International variations in childhood cancer in indigenous populations: a systematic review.
Identifieur interne : 003936 ( PubMed/Corpus ); précédent : 003935; suivant : 003937International variations in childhood cancer in indigenous populations: a systematic review.
Auteurs : Patricia C. Valery ; Suzanne P. Moore ; Judith Meiklejohn ; Freddie BraySource :
- The Lancet. Oncology [ 1474-5488 ] ; 2014.
English descriptors
- KwdEn :
- Adolescent, Age of Onset, Child, Child Mortality, Child, Preschool, Continental Population Groups (statistics & numerical data), Ethnic Groups (statistics & numerical data), Health Status Disparities, Healthcare Disparities (ethnology), Humans, Incidence, Infant, Infant, Newborn, Neoplasms (ethnology), Neoplasms (mortality), Neoplasms (pathology), Neoplasms (therapy), Prognosis, Residence Characteristics, Risk Assessment, Risk Factors, Survival Analysis, Survival Rate, Time Factors.
- MESH :
- ethnology : Healthcare Disparities, Neoplasms.
- mortality : Neoplasms.
- pathology : Neoplasms.
- statistics & numerical data : Continental Population Groups, Ethnic Groups.
- therapy : Neoplasms.
- Adolescent, Age of Onset, Child, Child Mortality, Child, Preschool, Health Status Disparities, Humans, Incidence, Infant, Infant, Newborn, Prognosis, Residence Characteristics, Risk Assessment, Risk Factors, Survival Analysis, Survival Rate, Time Factors.
Abstract
Although the cancer burden in indigenous children has been reported in some countries, up to now, no international comparison has been made. We therefore aimed to assess the available evidence of the burden of childhood cancer in indigenous populations. We did a systematic review of reports on cancer incidence, mortality, and survival in indigenous children worldwide. Our findings highlight the paucity of accessible information and advocate the pressing need for data by indigenous status in countries where population-based cancer registries are established. The true extent of disparities between the burden in the indigenous community needs to be measured so that targeted programmes for cancer control can be planned and implemented.
DOI: 10.1016/S1470-2045(13)70553-9
PubMed: 24480559
Links to Exploration step
pubmed:24480559Le document en format XML
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<author><name sortKey="Valery, Patricia C" sort="Valery, Patricia C" uniqKey="Valery P" first="Patricia C" last="Valery">Patricia C. Valery</name>
<affiliation><nlm:affiliation>Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia; Section of Cancer Information, International Agency for Research on Cancer, Lyon, France. Electronic address: Patricia.Valery@menzies.edu.au.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Moore, Suzanne P" sort="Moore, Suzanne P" uniqKey="Moore S" first="Suzanne P" last="Moore">Suzanne P. Moore</name>
<affiliation><nlm:affiliation>Section of Cancer Information, International Agency for Research on Cancer, Lyon, France.</nlm:affiliation>
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<author><name sortKey="Meiklejohn, Judith" sort="Meiklejohn, Judith" uniqKey="Meiklejohn J" first="Judith" last="Meiklejohn">Judith Meiklejohn</name>
<affiliation><nlm:affiliation>Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia.</nlm:affiliation>
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<author><name sortKey="Bray, Freddie" sort="Bray, Freddie" uniqKey="Bray F" first="Freddie" last="Bray">Freddie Bray</name>
<affiliation><nlm:affiliation>Section of Cancer Information, International Agency for Research on Cancer, Lyon, France.</nlm:affiliation>
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<author><name sortKey="Moore, Suzanne P" sort="Moore, Suzanne P" uniqKey="Moore S" first="Suzanne P" last="Moore">Suzanne P. Moore</name>
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<author><name sortKey="Bray, Freddie" sort="Bray, Freddie" uniqKey="Bray F" first="Freddie" last="Bray">Freddie Bray</name>
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<series><title level="j">The Lancet. Oncology</title>
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<term>Continental Population Groups (statistics & numerical data)</term>
<term>Ethnic Groups (statistics & numerical data)</term>
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<term>Age of Onset</term>
<term>Child</term>
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<term>Child, Preschool</term>
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<front><div type="abstract" xml:lang="en">Although the cancer burden in indigenous children has been reported in some countries, up to now, no international comparison has been made. We therefore aimed to assess the available evidence of the burden of childhood cancer in indigenous populations. We did a systematic review of reports on cancer incidence, mortality, and survival in indigenous children worldwide. Our findings highlight the paucity of accessible information and advocate the pressing need for data by indigenous status in countries where population-based cancer registries are established. The true extent of disparities between the burden in the indigenous community needs to be measured so that targeted programmes for cancer control can be planned and implemented.</div>
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