Abstract
BACKGROUND AND PURPOSE: Early assessment of treatment response is critical in patients with glioblastomas. A combination of DTI and DSC perfusion imaging parameters was evaluated to distinguish glioblastomas with true progression from mixed response and pseudoprogression.
MATERIALS AND METHODS: Forty-one patients with glioblastomas exhibiting enhancing lesions within 6 months after completion of chemoradiation therapy were retrospectively studied. All patients underwent surgery after MR imaging and were histologically classified as having true progression (>75% tumor), mixed response (25%–75% tumor), or pseudoprogression (<25% tumor). Mean diffusivity, fractional anisotropy, linear anisotropy coefficient, planar anisotropy coefficient, spheric anisotropy coefficient, and maximum relative cerebral blood volume values were measured from the enhancing tissue. A multivariate logistic regression analysis was used to determine the best model for classification of true progression from mixed response or pseudoprogression.
RESULTS: Significantly elevated maximum relative cerebral blood volume, fractional anisotropy, linear anisotropy coefficient, and planar anisotropy coefficient and decreased spheric anisotropy coefficient were observed in true progression compared with pseudoprogression (P < .05). There were also significant differences in maximum relative cerebral blood volume, fractional anisotropy, planar anisotropy coefficient, and spheric anisotropy coefficient measurements between mixed response and true progression groups. The best model to distinguish true progression from non–true progression (pseudoprogression and mixed) consisted of fractional anisotropy, linear anisotropy coefficient, and maximum relative cerebral blood volume, resulting in an area under the curve of 0.905. This model also differentiated true progression from mixed response with an area under the curve of 0.901. A combination of fractional anisotropy and maximum relative cerebral blood volume differentiated pseudoprogression from nonpseudoprogression (true progression and mixed) with an area under the curve of 0.807.
CONCLUSIONS: DTI and DSC perfusion imaging can improve accuracy in assessing treatment response and may aid in individualized treatment of patients with glioblastomas.
ABBREVIATIONS:
- AUC
- area under the curve
- CL
- linear anisotropy coefficient
- CP
- planar anisotropy coefficient
- CS
- spheric anisotropy coefficient
- FA
- fractional anisotropy
- LRM
- logistic regression model
- max
- maximum
- MD
- mean diffusivity
- PsP
- pseudoprogression
- rCBV
- relative cerebral blood volume
- TP
- true progression
The current standard of care for newly diagnosed glioblastomas is surgical resection and concurrent temozolomide radiation therapy, followed by at least 6 months of adjuvant temozolomide. Treatment outcome is generally monitored by using standard clinical MR imaging based on accepted guidelines such as the updated Response Assessment in Neuro-Oncology criteria.1,2 However, the appearance of enhancing lesions on MR imaging within the first 6 months after completion of chemoradiation therapy poses a challenge because it can reflect true progression (TP) or treatment-related changes known as pseudoprogression (PsP). PsP occurs in approximately a third of all patients with glioblastoma,3 in which lesions often decrease in size or stabilize without further treatment, resulting in a longer survival. Accurate identification of PsP and TP is critical because patients with TP may require a change in therapeutic strategy while those with PsP may not. While published reports have attempted to differentiate PsP from TP,4⇓⇓–7 these studies did not account for the common finding of a mixture of treatment-related changes and recurrent tumor. Management of these partial responders may be challenging, with short-interval imaging studies often required to determine clinical course. If identified early, these patients may benefit from novel therapeutics.
Mean diffusivity (MD), measured from diffusion imaging, has been used to diagnose and monitor treatment response in brain tumors.8,9 Both mean and minimum MD values have been used in differentiating PsP from TP.4⇓–6,10 However, due to the heterogeneity of treatment response, MD may have a limited role because reduced diffusion could represent not only highly cellular tumor areas but also inflammatory processes.9 DTI is increasingly being used in the characterization of glioblastomas9,11; anisotropy measures, including fractional anisotropy (FA), linear anisotropy (CL), planar anisotropy (CP), and spheric anisotropy (CS), have been used to differentiate glioblastomas from metastasis11⇓–13 and primary cerebral lymphomas.12,14 However, only 1 study has used DTI for differentiation of PsP and TP.15
Relative cerebral blood volume (rCBV) obtained from DSC perfusion imaging has been widely used for tumor grading,16 distinguishing recurrent tumor from radiation necrosis,17 and differentiating PsP from TP.18,19 Some studies have suggested that median rCBV and histogram analysis of rCBV can help differentiate PsP from TP.18,20⇓–22 However, rCBV has not been used to identify a mixed or partial response.
