第一民族澳大利亚人癌症诊断后的放射治疗和初始治疗时间:基于人群的分析结果

IF 3.2 3区 医学 Q2 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Sewunet Admasu Belachew, Ming Li, Shafkat Jahan, Siddhartha Baxi, Joan Cunningham, Kalinda E Griffiths, Gail Garvey
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引用次数: 0

摘要

背景:土著澳大利亚人患癌症的几率比其他澳大利亚人低。这可归因于多方面因素,包括在获得癌症服务和治疗方面的差异。放射治疗(RT)是癌症治疗的重要组成部分,但其在澳大利亚原住民中使用的证据有限。我们的目的是检查在澳大利亚昆士兰州被诊断为癌症的第一民族的放疗利用、治疗时间和相关因素。方法:使用癌症CostMod数据集确定2011年7月1日至2015年6月30日期间诊断为任何癌症的原住民昆士兰人(N = 1884)和其他昆士兰人(N = 104,204),以及2011年7月1日至2018年6月30日期间的RT详细信息,该数据集包括与昆士兰医院入院患者数据收集(QHAPDC)和医疗保险福利计划(MBS)相关的昆士兰癌症注册数据。分析仅限于与MBS和/或QHAPDC记录相关的非失踪土著身份(N = 105,983)。使用逻辑回归、非参数检验和分位数回归检验了原住民身份在RT利用和等待时间方面的差异。结果:在昆士兰州确诊的105,983例癌症患者中,有28.6%接受了放疗,其中外束放疗(EBRT)为主要类型(n = 29,387, 96.9%)。三分之一(33.5%)的原住民癌症患者至少接受过一次放射治疗,而其他昆士兰癌症患者的这一比例为28.5% (P结论:原住民癌症患者接受放射治疗的比例高于其他昆士兰癌症患者,特别是在诊断后的第一年。然而,所有癌症患者的放疗利用率(28.6%)明显低于48%的国家最佳放疗(EBRT)率。这一发现强调了放疗需要与最佳护理标准保持一致,这对改善癌症预后至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Radiotherapy and time to initial treatment following a cancer diagnosis among First Nations Australians: results from a population-based analysis.

Radiotherapy and time to initial treatment following a cancer diagnosis among First Nations Australians: results from a population-based analysis.

Radiotherapy and time to initial treatment following a cancer diagnosis among First Nations Australians: results from a population-based analysis.

Background: First Nations Australians experience poorer cancer outcomes than other Australians. This is attributable to multidimensional factors, including disparities in access to cancer services and treatments. Radiotherapy (RT) is an important component of cancer treatment yet evidence of its utilisation among First Nations Australians is limited. We aimed to examine RT utilisation, time to the treatment, and associated factors in First Nations Peoples diagnosed with cancer in Queensland, Australia.

Methods: First Nations Queenslanders (N = 1884) and other Queenslanders (N = 104,204) diagnosed with any cancer between 1st July 2011 and 30th June 2015 and their RT details between 1st July 2011 and 30th June 2018 were identified using the Cancer CostMod dataset, comprising Queensland Cancer Registry data linked with Queensland Hospital Admitted Patient Data Collection (QHAPDC) and Medicare Benefits Schedule (MBS). Analysis was limited to those with non-missing Indigenous status who linked to MBS and/or QHAPDC records (N = 105, 983). Differences in RT utilisation and waiting times by First Nations status were tested using logistic regressions, non-parametric tests, and quantile regression.

Results: Among 105, 983 people with a cancer diagnosis in Queensland, 28.6% had RT, with external Beam RT(EBRT) as the predominant type (n = 29,387, 96.9%). One-third (33.5%) of First Nations cancer patients received RT at least once, compared to 28.5% of other Queensland cancer patients (P < 0.001). After adjustment for covariates, First Nations cancer patients had a greater likelihood of RT utilisation than other Queenslanders (adjusted odds ratio(aOR): 1.15; 95% (confidence-interval (CI): 1.04-1.27) and more pronounced within the first year after diagnosis (aOR: 1.23: 95% CI:1.11-1.37). Among those receiving any RT, the median time from cancer diagnosis to first RT was 118 days (Interquartile-range (IQR): 55-232) for First Nations and 132 days (IQR: 59-258) for other Queenslanders (P = 0.034).

Conclusions: A higher proportion of First Nations cancer patients received RT than other Queensland cancer patients, particularly in the first year following diagnosis. However, RT utilisation for all cancer patients was notably lower (28.6%) than the national optimal RT(EBRT) rate of 48%. This finding highlights the need for RT to align with optimal care standards, which is crucial for improving cancer outcomes.

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来源期刊
Archives of Public Health
Archives of Public Health Medicine-Public Health, Environmental and Occupational Health
CiteScore
4.80
自引率
3.00%
发文量
244
审稿时长
16 weeks
期刊介绍: rchives of Public Health is a broad scope public health journal, dedicated to publishing all sound science in the field of public health. The journal aims to better the understanding of the health of populations. The journal contributes to public health knowledge, enhances the interaction between research, policy and practice and stimulates public health monitoring and indicator development. The journal considers submissions on health outcomes and their determinants, with clear statements about the public health and policy implications. Archives of Public Health welcomes methodological papers (e.g., on study design and bias), papers on health services research, health economics, community interventions, and epidemiological studies dealing with international comparisons, the determinants of inequality in health, and the environmental, behavioural, social, demographic and occupational correlates of health and diseases.
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