Faculty of Medicine, University of Toronto, Toronto, Canada.
Radiat Oncol. 2011 Sep 23;6:121. doi: 10.1186/1748-717X-6-121.
Early and accurate prediction of response to cancer treatment through imaging criteria is particularly important in rapidly progressive malignancies such as Glioblastoma Multiforme (GBM). We sought to assess the predictive value of structural imaging response criteria one month after concurrent chemotherapy and radiotherapy (RT) in patients with GBM.
Thirty patients were enrolled from 2005 to 2007 (median follow-up 22 months). Tumor volumes were delineated at the boundary of abnormal contrast enhancement on T1-weighted images prior to and 1 month after RT. Clinical Progression [CP] occurred when clinical and/or radiological events led to a change in chemotherapy management. Early Radiologic Progression [ERP] was defined as the qualitative interpretation of radiological progression one month post-RT. Patients with ERP were determined pseudoprogressors if clinically stable for ≥6 months. Receiver-operator characteristics were calculated for RECIST and MacDonald criteria, along with alternative thresholds against 1 year CP-free survival and 2 year overall survival (OS).
13 patients (52%) were found to have ERP, of whom 5 (38.5%) were pseudoprogressors. Patients with ERP had a lower median OS (11.2 mo) than those without (not reached) (p < 0.001). True progressors fared worse than pseudoprogressors (median survival 7.2 mo vs. 19.0 mo, p < 0.001). Volume thresholds performed slightly better compared to area and diameter thresholds in ROC analysis. Responses of > 25% in volume or > 15% in area were most predictive of OS.
We show that while a subjective interpretation of early radiological progression from baseline is generally associated with poor outcome, true progressors cannot be distinguished from pseudoprogressors. In contrast, the magnitude of early imaging volumetric response may be a predictive and quantitative metric of favorable outcome.
在快速进展的恶性肿瘤(如多形性胶质母细胞瘤,GBM)中,通过影像学标准尽早准确预测治疗反应尤为重要。我们旨在评估 GBM 患者在同步放化疗后一个月时的结构影像学反应标准的预测价值。
我们于 2005 年至 2007 年间入组了 30 名患者(中位随访时间 22 个月)。在放化疗前和放化疗后 1 个月,于 T1 加权图像上的异常对比增强边界勾画肿瘤体积。当临床和/或影像学事件导致化疗管理改变时,发生临床进展[CP]。早期影像学进展[ERP]定义为在 RT 后一个月对影像学进展的定性解释。如果患者在 6 个月以上的时间里保持临床稳定,则被确定为假性进展者。我们计算了 RECIST 和 MacDonald 标准以及针对 1 年无 CP 生存率和 2 年总生存率(OS)的替代阈值的接受者操作特征。
13 名患者(52%)被发现存在 ERP,其中 5 名(38.5%)为假性进展者。ERP 患者的中位 OS(11.2 个月)明显低于无 ERP 患者(未达到)(p < 0.001)。真正的进展者比假性进展者预后更差(中位生存时间 7.2 个月 vs. 19.0 个月,p < 0.001)。ROC 分析显示,与面积和直径阈值相比,体积阈值的性能略好。体积增加> 25%或面积增加> 15%与 OS 最相关。
我们表明,虽然基线时早期影像学进展的主观解释通常与不良预后相关,但无法将真正的进展者与假性进展者区分开来。相比之下,早期影像学体积反应的幅度可能是预后良好的预测和定量指标。