Diffusional kurtosis imaging for differentiating between high-grade glioma and primary central nervous system lymphoma
Haopeng Pang1, Yan Ren1, Zhenwei Yao1, Jingsong Wu1, Chengjun Yao1, Xuefei Dang2, Yong Zhang3, and Xiaoyuan Feng1

1Affiliated Huashan Hospital of Fudan University, Shanghai, China, People's Republic of, 2The 307th Hospital of Chinese People’s liberation Army, Beijing, China, People's Republic of, 3MR Research China, GE Healthcare, Beijing, China, People's Republic of

Synopsis

This study provided a new non-invasive method to better discriminate between high-grade gliomas and primary nervous system lymphomas. We found the kurtosis parameters (MK and K//) showed more obvious differences that can be used for differentiating between these two types of tumors than diffusion parameters (FA, MD, λ// and λ⊥). The ROC curve analysis showed MK and K// had the largest area under curve, which further confirmed that the kurtosis parameters MK and K// could better separate these tumors than traditional diffusion parameters.

Purpose

To assess the diagnostic accuracy of diffusion kurtosis magnetic resonance imaging parameters for differentiating high-grade gliomas (HGGs) from primary central nervous system lymphomas (PCNSLs).

Methods

Diffusion parameters, including fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (λ//), radial diffusivity (λ⊥); and kurtosis parameters, including mean kurtosis (MK), axial kurtosis (K//), and radial kurtosis (K⊥), were normalized to contralateral normal-appearing white matter (NAWMc) to decrease inter-individual and inter-regional changes across the entire brain, and then compared to the solid parts of 20 HGGs and 11 PCNSLs [median (95% confidence interval, 95% CI), P<0.004(0.05/14), significance level, Kolmogorov-Smirnov test, Bonferroni correction].

Results

FA, MD, λ//, and λ⊥ values were higher in HGGs than in PCNSLs, but not significantly [HGGs: 0.209 (95%CI: 0.134-0.338), 1.385 (95%CI:1.05-1.710), 1.655(95%CI:1.30-2.060), 1.228 (95%CI:0.932-1.480), respectively; PCNSLs: 0.143 (95%CI:0.110-0.317), 1.070 (95%CI:0.842-1.470), 1.260 (95%CI:0.960-1.930), 1.010 (95%CI:0.782-1.240), respectively; P=0.120, 0.010, 0.004, and 0.004, respectively]. However, MK and K// were significantly higher in PCNSLs compared to HGGs [PCNSLs: 0.765 (95%CI: 0.697-0.890), 0.787 (95%CI:0.615-1.030), respectively; HGGs: 0.531 (95%CI:0.402-0.766), 0.532 (95%CI:0.432-0.680), respectively; P=0.001, 0.000, respectively]; but not K⊥ [0.774 (95%CI:0.681-0.899) for PCNSLs; 0.554 (95%CI:0.389-0.954) for HGGs; P=0.024].

Discussion and Conclusion

The diffusional parameters FA, λ// and λ⊥ obtained on DKI did not show significant differences between HGGs and PCNSLs. Conversely, the kurtosis metrics MK and K// obtained on DKI in primary cerebral lymphoma were significantly higher than those of high-grade glioma. Thus, kurtosis parameters obtained on DKI are better for differentiating PCNSLs from HGGs than diffusional metrics.

Acknowledgements

No acknowledgement found.

References

1. Ricard D, Idbaih A, Ducray F, et al. Primary brain tumours in adults. The Lancet. 2012;379:1984-1996.

2. Van Cauter S, Veraart J, Sijbers J, et al. Gliomas: Diffusion Kurtosis MR Imaging in Grading. Radiology. 2012;263:492-501.

3. Jensen JH, Helpern JA, Ramani A, et al. Diffusional kurtosis imaging: The quantification of non-gaussian water diffusion by means of magnetic resonance imaging. Magn Reson Med. 2005;53:1432-1440.

Figures

ROI delineation for enhanced tumor regions

ROI delineation for unenhanced tumor regions and normal-appearing white matter

ROC curves and AUCs for average FA, MD, λ//, λ⊥, MK, K//, and K⊥ in solid tumors and average FA, MD, λ//, λ⊥, MK, K//, and K⊥ normalized to the age-corrected value in the NAWMc for differentiating between high-grade glioma and lymphoma



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
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