IN VIVO 1 H MAGNETIC RESONANCE SPECTROSCOPY IN EVALUATION OF HEPATOCELLULAR CARCINOMA AND ITS EARLY RESPONSE TO TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION
Chinese Medical Sciences JournalVol. 0, Issue 4, Pages: 258-264(2006)
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IN VIVO 1 H MAGNETIC RESONANCE SPECTROSCOPY IN EVALUATION OF HEPATOCELLULAR CARCINOMA AND ITS EARLY RESPONSE TO TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION
Affiliations:
Author bio:
Funds:
Supported by National Natural Sciences Foundation of China(30470503)
DOI:
CLC:R735.7
Published:2006
Accepted:
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IN VIVO 1 H MAGNETIC RESONANCE SPECTROSCOPY IN EVALUATION OF HEPATOCELLULAR CARCINOMA AND ITS EARLY RESPONSE TO TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION[J]. Chinese medical sciences journal, 2006, 0(4): 258-264.
DOI:
IN VIVO 1 H MAGNETIC RESONANCE SPECTROSCOPY IN EVALUATION OF HEPATOCELLULAR CARCINOMA AND ITS EARLY RESPONSE TO TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION[J]. Chinese medical sciences journal, 2006, 0(4): 258-264.DOI:
IN VIVO 1 H MAGNETIC RESONANCE SPECTROSCOPY IN EVALUATION OF HEPATOCELLULAR CARCINOMA AND ITS EARLY RESPONSE TO TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION
摘要
Abstract
Objective To investigate the value of in vivo proton magnetic resonance spectroscopy (MRS) in the assessment of hepatocellular carcinoma (HCC) and monitor its metabolic change shortly after transcatheter arterial chemoembolization (TACE). Methods In this prospective study
28 consecutive patients with large HCC (≥3 cm in diameter) confirmed by fine needle aspiration biopsy were recruited. The
1 H MRS of all hepatic lesions and some uninvolved liver parenchyma were performed with 1.5T whole body MR scanner. Among them
15 cases were evaluated again about one week after TACE. The main metabolites such as choline and lipid before and after interventional therapy were measured to assess the early response of the tumor. Results The technical success rate of
1 H MRS in liver was high (33/41
80%)
closely related to breath motion
location of lesion
and size of voxel. In spectra
the choline compound peak of HCC elevated compared with uninvolved liver parenchyma. After TACE
both the amplitude and the area of choline resonance peak significantly descended (choline-to-lipid ratios from 0.352±0.080 to 0.167±0.030
P=0.026; from 0.205±0.060 to 0.070±0.020
P=0.042
respectively); yet lipid resonance peak ascended. Conclusions In vivo
1 H MRS is technically feasible for the evaluation of large focal hepatic lesions
however
the reproducibility and stability are not as good as routine MR scan.
1 H MRS can monitor the early stage metabolic changes of HCC after TACE but limitation like quantification still exists.