de Jager Vincent D, Timens Wim, Bayle Arnaud, Botling Johan, Brcic Luka, Büttner Reinhard, Fernandes Maria Gabriela O, Havel Libor, Hochmair Maximilian, Hofman Paul, Janssens Annelies, van Kempen Léon, Kern Izidor, Machado José Carlos, Mohorčič Katja, Popat Sanjay, Ryška Aleš, Wolf Jürgen, Schuuring Ed, van der Wekken Anthonie J
Department of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Oncostat U1018, Inserm, Paris-Saclay University, Gustave Roussy, Villejuif, France.
Lancet Reg Health Eur. 2024 Mar 1;38:100839. doi: 10.1016/j.lanepe.2024.100839. eCollection 2024 Mar.
For patients with advanced stage non-small cell lung cancer (NSCLC), treatment strategies have changed significantly due to the introduction of targeted therapies and immunotherapy. In the last few years, we have seen an explosive growth of newly introduced targeted therapies in oncology and this development is expected to continue in the future. Besides primary targetable aberrations, emerging diagnostic biomarkers also include relevant co-occurring mutations and resistance mechanisms involved in disease progression, that have impact on optimal treatment management. To accommodate testing of pending biomarkers, it is necessary to establish routine large-panel next-generation sequencing (NGS) for all patients with advanced stage NSCLC. For cost-effectiveness and accessibility, it is recommended to implement predictive molecular testing using large-panel NGS in a dedicated, centralized expert laboratory within a regional oncology network. The central molecular testing center should host a regional Molecular Tumor Board and function as a hub for interpretation of rare and complex testing results and clinical decision-making.
对于晚期非小细胞肺癌(NSCLC)患者,由于靶向治疗和免疫治疗的引入,治疗策略发生了显著变化。在过去几年中,我们目睹了肿瘤学领域新引入的靶向治疗呈爆发式增长,并且预计这一发展在未来还将持续。除了主要的可靶向畸变外,新兴的诊断生物标志物还包括与疾病进展相关的同时出现的突变和耐药机制,这些对优化治疗管理具有影响。为了适应对待定生物标志物的检测,有必要为所有晚期NSCLC患者建立常规的大panel二代测序(NGS)。为了实现成本效益和可及性,建议在区域肿瘤网络内的一个专门的、集中的专家实验室中使用大panel NGS进行预测性分子检测。中央分子检测中心应设立一个区域分子肿瘤委员会,并作为罕见和复杂检测结果解读及临床决策的中心。