total of 6 institutions from 5 European countries (the Czech Republic, France, Germany, the Netherlands, and Switzerland) provided data on HRQoL assessed with the Short Form 36 and on relevant predictors. The central PanCareLIFE data center aggregated the data and harmonized the variables between the institutions. Survivors were eligible if they received a diagnosis of cancer according to the 12 main groups of the International Classification of Childhood Cancer, 3rd edition, or Langerhans cell histiocytosis; were aged ≤18 years at the time of diagnosis; were residents of the respective country at the time of diagnosis; had survived ≥5 years after cancer diagnosis; were aged ≥18 years at the time of the questionnaire survey; and did not refuse to registration in the national or local childhood cancer cohort. We identified 24,993 eligible survivors. Of those, 19,268 survivors received a questionnaire and 9871 survivors participated, resulting in response rates of 9871/24,993 (39.50%) of eligible survivors and of 9871/19,268 (51.23%) invited survivors. Most participants were diagnosed with cancer between the ages of 10 and 14 years (3448/9871, 34.93%) or <5 years (3201/9871, 32.43%). The median age was 8 years. Of the 9871 participants, 3157 (31.97%) were survivors of leukemia, 2075 (21.02%) lymphoma, and 1356 (13.7%) central nervous system (CNS) tumors. Most participants (9225/9871, 93.46%) had no history of a subsequent tumor; 77.45% (7645/9871) received chemotherapy with or without other treatments. More than half (5460/9871, 55.31%) were aged 25 to 34 years at the time of the HRQoL study. Participating survivors differed from nonparticipants; participants were more often women, survivors of leukemia or lymphoma, and less frequently, survivors of CNS tumors than nonparticipants. PanCareLIFE successfully assessed HRQoL and its predictors in 9871 European survivors of childhood cancer. This large population will permit detailed investigations of HRQoL after childhood cancer, particularly the impact of hearing and female fertility impairment on HRQoL. RR1-10.2196/21851.

Sections du résumé

BACKGROUND BACKGROUND
Survival after childhood cancer has improved to more than 80% during the last few years, leading to an increased number of childhood cancer survivors. Cancer itself, or its treatment, may cause chronic health conditions, including somatic and mental sequelae, which may affect survivors' health-related quality of life (HRQoL).
OBJECTIVE OBJECTIVE
The project PanCareLIFE aims to establish a large database with comprehensive data on childhood cancer survivors from different European countries, including data on HRQoL. Within PanCareLIFE, this study aims to describe HRQoL in survivors, investigate predictors of HRQoL, and describe the association of HRQoL with hearing and female fertility impairment. This paper describes the design of the HRQoL study, the origin of data, strategies for data collection, and sampling characteristics of survivors from each contributing country.
METHODS METHODS
A total of 6 institutions from 5 European countries (the Czech Republic, France, Germany, the Netherlands, and Switzerland) provided data on HRQoL assessed with the Short Form 36 and on relevant predictors. The central PanCareLIFE data center aggregated the data and harmonized the variables between the institutions. Survivors were eligible if they received a diagnosis of cancer according to the 12 main groups of the International Classification of Childhood Cancer, 3rd edition, or Langerhans cell histiocytosis; were aged ≤18 years at the time of diagnosis; were residents of the respective country at the time of diagnosis; had survived ≥5 years after cancer diagnosis; were aged ≥18 years at the time of the questionnaire survey; and did not refuse to registration in the national or local childhood cancer cohort.
RESULTS RESULTS
We identified 24,993 eligible survivors. Of those, 19,268 survivors received a questionnaire and 9871 survivors participated, resulting in response rates of 9871/24,993 (39.50%) of eligible survivors and of 9871/19,268 (51.23%) invited survivors. Most participants were diagnosed with cancer between the ages of 10 and 14 years (3448/9871, 34.93%) or <5 years (3201/9871, 32.43%). The median age was 8 years. Of the 9871 participants, 3157 (31.97%) were survivors of leukemia, 2075 (21.02%) lymphoma, and 1356 (13.7%) central nervous system (CNS) tumors. Most participants (9225/9871, 93.46%) had no history of a subsequent tumor; 77.45% (7645/9871) received chemotherapy with or without other treatments. More than half (5460/9871, 55.31%) were aged 25 to 34 years at the time of the HRQoL study. Participating survivors differed from nonparticipants; participants were more often women, survivors of leukemia or lymphoma, and less frequently, survivors of CNS tumors than nonparticipants.
CONCLUSIONS CONCLUSIONS
PanCareLIFE successfully assessed HRQoL and its predictors in 9871 European survivors of childhood cancer. This large population will permit detailed investigations of HRQoL after childhood cancer, particularly the impact of hearing and female fertility impairment on HRQoL.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID) UNASSIGNED
RR1-10.2196/21851.

Identifiants

pubmed: 33492237
pii: v10i1e21851
doi: 10.2196/21851
pmc: PMC7870350
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e21851

Informations de copyright

©Gabriele Calaminus, Katja Baust, Claire Berger, Julianne Byrne, Harald Binder, Leonie Casagranda, Desiree Grabow, Martha Grootenhuis, Peter Kaatsch, Melanie Kaiser, Tomas Kepak, Kateřina Kepáková, Leontien C M Kremer, Jarmila Kruseova, Ales Luks, Claudia Spix, Marleen van den Berg, Marry M M van den Heuvel-Eibrink, Eline van Dulmen-den Broeder, Rahel Kuonen, Grit Sommer, Claudia Kuehni. Originally published in JMIR Research Protocols (http://www.researchprotocols.org), 25.01.2021.

