Article

Detection of rectal cancer and response to concurrent chemoradiotherapy by proton magnetic resonance spectroscopy.

Department of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Ilwon-dong, Gangnam-gu, Seoul, South Korea.
Magnetic Resonance Imaging (impact factor: 1.99). 04/2012; 30(6):848-53. DOI:10.1016/j.mri.2012.02.013 pp.848-53
Source: PubMed

ABSTRACT To diagnose rectal cancer and monitor treatment response after preoperative concurrent chemoradiotherapy (CCRT) in rectal cancer patients using proton-1 magnetic resonance spectroscopy ((1)H-MRS).
We enrolled 134 rectal cancer patients before treatment, of whom 34 underwent preoperative CCRT and follow-up MR spectroscopy before surgery. (1)H-MRS was performed using a six-channel phased-array coil at 3.0 T. We evaluated the presence of a choline peak at 3.2 ppm, and lipid peaks at 0.9 and 1.3 ppm, and glutamine and glutamate peaks at 2.1-2.3 and 2.7 ppm seen at two TEs (40 and 135 ms). We divided MR spectra patterns into two groups (A and B).
A choline peak at 3.2 ppm seen in both TEs was characteristic for rectal cancer before treatment. Of 103 patients, 55 (53%) showed an elevated choline peak before treatment (type A). Type A spectra were seen in 68% of patients (23/34) before preoperative CCRT. After CCRT, the choline peak disappeared, resulting in only the lipid peak at 1.3 ppm (type B) in 97% of patients (33/34).
We optimized a localized in vivo(1)H-MRS method for detection of rectal adenocarcinoma and monitoring treatment response after preoperative CCRT. The method appears to be a promising and feasible noninvasive modality.

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Keywords

choline peak
 
diagnose rectal cancer
 
elevated choline peak
 
feasible noninvasive modality
 
follow-up MR spectroscopy
 
glutamate peaks
 
lipid peak
 
lipid peaks
 
monitoring treatment response
 
MR spectra patterns
 
preoperative CCRT
 
preoperative concurrent chemoradiotherapy
 
proton-1 magnetic resonance spectroscopy
 
rectal adenocarcinoma
 
rectal cancer
 
rectal cancer patients
 
six-channel phased-array coil
 
treatment response
 
type A
 
vivo(1)H-MRS method