Division of Clinical Neurooncology, Department of Neurology, University Hospital Bonn, Bonn, Germany.
Department of Neuroradiology, University Hospital Bonn, Bonn, Germany.
J Neurooncol. 2023 Sep;164(3):607-616. doi: 10.1007/s11060-023-04444-x. Epub 2023 Sep 20.
In the randomized CeTeG/NOA-09 trial, lomustine/temozolomide (CCNU/TMZ) was superior to TMZ therapy regarding overall survival (OS) in MGMT promotor-methylated glioblastoma. Progression-free survival (PFS) and pseudoprogression rates (about 10%) were similar in both arms. Further evaluating this discrepancy, we analyzed patterns of postprogression survival (PPS) and MRI features at first progression according to modified RANO criteria (mRANO).
We classified the patients of the CeTeG/NOA-09 trial according to long vs. short PPS employing a cut-off of 18 months and compared baseline characteristics and survival times. In patients with available MRIs and confirmed progression, the increase in T-enhancing, FLAIR hyperintense lesion volume and the change in ADC mean value of contrast-enhancing tumor upon progression were determined.
Patients with long PPS in the CCNU/TMZ arm had a particularly short PFS (5.6 months). PFS in this subgroup was shorter than in the long PPS subgroup of the TMZ arm (11.1 months, p = 0.01). At mRANO-defined progression, patients of the CCNU/TMZ long PPS subgroup had a significantly higher increase of mean ADC values (p = 0.015) and a tendency to a stronger volumetric increase in T-enhancement (p = 0.22) as compared to long PPS patients of the TMZ arm.
The combination of survival and MRI analyses identified a subgroup of CCNU/TMZ-treated patients with features that sets them apart from other patients in the trial: short first PFS despite long PPS and significant increase in mean ADC values upon mRANO-defined progression. The observed pattern is compatible with the features commonly observed in pseudoprogression suggesting mRANO-undetected pseudoprogressions in the CCNU/TMZ arm of CeTeG/NOA-09.
在随机对照 CeTeG/NOA-09 试验中,洛莫司汀/替莫唑胺(CCNU/TMZ)在 MGMT 启动子甲基化胶质母细胞瘤患者的总生存期(OS)方面优于 TMZ 治疗。无进展生存期(PFS)和假性进展率(约 10%)在两组中相似。为了进一步评估这种差异,我们根据改良的 RANO 标准(mRANO)分析了首次进展时的后进展生存(PPS)模式和 MRI 特征。
我们根据 18 个月的截止值将 CeTeG/NOA-09 试验的患者分为长 PPS 与短 PPS,比较了基线特征和生存时间。在有可用 MRI 且证实进展的患者中,确定了 T 增强、FLAIR 高信号病变体积的增加以及进展时增强肿瘤的 ADC 平均值的变化。
CCNU/TMZ 组中 PPS 较长的患者 PFS 特别短(5.6 个月)。该亚组的 PFS 短于 TMZ 组的长 PPS 亚组(11.1 个月,p=0.01)。在 mRANO 定义的进展时,CCNU/TMZ 长 PPS 亚组的患者 ADC 值的平均增加显著更高(p=0.015),并且 T 增强的体积增加趋势更强(p=0.22),与 TMZ 组的长 PPS 患者相比。
生存和 MRI 分析的结合确定了 CCNU/TMZ 治疗患者的亚组,这些特征将他们与试验中的其他患者区分开来:尽管 PPS 较长,但首次 PFS 较短,并且在 mRANO 定义的进展时平均 ADC 值显著增加。观察到的模式与假性进展中常见的特征一致,表明 CeTeG/NOA-09 中 CCNU/TMZ 臂的 mRANO 未检出假性进展。