The clinical management of patients with recurrent glioblastoma is rapidly changing because several alternative therapeutic options are being investigated, including bevacizumab,23 tumor treating fields,24 and immunotherapy.25 Increased incidence of PsP poses a dilemma for the treating physicians because determining the optimal therapeutic approach relies on a definitive diagnosis of TP, PsP, or mixed response. We hypothesize that DTI and DSC parameters have added value in making this differentiation and thus evaluated them for differentiating these 3 categories of treatment response.
Materials and Methods
Patients
This study was approved by the institutional review board and was compliant with the Health Insurance Portability and Accountability Act. MR imaging data from 41 patients with glioblastomas (14 women/27 men; 55.71 ± 11.83 years of age; age range, 23–80 years), who had initially undergone gross total resection of the tumor followed by standard radiation therapy and temozolomide chemotherapy and exhibited new enhancing lesions on follow-up MR imaging within 6 months after completion of radiation therapy, were retrieved from the University of Pennsylvania data base from May 2011 to May 2014 and retrospectively analyzed. All patients underwent repeat surgery within 2 weeks after the MR imaging study in which the new enhancing lesions were first observed.
MR Imaging Data Acquisition
MR imaging studies were performed on a Tim Trio 3T whole-body scanner (Siemens, Erlangen, Germany) by using a 12-channel phased array head coil. Routine sequences included axial T1-weighted 3D MPRAGE (TR/TE/TI = 1760/3.1/950 ms, 192 × 256 matrix size, 1-mm section thickness) and axial FLAIR (TR/TE/TI = 9420/141/2500 ms, 3-mm section thickness). DTI data were acquired by using a single-shot spin-echo EPI sequence with parallel imaging by using generalized autocalibrating partially parallel acquisition and an acceleration factor of 2. Diffusion weighting was applied in 30 isotropically distributed directions by using a b-value of 1000 s/mm2, with a total acquisition time of 8 minutes. For DSC imaging, a bolus of gadobenate dimeglumine (MultiHance; Bracco Diagnostics, Princeton, New Jersey) was injected with a preloading dose of 0.07 mmol/kg, which was used to reduce the effect of contrast agent leakage on CBV measurements.26 DSC imaging was performed by using a gradient-echo echo-planar imaging sequence during a second 0.07-mmol/kg bolus of contrast agent (TR/TE = 2000/45 ms, FOV = 22 × 22 cm2, resolution = 1.72 × 1.72 × 3 mm3, 20 sections, 45 measurements with at least 10 image volumes before bolus arrival, acquisition time = 1 minute 38 seconds). The injection rate was 5 mL/s for all patients and was immediately followed by a bolus injection of saline (total of 20 mL at the same rate). Postcontrast T1-weighted 3D MPRAGE images were acquired after completion of the DSC sequence.
Image Processing
The diffusion tensor datasets were coregistered to the b=0 s/mm2 images by using a 3D affine transformation estimated by maximizing the mutual information between the images.13 The corrected raw images were combined to estimate the DTI parametric maps by using in-house software (IDL; ITT Visual Information Solutions, Boulder, Colorado). Pixel-wise MD, FA, CL, CP, and CS maps were computed by using the methods described earlier.11,12 Leakage-corrected CBV maps using the γ variate function were generated by using NordicICE software (NordicNeuroLab, Bergen, Norway).
The DTI, CBV maps, and FLAIR images were coregistered to contrast-enhanced T1-weighted images. The CBV maps were normalized to the contralateral normal white matter to generate rCBV. A semiautomatic segmentation approach was used to generate a mask from the enhancing region by using the methods described earlier.11⇓–13 The median DTI metrics and rCBV values from the enhancing region were measured. In addition, the lower 10th percentile MD values were measured from the enhancing region and reported as minimum MD.27 The top 90th percentile rCBV values were measured from the enhancing region and reported as rCBVmax.12 Data analysis tools, including DTI computing, image coregistration, and segmentation, were implemented by using IDL routines. The total time for postprocessing was approximately 2 hours.
