University Hospital of Heraklion, Heraklion, Crete, Greece.
Ther Adv Med Oncol. 2011 Jul;3(4):185-205. doi: 10.1177/1758834011409973.
Although surgery is the only potentially curative treatment for early-stage non-small cell lung cancer (NSCLC), 5-year survival rates range from 77% for stage IA tumors to 23% in stage IIIA disease. Adjuvant chemotherapy has recently been established as a standard of care for resected stage II-III NSCLC, on the basis of large-scale clinical trials employing third-generation platinum-based regimens. As the overall absolute 5-year survival benefit from this approach does not exceed 5% and potential long-term complications are an issue of concern, the aim of customized adjuvant systemic treatment is to optimize the toxicity/benefit ratio, so that low-risk individuals are spared from unnecessary intervention, while avoiding undertreatment of high-risk patients, including those with stage I disease. Therefore, the application of reliable prognostic and predictive biomarkers would enable to identify appropriate patients for the most effective treatment.This is an overview of the data available on the most promising clinicopathological and molecular biomarkers that could affect adjuvant and neoadjuvant chemotherapy decisions for operable NSCLC in routine practice. Among the numerous candidate molecular biomarkers, only few gene-expression profiling signatures provide clinically relevant information warranting further validation. On the other hand, real-time quantitative polymerase-chain reaction strategy involving relatively small number of genes offers a practical alternative, with high cross-platform performance. Although data extrapolation from the metastatic setting should be cautious, the concept of personalized, pharmacogenomics-guided chemotherapy for early NSCLC seems feasible, and is currently being evaluated in randomized phase 2 and 3 trials. The mRNA and/or protein expression levels of excision repair cross-complementation group 1, ribonucleotide reductase M1 and breast cancer susceptibility gene 1 are among the most potential biomarkers for early disease, with stage-independent prognostic and predictive values, the clinical utility of which is being validated prospectively. Inter-assay discordance in determining the biomarker status and association with clinical outcomes is noteworthing.
虽然手术是治疗早期非小细胞肺癌(NSCLC)的唯一潜在治愈方法,但 5 年生存率从 IA 期肿瘤的 77%到 IIIA 期疾病的 23%不等。辅助化疗最近已被确立为可切除的 II-III 期 NSCLC 的标准治疗方法,这是基于采用第三代铂类方案的大规模临床试验。由于这种方法的总体绝对 5 年生存获益不超过 5%,并且潜在的长期并发症是一个令人关注的问题,因此,定制辅助全身治疗的目的是优化毒性/获益比,从而使低风险个体免受不必要的干预,同时避免对高危患者(包括 I 期疾病患者)治疗不足。因此,应用可靠的预后和预测生物标志物可以帮助识别适合最有效治疗的患者。本文概述了在常规实践中对可切除 NSCLC 进行辅助和新辅助化疗决策最有影响的最有前途的临床病理和分子生物标志物的相关数据。在众多候选分子生物标志物中,只有少数基因表达谱特征可提供有临床意义的信息,值得进一步验证。另一方面,涉及相对少数基因的实时定量聚合酶链反应策略提供了一种实用的替代方法,具有高的跨平台性能。虽然从转移性疾病中进行数据外推应该谨慎,但针对早期 NSCLC 的个性化、药物基因组学指导的化疗的概念似乎是可行的,目前正在随机 2 期和 3 期试验中进行评估。切除修复交叉互补组 1、核苷酸还原酶 M1 和乳腺癌易感基因 1 的 mRNA 和/或蛋白表达水平是早期疾病最有潜力的生物标志物之一,具有独立于分期的预后和预测价值,其临床应用正在前瞻性验证中。在确定生物标志物状态和与临床结局的相关性方面,不同检测方法之间的差异值得关注。