CT Texture Analysis Potentially Predicts Local Failure in Head and Neck Squamous Cell Carcinoma Treated with Chemoradiotherapy

H. Kuno; M.M. Qureshi; M.N. Chapman; B. Li; V.C. Andreu-Arasa; K. Onoue; M.T. Truong; O. Sakai

doi:10.3174/ajnr.A5407

Abstract

BACKGROUND AND PURPOSE: The accurate prediction of prognosis and failure is crucial for optimizing treatment strategies for patients with cancer. The purpose of this study was to assess the performance of pretreatment CT texture analysis for the prediction of treatment failure in primary head and neck squamous cell carcinoma treated with chemoradiotherapy.

MATERIALS AND METHODS: This retrospective study included 62 patients diagnosed with primary head and neck squamous cell carcinoma who underwent contrast-enhanced CT examinations for staging, followed by chemoradiotherapy. CT texture features of the whole primary tumor were measured using an in-house developed Matlab-based texture analysis program. Histogram, gray-level co-occurrence matrix, gray-level run-length, gray-level gradient matrix, and Laws features were used for texture feature extraction. Receiver operating characteristic analysis was used to identify the optimal threshold of any significant texture parameter. We used multivariate Cox proportional hazards models to examine the association between the CT texture parameter and local failure, adjusting for age, sex, smoking, primary tumor stage, primary tumor volume, and human papillomavirus status.

RESULTS: Twenty-two patients (35.5%) developed local failure, and the remaining 40 (64.5%) showed local control. Multivariate analysis revealed that 3 histogram features (geometric mean [hazard ratio = 4.68, P = .026], harmonic mean [hazard ratio = 8.61, P = .004], and fourth moment [hazard ratio = 4.56, P = .048]) and 4 gray-level run-length features (short-run emphasis [hazard ratio = 3.75, P = .044], gray-level nonuniformity [hazard ratio = 5.72, P = .004], run-length nonuniformity [hazard ratio = 4.15, P = .043], and short-run low gray-level emphasis [hazard ratio = 5.94, P = .035]) were significant predictors of outcome after adjusting for clinical variables.

CONCLUSIONS: Independent primary tumor CT texture analysis parameters are associated with local failure in patients with head and neck squamous cell carcinoma treated with chemoradiotherapy.

ABBREVIATIONS:

CRT: chemoradiotherapy
GLCM: gray-level co-occurrence matrix
GLN: gray-level nonuniformity
GLRL: gray-level run-length
HNSCC: head and neck squamous cell carcinoma
HPV: human papillomavirus
HR: hazard ratio
RLN: run-length nonuniformity
SRE: short-run emphasis
SRLGE: short-run low gray-level emphasis

Chemoradiotherapy (CRT) is the mainstay of treatment for early and locally advanced head and neck squamous cell carcinoma (HNSCC). The accurate prediction of prognosis and failure is crucial for optimizing treatment strategies for patients with cancer; however, it remains an area of ongoing controversy. Currently, the American Joint Committee on Cancer staging system, which uses unidimensional tumor size, local anatomic invasion, nodal involvement, and the presence of metastatic disease, is the most widely accepted and applied prognostic system in cancer management. Yet this classification is mainly based on surgical criteria rather than predictors of radiation or chemotherapy response, and this tumor node metastasis information sometimes fails to predict the response to nonsurgical therapy. Several studies have demonstrated a significant impact of primary tumor volume on treatment outcome in patients with HNSCC treated with radiation therapy.^{1⇓⇓⇓–5} More recent studies have also shown that patients with human papillomavirus (HPV)-positive HNSCCs have a better response to CRT than patients with HPV-negative tumors.^6⇓⇓–9 However, treatment failure still occurs in patients with HNSCC with small tumor volume and/or HPV-positive status.¹⁰

Image texture is defined as a complex visual pattern within an image, consisting of simpler subpatterns with characteristic features, and texture analysis allows the mathematic detection of the subtle spatial arrangement of the gray level among image pixels.^11,12 Texture analysis is a postprocessing technique and a new addition to the image-analysis armamentarium that extracts information native to image data that is not apparent on visual inspection of images. These techniques ultimately provide a quantitative means of extracting image features that are useful for comparative analyses. In the past several years, CT texture analysis has been investigated in oncology imaging for its ability to predict treatment outcome in patients with non-small cell lung cancer, esophageal cancer, and metastatic renal cell carcinoma.^{13⇓⇓⇓⇓–18} One study showed that CT texture and histogram analysis parameters of the primary mass were associated with overall survival in patients with HNSCC who were treated with induction chemotherapy followed by chemotherapy, radiation, and/or an operation.¹⁹ However, it is still unclear whether CT texture analysis can predict local failure to radiation therapy in patients with HNSCC, including with important clinical factors such as smoking history, tumor volume, and HPV status. Considering that texture analysis may detect subtle pathologic changes in an image,^20,21 we herein hypothesized that texture analysis on CT would enable assessment of radiosensitivity in a patient with HNSCC.

