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Prediction of Radiotherapy Response in Nasopharyngeal Carcinoma Patients Using Diffusion-Kurtosis Imaging
Weiyuan Huang1, Jiianjun Li2, Feng Chen3, Yingman Zhao4, and Xiaolei Zhu5

1Department of Radiology, Hainan General Hospital, Haikou, People's Republic of China, 2Department of Radiology, Hainan General Hospital, People's Republic of China, 3Department of Radiology, Hainan General Hospital, Haikou, China, People's Republic of China, 4department of Radiology, Hainan General Hospital, People's Republic of China, 5MR scientific marketing NE Asia, Siemens Healthcare

Synopsis

The first row: A 62-year-old man with NPC who was a nonresponder. The lesions located at the left nasopharyngeal wall and cavum. Manual draw an ROI within the boundaries of the NPC on Kmean map. The tumor’s maximum diameter was 3.5 before radiotherapy. Residual tumor was detected after radiotherapy. Mean Dmean and Kmean values were 1.48 10-3 mm2/s and 0.72 before treatment. The second row: A 63–year-old man with NPC who was a responder. The lesion affect the bilateral mucous membrane of the nasopharynx. The tumor’s maximum diameter was 3.09 before radiotherapy. No residual tumor was detected after radiotherapy. Mean Dmean and Kmean values were 1.22 10-3 mm2/s and 0.83 before treatment. NRG: non response group RG: reponse group

Introduction

Nasopharyngeal carcinoma (NPC) is one of the most common malignancies in Southeast Asia[1]. Early prediction of radiotherapy response to NPC may help clinicians to carry out individual treatment and avoid unnecessary systemic toxicity[2]. A number of studies have shown the possibility of diffusion weighted imaging (DWI)-MRI to prospectively predict the treatment response in different tumors[3-6]. The premise of monoexponential DWI is that water diffusion in vivo obeys standard Gaussian distribution[7]. However, water diffusion in vivo is much more complex than standard Gaussian distribution due to diffusion barriers like cell membranes. Diffusion kurtosis imaging (DKI) is an emerging new technique, based on a non-Gaussian diffusion model that should better account for restricted water diffusion within the complex microstructure of most tissues[8]. This study aimed to explore the clinical application of DKI in the early prediction of the response to radiotherapy of NPC.

Methods

Twenty-six patients with NPC were consecutively recruited in this prospective study. All the TNM statuses were determined according to the latest 7th edition of the American Joint Committee on Cancer (AJCC) staging system[9]. All patients were imaged by using a 3T MR scanner (MAGNETOM Skyra, Siemens Healthcare, Erlangen, Germany) with 8-channel head and neck array coil pretreatment and 3th months after radiotherapy. MR imaging examinations included T1-weighted imaging, proton density-weighted imaging, DWI and DKI sequences. A fat-suppressed single-shot spin echo EPI sequence was used in the axial plane, TR/TE=8300/72 msec, Slice thickness=4 mm, FOV=230*240 mm, scan time =10:57 min, using thirty orthogonal diffusion directions for DKI examination with b values (0, 500, 1000, 1500 sec/mm2). DKI parameters (including fractional anisotropy (FA), apparent diffusion coefficient (D), and principle kurtosis eigenvectors (K)) were measured pretreatment using in-house software based on the formula: Sb/S0=exp[-b*ADC0+K*(bADC0)2/6]. Three months after the end of radiotherapy, patients were classified as response group and non-response group according to the assessment of short-time radiotherapeutic effect by Word Health Organization's response evaluation criteria. Mann-Whitney U-test was used to compare DKI parameters between groups. The performance of DKI parameters in prediction of radiotherapy responses was evaluated using receiver operating characteristic curve analyses and binary logistic regression.

Results

Three months after radiotherapy, residual local tumors were detected in 7 (30.4%) cases, and no residual tumors in 16 (69.6%) cases. The maximum diameter of tumors in response group was lower than non-response group before radiotherapy, but there was no statistically difference (p=0.103). All DKI parameters were statistically different between groups (p<.05), and the differences in Kax, Kmean, Krad, and FA were statistically significant (p<.01). Krad at 0.76 was the best parameter to predict radiotherapy response with 71.4% sensitivity, 93.7% specificity (AUC:0.897, 95% CI, 0.756-1). Binary logistic regression showed age, T staging and DKI parameters were considered as the independent factors for response to radiotherapy.

Discussion and Conclusion

The K(Kax, Kfa, Kmean and Krad) parameters represent the excess diffusion kurtosis in the tissue and are believed to be associated with microstructural complexity in vivo. Our result documented pretreatment values of DKI were found to correlate significantly with later tumor response/nonresponse. This correlation implies that NPC lesions with high pretreatment diffusivity (Dax, Dmean and Drad) values and low pretreatment kurtosis (Kax, Kfa, Kmean and Krad) values, indicating high viability and low heterogeneity, will respond better to radiotherapy. Our results demonstrate the feasibility of using DKI for pretreatment prediction of response to therapy in patients with NPCs undergoing radiotherapy.

Acknowledgements

No acknowledgement found.

References

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Figures

The first row: A 62-year-old man with NPC who was a nonresponder. The lesions located at the left nasopharyngeal wall and cavum. Manual draw an ROI within the boundaries of the NPC on Kmean map. The tumor’s maximum diameter was 3.5cm before radiotherapy. Residual tumor was detected after radiotherapy. Dmean and Kmean values were 1.48 and 0.72 before treatment. The second row: A 63–year-old man with NPC who was a responder. The tumor’s maximum diameter was 3.09cm before radiotherapy. No residual tumor was detected after radiotherapy. Dmean and Kmean values were 1.22and 0.83 before treatment.

Specificity and sensibility of DKI in radiotherapy: AUC=0.844; 95% CI=0.679-1 for FA; AUC=0.804; 95% CI=0.578-1 for Kax; AUC=0.871; 95% CI=0.722-1 for Kmean and AUC=0.897; 95% CI=0.756-1 for Krad.

Proc. Intl. Soc. Mag. Reson. Med. 25 (2017)
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