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Family history of cancer in children and adolescents with germ cell tumours: a report from the Children’s Oncology Group
BACKGROUND: Studies of family history of cancer in paediatric germ cell tumours (GCTs) are few, and none has had sufficient sample size to specifically evaluate family history of GCT. METHODS: We utilised family history data from a paediatric GCT study to calculate standardised incidence ratios (SIR...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765220/ https://www.ncbi.nlm.nih.gov/pubmed/29065103 http://dx.doi.org/10.1038/bjc.2017.358 |
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author | Poynter, Jenny N Richardson, Michaela Roesler, Michelle Krailo, Mark Amatruda, James F Frazier, A Lindsay |
author_facet | Poynter, Jenny N Richardson, Michaela Roesler, Michelle Krailo, Mark Amatruda, James F Frazier, A Lindsay |
author_sort | Poynter, Jenny N |
collection | PubMed |
description | BACKGROUND: Studies of family history of cancer in paediatric germ cell tumours (GCTs) are few, and none has had sufficient sample size to specifically evaluate family history of GCT. METHODS: We utilised family history data from a paediatric GCT study to calculate standardised incidence ratios (SIR) for GCT and other cancers using age- and sex-specific incidence rates from the SEER Program. RESULTS: This analysis included 7998 relatives of paediatric GCT probands. We observed a higher number of GCT cases than expected in male and female relatives of probands (SIR=2.38, 95% CI 1.25, 3.51 for males; SIR=14.3, 95% CI 0.29, 28.4 for females). Further, we observed a particularly strong SIR for relatives of probands with intracranial GCT (SIR=8.07, 95% CI 3.51, 12.6). The SIR for relatives of probands with ovarian GCT was also elevated but did not reach statistical significance (SIR 4.35, 95% CI 0-9.27). Other notable associations include elevated SIRs for melanoma in male relatives and reduced SIRs for lymphatic/haematologic malignancies in male and female relatives. CONCLUSIONS: These results support the hypothesis that familial aggregation of GCT occurs in males and females. |
format | Online Article Text |
id | pubmed-5765220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-57652202019-01-01 Family history of cancer in children and adolescents with germ cell tumours: a report from the Children’s Oncology Group Poynter, Jenny N Richardson, Michaela Roesler, Michelle Krailo, Mark Amatruda, James F Frazier, A Lindsay Br J Cancer Epidemiology BACKGROUND: Studies of family history of cancer in paediatric germ cell tumours (GCTs) are few, and none has had sufficient sample size to specifically evaluate family history of GCT. METHODS: We utilised family history data from a paediatric GCT study to calculate standardised incidence ratios (SIR) for GCT and other cancers using age- and sex-specific incidence rates from the SEER Program. RESULTS: This analysis included 7998 relatives of paediatric GCT probands. We observed a higher number of GCT cases than expected in male and female relatives of probands (SIR=2.38, 95% CI 1.25, 3.51 for males; SIR=14.3, 95% CI 0.29, 28.4 for females). Further, we observed a particularly strong SIR for relatives of probands with intracranial GCT (SIR=8.07, 95% CI 3.51, 12.6). The SIR for relatives of probands with ovarian GCT was also elevated but did not reach statistical significance (SIR 4.35, 95% CI 0-9.27). Other notable associations include elevated SIRs for melanoma in male relatives and reduced SIRs for lymphatic/haematologic malignancies in male and female relatives. CONCLUSIONS: These results support the hypothesis that familial aggregation of GCT occurs in males and females. Nature Publishing Group 2018-01 2017-10-24 /pmc/articles/PMC5765220/ /pubmed/29065103 http://dx.doi.org/10.1038/bjc.2017.358 Text en Copyright © 2018 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Epidemiology Poynter, Jenny N Richardson, Michaela Roesler, Michelle Krailo, Mark Amatruda, James F Frazier, A Lindsay Family history of cancer in children and adolescents with germ cell tumours: a report from the Children’s Oncology Group |
title | Family history of cancer in children and adolescents with germ cell tumours: a report from the Children’s Oncology Group |
title_full | Family history of cancer in children and adolescents with germ cell tumours: a report from the Children’s Oncology Group |
title_fullStr | Family history of cancer in children and adolescents with germ cell tumours: a report from the Children’s Oncology Group |
title_full_unstemmed | Family history of cancer in children and adolescents with germ cell tumours: a report from the Children’s Oncology Group |
title_short | Family history of cancer in children and adolescents with germ cell tumours: a report from the Children’s Oncology Group |
title_sort | family history of cancer in children and adolescents with germ cell tumours: a report from the children’s oncology group |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765220/ https://www.ncbi.nlm.nih.gov/pubmed/29065103 http://dx.doi.org/10.1038/bjc.2017.358 |
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