The purpose of this study was to assess the utility of texture analysis for the prediction of treatment failure in primary HNSCC treated with CRT.

Materials and Methods

Patients

The institutional review board at Boston Medical Center approved this study. The requirement to obtain written informed consent was waived for this retrospective analysis.

Between February 2008 and February 2015, one hundred sixty-five consecutive newly diagnosed patients with histologically proved HNSCCs (oropharynx, larynx, hypopharynx, and oral cavity) underwent contrast-enhanced CT before treatment. Eighty-six of the 165 patients (52%) were excluded because they were treated surgically. We excluded an additional 13 patients: 3 patients due to significant artifacts from motion or dental hardware on CT that may have influenced the texture analysis, 5 patients with very small primary tumors (tumor volume <0.4 cm³) that were difficult to contour, and 5 patients due to an inability to complete treatment. Three patients showing local control were excluded because follow-up periods were <12 months due to other causes of death (2 patients) or transfer to hospice care for distant metastatic disease. One patient who developed metachronous multiple HNSCC was also excluded due to additional treatment with CyberKnife stereotactic radiosurgery (Accuray, Sunnyvale, California) in the same region for a secondary squamous cell carcinoma. The remaining 62 patients (53 men, 9 women; age 31–80 years; median age, 58 years) diagnosed with primary HNSCC were enrolled in this study. Of 62 patients, 31 (50%) had oropharyngeal squamous cell carcinomas, 9 (15%) had hypopharyngeal squamous cell carcinomas, 19 (31%) had laryngeal squamous cell carcinomas, and 3 (5%) had oral cavity squamous cell carcinomas.

Treatment and Follow-Up

All patients were treated with definitive intensity-modulated radiation therapy. The primary gross tumor volume was treated to a median dose of 69.96 Gy (range, 60.0–69.96 Gy), over a median of 33 fractions (range, 30–33 fractions) and a median of 47 days (range, 40–102 days). Concurrent chemotherapy was given to 60 (96.8%) patients, but 1 patient was changed to radiation therapy alone due to stomatitis. Of these 60 patients, 33 also received induction chemotherapy. The remaining 2 patients underwent radiation therapy alone.

Patients were followed after the conclusion of treatment to evaluate local control. All patients were followed clinically for at least 12 months after completion of radiation therapy. The follow-up evaluation included physical and endoscopic examinations. In addition to the clinical examination, CT, MR imaging, and [¹⁸F] FDG PET/CT were used to assess the clinical response as part of standard treatment care. Local failures were confirmed by biopsy except in cases of significant progressive disease by clinical examination and imaging assessment with [¹⁸F] FDG PET/CT or MR imaging. The follow-up period was designated as the total time of follow-up, starting at treatment initiation and ending either at histologically confirmed local failure or at last patient contact without local failure.

CT Imaging Protocol

Contrast-enhanced CT examinations were performed either independently or combined with [¹⁸F] FDG PET examination, acquired by 64- or 16-detector row CT scanners (LightSpeed VCT or Discovery STE-16 PET/CT; GE Healthcare, Milwaukee, Wisconsin). Dedicated neck CT studies were helically acquired (120 kV[peak], gantry rotation time = 0.5 second, automatic tube current modulation on with 10% adaptive statistical iterative reconstruction, helical pitch factor = 0.937:1, scan FOV = 300 mm, reconstructed section thickness = 1.25 or 3.75 mm, image matrix = 512 × 512) extending from the skull base to the thoracic inlet following a 60-second delay after intravenous contrast injection (80–160 mL; ioversol, Optiray 350, Mallinckrodt, St. Louis, Missouri; or iopamidol, Isovue 370, Bracco, Princeton, New Jersey). The images were reviewed in soft-tissue algorithms.

