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Survival Differences Between Males and Females Diagnosed With Childhood Cancer

BACKGROUND: Males have worse survival for childhood cancer, but whether this disparity exists among all childhood cancer types is undescribed. METHODS: We estimated sex differences in survival for 18 cancers among children (0–19 years) in Surveillance, Epidemiology, and End Results 18 (2000–2014). W...

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Autores principales: Williams, Lindsay A, Spector, Logan G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580869/
https://www.ncbi.nlm.nih.gov/pubmed/31259303
http://dx.doi.org/10.1093/jncics/pkz032
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author Williams, Lindsay A
Spector, Logan G
author_facet Williams, Lindsay A
Spector, Logan G
author_sort Williams, Lindsay A
collection PubMed
description BACKGROUND: Males have worse survival for childhood cancer, but whether this disparity exists among all childhood cancer types is undescribed. METHODS: We estimated sex differences in survival for 18 cancers among children (0–19 years) in Surveillance, Epidemiology, and End Results 18 (2000–2014). We used Kaplan-Meier survival curves (log-rank P values) to characterize sex differences in survival and Cox proportional hazards models to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for the association between sex and death for each cancer type. We used an inverse odds weighting method to determine whether the association between sex and death was mediated by stage of disease for solid tumors. RESULTS: Males had worse overall survival and a higher risk of death for acute lymphoblastic leukemia (HR = 1.24, 95% CI = 1.12 to 1.37), ependymoma (HR = 1.36, 95% CI = 1.05 to 1.77), neuroblastoma (HR = 1.28, 95% CI = 1.09 to 1.51), osteosarcoma (HR = 1.29, 95% CI = 1.08 to 1.53), thyroid carcinoma (HR = 3.25, 95% CI = 1.45 to 7.33), and malignant melanoma (HR = 1.97, 95% CI = 1.33 to 2.92) (all log-rank P values < .02). The association between sex and death was mediated by stage of disease for neuroblastoma (indirect HR = 1.12, 95% CI = 1.05 to 1.19), thyroid carcinoma (indirect HR = 1.24, 95% CI = 1.03 to 1.48), and malignant melanoma (indirect HR = 1.28, 95% CI = 1.10 to 1.49). For these six tumors, if male survival had been as good as female survival, 21% of male deaths and 13% of total deaths after these cancer diagnoses could have been avoided. CONCLUSIONS: Consideration of molecular tumor and clinical data may help identify mechanisms underlying the male excess in death after childhood cancer for the aforementioned cancers.
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spelling pubmed-65808692019-06-27 Survival Differences Between Males and Females Diagnosed With Childhood Cancer Williams, Lindsay A Spector, Logan G JNCI Cancer Spectr Article BACKGROUND: Males have worse survival for childhood cancer, but whether this disparity exists among all childhood cancer types is undescribed. METHODS: We estimated sex differences in survival for 18 cancers among children (0–19 years) in Surveillance, Epidemiology, and End Results 18 (2000–2014). We used Kaplan-Meier survival curves (log-rank P values) to characterize sex differences in survival and Cox proportional hazards models to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for the association between sex and death for each cancer type. We used an inverse odds weighting method to determine whether the association between sex and death was mediated by stage of disease for solid tumors. RESULTS: Males had worse overall survival and a higher risk of death for acute lymphoblastic leukemia (HR = 1.24, 95% CI = 1.12 to 1.37), ependymoma (HR = 1.36, 95% CI = 1.05 to 1.77), neuroblastoma (HR = 1.28, 95% CI = 1.09 to 1.51), osteosarcoma (HR = 1.29, 95% CI = 1.08 to 1.53), thyroid carcinoma (HR = 3.25, 95% CI = 1.45 to 7.33), and malignant melanoma (HR = 1.97, 95% CI = 1.33 to 2.92) (all log-rank P values < .02). The association between sex and death was mediated by stage of disease for neuroblastoma (indirect HR = 1.12, 95% CI = 1.05 to 1.19), thyroid carcinoma (indirect HR = 1.24, 95% CI = 1.03 to 1.48), and malignant melanoma (indirect HR = 1.28, 95% CI = 1.10 to 1.49). For these six tumors, if male survival had been as good as female survival, 21% of male deaths and 13% of total deaths after these cancer diagnoses could have been avoided. CONCLUSIONS: Consideration of molecular tumor and clinical data may help identify mechanisms underlying the male excess in death after childhood cancer for the aforementioned cancers. Oxford University Press 2019-05-11 /pmc/articles/PMC6580869/ /pubmed/31259303 http://dx.doi.org/10.1093/jncics/pkz032 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com.
spellingShingle Article
Williams, Lindsay A
Spector, Logan G
Survival Differences Between Males and Females Diagnosed With Childhood Cancer
title Survival Differences Between Males and Females Diagnosed With Childhood Cancer
title_full Survival Differences Between Males and Females Diagnosed With Childhood Cancer
title_fullStr Survival Differences Between Males and Females Diagnosed With Childhood Cancer
title_full_unstemmed Survival Differences Between Males and Females Diagnosed With Childhood Cancer
title_short Survival Differences Between Males and Females Diagnosed With Childhood Cancer
title_sort survival differences between males and females diagnosed with childhood cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580869/
https://www.ncbi.nlm.nih.gov/pubmed/31259303
http://dx.doi.org/10.1093/jncics/pkz032
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