Abstract
Purpose was to assess predictive power for overall survival (OS) and diagnostic performance of combination of susceptibility-weighted MRI sequences (SWMRI) and dynamic susceptibility contrast (DSC) perfusion-weighted imaging (PWI) for differentiation of recurrence and radionecrosis in high-grade glioma (HGG). We enrolled 51 patients who underwent radiation therapy or gamma knife surgeryfollowed by resection for HGG and who developed new measurable enhancement more than six months after complete response. The lesions were confirmed as recurrence (n = 32) or radionecrosis (n = 19). The mean and each percentile value from cumulative histograms of normalized CBV (nCBV) and proportion of dark signal intensity on SWMRI (proSWMRI, %) within enhancement were compared. Multivariate regression was performed for the best differentiator. The cutoff value of best predictor from ROC analysis was evaluated. OS was determined with Kaplan-Meier method and log-rank test. Recurrence showed significantly lower proSWMRI and higher mean nCBV and 90th percentile nCBV (nCBV90) than radionecrosis. Regression analysis revealed both nCBV90 and proSWMRI were independent differentiators. Combination of nCBV90 and proSWMRI achieved 71.9% sensitivity (23/32), 100% specificity (19/19) and 82.3% accuracy (42/51) using best cut-off values (nCBV90 > 2.07 and proSWMRI≤15.76%) from ROC analysis. In subgroup analysis, radionecrosis with nCBV > 2.07 (n = 5) showed obvious hemorrhage (proSWMRI > 32.9%). Patients with nCBV90 > 2.07 and proSWMRI≤15.76% had significantly shorter OS. In conclusion, compared with DSC PWI alone, combination of SWMRI and DSC PWI have potential to be prognosticator for OS and lower false positive rate in differentiation of recurrence and radionecrosis in HGG who develop new measurable enhancement more than six months after complete response.
Highlights
High-grade glioma accounts for approximately 50 % of primary malignant cerebral tumors and includes glioblastoma [World Health Organization (WHO) grade IV], anaplastic astrocytoma, mixed anaplastic oligoastrocytoma and anaplastic oligodendroglioma (WHO grade III) [1, 2]
We hypothesized that the combined use of SWMRI and dynamic susceptibility contrast (DSC) perfusion-weighted imaging (PWI) could have the potential as prognostic factor for overall survival (OS) and improve the accuracy of the differential diagnosis of recurrence from radionecrosis in high-grade glioma patients
We found that the mean normalized CBV (nCBV) and nCBV90 were higher, and the proSWMRI was lower in the contrast-enhanced regions of recurrence compared with those of radionecrosis
Summary
High-grade glioma accounts for approximately 50 % of primary malignant cerebral tumors and includes glioblastoma [World Health Organization (WHO) grade IV], anaplastic astrocytoma, mixed anaplastic oligoastrocytoma and anaplastic oligodendroglioma (WHO grade III) [1, 2]. Several characteristic imaging features of radiationrelated changes on MRI have been identified, including diffuse white matter edema-like changes, cysts and contrast-enhancing lesions [6,7,8]. Among these changes, newly appearing contrast-enhancing lesions, usually termed as pseudoprogression or radionecrosis, receive the attention of both clinicians and neuroradiologists because these MRI lesions can mimic the recurrence of tumors. Pseudoprogression refers to acute to subacute radiation-related changes; it typically occurs within 12 weeks and may occur up to 6 months after post-irradiation. Radionecrosis, on the other hand, encompasses late radiation-related changes occurring months to years’ post-irradiation [9]. The incidence of radionecrosis is reported between 3 % - 24 % [11]
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