Image Segmentation

The primary tumor was manually contoured by a neuroradiologist with 9 years of experience who was blinded to patient history. Segmentation of the whole primary lesion for each section was performed with a dedicated AW workstation (GE Healthcare) with a semiautomated graphic user interface. We used axial images for the segmentation. If the tumor border was unclear on the axial images, coronal or sagittal reformatted sections were used to guide segmentation. We manually excluded obvious necrotic and cystic areas, regions of ulceration of the tumor, calcification, and areas of artifacts from the contoured tumor volume (On-line Figure). The most solid component of the tumor was contoured. When severe streak artifacts within the tumor were seen, we excluded the artifact section and used only artifact-free sections for texture analysis. The full processing time of image segmentation and texture analysis per subject was approximately 10 minutes.

Texture Analysis

In this work, we measured 42 features from each segmented tissue volume using an in-house-developed Matlab (MathWorks, Natick, Massachusetts) texture analysis software.^20,22 The mean value of the textural features on an ROI basis was estimated. The volume of each primary tumor was also calculated. The 42 features included the following:

Thirteen histogram features
Five gray-level co-occurrence matrix (GLCM) features
Eleven gray-level run-length (GLRL) features
Four gray-level gradient matrix features
Nine Laws features.

We discuss the extraneous math behind each texture feature in detail in a subsequent On-line Appendix.^{11,12,20,22⇓⇓–25}

Statistical Analysis

First, associations of demographic and clinical characteristics with local control status were tested with the Pearson χ² test or Mann-Whitney U test. Texture parameters were then compared in patients with local control against patients who developed local failure using the Mann-Whitney U test to select significant texture parameters. Second, receiver operating characteristic analysis was used to identify the optimal threshold of any significant texture parameter. The point on the receiver operating characteristic curve farthest from the 45-degree reference line with the best combination of sensitivity and specificity was considered the optimum threshold. The area under the receiver operating characteristic curve was also measured for the selected parameters. Third, Cox proportional hazards models were used to examine the association between each selected CT texture parameter and local failure. The local control time was defined as the time between the start of treatment and the date on which local recurrence was found or the last follow-up. Furthermore, we used multivariate Cox proportional hazards models to examine the association between CT texture parameters and local failure, adjusting for age, sex, smoking (pack-year), primary tumor stage, primary tumor volume, and HPV status. Because 15 of 62 subjects had unknown HPV status, we used 47 subjects with HPV data for multivariate models.

All statistical analyses were performed by using STATA (Version 12.1; StataCorp, College Station, Texas). A P value < .05 was considered statistically significant.

Results

At a median follow-up of 29 months (range, 7–88 months) for included subjects, 22 patients (35.5%) developed local failure and the remaining 40 patients (64.5%) showed local control. The follow-up time of patients with local failure ranged from 3.7 to 14.4 months (median, 4.6 months), and the follow-up time of patients with local control ranged from 16.8 to 88.4 months (median, 35 months). Among 24 patients positive for HPV, 8 patients (33.3%; 5 oropharynx, 2 larynx, and 1 oral tongue carcinoma) developed local failure. Complete patient demographics and tumor characteristics are described in Table 1. Primary tumor volume of the local control group was significantly smaller than that in the failure group (median, 4.56 versus 15.07 mL, P = .007). The primary T-stage was also significantly different between the local control and failure groups (P = .037). There was no significant difference in the age (P = .205), sex (P = .098), primary site (P = .515), N-stage (P = .914), histopathologic grade (P = .927), smoking pack-years (P = .947), and HPV status (P = .917) between the 2 groups. The distributions of the CT scanner, section thickness, and the use of adaptive statistical iterative reconstruction of these study subjects were not different between local control and failure groups (P = .618 for CT scanner, P = .689 for section thickness, and P = .655 for adaptive statistical iterative reconstruction).

View this table:

Table 1:

Demographics and tumor characteristics of patients with head and neck cancer^{^a}

Results of 42 texture parameters differentiating local control and local failure are shown in the On-line Table. The Mann-Whitney U test revealed that 13 parameters, including 5 histogram features (mean, SD, geometric mean, harmonic mean, fourth moment) and 8 GLRL features (short-run emphasis [SRE], long-run emphasis, gray-level nonuniformity [GLN], run-length nonuniformity [RLN], run percentage, low gray-level run emphasis, high gray-level run emphasis, and short-run low gray-level emphasis [SRLGE]) showed significant differences between the local failure and local control groups.

