Childhood and adolescent cancer in Germany - an overview.

ADOLESCENTS CANCER CHILDREN EPIDEMIOLOGY GERMANY LONG-TERM FOLLOW-UP PROGNOSIS

Journal

Journal of health monitoring
ISSN: 2511-2708
Titre abrégé: J Health Monit
Pays: Germany
ID NLM: 101757730

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 15 12 2022
accepted: 21 03 2023
medline: 6 7 2023
pubmed: 6 7 2023
entrez: 6 7 2023
Statut: epublish

Résumé

Childhood and adolescent cancer constitutes only a very small fraction of the cancer cases in Germany and throughout the world, but it is the most frequent cause of disease-related death in children. The diagnostic spectrum differs markedly from that of adults. More than 90% of all cases of childhood and adolescent cancer in Germany are treated according to centralised protocols or in therapy studies. The main epidemiological data for this group are collected by the German Childhood Cancer Registry (GCCR) since 1980. Based on this data, three typical diagnoses and their incidence and prognosis are described in exemplary manner: Lymphoid leukaemia (LL), astrocytoma and neuroblastoma. Approximately 2,250 new cancers are diagnosed in children and adolescents under the age of 18 in Germany every year. In this age group, leukaemia and lymphoma account for almost 50% of all new cancer cases, predominately acute forms. Overall, the prognosis is considerably better than in adults. There is relatively little consistent evidence available on external factors as risk factors for childhood cancer, despite decades of research. For LL, the immune system and infections are assumed to play a role, as early training of the immune system appears to be protective. To an increasing degree, research is identifying genetic risk factors for many types of childhood and adolescent cancer. The therapy is sometimes very intensive and leads to a variety of late effects for at least 75% of the survivors, which may occur soon after the primary diagnosis, but also decades later.

Sections du résumé

Background UNASSIGNED
Childhood and adolescent cancer constitutes only a very small fraction of the cancer cases in Germany and throughout the world, but it is the most frequent cause of disease-related death in children. The diagnostic spectrum differs markedly from that of adults. More than 90% of all cases of childhood and adolescent cancer in Germany are treated according to centralised protocols or in therapy studies.
Methods UNASSIGNED
The main epidemiological data for this group are collected by the German Childhood Cancer Registry (GCCR) since 1980. Based on this data, three typical diagnoses and their incidence and prognosis are described in exemplary manner: Lymphoid leukaemia (LL), astrocytoma and neuroblastoma.
Results UNASSIGNED
Approximately 2,250 new cancers are diagnosed in children and adolescents under the age of 18 in Germany every year. In this age group, leukaemia and lymphoma account for almost 50% of all new cancer cases, predominately acute forms. Overall, the prognosis is considerably better than in adults.
Conclusions UNASSIGNED
There is relatively little consistent evidence available on external factors as risk factors for childhood cancer, despite decades of research. For LL, the immune system and infections are assumed to play a role, as early training of the immune system appears to be protective. To an increasing degree, research is identifying genetic risk factors for many types of childhood and adolescent cancer. The therapy is sometimes very intensive and leads to a variety of late effects for at least 75% of the survivors, which may occur soon after the primary diagnosis, but also decades later.

Identifiants

pubmed: 37408714
doi: 10.25646/11438
pmc: PMC10318562
doi:

Types de publication

Journal Article

Langues

eng

Pagination

79-94

Informations de copyright

© Robert Koch Institute. All rights reserved unless explicitly granted.

Déclaration de conflit d'intérêts

Conflicts of Interest The authors declared no conflicts of interest.

