关于肿瘤基因组测序和基因检测,癌症患者知道或想知道什么?最新的评论。

Lisa Stewart, Linda D Ward
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引用次数: 0

摘要

分子谱分析(MP)涉及检测组织、血液或其他体液以识别生物标志物,在癌症治疗中变得越来越重要。肿瘤基因组测序是一种特殊类型的MP,通常用于识别可靶向治疗的特定基因变异或蛋白质。生殖系检测也被常规推荐用于某些癌症。癌症患者的基因组知识水平较低,再加上检测结果越来越复杂,这给临床医生传达结果和提供适当的教育带来了挑战。此外,患者可能对他们想要和能够处理的信息水平有不同的偏好。这篇最新的综述探讨了癌症患者在接受分子谱分析时的期望、态度、知识、满意度和关注点。通过四个数据库进行了搜索,以确定2016年至2022年期间的研究,以探索癌症患者对基因组检测的知识和偏好。19项研究符合纳入标准。大多数研究表明,尽管存在显著差异,但癌症患者对MP的了解程度较低。患者主要希望MP能够确定新的治疗方案并提高生存率。虽然患者依赖于他们的提供者来解释测试结果,但他们希望被告知所有的结果,主要是如果这些结果可能指导治疗决策或未来的护理计划。大多数患者,特别是那些基因组/遗传知识较低的患者,倾向于高估MP的个人益处。需要进一步的研究来提供量身定制的教育,以满足患者的信息需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
What Do Patients With Cancer Know, or Want to Know, About Genomic Tumor Sequencing and Genetic Testing? A State-of-the-Art Review.

Molecular profiling (MP), which involves testing tissue, blood, or other body fluids to identify biomarkers, has become increasingly important in cancer treatment. Genomic tumor sequencing, a specific type of MP, is commonly used to identify specific gene variants or proteins that can be targeted for treatment. Germline testing is also routinely recommended for certain cancers. Low levels of genomic literacy among cancer patients, coupled with increasingly complex test results, challenge clinicians to communicate results and provide appropriate education. In addition, patients may have varying preferences for the level of information they desire and are able to process. This state-of-the-art review explores cancer patients' expectations, attitudes, knowledge, satisfaction, and concerns as they undergo molecular profiling. A search was conducted through four databases to identify studies from 2016 to 2022 to explore cancer patients' knowledge and preferences regarding genomic testing. Nineteen studies met the inclusion criteria. Most studies revealed that people with cancer have low levels of knowledge regarding MP, albeit with significant variability. Patients primarily desired MP to identify new treatment options and increase survival. While patients relied on their providers to interpret test results, they wanted to be informed of all results, mainly if those results might guide treatment decisions or future care planning. Most patients, especially those with low genomic/genetic knowledge, tended to overestimate the personal benefits of MP. Further study is needed to provide tailored education to fulfill patients' information needs.

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