Department of Pulmonology, St. Antonius Hospital Utrecht/Nieuwegein, Utrecht.
Department of Thoracic Oncology, The Netherlands Cancer Institute, Antoni van Leeuwenhoek Hospital, Amsterdam.
Curr Opin Pulm Med. 2019 May;25(3):300-307. doi: 10.1097/MCP.0000000000000572.
With the development of targeted therapies, the treatment strategy of patients with advanced or metastatic non-small cell lung cancer (NSCLC) has changed tremendously. In this review, we focus on the different aspects of the treatment of oncogene-driven NSCLC.
Patients with an EGFR or ALK alteration show a better clinical outcome with tyrosine kinase inhibitor (TKI) treatment compared to chemotherapy.Patients with a ROS1 rearrangement or a BRAF V600E mutation show favorable clinical outcome with TKI treatment compared to chemotherapy, although randomized trials are not available.Patients on TKIs will eventually develop disease progression because of acquired resistance.The treatment with immunotherapy in EGFR and ALK-positive NSCLC patients did not improve overall survival over that of chemotherapy.Blood-based genetic analysis provides the opportunity to noninvasively screen patients for the presence of oncogenic drivers and to monitor resistance during TKI treatment.
Targeted molecular therapies are now standard of care for patients with oncogene-driven NSCLC with a good clinical benefit and minimal toxicity. The role of immunotherapy in patients with molecular alterations is still unclear. Blood-based genotyping has gained interest in the diagnostic and resistance monitoring setting for patients with NSCLC.
随着靶向治疗的发展,晚期或转移性非小细胞肺癌(NSCLC)患者的治疗策略发生了巨大变化。在这篇综述中,我们重点关注驱动基因 NSCLC 的治疗的不同方面。
与化疗相比,携带 EGFR 或 ALK 突变的患者接受酪氨酸激酶抑制剂(TKI)治疗的临床结局更好。与化疗相比,携带 ROS1 重排或 BRAF V600E 突变的患者接受 TKI 治疗具有更好的临床结局,尽管尚无随机试验。接受 TKI 治疗的患者最终会因获得性耐药而出现疾病进展。在 EGFR 和 ALK 阳性 NSCLC 患者中,免疫治疗并未改善总生存期,优于化疗。基于血液的基因分析为非侵入性筛选患者是否存在致癌驱动基因以及在 TKI 治疗期间监测耐药性提供了机会。
针对携带驱动基因 NSCLC 的患者,靶向分子治疗现在是标准治疗方法,具有良好的临床获益和最小的毒性。免疫治疗在分子改变患者中的作用仍不清楚。基于血液的基因分型在 NSCLC 患者的诊断和耐药监测中引起了关注。