The results of optimal thresholds for selected texture features obtained from receiver operating characteristic curves and sensitivity/specificity with area under the receiver operating characteristic curve to predict local failure are shown in Table 2. The highest area under the receiver operating characteristic curve was 0.82, with a sensitivity of 77.3% and a specificity of 77.5% in RLN (one of the GLRL features). In subgroup analysis based on the HPV status, the area under the receiver operating characteristic curve was 0.80, with a sensitivity of 87.5% and a specificity of 68.8% for the HPV-positive group and the area under the receiver operating characteristic curve was 0.75 with a sensitivity of 75.0% and a specificity of 73.3% for the HPV-negative group in RLN.

View this table:

Table 2:

Optimal thresholds obtained from ROC curves and sensitivity/specificity to predict local failure^{^a}

The results of Cox proportional hazards model of selected CT texture parameters and clinical factors for predicting local failure are shown in Table 3. The multivariate Cox proportional hazards model revealed that 3 histogram features [geometric mean (hazard ratio [HR] = 4.68, P = .026), harmonic mean (HR = 8.61, P = .004), fourth moment (HR = 4.56, P = .048)], and 4 GLRL features [SRE (HR = 3.75, P = .044), GLN (HR = 5.72, P = .004), RLN (HR = 4.15; P = .043), and SRLGE (HR = 5.94, P = .035)] remained significant predictors of outcome after adjusting for clinical variables. Representative examples of patients positive for HPV with oropharyngeal squamous cell carcinomas with local failure and local control are shown in the Figure.

View this table:

Table 3:

Cox proportional hazards model of selected CT texture parameters for predicting local failure

FIGURE.

Representative axial contrast-enhanced CT images (A and C) and corresponding axial section ROI mask-segmented primary tumor (B and D) for 2 different patients with oropharyngeal squamous cell carcinoma. Segmented tumor is from a 75-year-old man (B) with right tonsil squamous cell carcinoma (HPV-positive; smoking, 0 pack-year; tumor volume, 16.4 mL; clinical T-stage, T4) who developed local failure and a 43-year-old woman (D) with squamous cell carcinoma of the right base of tongue (HPV- positive; smoking, 0 pack-year; tumor volume, 20.6 mL; clinical T-stage, T4) who showed local control. Representative texture features of each patients are as follows; for geometric mean, 973.2 (local failure, B) and 906.6 (local control, D); for harmonic mean, 285.1 (local failure, B) and 210.3 (local control, D); for SRE, 0.026 (local failure, B) and 0.043 (local control, D); for GLN, 0.026 (local failure, B) and 0.042 (local control, D); for RLN, 0.019 (local failure, B) and 0.032 (local control, D); and for SRLGE, 479.1 (local failure, B) and 459.1 (local control, D).

Discussion

In our study, we measured volumetric texture features of the whole primary HNSCC tumor using pretreatment contrast-enhanced CT. Three histogram features and 4 GLRL features have been associated with local failure in patients treated with CRT after adjusting for clinical variables, including smoking history, HPV status, T-stage, and tumor volume. The results suggest that CT texture analysis may serve as an independent indicator of local failure regardless of tumor status, including HPV infection.

In recent years, the measurement of spatial heterogeneity by CT textural analysis has gained acceptance as a means to extract information from imaging of primary tumors to predict treatment outcome in oncology patients.^{13⇓⇓⇓⇓–18} In the head and neck, Zhang et al¹⁹ analyzed the predictive value of texture and histogram features in 72 patients with HNSCC treated with induction chemotherapy (TPF; docetaxel, cisplatin, and fluouracil) and found that in addition to expected factors such as tumor volume and N stage, primary mass entropy (HR = 2.10 for each 0.5-unit increase; P = .036) and histogram skewness (HR = 3.67 for each 1.0-unit increase; P = .009) were independent predictors of overall survival in multivariate Cox regression analysis. However, their study included patients treated with an operation followed by chemotherapy, and HPV status was not provided in their analysis. In our study, we focused on the chemoradiosensitivity of the primary tumor using whole-tumor primary HNSCC volume texture analysis, and the results demonstrated that CT texture analysis parameters such as histogram and GLRL features are associated with local failure in patients with HNSCC treated with CRT.