Références

Klin Padiatr. 2009 Nov-Dec;221(6):362-8
pubmed: 19890788
Eur J Cancer. 2017 Sep;82:137-148
pubmed: 28689091
BMJ. 2016 Sep 07;354:i4567
pubmed: 27604249
Eur J Epidemiol. 2018 Mar;33(3):335-349
pubmed: 29497894
Br J Cancer. 2012 Sep 25;107(7):1163-8
pubmed: 22955857
Endocr Connect. 2022 Aug 11;11(9):
pubmed: 35900792
Am J Med Genet A. 2017 Apr;173(4):1017-1037
pubmed: 28168833
Acta Neuropathol. 2005 Jan;109(1):93-108
pubmed: 15685439
Eur J Cancer. 2013 Apr;49(6):1437-47
pubmed: 23266048
Mol Med. 2022 Sep 6;28(1):105
pubmed: 36068491
Cancer Causes Control. 2020 May;31(5):491-501
pubmed: 32144681
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2022 Apr;65(4):453-461
pubmed: 35294562
Lancet. 2004 Dec 11-17;364(9451):2097-105
pubmed: 15589307
Med Pediatr Oncol. 2002 Apr;38(4):229-39
pubmed: 11920786
Fam Cancer. 2021 Oct;20(4):263-271
pubmed: 33686467
Lancet Oncol. 2022 Dec;23(12):1525-1536
pubmed: 36400102
Am J Epidemiol. 2007 Mar 1;165(5):496-504
pubmed: 17182983
Int J Cancer. 2008 Apr 15;122(8):1859-67
pubmed: 18076067
JNCI Cancer Spectr. 2021 May 05;5(4):
pubmed: 34240006
Pediatrics. 2015 Sep;136(3):e623-32
pubmed: 26304823
J Clin Oncol. 2022 Jan 1;40(1):32-39
pubmed: 34597127
Echocardiography. 2021 Jun;38(6):951-963
pubmed: 34013999
Lancet Oncol. 2017 Jun;18(6):719-731
pubmed: 28410997
Int J Cancer. 2022 Feb 1;150(3):406-419
pubmed: 34551126
Pediatr Blood Cancer. 2013 Oct;60(10):1574-81
pubmed: 23737479
Eur J Cancer. 2015 Jul;51(10):1203-11
pubmed: 25958037
JAMA. 2010 Jul 14;304(2):172-9
pubmed: 20628130
BMJ. 2016 Sep 01;354:i4351
pubmed: 27586237
Int J Cancer. 2021 May 1;148(9):2227-2240
pubmed: 33210292
Br J Cancer. 2011 Nov 22;105(11):1783-7
pubmed: 22027710
N Engl J Med. 2002 Apr 4;346(14):1047-53
pubmed: 11932471
Cancer. 2005 Apr 1;103(7):1457-67
pubmed: 15712273
Cancer Lett. 2003 Jul 18;197(1-2):11-7
pubmed: 12880954
Stat Med. 2003 Sep 30;22(18):2877-92
pubmed: 12953286
Br J Haematol. 2004 Nov;127(3):243-63
pubmed: 15491284
Pediatr Blood Cancer. 2019 Aug;66(8):e27774
pubmed: 31033160
Cancers (Basel). 2022 Jan 13;14(2):
pubmed: 35053543
Br J Cancer. 2015 Apr 14;112(8):1392-7
pubmed: 25742478
Paediatr Drugs. 2017 Dec;19(6):577-593
pubmed: 28786082
N Engl J Med. 2002 Apr 4;346(14):1041-6
pubmed: 11932470
Lancet Oncol. 2018 Sep;19(9):1159-1169
pubmed: 30098952
Oncol Res Treat. 2020;43(3):61-69
pubmed: 31931503
J Natl Cancer Inst. 2006 Mar 15;98(6):417-20
pubmed: 16537835
BMC Health Serv Res. 2022 Sep 20;22(1):1176
pubmed: 36127717
JAMA. 2007 Jun 27;297(24):2705-15
pubmed: 17595271
Eur J Cancer. 2017 Jul;80:48-54
pubmed: 28544908
Pediatr Blood Cancer. 2018 Jan;65(1):
pubmed: 28834056
Acta Oncol. 2015 May;54(5):655-68
pubmed: 25813473
Cancer Epidemiol. 2021 Aug;73:101968
pubmed: 34174725
Cell Tissue Res. 2018 May;372(2):211-221
pubmed: 29445860
Dtsch Arztebl Int. 2018 Jun 8;115(23):385-392
pubmed: 29960606
Br J Cancer. 2020 Aug;123(4):619-623
pubmed: 32451468

Auteurs

Claudia Spix (C)

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

Friederike Erdmann (F)

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

Desiree Grabow (D)

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

Cécile Ronckers (C)

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

Classifications MeSH