Dept. of Oncology, Finsen Centre, National University Hospital, 9 Blegdamsvej, Copenhagen, Denmark.
Eur Respir Rev. 2011 Mar;20(119):45-52. doi: 10.1183/09059180.00007310.
Treating patients with advanced nonsmall cell lung cancer (NSCLC) is a daunting task but during recent years new options have emerged. By tailoring treatment using either information on histological subtypes of NSCLC or biomarkers it is now possible to improve outcome and maintain stable quality of life. We conducted a literature search of tailored treatment already implemented in advanced NSCLC in order to highlight the information required to decide on the optimal oncological treatment for individual patients. 16 studies were identified by literature review. Significantly improved outcome was demonstrated in patients with nonsquamous NSCLC treated with cisplatin/pemetrexed in pre-planned, exploratory and retrospective analysis from large-scale, randomised trials. Level 1 evidence showed significantly better progression-free survival when patients carrying an epidermal growth factor receptor (EGFR) mutation were treated with gefitinib compared to standard chemotherapy. Retrospective, unplanned analysis of excision repair cross complementation group 1 (ERCC1) and betatubulin III upregulation demonstrated poorer outcome in NSCLC patients treated with platinum-doublets and vinorelbine-based chemotherapy, respectively. In conclusion, tailoring treatment according to either histological subtype or EGFR mutation status in advanced NSCLC should today be part of daily practice based on current evidence. Future biomarkers need optimisation of methodology and prospective validation before clinical implementation.
治疗晚期非小细胞肺癌(NSCLC)患者是一项艰巨的任务,但近年来出现了新的选择。通过针对 NSCLC 的组织学亚型或生物标志物的信息来定制治疗,现在可以改善预后并保持稳定的生活质量。我们对已经在晚期 NSCLC 中实施的针对性治疗进行了文献检索,以突出为个别患者确定最佳肿瘤治疗所需的信息。通过文献回顾,确定了 16 项研究。来自大型随机试验的预先计划、探索性和回顾性分析表明,顺铂/培美曲塞治疗非鳞状 NSCLC 患者的结果显著改善。1 级证据表明,与标准化疗相比,携带表皮生长因子受体(EGFR)突变的患者接受吉非替尼治疗时,无进展生存期显著延长。对切除修复交叉互补组 1(ERCC1)和β-微管蛋白 III 上调的回顾性、非计划性分析表明,接受铂类双联和长春瑞滨为基础的化疗的 NSCLC 患者的预后较差。总之,根据晚期 NSCLC 的组织学亚型或 EGFR 突变状态进行针对性治疗,目前应基于现有证据成为日常实践的一部分。未来的生物标志物需要优化方法和前瞻性验证,然后才能临床实施。