Yoshiharu Ohno1,2,3, Masao Yui4, Takeshi Yoshikawa3,5, Daisuke Takenaka5, Kaori Yamamoto4, Yoshimori Kassai4, Kazuhiro Murayama2, and Hiroshi Toyama1
1Radiology, Fujita Health University School of Medicine, Toyoake, Japan, 2Joint Research Laboratory of Advanced Medical Imaging, Fujita Health University School of Medicine, Toyoake, Japan, 3Division of Functional and Diagnostic Imaging Research, Department of Radiology, Kobe University Graduate School of Medicine, Kobe, Japan, 4Canon Medical Systems Corporation, Otawara, Japan, 5Diagnostic Radiology, Hyogo Cancer Center, Akashi, Japan
Synopsis
No
major papers that directly compared the capability for N-stage evaluation among
cDWIs with different b values, aDWI and FDG-PET/CT in NSCLC patients. We hypothesize that cDWI has a potential for
improving diagnostic performance of N-stage in NSCLC patients as compared with
aDWI as well as FDG-PET/CT, when set appropriate b value. The purpose of this study is to directly
compare the capability for N-stage evaluation among cDWI with different b
values, aDWI and FDG-PET/CT in NSCLC patients.
Introduction
Accurate
TNM staging in non-small cell lung cancer (NSCLC) is fundamental clinical
question from clinicians to determine appropriate therapeutic strategy. Since 1990s, positron emission tomography (PET) or PET fused with
CT (PET/CT) combined with [18F] fluoro-2-D-glucose (FDG) has been applied to answer this question, although the diagnostic
accuracy of PET or PET/CT is recently suggested as having some limitations. Since 2000s, magnetic resonance imaging (MRI)
has also been suggested as another promising modality in this setting by means
of short TI inversion recovery (STIR) turbo spin-echo (SE) imaging as well as
diffusion-weighted imaging (DWI) (1-3). In
addition, DWI has been widely applied for N-stage assessment in non-small cell
lung cancer (NSCLC) patients (2-4).
However, image quality of DWI at 3T MR system is relatively lower than
that at 1.5T MR system (3). Recently,
computed DWI (cDWI) generated from actually obtained DWI (aDWI) at two
different b values has been reported as useful for improving image quality and improving
diagnostic performance in prostatic cancer (5).
However, there are no major papers that directly compared the capability
for N-stage evaluation among cDWIs with different b values, aDWI and FDG-PET/CT
in NSCLC patients. We hypothesize that cDWI
has a potential for improving diagnostic performance of N-stage in NSCLC
patients as compared with aDWI as well as FDG-PET/CT, when set appropriate b
value. The purpose of this study is to directly
compare the capability for N-stage evaluation among cDWIs with different b
values, aDWI and FDG-PET/CT in NSCLC patients. Materials and Methods
245 consecutive operable
NSCLC patients (127 men, 118 women; mean age 75 years) prospectively underwent
actual DWI (aDWI) on a
3T system (Vantage Titan 3T, Canon Medical Systems Corporation, Otawara, Japan)
with b value
at 0 and 1000 s/mm2, FDG-PET/CT, surgical treatment and pathological
and follow-up examinations. In each
subject, computed DWIs were generated at 400 (cDWI400), 600 (cDWI600)
and 800 (cDWI800) s/mm2.
According to pathological examination results, 114 metastatic nodes and
114 out of 2581 non-metastatic nodes were measured contrast ratio (CR) on each
computed DWI between each lymph node and chest wall muscle, ADC on aDWI and SUVmax
by ROI measurements. To compare
differentiation capability on a per node basis, ROC analysis was
performed. Then, diagnostic performance was
compared among all methods by McNemar’s test.
On a per patient basis, agreement of N-stage classification between each
index and pathological examination result was evaluated by kappa
statistics. Finally, accuracy of N-stage
classification was also compared among all methods by McNemar’s test. Results
Representative
case is shown in Figure 1. All CR, ADC
and SUVmax had significant differences between metastatic and
non-metastatic lymph nodes (p<0.05).
Figure 2 shows the results of ROC analysis for differentiating
metastatic from non-metastatic lymph nodes.
Area under the curve (AUC) of CR600 (AUC=0.86) was
significantly larger than that of SUVmax (AUC=0.77, p=0.003), CR400
(AUC=0.79, p<0.0001) and CR800 (AUC=0.81, p<0.0001). AUC of CR800 was also
significantly larger than that of CR400 (p=0.02). Figure 3 shows the results of compared
differentiation capability for metastatic from non-metastatic lymph nodes on a
per node basis. Sensitivity of each CR
was significantly higher than that of SUVmax (p<0.05). Specificity of SUVmax was
significantly higher than that of CR400 and CR800 (p<0.05). Accuracy of CR600 was
significantly higher than that of other CRs, ADC and SUVmax
(p<0.05). Figure 4 demonstrates
agreement of N-stage between evaluated and final N-stage and compared
diagnostic accuracy for N-stage on a per patient basis. Agreement with final diagnosis by each index
was significant and substantial (0.71<κ<0.79, p<0.0001). Accuracy of CR600 was
significantly higher than that of CR400 and CR800
(p<0.05). Conclusion
cDWI is considered as the new promising method for improving diagnostic
performance of lymph node metastasis and N-stage evaluation, when compared with
aDWI and FDG-PET/CT in NSCLC patients. In
addition, b value at 600s/mm2 would be better to be applied for generating
cDWI rather than other b values in this setting.
Acknowledgements
This study is technically and financially supported by Canon Medical Systems Corporation. References
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