Histologic Analysis
Pathologic samples were originally cut, mounted, and stained with hematoxylin-eosin by standard methods. Immunohistochemistry for Ki-67 (mouse monoclonal, MIB-1, IR62661; Dako, Carpinteria, California) and p53 (mouse monoclonal, 1:60; DO-7, M7001; Dako) was performed by using a Bond III automated system (Leica Biosystems, Buffalo Grove, Illinois). The entirety of submitted material for each case was examined by a board-certified neuropathologist (M.M.-L.) who was blinded to the results of the MR imaging studies. The slides were examined to determine the relative degree of recurrent glioma and treatment-related changes. The percentage of geographic tissue necrosis across the specimen was assessed in an initial approach, excluding normal or quasinormal brain parenchyma. Histologic features associated with treatment, including vascular necrosis, hyalinization, hemosiderin, lymphocyte and macrophage infiltrates, gliosis, fibrosis, and dystrophic calcification, were also documented. Tumor-specific characteristics within the specimen, including neoplastic high cellularity, the presence of pseudopalisading necrosis, endothelial cell proliferation, and increased mitotic activity were additionally used to either increase or decrease the weightage for the presence of overall malignant features. The patients were grouped in 3 categories: <25% malignant features, PsP (8 patients; 3 women/5 men; 48.5 ± 12.72 years of age); 25%–75% malignant features, mixed tumor with treatment response (12 patients; 5 women/7 men; 58.25 ± 7.47 years of age); and >75% malignant features, TP (21 patients; 6 women/15 men; 57.0 ± 12.9 years of age). Strong and diffuse nuclear staining for p53 was used as supportive evidence of the presence of tumor, but the lack of staining did not reject the presence of recurrent glioma. We calculated the proliferative index with Ki-67 for each case as a percentage of positive tumor cells, avoiding areas of inflammatory infiltrates.
Statistical Analysis
A Mann-Whitney U test was used to compare the difference in the median MD, FA, CL, CP, CS, and rCBV values and minimum MD and rCBVmax among PsP, mixed, and TP groups. Bonferroni correction was used to adjust for multiple comparisons, and a P value < .05 was considered significant. A multivariate logistic regression model (LRM) was used to determine the best classification model, and a leave-one-out cross-validation approach was applied to estimate the accuracy of the LRM. Areas under the receiver operating characteristic curves (AUCs) were computed by using the selected parameters and the LRM output. A cutoff value for each parameter was determined by maximizing the sum of sensitivity and specificity. All statistical analyses were conducted by using PASW Statistics, Version 18 (IBM, Armonk, New York).
Results
Representative MR images and histologic photomicrographs from patients with PsP, mixed, and TP features are shown in Figs 1⇓–3, respectively. MD maps demonstrate variable degrees of diffusivity from the enhancing parts of the tumor. Anisotropy and rCBV maps also show variability. However, quantitative analysis revealed significantly higher median FA, CL, and CP values and higher rCBV in patients with TP compared with PsP and mixed response (Fig 4).
A pair-wise comparison of DTI and DSC parameters from enhancing tissue is shown in Fig 4. While median MD values did not show significant differences between groups (P > .05), significantly higher rCBVmax (4.75 versus 2.90, P = .007), FA (0.14 versus 0.11, P = .008), CL (0.05 versus 0.04, P = .04), and CP (0.08 versus 0.06, P = .002), and decreased CS (0.87 versus 0.90, P = .004) were observed in TP compared with PsP. There were also significant differences between mixed and TP groups in rCBVmax (4.75 versus 3.31, P = .02), FA (0.14 versus 0.11, P = .01), CP (0.08 versus 0.06, P = .001), and CS (0.87 versus 0.89, P = .02) measurements. None of the parameters demonstrated a significant difference between PsP and mixed response. Of all the parameters, CP and CS showed a significant difference between PsP and TP, and CP showed a significant difference between mixed and TP after Bonferroni correction (P < .006).
Discrimination of TP versus PsP and Mixed Response
The discrimination analysis was first performed to distinguish TP from PsP and mixed response. CP was the single best predictor for classification (AUC = 0.84), followed by FA and rCBVmax (AUC = 0.78, Table). The imaging parameters were then used for a multivariate logistic regression analysis with backward stepwise selection, which indicated that the best classification of TP from non-TPs, including PsP and mixed, was achieved with 3 parameters, FA, CL, and rCBVmax, as follows: where β0 = −16.17, β1 = 194.01, β2 = −285.65, and β3 = 1.21. Figure 5A shows the receiver operating characteristic curves for the best LRM and selected parameters. The cutoff value for the LRM was 0.55 with a sensitivity = 76%, specificity = 95%, and AUC = 0.905 (Table). Leave-one-out cross-validation analysis revealed that 78% of cases were correctly classified by using the LRM. Although CP was the single best predictor, it was not selected by the statistical model for highest sensitivity. Using forward stepwise selection, the best model included CP and rCBVmax, resulting in an AUC of 0.89, similar to the model FA, CL, and rCBVmax. In addition, there was a high correlation (r = 0.84) between FA and CP (On-line Figure), suggesting that the results from either model were similar.
