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首页> 外文期刊>Radiation and Environmental Biophysics >Boron neutron capture therapy (BNCT) for liver metastasis in an experimental model: dose-response at five-week follow-up based on retrospective dose assessment in individual rats
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Boron neutron capture therapy (BNCT) for liver metastasis in an experimental model: dose-response at five-week follow-up based on retrospective dose assessment in individual rats

机译:硼中子俘获疗法(BNCT)在实验模型中用于肝转移:基于对每只大鼠的回顾性剂量评估,在五周随访中的剂量反应

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Boron neutron capture therapy (BNCT) was proposed for untreatable colorectal liver metastases. Employing an experimental model of liver metastases in rats, we recently demonstrated that BNCT mediated by boron-ophenylalanine (BPA-BNCT) at 13 Gy prescribed to tumor is therapeutically useful at 3-week follow-up. The aim of the present study was to evaluate dose-response at 5-week follow-up, based on retrospective dose assessment in individual rats. BDIX rats were inoculated with syngeneic colon cancer cells DHD/K12/TRb. Tumor-bearing animals were divided into three groups: BPA-BNCT (n = 19), Beam only (n = 8) and Sham (n = 7) (matched manipulation, no treatment). For each rat, neutron flux was measured in situ and boron content was measured in a pre-irradiation blood sample for retrospective individual dose assessment. For statistical analysis (ANOVA), individual data for the BPA-BNCT group were pooled according to absorbed tumor dose, BPA-BNCT I: 4.5-8.9 Gy and BPA-BNCT II: 9.2-16 Gy. At 5 weeks post-irradiation, the tumor surface area post-treatment/pre-treat-ment ratio was 12.2 ± 6.6 for Sham, 7.8 ± 4.1 for Beam only, 4.4 ± 5.6 for BPA-BNCT I and 0.45 ± 0.20 for BPA-BNCT II; tumor nodule weight was 750 ± 480 mg for Sham, 960 ± 620 mg for Beam only, 380 ± 720 mg for BPA-BNCT I and 7.3 ± 5.9 mg for BPA-BNCT II. The BPA-BNCT II group exhibited statistically significant tumor control with no contributory liver toxicity. Potential threshold doses for tumor response and significant tumor control were established at 6.1 and 9.2 Gy, respectively.
机译:硼中子俘获疗法(BNCT)被提议用于不可治愈的大肠肝转移。利用大鼠肝转移的实验模型,我们最近证明了在指定给肿瘤的13 Gy剂量下由硼-邻苯丙氨酸(BPA-BNCT)介导的BNCT在3周的随访中具有治疗作用。本研究的目的是基于对每只大鼠的回顾性剂量评估,评估5周随访时的剂量反应。用同系结肠癌细胞DHD / K12 / TRb接种BDIX大鼠。荷瘤动物分为三组:BPA-BNCT(n = 19),仅束(n = 8)和Sham(n = 7)(匹配处理,未治疗)。对于每只大鼠,原位测量中子通量,并在辐射前血样中测量硼含量,以进行回顾性个人剂量评估。为了进行统计分析(ANOVA),根据吸收的肿瘤剂量汇总BPA-BNCT组的个人数据,BPA-BNCT I:4.5-8.9 Gy,BPA-BNCT II:9.2-16 Gy。放疗后5周,治疗后/治疗前的肿瘤表面积比值:假手术为12.2±6.6,仅射线为7.8±4.1,BPA-BNCT I为4.4±5.6,BPA-0.44±0.20 BNCT II; Sham的瘤结节重量为750±480 mg,仅Beam肿瘤结节重量为960±620 mg,BPA-BNCT I为380±720 mg,BPA-BNCT II为7.3±5.9 mg。 BPA-BNCT II组显示出统计学上显着的肿瘤控制,无肝毒性。用于肿瘤应答和显着肿瘤控制的潜在阈值剂量分别确定为6.1 Gy和9.2 Gy。

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