Bodén Embla, Sveréus Fanny, Olm Franziska, Lindstedt Sandra
Department of Clinical Sciences, Lund University, 22184 Lund, Sweden.
Wallenberg Center for Molecular Medicine, Lund University, 22184 Lund, Sweden.
Cancers (Basel). 2023 Jul 27;15(15):3827. doi: 10.3390/cancers15153827.
Lung cancer represents the leading cause of annual cancer-related deaths worldwide, accounting for 12.9%. The available treatment options for patients who experience disease progression remain limited. Targeted therapeutic approaches are promising but further understanding of the role of genetic alterations in tumorigenesis is imperative. The gene has garnered great interest in this regard. The aim of this systematic review was to analyze the findings from multiple studies to provide a comprehensive and unbiased summary of the evidence. A systematic search was conducted in the reputable scientific databases Embase and PubMed, leading to the inclusion of twenty-two articles, following the PRISMA guidelines, elucidating the biological role of in lung cancer and targeted therapies. The systematic review was registered in PROSPERO with registration ID: CRD42023437714. mutations were detected in 7.6-11.0% of cases while gene amplification was observed in 3.9-22.0%. Six studies showed favorable treatment outcomes utilizing inhibitors compared to standard treatment or placebo, with increases in PFS and OS ranging from 0.9 to 12.4 and 7.2 to 24.2 months, respectively, and one study reporting an increase in ORR by 17.3%. Furthermore, patients with a higher mutational burden may derive greater benefit from treatment with tyrosine kinase inhibitors (TKIs) than those with a lower mutational burden. Conversely, two studies reported no beneficial effect from adjunctive treatment with a targeted therapy. Given these findings, there is an urgent need to identify effective therapeutic strategies specifically targeting the gene in lung cancer patients.
肺癌是全球每年癌症相关死亡的主要原因,占比12.9%。对于疾病进展的患者,可用的治疗选择仍然有限。靶向治疗方法很有前景,但进一步了解基因改变在肿瘤发生中的作用至关重要。该基因在这方面引起了极大的关注。本系统评价的目的是分析多项研究的结果,以提供全面且无偏倚的证据总结。按照PRISMA指南,在著名的科学数据库Embase和PubMed中进行了系统检索,纳入了22篇文章,阐明了该基因在肺癌中的生物学作用和靶向治疗。该系统评价已在PROSPERO注册,注册号为:CRD42023437714。在7.6%-11.0%的病例中检测到该基因突变,而在3.9%-22.0%的病例中观察到该基因扩增。六项研究表明,与标准治疗或安慰剂相比,使用该基因抑制剂可获得良好的治疗效果,无进展生存期(PFS)和总生存期(OS)分别增加0.9至12.4个月和7.2至24.2个月,一项研究报告客观缓解率(ORR)提高了17.3%。此外,与突变负担较低的患者相比,突变负担较高的患者可能从该基因酪氨酸激酶抑制剂(TKIs)治疗中获益更大。相反,两项研究报告该基因靶向辅助治疗无有益效果。鉴于这些发现,迫切需要确定专门针对肺癌患者该基因的有效治疗策略。