Quantitative perfusion- and diffusion-weighted magnetic resonance imaging of gastrointestinal cancers treated with multikinase inhibitors: a pilot study.

Hyunki Kim, Kimberly S Keene, David B Sarver, S Kyle Lee, T Mark Beasley, Desiree E Morgan, James A Posey
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Abstract

Background: Dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) and diffusion-weighted imaging (DWI) are often used to detect the early response of solid tumors to an effective therapy. The early changes in intratumoral physiological parameters measured by DCE-MRI/DWI have been evaluated as surrogate biomarkers allowing a tailored treatment for the individual patient.

Methods: Patients with newly diagnosed, biopsy-proven, treatment-naïve gastrointestinal stromal tumor (GIST) or hepatocellular carcinoma (HCC) were enrolled prospectively after institutional review board (IRB)-approved informed consent (5 patients per tumor type). Patients with GIST were treated with sunitinib over 6 weeks. DCE-MRI/DWI was applied before therapy (baseline imaging) and at 2 and 6 weeks after therapy initiation. Patients with HCC were treated with radiation during the first 2 weeks and then with sorafenib for the next 6 weeks. DCE-MRI/DWI was applied in all patients with HCC before and after radiation therapy and at the end of sorafenib therapy. Tumor volume, perfusion parameters (K (trans), the forward volume-transfer constant, and k ep, the reverse reflux-rate constant) and the apparent diffusion coefficient (ADC) were measured.

Results: During 2 weeks of sunitinib therapy, GIST volume, K (trans), and k ep decreased 32 ± 13, 45 ± 24, and 42 ± 15%, respectively, whereas ADC increased 76 ± 24%. After 6 weeks of sunitinib therapy, GIST volume, K (trans), and k ep decreased 56 ± 7, 70 ± 7, and 50 ± 12%, respectively, whereas ADC increased 85 ± 33%. After completion of radiation therapy, HCC volume, K (trans), and k ep decreased 34 ± 14, 35 ± 12, and 4 ± 21%, respectively, but ADC increased 21 ± 9%. During the entire 10-week therapeutic period, HCC volume, K (trans), and k ep decreased 65 ± 15, 40 ± 9, and 26 ± 2%, respectively, whereas ADC increased 28 ± 10%.

Conclusion: DCE-MRI/DWI can measure the perfusion and diffusion changes in GISTs or HCCs treated with multikinase inhibitors.

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多激酶抑制剂治疗胃肠道癌症的定量灌注和扩散加权磁共振成像:一项初步研究。
背景:动态对比增强磁共振成像(DCE-MRI)和弥散加权成像(DWI)通常用于检测实体瘤对有效治疗的早期反应。通过DCE-MRI/DWI测量的肿瘤内生理参数的早期变化已被评估为替代生物标志物,允许针对个体患者进行定制治疗。方法:经机构审查委员会(IRB)批准的知情同意后,前瞻性纳入新诊断、活检证实的treatment-naïve胃肠道间质瘤(GIST)或肝细胞癌(HCC)患者(每种肿瘤类型5例)。GIST患者接受舒尼替尼治疗超过6周。在治疗前(基线成像)和治疗开始后2周和6周分别应用DCE-MRI/DWI。HCC患者在前2周接受放射治疗,然后在接下来的6周使用索拉非尼。所有HCC患者放疗前后及索拉非尼治疗结束时均行DCE-MRI/DWI检查。测定肿瘤体积、灌注参数(正向体积传递常数K (trans)、反向回流速率常数K ep)和表观扩散系数(ADC)。结果:舒尼替尼治疗2周,GIST体积、K (trans)和K - ep分别下降32±13%、45±24%和42±15%,而ADC增加76±24%。舒尼替尼治疗6周后,GIST体积、K(反式)和K - ep分别下降56±7%、70±7%和50±12%,而ADC增加85±33%。放疗结束后,HCC体积、K(反式)和K - ep分别下降34±14%、35±12%和4±21%,而ADC增加21±9%。在整个10周的治疗期间,HCC体积、K(反式)和K - ep分别下降65±15%、40±9%和26±2%,而ADC增加28±10%。结论:DCE-MRI/DWI可以测量多激酶抑制剂治疗后的gist或hcc灌注和弥散的变化。
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