The GLRL features are one of the categories of spatially dependent texture features based on the length and quantity of runs of adjacent pixels with similar intensity values.^11,12,20 The significant difference in the texture features between local control and local failure groups suggests a different degree of uniformity within the tumors along both long and short matrix runs. Increased heterogeneity of the primary mass on contrast-enhanced CT images indicates that the tumor blood supply is heterogeneous, with some areas having increased vascular supply and others having hypoxic voids.^{26⇓⇓–29} Although there is no direct comparison between the underlying tumor histopathology and correlation to the mathematic significance of these features on texture analysis, the texture features may potentially reflect increased heterogeneity or hypoxic voids of the primary mass on contrast-enhanced CT images.^19,30

Other pretreatment predictive imaging biomarkers of local control for HNSCC have been investigated using advanced imaging techniques, albeit with variable results. CT perfusion has been reported to obtain measures of tumor vascular physiology and hemodynamics, and some investigators demonstrated that CT-determined tumor perfusion was an independent predictor of local control in HNSCC treated by definitive radiation therapy with or without chemotherapy.^{29,31⇓–33} Diffusion-weighted imaging^{34⇓⇓–37} and dynamic contrast-enhanced MR imaging^{38⇓⇓–41} have also been used as functional imaging techniques as predictive biomarkers of radiation therapy. One recently published study showed preliminary results exploring the value of assessing texture features with intratreatment dynamic contrast-enhanced MR imaging for patients with HNSCC.⁴² Functional imaging studies including perfusion are useful tools for mapping the vascularity of the tumor environment at baseline. However, these techniques are not routinely used in the clinical protocol for staging of HNSCC, and recently, there are increasing concerns for additional exposure to radiation or gadolinium-based contrast agents.^43,44 [¹⁸F] FDG PET/CT is another imaging technique widely used in the evaluation of patients with HNSCC, and its clinical utility for predicting treatment outcome of HNSCC has been previously investigated.^5,45⇓–47 However, [¹⁸F] FDG PET/CT examinations are used only in advanced-stage HNSCC when management may be altered due to detection of distant metastases. Contrast-enhanced CT is widely used to stage HNSCC before treatment; therefore, CT texture analysis could be potentially useful for predicting local failure without additional exposure to radiation or contrast material.

There are several limitations to this study. First, CT protocols including the types of CT scanners, section thickness, and adaptive statistical iterative reconstruction were not identical in this population, which may potentially affect the texture analysis.⁴⁸ These problems remain to be solved in future validation studies using identical CT parameters. However, the distribution of subjects between local control and failure groups was almost the same for both types of CT scanners, different section thicknesses, and the use of adaptive statistical iterative reconstruction. Additionally, CT texture analysis parameters have been shown to be highly reproducible in multiple kilovolt peaks and milliampere-second settings in a water phantom.¹⁹ We therefore believe that the differences in scanners have little, if any, influence on our presented results. Second, a single user performed the semiautomated segmentation and workflow for this CT texture analysis. The generalizability of our results to other institutions and users is unknown, though the semiautomated nature of the software has the potential to reduce interobserver variation. Third, we contoured areas of obvious necrotic and cystic changes as well as ulceration out of the final contours that were imported into the texture analysis program, because including foci of air would not accurately reflect the underlying texture features within the solid portion of the tumors. However, the necrosis or ulceration within the tumor has a potential impact on hypoxia/radiosensitivity. This issue needs to be further evaluated in a future study assessing whether the region of necrosis should be included or excluded for texture analysis. Finally, the study subjects included heterogeneous groups of patients with HNSCC of different primary sites. Further studies with a larger number of patients are needed to validate the performance of the predictive model for each subsite.

Conclusions

Independent primary tumor CT texture analysis parameters are associated with local failure in patients with HNSCC treated with CRT. CT is noninvasive, widely available, and frequently used to stage early and locally advanced HNSCC before treatment. Therefore, CT texture analysis could serve as a widely applicable pretreatment noninvasive biomarker for predicting local failure with the potential to assist in treatment decisions in patients with HNSCC. Further testing using a larger sample size is needed to validate the performance of the predictive model.

Footnotes

Disclosures: Hirofumi Kuno—UNRELATED: Grants/Grants Pending: Grant-in-Aid for Young Scientists (B) KAKEN (No. 26861033), 2014–2015; Payment for Lectures Including Service on Speakers Bureaus: Toshiba Medical Systems, 2014. Osamu Sakai—UNRELATED: Consultancy: Guerbet; Payment for Lectures Including Service on Speakers Bureaus: Bracco Diagnostics, Eisai.

