Roldán Gloria B, Scott James N, McIntyre John B, Dharmawardene Marisa, de Robles Paula A, Magliocco Anthony M, Yan Elizabeth S Y, Parney Ian F, Forsyth Peter A, Cairncross J Gregory, Hamilton Mark G, Easaw Jacob C
Department of Oncology, Tom Baker Cancer Centre, Alberta Cancer Board, Department of Clinical Neurosciences, University of Calgary, Calgary, AB, Canada.
Can J Neurol Sci. 2009 Sep;36(5):617-22. doi: 10.1017/s0317167100008131.
Chemoradiotherapy followed by monthly temozolomide (TMZ) is the standard of care for patients with glioblastoma multiforme (GBM). Case reports have identified GBM patients who experienced transient radiological deterioration after concurrent chemoradiotherapy which stabilized or resolved after additional cycles of adjuvant TMZ, a phenomenon known as radiographic pseudoprogression. Little is known about the natural history of radiographic pseudoprogression.
We retrospectively evaluated the incidence of radiographic pseudoprogression in a population-based cohort of GBM patients and determined its relationship with outcome and MGMT promoter methylation status.
Out of 43 evaluable patients, 25 (58%) exhibited radiographic progression on the first MRI after concurrent treatment. Twenty of these went on to receive adjuvant TMZ, and subsequent investigation demonstrated radiographic pseudoprogression in 10 cases (50%). Median survival (MS) was better in patients with pseudoprogression (MS 14.5 months) compared to those with true radiologic progression (MS 9.1 months, p=0.025). The MS of patients with pseudoprogression was similar to those who stabilized/responded during concurrent treatment (p=0.31). Neither the extent of the initial resection nor dexamethasone dosing was associated with pseudoprogression.
These data suggest that physicians should continue adjuvant TMZ in GBM patients when early MRI scans show evidence of progression following concurrent chemoradiotherapy, as up to 50% of these patients will experience radiologic stability or improvement in subsequent treatment cycles.
同步放化疗后每月给予替莫唑胺(TMZ)是多形性胶质母细胞瘤(GBM)患者的标准治疗方案。病例报告显示,GBM患者在同步放化疗后出现短暂的影像学恶化,在辅助TMZ的额外疗程后病情稳定或缓解,这一现象称为影像学假性进展。关于影像学假性进展的自然病程知之甚少。
我们回顾性评估了基于人群的GBM患者队列中影像学假性进展的发生率,并确定其与预后及O6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子甲基化状态的关系。
在43例可评估的患者中,25例(58%)在同步治疗后的首次磁共振成像(MRI)上显示影像学进展。其中20例继续接受辅助TMZ治疗,后续检查显示10例(50%)存在影像学假性进展。假性进展患者的中位生存期(MS)(14.5个月)优于真正影像学进展的患者(MS 9.1个月,p = 0.025)。假性进展患者的MS与同步治疗期间病情稳定/缓解的患者相似(p = 0.31)。初始切除范围和地塞米松剂量均与假性进展无关。
这些数据表明,当早期MRI扫描显示同步放化疗后有进展迹象时,医生应继续对GBM患者进行辅助TMZ治疗,因为这些患者中高达一半将在后续治疗周期中出现影像学稳定或改善。