Wu Yu-Cheng, Hsu Hsian-He, Chang Wei-Chou, Tung Ho-Jui, Ko Kai-Hsiung, Hsu Yi-Chih, Huang Tsai-Wang, Ho Ching-Liang, Chang Hung
Department of Radiology, Tri-Service General Hospital, National Defense Medical Center, 325, Section 2, Cheng-Gong Road, Nei-Hu, Taipei, 114, Taiwan, Republic of China.
Eur Radiol. 2015 Jun;25(6):1801-13. doi: 10.1007/s00330-014-3579-x. Epub 2015 Jan 11.
We aimed to determine whether initial tumour responses measured during short-term follow-up computed tomography (CT) examinations after baseline examinations would correlate with clinical outcomes in patients with non-small cell lung cancer (NSCLC) who received epidermal growth factor receptor (EGFR)-targeted therapy.
A total of 86 gefitinib-treated patients with advanced adenocarcinoma of the lung were retrospectively reviewed. All patients underwent baseline and short-term follow-up CT examinations. The new response criteria (NRC) by Lee et al. were used for the response evaluations. A Cox proportional hazards multiple regression model and Kaplan-Meier survival analyses were used to evaluate correlations between the initial tumour changes and progression-free and overall survival (PFS, OS).
Better separation and smaller p values were observed for both PFS and OS when good and poor disease responses (as defined by NRC) were compared after excluding tumours with characteristic morphologies. Early tumour changes correlated with PFS in a size-dependent manner. Moreover, a stronger association was observed between size changes and PFS when characteristic morphology was also considered.
Initial changes in tumour size during short-term post-treatment CT examinations could act as a potential prognostic imaging surrogate for PFS in gefitinib-treated patients with advanced adenocarcinoma of the lung.
• Initial responses to gefitinib on computed tomography significantly correlate with clinical outcomes. • Regardless of morphology, size decrease greater than 30 % predicts prolonged progression-free and overall survival. • Combination of size and morphological changes yields prognostic independence regarding progression-free survival.
我们旨在确定在基线检查后的短期随访计算机断层扫描(CT)检查中测得的初始肿瘤反应是否与接受表皮生长因子受体(EGFR)靶向治疗的非小细胞肺癌(NSCLC)患者的临床结局相关。
回顾性分析了86例接受吉非替尼治疗的晚期肺腺癌患者。所有患者均接受了基线和短期随访CT检查。采用Lee等人提出的新反应标准(NRC)进行反应评估。使用Cox比例风险多元回归模型和Kaplan-Meier生存分析来评估初始肿瘤变化与无进展生存期和总生存期(PFS、OS)之间的相关性。
在排除具有特征性形态的肿瘤后,比较良好和不良疾病反应(根据NRC定义)时,PFS和OS均观察到更好的区分度和更小的p值。早期肿瘤变化与PFS呈大小依赖性相关。此外,当同时考虑特征性形态时,大小变化与PFS之间的关联更强。
治疗后短期CT检查中肿瘤大小的初始变化可作为接受吉非替尼治疗的晚期肺腺癌患者PFS的潜在预后影像替代指标。
• 吉非替尼在计算机断层扫描上的初始反应与临床结局显著相关。• 无论形态如何,大小减小超过30%可预测无进展生存期和总生存期延长。• 大小和形态变化的组合在无进展生存期方面具有预后独立性。