BC Cancer-Vancouver Centre, Vancouver, BC.
CancerCare Manitoba, University of Manitoba, Winnipeg, MB.
Curr Oncol. 2020 Apr;27(2):e146-e155. doi: 10.3747/co.27.6007. Epub 2020 May 1.
Multiple clinical trials for the treatment of advanced mutated non-small-cell lung cancer (nsclc) have recently been reported. As a result, the treatment algorithm has changed, and many important clinical questions have been raised:■ What is the optimal first-line treatment for patients with mutated nsclc?■ What is preferred first-line treatment for patients with brain metastasis?■ What is the preferred second-line treatment for patients who received first-line first- or second-generation tyrosine kinase inhibitors (tkis)?■ What is the preferred treatment after osimertinib?■ What evidence do we have for treating patients whose tumours harbour uncommon mutations?
A Canadian expert panel was convened to define the key clinical questions, review recent evidence, and discuss and agree on practice recommendations for the treatment of advanced mutated nsclc.
The published overall survival results for osimertinib, combined with its central nervous system activity, have led to osimertinib becoming the preferred first-line treatment for patients with common mutations, including those with brain metastasis. Other agents could still have a role, especially when osimertinib is not available or not tolerated. Treatment in subsequent lines of therapy depends on the first-line therapy or on T790M mutation status. Treatment recommendations for patients whose tumours harbour uncommon mutations are guided mainly by retrospective and limited prospective evidence. Finally, the evidence for sequencing and combining tkis with chemotherapy, angiogenesis inhibitors, checkpoint inhibitors, and other new therapeutics is reviewed.
This Canadian expert consensus statement and algorithm were driven by significant advances in the treatment of mutated nsclc.
最近有多项针对晚期突变型非小细胞肺癌(nsclc)治疗的临床试验报告。因此,治疗方案发生了变化,提出了许多重要的临床问题:
突变型 nsclc 患者的最佳一线治疗方法是什么?
有脑转移的患者首选的一线治疗方法是什么?
接受一线第一代或第二代酪氨酸激酶抑制剂(tkis)治疗的患者首选的二线治疗方法是什么?
奥希替尼治疗后的首选治疗方法是什么?
我们有治疗肿瘤携带罕见突变患者的证据吗?
召集加拿大专家小组,确定关键的临床问题,回顾最新的证据,并就治疗晚期突变型 nsclc 的实践建议进行讨论和达成一致。
奥希替尼的发表总生存结果,加上其对中枢神经系统的活性,使其成为常见 突变患者的首选一线治疗药物,包括有脑转移的患者。其他药物仍可能有作用,特别是在奥希替尼不可用或不能耐受的情况下。后续治疗线的治疗取决于一线治疗或 T790M 突变状态。对于肿瘤携带罕见 突变的患者,治疗建议主要是基于回顾性和有限的前瞻性证据。最后,对 tkis 与化疗、血管生成抑制剂、检查点抑制剂和其他新疗法联合进行测序的证据进行了综述。
本加拿大专家共识声明和算法是由突变型 nsclc 治疗的显著进展驱动的。