Department of Radiation Oncology, Hyogo Cancer Center, Akashi, Hyogo, Japan.
Department of Diagnostic Radiology, Hyogo Cancer Center, Akashi, Hyogo, Japan.
J Thorac Oncol. 2014 Jul;9(7):983-990. doi: 10.1097/JTO.0000000000000187.
We aimed to develop a more accurate model for predicting severe radiation pneumonitis (RP) after concurrent chemoradiotherapy for non-small-cell lung cancer.
We retrospectively analyzed data from 122 patients with locally advanced non-small-cell lung cancer treated with concurrent chemoradiotherapy. Several dose-volume histogram metrics including absolute lung volume spared from a 5 Gy dose (VS5) were analyzed for an association with RP above NCI-CTC grade 3 (RP ≥ G3). Clinical factors including pulmonary fibrosis score (PFS) and pulmonary emphysema score on baseline chest computed tomography (CT) were also analyzed.
Fourteen patients (11.4%) developed RP greater than or equal to G3. On univariate analysis, all dose-volume histogram metrics, sex, and PFS on baseline CT were significantly (p < 0.05) associated with occurrence of RP greater than or equal to G3. Multivariate analysis revealed that V20 greater than or equal to 26%, VS5 less than 1500 cc, age greater than or equal to 68 years, and PFS on baseline CT greater than or equal to 2 were significant risk factors. Thus, we defined a new predictive risk score (PRS) that combines these factors. The cumulative incidence of RP greater than or equal to G3 at 12 months were 0%, 7.8%, 26.6%, and 71.4% when the PRS was 0, 3-5, 6-8, and 9-14, respectively (p < 0.001). This PRS was superior at predicting RP than both V20 and VS5 combined, or V20 alone by receiver operating characteristic analysis (area under the curve, 0.888 versus 0.779 versus 0.678).
V20, VS5, age, and PFS on baseline CT are independent and significant risk factors for occurrence of severe RP. Combining these factors may improve the predictability of severe RP.
我们旨在开发一种更准确的模型,以预测非小细胞肺癌同步放化疗后严重放射性肺炎(RP)。
我们回顾性分析了 122 例局部晚期非小细胞肺癌患者同步放化疗的数据。分析了多个剂量-体积直方图指标,包括从 5 Gy 剂量中保留的绝对肺体积(VS5),以与 NCI-CTC 分级 3 以上的 RP(RP≥G3)相关。还分析了临床因素,包括基线胸部 CT 上的肺纤维化评分(PFS)和肺气肿评分。
14 例(11.4%)患者发生≥G3 级 RP。单因素分析显示,所有剂量-体积直方图指标、性别和基线 CT 上的 PFS 均与≥G3 级 RP 的发生显著相关(p<0.05)。多因素分析显示,V20≥26%、VS5<1500cc、年龄≥68 岁和基线 CT 上的 PFS≥2 是显著的危险因素。因此,我们定义了一个新的预测风险评分(PRS),将这些因素结合在一起。当 PRS 为 0、3-5、6-8 和 9-14 时,12 个月时≥G3 级 RP 的累积发生率分别为 0%、7.8%、26.6%和 71.4%(p<0.001)。与 V20 和 VS5 联合或 V20 单独相比,该 PRS 在预测 RP 方面更优(曲线下面积,0.888 对 0.779 对 0.678)。
V20、VS5、年龄和基线 CT 上的 PFS 是发生严重 RP 的独立和显著危险因素。结合这些因素可以提高严重 RP 的预测能力。