Department of Medicine, University of Wisconsin, Madison, Wisconsin 53705, USA.
J Thorac Oncol. 2012 Sep;7(9):1361-8. doi: 10.1097/JTO.0b013e318260e106.
To determine prognostic factors and build a model to predict 1-year overall survival (OS) and 6-month progression-free survival (PFS) in advanced non-small-cell lung cancer (NSCLC) patients treated with first-line paclitaxel and carboplatin with or without bevacizumab.
We analyzed 26 pretreatment clinical variables in 850 NSCLC patients treated in the randomized Eastern Cooperative Oncology Group 4599 study. Univariate and multivariate analyses were performed to identify prognostic factors. Cox regression with 50% randomly sampled data was used to build nomograms with a prognostic score assigned to each factor. The model was validated with the remaining 50% of data.
Eleven poor factors for OS (hazard ratio) were as follows: skin metastasis (4.49), body mass index less than 18.5 (2.09), increased serum lactate dehydrogenase (1.74), adrenal metastasis (1.52), performance status greater than 0 (1.45), low serum albumin (1.45), men (1.39), bone metastasis (1.39), large cell/not otherwise specified histology (1.29), mediastinal nodal metastasis (1.23), and treatment without bevacizumab (1.18). Seven poor factors for PFS were as follows: skin metastasis (3.13), treatment without bevacizumab (1.52), bone metastasis (1.41), liver metastasis (1.40), low serum albumin (1.39), performance status greater than 0 (1.21), and mediastinal nodal metastasis (1.14). Based on these factors, we built and validated two nomograms predicting 1-year OS and 6-month PFS.
Using our proposed models, the probability of survival with first-line paclitaxel and carboplatin with or without bevacizumab in nonsquamous NSCLC patients can be estimated. These prognostic models provide a tool for research design and clinical decision making, such as patient stratification and therapy selection.
为了确定预测因素,并建立一个模型来预测接受一线紫杉醇和卡铂联合或不联合贝伐珠单抗治疗的晚期非小细胞肺癌(NSCLC)患者的 1 年总生存期(OS)和 6 个月无进展生存期(PFS)。
我们分析了 850 例接受随机东部合作肿瘤学组 4599 研究治疗的 NSCLC 患者的 26 项治疗前临床变量。进行单变量和多变量分析以确定预后因素。使用 Cox 回归对 50%随机抽样数据进行分析,以建立每个因素的预后评分分配的列线图。使用剩余的 50%数据验证模型。
11 个与 OS(风险比)相关的不良因素如下:皮肤转移(4.49)、体质指数小于 18.5(2.09)、血清乳酸脱氢酶升高(1.74)、肾上腺转移(1.52)、表现状态大于 0(1.45)、血清白蛋白低(1.45)、男性(1.39)、骨转移(1.39)、大细胞/非特指组织学(1.29)、纵隔淋巴结转移(1.23)、未接受贝伐珠单抗治疗(1.18)。7 个与 PFS 相关的不良因素如下:皮肤转移(3.13)、未接受贝伐珠单抗治疗(1.52)、骨转移(1.41)、肝转移(1.40)、血清白蛋白低(1.39)、表现状态大于 0(1.21)、纵隔淋巴结转移(1.14)。基于这些因素,我们建立并验证了两个预测 1 年 OS 和 6 个月 PFS 的列线图。
使用我们提出的模型,可以估计非鳞状 NSCLC 患者接受一线紫杉醇和卡铂联合或不联合贝伐珠单抗治疗的生存概率。这些预后模型为研究设计和临床决策提供了工具,例如患者分层和治疗选择。