Quantitative in vivo assessment of radiation injury of the liver using Gd-EOB-DTPA enhanced MRI: tolerance dose of small liver volumes

被引:45
|
作者
Seidensticker, Max [1 ]
Seidensticker, Ricarda [1 ]
Mohnike, Konrad [1 ]
Wybranski, Christian [1 ]
Kalinski, Thomas [2 ]
Luess, Sebastian [1 ]
Pech, Maciej [1 ]
Wust, Peter [3 ]
Ricke, Jens [1 ]
机构
[1] Univ Magdeburg, Univ Klinikum Magdeburg, Klin Radiol & Nukl Med, D-39106 Magdeburg, Germany
[2] Univ Magdeburg, Univ Klinikum Magdeburg, Inst Pathol, D-39106 Magdeburg, Germany
[3] Charite Univ Med Berlin, Klin Strahlentherapie, Berlin, Germany
来源
RADIATION ONCOLOGY | 2011年 / 6卷
关键词
BONE-MARROW-TRANSPLANTATION; VENO-OCCLUSIVE DISEASE; PHASE-I/II TRIAL; CONTRAST AGENT; CLINICAL-EVALUATION; HEPATIC-UPTAKE; NORMAL TISSUE; IRRADIATION; CT; PHARMACOKINETICS;
D O I
10.1186/1748-717X-6-40
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Backround: Hepatic radiation toxicity restricts irradiation of liver malignancies. Better knowledge of hepatic tolerance dose is favourable to gain higher safety and to optimize radiation regimes in radiotherapy of the liver. In this study we sought to determine the hepatic tolerance dose to small volume single fraction high dose rate irradiation. Materials and methods: 23 liver metastases were treated by CT-guided interstitial brachytherapy. MRI was performed 3 days, 6, 12 and 24 weeks after therapy. MR-sequences were conducted with T1-w GRE enhanced by hepatocyte-targeted Gd-EOB-DTPA. All MRI data sets were merged with 3D-dosimetry data. The reviewer indicated the border of hypointensity on T1-w images (loss of hepatocyte function) or hyperintensity on T2-w images (edema). Based on the volume data, a dose-volume-histogram was calculated. We estimated the threshold dose for edema or function loss as the D(90), i.e. the dose achieved in at least 90% of the pseudolesion volume. Results: At six weeks post brachytherapy, the hepatocyte function loss reached its maximum extending to the former 9.4Gy isosurface in median (i.e., >= 9.4Gy dose exposure led to hepatocyte dysfunction). After 12 and 24 weeks, the dysfunctional volume had decreased significantly to a median of 11.4Gy and 14Gy isosurface, respectively, as a result of repair mechanisms. Development of edema was maximal at six weeks post brachytherapy (9.2Gy isosurface in median), and regeneration led to a decrease of the isosurface to a median of 11.3Gy between 6 and 12 weeks. The dose exposure leading to hepatocyte dysfunction was not significantly different from the dose provoking edema. Conclusion: Hepatic injury peaked 6 weeks after small volume irradiation. Ongoing repair was observed up to 6 months. Individual dose sensitivity may differ as demonstrated by a relatively high standard deviation of threshold values in our own as well as all other published data.
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页数:13
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