Northern Sydney Cancer Centre, Royal North Shore Hospital, Sydney, NSW, Australia; Central Coast Cancer Centre, Gosford Hospital, Gosford, NSW, Australia; Sydney Medical School, University of Sydney, Sydney, NSW, Australia; Sydney NeuroOncology Group, Sydney, NSW, Australia.
Sydney NeuroOncology Group, Sydney, NSW, Australia.
Clin Oncol (R Coll Radiol). 2018 Sep;30(9):556-562. doi: 10.1016/j.clon.2018.06.005. Epub 2018 Jul 3.
The recognition of specific molecular prognostic factors has altered the management of primary brain tumours over the past decade. These factors have allowed stratification of morphologically similar tumours into different prognostic groups and are now also being used to determine clinical trial eligibility. Many of these factors have been included in the revised fourth edition of the World Health Organization (WHO) Classification of Tumours of the Central Nervous System, released in May 2016. This revised edition places greater emphasis on molecular testing and, for certain tumour types, molecular testing is required for diagnosis. Many pathology departments have also adopted the four-tiered report format suggested in the Haarlem guidelines, and provide a final 'integrated diagnosis' incorporating a morphological diagnosis, the WHO grade and molecular findings. Pathologists need to perform and report these molecular tests in a timeframe that is relevant for clinical decision-making. Clinicians need to understand and incorporate these changes into their daily practice, as they have direct effects on both the type and intent of therapeutic interventions.
过去十年中,对特定分子预后因素的认识改变了原发性脑肿瘤的治疗方式。这些因素使形态相似的肿瘤能够分为不同的预后组,现在也被用于确定临床试验的入选资格。许多这些因素已被纳入 2016 年 5 月发布的世界卫生组织(WHO)中枢神经系统肿瘤分类的第四版修订版中。该修订版更加重视分子检测,对于某些肿瘤类型,诊断需要进行分子检测。许多病理科也采用了 Haarlem 指南中建议的四级报告格式,并提供最终的“综合诊断”,其中包括形态学诊断、WHO 分级和分子发现。病理学家需要在与临床决策相关的时间范围内进行这些分子检测并报告结果。临床医生需要理解并将这些变化纳入他们的日常实践中,因为它们直接影响治疗干预的类型和意图。