Perelini Olivia M, Nosa Vili H, Wilson Michelle K, Lawrence Nicola J, McNeill Rob B, Wilson Sheridan
Auckland Regional Cancer and Blood Service, Te Toka Tumai Auckland, Health New Zealand, Te Whatu Ora, Auckland, New Zealand.
University of Auckland, Auckland, New Zealand.
JCO Glob Oncol. 2025 Jan;11:e2400133. doi: 10.1200/GO.24.00133. Epub 2025 Jan 3.
In Aotearoa New Zealand, there are inequitable outcomes for Pacific peoples who experience higher rates of preventable cancers and poorer survival compared with other ethnicities. The aim of this study was to explore Pacific peoples lived experience of cancer and its treatment in the Auckland setting.
Data were collected through semistructured interviews (talanoa) with Pacific patients under the Auckland Regional Cancer and Blood Service. A general inductive approach was used to analyze the data. Ethical approval was granted by the Auckland Health Research Ethics Committee (reference number AH24086).
Thirteen participants of Samoan and Tongan ethnicity were interviewed. Participants had a range of tumor diagnoses and were receiving curative and noncurative treatments. Five key themes were identified, giving insight into beliefs around cancer, struggles faced by patients, and potential areas of priority. These include (1) cancer means death, (2) holistic and collective approach to support, (3) communication and trust, (4) cost in accessing cancer care and treatment, and (5) Pacific representation.
This study sheds light on both positive and negative experiences of Pacific peoples living with cancer in Aotearoa New Zealand. It highlights gaps in the current model of oncology care for this population, which are multilevel and therefore require a multifaceted approach. It calls for priority toward reducing barriers to access of care and creating a more culturally safe pathway.
在新西兰奥特亚罗瓦,太平洋岛民面临着不公平的结果,与其他种族相比,他们患可预防癌症的几率更高,生存率更低。本研究的目的是探索太平洋岛民在奥克兰地区患癌症及其治疗的生活经历。
通过对奥克兰地区癌症与血液服务中心的太平洋岛民患者进行半结构化访谈(talanoa)收集数据。采用一般归纳法对数据进行分析。奥克兰健康研究伦理委员会批准了该研究(参考编号AH24086)。
对13名萨摩亚族和汤加族参与者进行了访谈。参与者有一系列肿瘤诊断,正在接受根治性和非根治性治疗。确定了五个关键主题,深入了解了围绕癌症的信念、患者面临的困难以及潜在的优先领域。这些主题包括:(1)癌症意味着死亡;(2)支持的整体和集体方法;(3)沟通与信任;(4)获得癌症护理和治疗的成本;(5)太平洋岛民的代表性。
本研究揭示了新西兰奥特亚罗瓦癌症患者的太平洋岛民的积极和消极经历。它突出了目前针对这一人群的肿瘤护理模式中的差距,这些差距是多层面的,因此需要多方面的方法。它呼吁优先减少获得护理的障碍,并创造一条更具文化安全性的途径。