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芬兰 - 突变型非小细胞肺癌患者的真实世界证据研究。

Real-World Evidence Study of Patients with -Mutated NSCLC in Finland.

机构信息

Medaffcon Oy, 02130 Espoo, Finland.

Amgen AB, 02150 Espoo, Finland.

出版信息

Curr Oncol. 2024 May 11;31(5):2700-2712. doi: 10.3390/curroncol31050205.

Abstract

While is the most frequently mutated oncogene in non-small cell lung cancer (NSCLC), -mutant tumors have long been considered difficult to treat and thus, an unmet need still remains. Partly due to the lack of targeted treatments, comprehensive real-world description of NSCLC patients with mutation is still largely missing in Finland. In this study, all adult patients diagnosed with locally advanced and unresectable or metastatic NSCLC from 1 January 2018 to 31 August 2020 at the Hospital District of Helsinki and Uusimaa were first identified in this retrospective registry-based real-world study. The final cohort included only patients tested with next generation sequencing (NGS) and was stratified by the mutation status. A total of 383 patients with locally advanced and unresectable or metastatic NSCLC and with NGS testing performed were identified. Patients with mutation ( G12C = 35, other = 74) were younger than patients without mutations, were all previous or current smokers, and had more often metastatic disease at diagnosis. Also, these patients had poorer survival, with higher age, Charlson comorbidity index (CCI) being 5 or above, and G12C being the most significant risk factors associated with poorer survival. This suggests that the patients with mutation have a more aggressive disease and/or tumors with mutation are more difficult to treat, at least without effective targeted therapies.

摘要

虽然 是最常见的非小细胞肺癌(NSCLC)中的致癌基因突变,但 - 突变肿瘤一直被认为难以治疗,因此仍然存在未满足的需求。部分由于缺乏靶向治疗,芬兰对 突变的 NSCLC 患者的全面真实世界描述在很大程度上仍然缺失。在这项研究中,所有在 2018 年 1 月 1 日至 2020 年 8 月 31 日期间在赫尔辛基和乌西玛地区医院区被诊断为局部晚期、不可切除或转移性 NSCLC 的成年患者均在这项回顾性基于登记的真实世界研究中首次被确定。最终队列仅包括接受下一代测序(NGS)检测的患者,并根据 突变状态进行分层。共确定了 383 名接受局部晚期、不可切除或转移性 NSCLC 且进行 NGS 检测的患者。携带 突变(G12C=35,其他=74)的患者比未携带 突变的患者更年轻,均为既往或当前吸烟者,且在诊断时更常发生转移性疾病。此外,这些患者的生存情况更差,年龄较大、Charlson 合并症指数(CCI)为 5 或更高,以及 G12C 是与较差生存相关的最显著危险因素。这表明携带 突变的患者具有更具侵袭性的疾病,或者 突变的肿瘤更难以治疗,至少在没有有效靶向治疗的情况下是这样。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94a9/11120216/8a4de664c0eb/curroncol-31-00205-g001.jpg

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