Medical Oncology/Hematology, William Osler Health System, Brampton, ON L6R 3J7, Canada.
Faculty of Medicine, University of Toronto, Toronto, ON M5S 1A8, Canada.
Curr Oncol. 2021 Nov 9;28(6):4552-4576. doi: 10.3390/curroncol28060386.
In Canada, the therapeutic management of patients with advanced non-small cell lung cancer (NSCLC) with rare actionable mutations differs between provinces, territories, and individual centres based on access to molecular testing and funded treatments. These variations, together with the emergence of several novel mesenchymal-epithelial transition () factor-targeted therapies for the treatment of NSCLC, warrant the development of evidence-based consensus recommendations for the use of these agents. A Canadian expert panel was convened to define key clinical questions, review evidence, discuss practice recommendations and reach consensus on the treatment of advanced -altered NSCLC. Questions addressed by the panel include: 1. How should the patients most likely to benefit from targeted therapies be identified? 2. What are the preferred first-line and subsequent therapies for patients with exon 14 skipping mutations? 3. What are the preferred first-line and subsequent therapies for advanced NSCLC patients with de novo amplification? 4. What is the preferred therapy for patients with advanced epidermal growth factor receptor ()-mutated NSCLC with acquired amplification progressing on EGFR inhibitors? 5. What are the potential strategies for overcoming resistance to inhibitors? Answers to these questions, along with the consensus recommendations herein, will help streamline the management of -altered NSCLC in routine practice, assist clinicians in therapeutic decision-making, and help ensure optimal outcomes for NSCLC patients with alterations.
在加拿大,针对罕见可操作突变的晚期非小细胞肺癌(NSCLC)患者的治疗管理,因各省、地区和各中心的分子检测和已获资助治疗的可及性不同而存在差异。这些差异,加上针对 NSCLC 治疗的几种新型间质-上皮转化(MET)因子靶向治疗药物的出现,需要制定基于证据的共识推荐意见,以规范这些药物的使用。召集了一个加拿大专家小组来确定关键的临床问题,审查证据,讨论实践建议,并就晚期 MET 改变 NSCLC 的治疗达成共识。小组提出的问题包括:1. 如何识别最有可能从靶向治疗中获益的患者?2. 对于携带外显子 14 跳跃突变的患者,首选的一线和后续治疗方法是什么?3. 对于初诊 MET 扩增的晚期 NSCLC 患者,首选的一线和后续治疗方法是什么?4. 对于接受 EGFR 抑制剂治疗后出现获得性 MET 扩增的晚期 EGFR(EGFR)突变型 NSCLC 患者,首选的治疗方法是什么?5. 克服 MET 抑制剂耐药的潜在策略有哪些?这些问题的答案以及本文中的共识推荐意见将有助于简化 MET 改变 NSCLC 的常规治疗管理,帮助临床医生做出治疗决策,并确保 MET 改变的 NSCLC 患者获得最佳治疗效果。