Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Expert Opin Emerg Drugs. 2024 Jun;29(2):139-154. doi: 10.1080/14728214.2024.2331139. Epub 2024 Apr 8.
Current research in EGFR-mutated NSCLC focuses on the management of drug resistance and uncommon mutations, as well as on the opportunity to extend targeted therapies' field of action to earlier stages of disease.
We conducted a review analyzing literature from the PubMed database with the aim to describe the current state of art in the management of EGFR-mutated NSCLC, but also to explore new strategies under investigation. To this purpose, we collected recruiting phase II-III trials registered on Clinicaltrials.govand conducted on EGFR-mutated NSCLC both in early and advanced stage.
With this review, we want to provide an exhaustive overview of current and new potential treatments in EGFR-mutated NSCLC, with emphasis on the most promising newly investigated strategies, such as association therapies in the first-line setting involving EGFR-TKIs and chemotherapy (FLAURA2) or drugs targeting different driver pathways (MARIPOSA). We also aimed at unearthing challenges to achieve in this field, specifically the need to fully exploit already available compounds while developing new ones, the management of new emerging toxicities and the necessity to improve our biological understanding of the disease to design trials with a solid scientific rationale and to allow treatment personalization such in case of uncommon mutations.
目前针对 EGFR 突变型非小细胞肺癌的研究集中于耐药和罕见突变的管理,以及将靶向治疗的作用范围扩展到疾病的早期阶段的机会。
我们进行了一项文献综述,分析了 PubMed 数据库中的文献,旨在描述 EGFR 突变型非小细胞肺癌管理的当前现状,同时还探讨了正在研究的新策略。为此,我们收集了在 Clinicaltrials.gov 上注册的针对 EGFR 突变型非小细胞肺癌的招募阶段 II-III 期临床试验,并对早期和晚期的 EGFR 突变型非小细胞肺癌进行了研究。
通过本次综述,我们旨在全面概述 EGFR 突变型非小细胞肺癌的现有和新的潜在治疗方法,重点关注最有前途的新研究策略,如在一线治疗中联合使用 EGFR-TKIs 和化疗的联合治疗(FLAURA2)或针对不同驱动途径的药物(MARIPOSA)。我们还旨在发现该领域需要克服的挑战,特别是需要在开发新药的同时充分利用已有的化合物,管理新出现的毒性,以及提高我们对疾病的生物学认识,以便设计具有坚实科学依据的试验,并允许进行个体化治疗,例如针对罕见突变。