Can Diffusion Weighted MRI Assess Early Response of Lymphadenopathy to Induction Chemotherapy in Nasopharyngeal Cancer: A Heterogeneity Analysis Approach
Manijeh Beigi1, Anahita Fathi Kazerooni1, Mojtaba Safari2, Marzieh Alamolhoda3, Ahmad Ameri4, Shiva Moghadam5, Mohsen Shojaee Moghadam6, and Hamidreza SalighehRad2

1, Tehran University of Medical Sciences, Quantitative MR Imaging and Spectroscopy Group, Research Center for Cellular and Molecular Imaging, Institute for Advanced Medical Imaging, Tehran, Iran, 2Tehran University of Medical Sciences, Quantitative MR Imaging and Spectroscopy Group, Research Center for Cellular and Molecular Imaging, Institute for Advanced Medical Imaging, Tehran, Iran, 3Statistics, Shiraz University of Medical Science, Shiraz, Iran, 4Jorjani Radiotherapy Center, Shahid Beheshti of Medical Sciense, Tehran, Iran, 5Shahid Beheshti University of Medical Science, Tehran, Iran, 6Payambaran MRI center, Tehran, Iran

Synopsis

Induction chemotherapy is an effective way to control subclinical metastasis in locally-advanced nasopharyngeal cancer patients. Diffusion-weighted MRI is a noninvasive imaging technique allowing some degree of tissue characterization by showing and quantifying molecular diffusion. Histogram analysis on ADC map could be carried out to reveal physiological alterations early after IC. For this purpose, several quantitative metrics from ADC-map were explored to obtain the most accurate feature(s) as potential predictive biomarker for early response of the lymphnode to IC. If the outcome can be predicted at an early stage of the treatment, the patient could be spared from unnecessary treatment toxicity.

Purpose

Induction chemotherapy (IC) is an effective way to control subclinical metastasis in locally-advanced nasopharyngeal cancer patients. If the outcome can be predicted at an early stage of the treatment, the patient could be spared from unnecessary treatment toxicity. In this light, the aim of the present study is to find appropriate metrics for assessing the response of Adenopathy through quantification of the heterogeneity in diffusion-weighted images (DWI) of lymph nodes (LN) early after initiation of chemotherapy.1,2,3

Methods

The study group consisted of 7 patients. DWI was performed before and ten days after the initiation of injection in the first cycle of induction chemotherapy on 1.5T Avanto Siemens scanner. Patient characteristics and imaging parameters are demonstrated in Tables 1 and 2. Apparent diffusion coefficient (ADC) maps were generated from DW images on the system workstation. LNs, diagnosed as malignant on pre-therapeutic clinical and imaging assessment, were included for response assessment. Regions of interest (ROIs) containing the malignant LNs were delineated on the ADC-maps and Gd-enhanced T1-weighted images for each patient at two different time points. The LN volumes were calculated for the selected area on T1C images. Several commonly-used quantitative parameters, including mean-, max-, min-, and median-ADC were calculated for the defined ROIs on ADC-maps. Moreover, first-order histogram analysis was applied on the ROIs to derive the following features: (1) histogram standard deviation, representing average contrast, (2) normalized variance, as a measure of smoothness, (3) skewness, denoting the third moment, (4) energy, as a measure of uniformity or homogeneity, and (5) entropy, a statistical measure of irregularities of ADC-values.

Results

For each quantitative parameter, differences between two time-points were compared with Wilcoxon non-parametric test. A level of p-value less than 0.05 was regarded as statistically significant. As indicated in Table 3, mean, median, smoothness, third moment and uniformity indicate statistically significant difference (p-value< 0.05) for early changes of LN structures following induction chemotherapy. No significant change was observed in the volume of LNs (p-value = 0.128). Uniformity metric decreased in the second time-point (after IC) for all patients.

Discussion/Conclusion

For nasopharyngeal patients with involved LN, the standard determination of the response of LN is based on conventional MRI. In this study, histogram analysis was carried out in manually-defined ROIs selected within the tumor on ADC-maps to reveal physiological alterations early after IC. For this purpose, several quantitative metrics derived from ADC-map were explored to obtain the most accurate feature(s) as potential predictive biomarker(s) for early response of the lymph node to IC. The initial results showed that mean, smoothness, third moment and uniformity metrics, which are indicators of heterogeneity, could detect early response of the lymph node to treatment. This is in the meantime that the volume of the lymph nodes could not exhibit significant differences (p-value=: 0.128) for early response assessment. Finally, the results reported in this abstract will be validated in a larger patient population to determine the optimum heterogeneity features that can be adopted as relevant biomarkers for response assessment of lymph nodes to IC. Furthermore, serial DWI will be acquired to find correlation between changes of extracted heterogeneity metrics and the tumor residue after completion of the IC. .

Acknowledgements

We gratefully acknowledge the support of Payambaran MRI center.

References

1. Ceri P, Maria S, Marco B, et al. Changes in functional imaging parameters following induction chemotherapy have important implications for individualised patient-based treatment regimens for advanced head and neck cancer. Radiotherapy and Oncology. 2013; 106: 112-117.

2. Sanjeev C, Sungheon K, Lawrence D. Pretreatment Diffusion-Weighted and Dynamic Contrast- Enhanced MRI for Prediction of Local Treatment Response in Squamous Cell Carcinomas of the Head and Neck. Am J Roentgenol. 2013; 200(1): 35-43.

3. Devin F, Kunwar B, David Y, et al. Diagnostic accuracy of diffusion-weighted MR imaging for nasopharyngeal carcinoma, head and neck lymphoma and squamous cell carcinoma at the primary site. 2010; 46: 603-606.

Figures

Table1: Imaging parameters

Table2: Patients Characteristic

Table3: p value of all quantitative parameters



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