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. Can pretreatment CT perfusion predict response of advanced squamous cell carcinoma of the upper aerodigestive tract treated with induction chemotherapy? AJNR Am J Neuroradiol 2007;28:328–34 pmid:17297007
Abstract/FREE Full Text
32.↵
2. Bisdas S,
3. Nguyen SA,
4. Anand SK, et al
. Outcome prediction after surgery and chemoradiation of squamous cell carcinoma in the oral cavity, oropharynx, and hypopharynx: use of baseline perfusion CT microcirculatory parameters vs. tumor volume. Int J Radiat Oncol Biol Phys 2009;73:1313–18 doi:10.1016/j.ijrobp.2008.06.1956 pmid:18963541
CrossRef PubMed
33.↵
2. Truong MT,
3. Saito N,
4. Ozonoff A, et al
. Prediction of locoregional control in head and neck squamous cell carcinoma with serial CT perfusion during radiotherapy. AJNR Am J Neuroradiol 2011;32:1195–201 doi:10.3174/ajnr.A2501 pmid:21757530
Abstract/FREE Full Text
34.↵
2. Hatakenaka M,
3. Nakamura K,
4. Yabuuchi H, et al
. Apparent diffusion coefficient is a prognostic factor of head and neck squamous cell carcinoma treated with radiotherapy. Jpn J Radiol 2014;32:80–89 doi:10.1007/s11604-013-0272-y pmid:24408077
CrossRef PubMed
35.↵
2. King AD,
3. Chow KK,
4. Yu KH, et al
. Head and neck squamous cell carcinoma: diagnostic performance of diffusion-weighted MR imaging for the prediction of treatment response. Radiology 2013;266:531–38 doi:10.1148/radiol.12120167 pmid:23151830
CrossRef PubMed
36.↵
2. Ohnishi K,
3. Shioyama Y,
4. Hatakenaka M, et al
. Prediction of local failures with a combination of pretreatment tumor volume and apparent diffusion coefficient in patients treated with definitive radiotherapy for hypopharyngeal or oropharyngeal squamous cell carcinoma. J Radiat Res 2011;52:522–30 doi:10.1269/jrr.10178 pmid:21905311
CrossRef PubMed
37.↵
2. Ng SH,
3. Liao CT,
4. Lin CY, et al
. Dynamic contrast-enhanced MRI, diffusion-weighted MRI and (18)F-FDG PET/CT for the prediction of survival in oropharyngeal or hypopharyngeal squamous cell carcinoma treated with chemoradiation. Eur Radiol 2016;26:4162–72 doi:10.1007/s00330-016-4276-8 pmid:26911889
CrossRef PubMed
38.↵
2. Ng SH,
3. Lin CY,
4. Chan SC, et al
. Dynamic contrast-enhanced MR imaging predicts local control in oropharyngeal or hypopharyngeal squamous cell carcinoma treated with chemoradiotherapy. PLoS One 2013;8:e72230 doi:10.1371/journal.pone.0072230 pmid:23951300
CrossRef PubMed
39.↵
2. Chawla S,
3. Kim S,
4. Dougherty L, et al
. Pretreatment diffusion-weighted and dynamic contrast-enhanced MRI for prediction of local treatment response in squamous cell carcinomas of the head and neck. AJR Am J Roentgenol 2013;200:35–43 doi:10.2214/AJR.12.9432 pmid:23255739
CrossRef PubMed
40.↵
2. Jansen JF,
3. Schöder H,
4. Lee NY, et al
. Tumor metabolism and perfusion in head and neck squamous cell carcinoma: pretreatment multimodality imaging with 1H magnetic resonance spectroscopy, dynamic contrast-enhanced MRI, and [18 F]FDG-PET. Int J Radiat Oncol Biol Phys 2012;82:299–307 doi:10.1016/j.ijrobp.2010.11.022 pmid:21236594
CrossRef PubMed
41.↵
2. Kim S,
3. Loevner L,
4. Quon H, et al
. Prediction of response to chemoradiation therapy in squamous cell carcinomas of the head and neck using dynamic contrast-enhanced MR imaging. AJNR Am J Neuroradiol 2010;31:262–68 doi:10.3174/ajnr.A1817 pmid:19797785
Abstract/FREE Full Text
42.↵
2. Jansen JF,
3. Lu Y,
4. Gupta G, et al
. Texture analysis on parametric maps derived from dynamic contrast-enhanced magnetic resonance imaging in head and neck cancer. World J Radiol 2016;8:90–97 doi:10.4329/wjr.v8.i1.90 pmid:26834947
CrossRef PubMed
43.↵
2. Kanda T,
3. Ishii K,
4. Kawaguchi H, et al
. High signal intensity in the dentate nucleus and globus pallidus on unenhanced T1-weighted MR images: relationship with increasing cumulative dose of a gadolinium-based contrast material. Radiology 2014;270:834–41 doi:10.1148/radiol.13131669 pmid:24475844
CrossRef PubMed
44.↵
2. Kuno H,
3. Jara H,
4. Buch K, et al
. Global and regional brain assessment with quantitative MR imaging in patients with prior exposure to linear gadolinium-based contrast agents. Radiology 2017;283:195–204 doi:10.1148/radiol.2016160674 pmid:27797676
CrossRef PubMed
45.↵
2. Chung MK,
3. Jeong HS,
4. Park SG, et al
. Metabolic tumor volume of [18F]-fluorodeoxyglucose positron emission tomography/computed tomography predicts short-term outcome to radiotherapy with or without chemotherapy in pharyngeal cancer. Clin Cancer Res 2009;15:5861–68 doi:10.1158/1078-0432.CCR-08-3290 pmid:19737951
Abstract/FREE Full Text
46.↵
2. Kao CH,
3. Lin SC,
4. Hsieh TC, et al
. Use of pretreatment metabolic tumour volumes to predict the outcome of pharyngeal cancer treated by definitive radiotherapy. Eur J Nucl Med Mol Imaging 2012;39:1297–305 doi:10.1007/s00259-012-2127-7 pmid:22532254
CrossRef PubMed
47.↵
2. Hanamoto A,
3. Tatsumi M,
4. Takenaka Y, et al
. Volumetric PET/CT parameters predict local response of head and neck squamous cell carcinoma to chemoradiotherapy. Cancer Med 2014;3:1368–76 doi:10.1002/cam4.295 pmid:25045041
CrossRef PubMed
48.↵
2. Buch K,
3. Li B,
4. Qureshi MM, et al
. Quantitative assessment of variation in CT parameters on texture features: pilot study using a nonanatomic phantom. AJNR Am J Neuroradiol 2017;38:981–85 doi:10.3174/ajnr.A5139 pmid:28341714
Abstract/FREE Full Text

