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澳大利亚土著乳腺癌女性患者的预后差异:一项系统综述。

Variations in outcomes for Indigenous women with breast cancer in Australia: A systematic review.

作者信息

Dasgupta P, Baade P D, Youlden D R, Garvey G, Aitken J F, Wallington I, Chynoweth J, Zorbas H, Roder D, Youl P H

机构信息

Viertel Cancer Research Centre, Cancer Council Queensland, Brisbane, Australia.

School of Mathematical Sciences, Queensland University of Technology, Brisbane, QLD, Australia.

出版信息

Eur J Cancer Care (Engl). 2017 Nov;26(6). doi: 10.1111/ecc.12662. Epub 2017 Feb 10.

DOI:10.1111/ecc.12662
PMID:28186346
Abstract

This systematic review examines variations in outcomes along the breast cancer continuum for Australian women by Indigenous status. Multiple databases were systematically searched for peer-reviewed articles published from 1 January 1990 to 1 March 2015 focussing on adult female breast cancer patients in Australia and assessing survival, patient and tumour characteristics, diagnosis and treatment by Indigenous status. Sixteen quantitative studies were included with 12 rated high, 3 moderate and 1 as low quality. No eligible studies on referral, treatment choices, completion or follow-up were retrieved. Indigenous women had poorer survival most likely reflecting geographical isolation, advanced disease, patterns of care, comorbidities and disadvantage. They were also more likely to be diagnosed when younger, have advanced disease or comorbidities, reside in disadvantaged or remote areas, and less likely to undergo mammographic screening or surgery. Despite wide heterogeneity across studies, an overall pattern of poorer survival for Indigenous women and variations along the breast cancer continuum of care was evident. The predominance of state-specific studies and small numbers of included Indigenous women made forming a national perspective difficult. The review highlighted the need to improve Indigenous identification in cancer registries and administrative databases and identified key gaps notably the lack of qualitative studies in current literature.

摘要

本系统评价研究了澳大利亚女性乳腺癌患者在整个病程中因原住民身份而产生的结局差异。系统检索了多个数据库,以查找1990年1月1日至2015年3月1日发表的同行评审文章,重点关注澳大利亚成年女性乳腺癌患者,并按原住民身份评估生存情况、患者和肿瘤特征、诊断及治疗情况。纳入了16项定量研究,其中12项质量评级为高,3项为中等,1项为低。未检索到关于转诊、治疗选择、治疗完成情况或随访的符合条件的研究。原住民女性的生存情况较差,这很可能反映了地理隔离、疾病进展、护理模式、合并症和不利条件。她们也更有可能在年轻时被诊断出患有癌症,患有晚期疾病或合并症,居住在条件不利或偏远的地区,并且接受乳房X光筛查或手术的可能性较小。尽管各研究之间存在很大异质性,但原住民女性生存情况较差以及在乳腺癌连续护理过程中存在差异的总体模式是明显的。以州为特定对象的研究占主导地位且纳入的原住民女性数量较少,这使得难以形成全国性的观点。该评价强调了改善癌症登记处和行政数据库中原住民身份识别的必要性,并指出了关键差距,特别是当前文献中缺乏定性研究。

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