State Key Laboratory of Oncology in Southern China & Department of Medical Oncology, Cancer Center, Sun Yat-sen University, 510060 Guangzhou, Guangdong Province, China.
Med Oncol. 2011 Mar;28(1):331-5. doi: 10.1007/s12032-010-9451-1. Epub 2010 Mar 4.
A clinical prognostic model derived from BR.21 trial was established by Florescu et al., which helped to identify a small group of patients with non-small cell lung cancer (NSCLC) who might be less likely to benefit from erlotinib therapy. Whether the prognostic model derived from Caucasian patients treated with erlotinib will be applied to Asian patients treated with gefitinib is still an open question. We reviewed a multi-center clinical trial of Chinese patients with NSCLC treated with gefitinib. The data were collected and analyzed according to the prognostic model reported by Florescu et al. One hundred and nineteen patients were included in the validation study. Twenty-eight patients, 61 patients, 27 patients, and 3 patients were classified into the Low Risk (LR) group, Intermediate Low Risk (ILR) group, Intermediate High Risk/High Risk (IHR/HR) group, respectively. The median overall survival of LR group was not reached, ILR and IHR/HR group was 8.9 months and 4.5 months, respectively. There was a significant difference in overall survival between LR group versus ILR group and IHR/HR group (P = 0.0003 and 0.0001, respectively). While IHR/HR group appeared to have less survival benefit than ILR group, the difference was not statistically significant (P = 0.148). The result has shown a similar effect as that seen by Florescu et al. in differentiating patient risk groups. Our study provides the potential evidence that the prognostic model might be applied to Asian patients with NSCLC treated with gefitinib and helps clinicians to select patients for gefitinib therapy and stratify patients within second-line clinical trials.
弗洛雷斯库等人建立了一个源自 BR.21 试验的临床预后模型,该模型有助于识别一小部分非小细胞肺癌(NSCLC)患者,他们可能不太可能从厄洛替尼治疗中获益。源自接受厄洛替尼治疗的白种人群的预后模型是否适用于接受吉非替尼治疗的亚洲患者,仍然是一个悬而未决的问题。我们回顾了一项针对接受吉非替尼治疗的中国 NSCLC 患者的多中心临床试验。根据弗洛雷斯库等人报告的预后模型收集和分析数据。验证研究纳入了 119 例患者。28 例、61 例、27 例和 3 例患者分别归入低危(LR)组、中低危(ILR)组、中高危/高危(IHR/HR)组。LR 组的中位总生存期未达到,ILR 和 IHR/HR 组分别为 8.9 个月和 4.5 个月。LR 组与 ILR 组和 IHR/HR 组的总生存期有显著差异(P = 0.0003 和 0.0001)。虽然 IHR/HR 组的生存获益似乎低于 ILR 组,但差异无统计学意义(P = 0.148)。结果显示出与弗洛雷斯库等人在区分患者风险组方面相似的效果。我们的研究提供了潜在的证据,表明该预后模型可能适用于接受吉非替尼治疗的亚洲 NSCLC 患者,并有助于临床医生选择接受吉非替尼治疗的患者,并对二线临床试验中的患者进行分层。