Références

JAMA. 2013 Jun 12;309(22):2371-2381
pubmed: 23757085
Klin Padiatr. 2011 May;223(3):159-64
pubmed: 21472636
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2013 May;56(5-6):643-9
pubmed: 23703481
Eur J Cancer. 2019 Jan;107:153-163
pubmed: 30576971
Cancer. 2005 Apr 1;103(7):1457-67
pubmed: 15712273
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2012 Jun;55(6-7):843-51
pubmed: 22736166
Int J Epidemiol. 2012 Dec;41(6):1553-64
pubmed: 22736394
Stroke. 1993 Feb;24(2):320-7
pubmed: 8421836
Lancet Oncol. 2014 Jan;15(1):35-47
pubmed: 24314616
J Adolesc Young Adult Oncol. 2018 Aug;7(4):415-423
pubmed: 29851372
Swiss Med Wkly. 2015 Dec 23;145:w14225
pubmed: 26700416
Lancet. 2017 Dec 9;390(10112):2569-2582
pubmed: 28890157
J Clin Oncol. 2017 Jul 10;35(20):2288-2298
pubmed: 28530852
JAMA. 2003 Sep 24;290(12):1583-92
pubmed: 14506117
Gesundheitswesen. 1999 Dec;61 Spec No:S184-90
pubmed: 10726419
Qual Life Res. 2019 Jul;28(7):1963-1977
pubmed: 30848444
Int J Cancer. 2007 Aug 1;121(3):633-40
pubmed: 17405119
Pediatr Blood Cancer. 2011 Apr;56(4):532-43
pubmed: 21298737
J Clin Epidemiol. 1998 Nov;51(11):903-12
pubmed: 9817107
JMIR Res Protoc. 2018 Sep 14;7(9):e10824
pubmed: 30215599
J Cancer Surviv. 2013 Dec;7(4):511-22
pubmed: 23784593
Psychooncology. 2004 Dec;13(12):867-81
pubmed: 15386796
Int J Cancer. 2018 Sep 15;143(6):1279-1286
pubmed: 29468674
Oncol Res Treat. 2020;43(3):61-69
pubmed: 31931503
Acta Oncol. 2015 May;54(5):655-68
pubmed: 25813473
Eur J Cancer. 2018 Nov;103:227-237
pubmed: 30273888

Auteurs

Gabriele Calaminus (G)

Department of Paediatric Haematology and Oncology, University Hospital Bonn, Bonn, Germany.
Department of Paediatric Haematology and Oncology, University Hospital Münster, Münster, Germany.

Katja Baust (K)

Department of Paediatric Haematology and Oncology, University Hospital Bonn, Bonn, Germany.

Claire Berger (C)

Department of Paediatric Hematology and Oncology Unit, University Hospital of Saint-Étienne, Saint-Étienne, France.

Julianne Byrne (J)

Boyne Research Institute, Drogheda, Ireland.

Harald Binder (H)

Institute of Medical Biometry and Statistics, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.

Leonie Casagranda (L)

Department of Paediatric Hematology and Oncology Unit, University Hospital of Saint-Étienne, Saint-Étienne, France.
Host Research Team EA4607 SNA-EPIS (Autonomic Nervous System, Epidemiology, Physiology, Exercise, and Health), Jean Monnet University of Saint-Etienne, PRES (Education and Research Cluster) Lyon, St. Etienne, France.

Desiree Grabow (D)

Division of Childhood Cancer Epidemiology, German Childhood Cancer Registry, Institute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Martha Grootenhuis (M)

Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.

Peter Kaatsch (P)

Division of Childhood Cancer Epidemiology, German Childhood Cancer Registry, Institute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Melanie Kaiser (M)

Division of Childhood Cancer Epidemiology, German Childhood Cancer Registry, Institute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Tomas Kepak (T)

University Hospital Brno, Masaryk University, Brno, Czech Republic.
International Clinical Research Center (FNUSA-ICRC), Masaryk University, Brno, Czech Republic.

Kateřina Kepáková (K)

University Hospital Brno, Masaryk University, Brno, Czech Republic.

Leontien C M Kremer (LCM)

Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
DCOG LATER, Utrecht, Netherlands.

Jarmila Kruseova (J)

Department of Paediatric Haematology/Oncology, Second Faculty of Medicine, Charles University, Prague, Czech Republic.

Ales Luks (A)

Department of Paediatric Haematology/Oncology, Second Faculty of Medicine, Charles University, Prague, Czech Republic.

Claudia Spix (C)

Division of Childhood Cancer Epidemiology, German Childhood Cancer Registry, Institute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.

Marleen van den Berg (M)

Department of Paediatric Oncology, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.

Marry M M van den Heuvel-Eibrink (MMM)

Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
DCOG LATER, Utrecht, Netherlands.
Sophias Childrens Hospital, Erasmus MC, Rotterdam, Netherlands.

Eline van Dulmen-den Broeder (E)

Department of Paediatric Oncology, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.

Rahel Kuonen (R)

Swiss Childhood Cancer Registry, Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.

Grit Sommer (G)

Swiss Childhood Cancer Registry, Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
Pediatric Endocrinology, Diabetology and Metabolism, Department of Pediatrics, Inselspital, Bern University Hospital, Bern, Switzerland.

Claudia Kuehni (C)

Swiss Childhood Cancer Registry, Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
Pediatric Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Classifications MeSH