Department of Experimental Medicine, La Sapienza University of Rome, Viale Regina Elena 324, 00161 Rome, Italy.
Lung Cancer. 2010 Nov;70(2):200-4. doi: 10.1016/j.lungcan.2010.02.003. Epub 2010 Mar 15.
Until recently, histology has not been clearly or consistently described in the literature as a prognostic or predictive variable in advanced NSCLC studies. We have categorised patients treated with vinorelbine and gemcitabine based first line chemotherapy regimes for advanced NSCLC as either squamous or non-squamous, and also as either adenocarcinoma and non-adenocarcinoma, and compared outcome.
420 patients treated with platinum/gemcitabine, platinum/vinorelbine or single agent gemcitabine or vinorelbine as first line chemotherapy for advanced NSCLC were identified. The influence of pathology on progression free survival (PFS) and overall survival (OS) has been investigated by means of a Cox regression analysis. Hazard ratios with 95% CIs have been given for each pathological type after adjusting for the effects of age, gender, stage (III vs. IV), PS (0/1 vs. 2/3) and treatment type (platinum doublet vs. single agent).
Neither univariate nor multivariate analysis suggested that there was a significant difference in the response rates for adenocarcinoma vs. non-adenocarcinoma or between squamous and non-squamous pathology. There was no difference in PFS between adenocarcinoma and non-adenocarcinoma pathologies until 8 months (p = 0.98), and there was a statistically significant advantage in PFS for squamous vs. non-squamous pathologies (p = 0.04). Using multivariate Cox regression analysis to adjust for the effects of age, gender, stage, PS, and treatment type, the pathology subtype was not significant. There was no difference in OS in any group.
These results suggest that histology may not be considered as a predictor of clinical outcome using these drugs.
直到最近,组织学在晚期 NSCLC 研究的文献中并未被明确或一致地描述为预后或预测变量。我们根据一线化疗方案将接受长春瑞滨和吉西他滨治疗的晚期 NSCLC 患者分为鳞癌或非鳞癌,也分为腺癌和非腺癌,并比较了结果。
确定了 420 例接受铂类/吉西他滨、铂类/长春瑞滨或单药吉西他滨或长春瑞滨治疗晚期 NSCLC 的患者。通过 Cox 回归分析研究了病理学对无进展生存期(PFS)和总生存期(OS)的影响。在调整年龄、性别、分期(III 期与 IV 期)、PS(0/1 与 2/3)和治疗类型(铂类双药与单药)的影响后,为每种病理类型提供了具有 95%CI 的风险比。
单因素和多因素分析均表明,腺癌与非腺癌或鳞癌与非鳞癌之间的客观缓解率无显著差异。腺癌和非腺癌之间的 PFS 差异直到 8 个月时才具有统计学意义(p = 0.98),而鳞癌与非鳞癌之间的 PFS 具有统计学显著优势(p = 0.04)。使用多因素 Cox 回归分析调整年龄、性别、分期、PS 和治疗类型的影响,病理亚型无显著意义。任何组别的 OS 均无差异。
这些结果表明,使用这些药物时,组织学可能不能被视为临床结果的预测因子。