当遗传学与小儿癌症发生冲突时:了解并优化家庭的经历。

IF 3.7 Q1 CLINICAL NEUROLOGY
Neuro-oncology advances Pub Date : 2024-07-31 eCollection Date: 2024-01-01 DOI:10.1093/noajnl/vdae133
Kate Hetherington, Claire E Wakefield, Brittany C McGill, Katherine M Tucker, Mark W Donoghoe, Rebecca Daly, Jacqueline D Hunter, Mandy Ballinger, Noemi A Fuentes-Bolanos, David S Ziegler
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引用次数: 0

摘要

背景:我们对儿童癌症(包括原发性中枢神经系统癌症)遗传基础的认识取得了进展,从而改善了儿科患者的诊断、治疗和临床管理。为了有效地将科学突破转化为更好的临床治疗,我们必须了解并学习患者、家属和医疗专业人员的经验:本报告总结了澳大利亚 4 项社会心理子研究的结果,这些研究探讨了参与儿童癌症遗传学相关研究的患者、家长、临床医生和科学家的观点。具体而言,这些研究重点关注儿童种系检测的社会心理影响、对患有癌症易感综合征儿童的监控以及提供检测和监控的医疗保健专业人员的观点:所提供的数据突显了与儿童、青少年和成年癌症患者遗传易感性检测不断变化的环境相关的一些机遇和挑战,并说明了将社会心理数据收集纳入临床研究可如何回答该领域的重要问题,以及如何为设计以患者为中心的护理模式、资源和劳动力培训提供信息:通过接受这些观点,我们可以确保基因研究的进展转化为家庭体验的改善,并最终改善癌症儿童和青少年及其家庭的治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
When genetics and pediatric cancer collide: Understanding and optimizing families' experiences.

Background: Advances in our understanding of the genetic basis of childhood cancer, including primary central nervous system cancers, are improving the diagnosis, treatment, and clinical management of pediatric patients. To effectively translate scientific breakthroughs into enhanced clinical care, it is essential we understand and learn from the experiences of patients, families, and health professionals.

Methods: This report summarizes findings from 4 Australian psychosocial substudies exploring the perspectives of patients, parents, clinicians, and scientists participating in research related to childhood cancer genetics. Specifically, these studies focus on the psychosocial impact of germline testing in children, surveillance for children with a cancer predisposition syndrome and the perspectives of healthcare professionals who deliver this testing and surveillance.

Results: Data presented highlight some of the opportunities and challenges associated with the changing context of genetic predisposition testing for children, adolescents and yound adults with cancer and illustrate how embedding psychosocial data collection in clinical research can answer important questions in the field and inform the design of patient-centric models of care, resources, and workforce training.

Conclusions: By embracing these perspectives, we can ensure that advances in genetic research translate into enhanced family experiences, and, ultimately, improved outcomes for children and young people with cancer, and their families.

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CiteScore
6.20
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