Discrimination of PsP versus TP and Mixed Response
The single best predictor for classification was CP (AUC = 0.74), followed by rCBVmax (AUC = 0.73) and FA (AUC = 0.70, Table). The best LRM for classification of PsP from non-PsPs, including TP and mixed response, was achieved with 2 parameters, FA and rCBVmax, as follows: where β0 = −3.59, β1 = 23.52, and β2 = 0.62. Figure 5B shows the receiver operating characteristic curves for the best LRM and selected parameters. The cutoff value for the LRM was 0.77 with sensitivity = 79%, specificity = 75%, and AUC = 0.807 (Table). Leave-one-out cross-validation analysis revealed that 63.4% of cases were correctly classified by using the LRM.
Discrimination between TP and Mixed Response
A subanalysis was performed to differentiate TP from mixed response so that the patients with mixed response could be closely monitored with short-interval imaging scans or enrolled in novel therapeutic trials. CP was again the single best predictor for classification (AUC = 0.83), followed by FA (AUC = 0.76) and rCBVmax (AUC = 0.74, Table). The LRM for classification of TP from mixed response was achieved with 3 parameters, including FA, CL, and rCBVmax, as follows: where β0 = −15.43, β1 = 202.14, β2 = −313.99, and β3 = 1.20. Figure 5C shows the receiver operating characteristic curves for the best LRM and selected parameters. The cutoff value for the LRM was 0.65 with sensitivity = 76%, specificity = 100%, and AUC = 0.901 (Table). Leave-one-out cross-validation analysis revealed that 72.7% of cases were correctly classified by using the LRM.
Discrimination of PsP from Mixed Response
A final analysis to differentiate patients with PsP from those with mixed response showed a significant overlap between the 2 groups, with only MD having some predictive value with an AUC = 0.62 followed by rCBVmax (AUC = 0.57).
Discussion
The heterogeneity and variability in response did not allow differentiating TP from PsP simply by visual inspection of the parametric maps. However, a quantitative analysis of DTI parameters and rCBVmax from the enhancing regions of the lesion demonstrated better assessment of treatment response in patients with glioblastomas. Such a categorization is clinically feasible because the postprocessing time was only approximately 2 hours, indicating that our proposed analytic approach may aid in individualized treatment management and better clinical decision-making.
Identification of TP
Early identification of TP could prevent further delays in repeat surgery or enrollment in alternative clinical trials. The LRM analysis indicated that the best model to distinguish TP from PsP or mixed responses was based on FA, CL, and rCBVmax. Higher anisotropy values have been reported in glioblastomas compared with brain metastases and primary cerebral lymphomas.11⇓–13 High FA in glioblastomas is probably related to the orientation of overproduced extracellular matrix.11,28 Glioblastoma tumor cells produce large amounts of tumor-specific extracellular matrix components, which can serve as a substrate for adhesion and subsequent migration of the tumor cells through the enlarged extracellular space,28 which may explain the elevated anisotropy observed in patients with TP. However, a previous study reported no difference in anisotropy measures between PsP and TP.15 Potential reasons for this discrepancy may be because we divided the patients on the basis of the histologic features as opposed to grouping on the basis of follow-up imaging used in the previous study.15 In addition, we assessed 3 categories, including mixed response, instead of just separating PsP and TP.
DSC imaging can be helpful in differentiating tumor recurrence from radiation necrosis.17,29 Recent studies have also used DSC imaging18,19,21 to detect TP from PsP. Kong et al18 reported that a mean rCBV value of 1.47 had 81.5% sensitivity and 77.8% specificity in differentiating PsP from TP, while Kim et al20 reported a histogram analysis of rCBV, in which a peak height position of 1.7 showed 90.2% sensitivity and 91.1% specificity for differentiating tumor recurrence from treatment changes. In comparison, we used rCBVmax and observed that a threshold rCBVmax value of 4.06 led to a sensitivity of 62% and specificity of 80% in differentiating TP from PsP and mixed tumors.