Received March 6, 2017.
Accepted after revision July 16, 2017.

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Schöder H,
Lee NY, et al
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Abstract/FREE Full Text

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Jansen JF,
Lu Y,
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Jara H,
Buch K, et al
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Abstract/FREE Full Text

[218] Chung MK,

[219] Jeong HS,

[220] Park SG, et al

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Kao CH,
Lin SC,
Hsieh TC, et al
. Use of pretreatment metabolic tumour volumes to predict the outcome of pharyngeal cancer treated by definitive radiotherapy. Eur J Nucl Med Mol Imaging 2012;39:1297–305 doi:10.1007/s00259-012-2127-7 pmid:22532254
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Hanamoto A,
Tatsumi M,
Takenaka Y, et al
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CrossRef PubMed

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[230] Takenaka Y, et al

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Buch K,
Li B,
Qureshi MM, et al
. Quantitative assessment of variation in CT parameters on texture features: pilot study using a nonanatomic phantom. AJNR Am J Neuroradiol 2017;38:981–85 doi:10.3174/ajnr.A5139 pmid:28341714
Abstract/FREE Full Text

[233] Buch K,

[234] Li B,

[235] Qureshi MM, et al

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CT Texture Analysis Potentially Predicts Local Failure in Head and Neck Squamous Cell Carcinoma Treated with Chemoradiotherapy

Abstract

ABBREVIATIONS:

Materials and Methods

Patients

Treatment and Follow-Up

CT Imaging Protocol

Image Segmentation

Texture Analysis

Statistical Analysis

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CT Texture Analysis Potentially Predicts Local Failure in Head and Neck Squamous Cell Carcinoma Treated with Chemoradiotherapy

Abstract

ABBREVIATIONS:

Materials and Methods

Patients

Treatment and Follow-Up

CT Imaging Protocol

Image Segmentation

Texture Analysis

Statistical Analysis

Results

Discussion

Conclusions

Footnotes

References

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