Identification of PsP
Accurate identification of PsP is critical for patient management because unnecessary repeat surgery/biopsy can be avoided in these patients and they can continue on an effective temozolomide regimen with standard imaging follow-up of 3–6 months, thereby reducing patient care costs. Logistic regression analysis showed that the best model to differentiate PsP from TP and mixed response included FA and rCBVmax.
Pseudoprogression is predominantly a subacute treatment-related reaction. Pathologically, it corresponds to gliosis and radiation-induced reactive changes including disruption of the BBB, inflammation, increased permeability, and edema. These changes cause increased enhancement on MR imaging and can mimic TP.9 Several studies have reported that PsP exhibits higher MD values from the enhancing region than TP, partly due to the extent of cellular death and vascular changes in PsP.4,6 Minimum MD values have been reported to be prognostic of outcomes in gliomas.30 Chu et al5 reported that the fifth percentile of the cumulative MD histogram was the most promising parameter in the differentiation of TP and PsP. Although we found a similar trend for minimum MD, calculated from the 10th percentile of the MD value, it did not reach statistical significance. There are a limited number of studies regarding the role of FA in the evaluation of treatment response.15,31 Xu et al31 reported a low FA ratio in radiation necrosis compared with recurrent tumor. rCBV measurements have also been used in identifying PsP.9,32 The inflammation/necrotic processes involved in PsP result in lower rCBV values,9,32 and our results confirm this hypothesis. In addition, our study showed that a combination of FA and rCBVmax can help in identifying PsP from TP or mixed response.
Identification of Mixed Response
On a practical level, posttreatment new enhancing lesions usually contain a mixture of viable neoplasm and treatment-induced changes, and a more accurate assessment of the relative contribution of each entity can guide clinical decision-making. However, most previous studies have attempted to only differentiate between PsP and TP.4,6,15,19 DTI and DSC imaging findings between viable neoplasm and treatment-induced changes are variable and difficult to synthesize on routine visual inspection. We believe the quantitative analysis of imaging parameters8,33 should yield a better estimate of each component. Our findings indicate that DTI and perfusion may have a complementary predictive value for the evaluation of treatment response and demonstrate that a combination of FA, CL and rCBVmax can differentiate mixed response from TP with high sensitivity. Although similar trends were observed between PsP and mixed response, DTI and DSC parameters had relatively modest utility in distinguishing mixed response from PsP. Because dynamic contrast-enhanced MR imaging is increasingly being used to assess brain tumors, we believe future studies including quantitative dynamic contrast-enhanced–based parameters may further enhance the sensitivity of our method in differentiating PsP from mixed response.
While these results are promising, the study has some limitations, including a retrospective analysis design and a relatively smaller sample size. In addition, image-guided biopsy may be necessary to evaluate the pathophysiologic basis of higher CP and FA in TP. A clinical follow-up study by using progression-free or overall analysis as end points for determination of PsP and TP at the time of initial MR imaging is desirable because not all patients will undergo repeat surgery for confirmation of imaging findings.
Conclusions
Our study shows that a combination of DTI and DSC perfusion parameters can help in the evaluation of treatment response in glioblastomas and may aid in the optimal management of these patients.
Acknowledgments
We acknowledge Tianyu Yin for assistance in data analysis; Dr Ruyun Jin, Medical Data Research Center, Providence Health & Services, Portland, Oregon, for statistical analysis; and research coordinators Lisa Desiderio, Katelyn Reilly, and Krista Huff.
Footnotes
Disclosures: Maria Martinez-Lage—RELATED: National Institutes of Health (Principal Investigator: Harish Poptani).* Suyash Mohan—RELATED: Grant: National Institutes of Health (R21 grant).* Ronald L. Wolf—RELATED: Grant: National Institutes of Health,* Comments: 5-R21-CA-170284–02 direct/indirect support. I get a small amount of salary support under this grant (<$10,000); previous Principal Investigator H. Poptani, but now I am the Principal Investigator on behalf of the University of Pennsylvania. Arati Desai—RELATED: Grant: National Institutes of Health (R21).* Harish Poptani—RELATED: Grant: National Institutes of Health*; UNRELATED: Consultancy: American College of Radiology Image Metrix, Comments: consulting for MRS study trials; Grants/Grants Pending: National Institutes of Health.* *Money paid to the institution.
This work was supported by National Institutes of Health grant 1R21CA170284.
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References
- Received March 10, 2015.
- Accepted after revision June 2, 2015.
- © 2016 by American Journal of Neuroradiology