中文摘要：

目的探讨18F-FDGMicro—PET／CT对125I粒子组织间植入治疗胰腺癌裸鼠移植瘤疗效进行早期评价的应用价值。方法人胰腺癌SW1990细胞株接种于BABL／c裸鼠右后肢，2周后成瘤大小8～10mm。12只荷瘤裸鼠随机分为空白对照组、空载粒子组和125I粒子植入组，每组4只。治疗前及治疗后1周行”F-FDGMicro—PET／CT检查，计算最大标准摄取值（SUVmax）、平均标准摄取值（SUVmax）、肿瘤体积及坏死率。瘤体标本行HE染色和细胞质胸腺嘧啶核苷激酶（TK1）免疫组织化学检查。结果3组治疗前SUVmax和SUVmax值差异无统计学意义，治疗后1周3组SUVmax和SUVmean。分别为3．53±1．20和0．57±0．26、3．83±2．13和0．59±0．24、0．29±0．23和0．02±0．01，差异有统计学意义（F=7．62、10．34，P〈0．01）。125I粒子植入组SUVmax和SUVmean。明显低于空载粒子植入组及空白对照组，且明显低于治疗前。3组治疗前肿瘤坏死率无明显差异，免疫组织化学染色发现，3组TK1阳性染色指数分别为（64．25±1．71）％、（62．25±2．22）％和（38．25±1．71）％，差异有统计学意义（F=233．67，P〈0．01），125I粒子植入组明显低于空载粒子植入组及空白对照组。SUVmax与TK1阳性染色指数有一定的正相关性（r=0．85，P〈0．01）。结论18F-FDGMicro．PET／CT是监测125I粒子治疗胰腺癌早期疗效的有效方法。

英文摘要：

Objective To investigate the application value of early evaluation and monitoring of 125I interstitial implantation in a pancreatic cancer xenograft. Methods Xenograft models were created by subcutaneous injection of Sw 1990 human pancreatic cancer cell suspensions into the right hind limbs of the immunodeficient BABL/c nude mice. The tumors size were about 8-10 mm after two weeks. The mice were randomly divided into 5 groups, including control group （ n = 4）, empty seed implantation group （ n = 4） and 125I implantation group （n = 4）. Before treatment and one week after treatment, 18F-FDG Micro-PET/ CT scan was performed and then maximum standardized uptake values （SUVmax）, mean standardized uptake values （SUV ）, tumor size and necrosis rate were measured. HE staining and TK1 immunohistochemistry examination were carried out in the paraffin-embedded sample. Results Before treatment the SUVx and SUV values of three groups did not reach statistical significance. One week after treatment the SUVmax and SUV values of three groups were 3.53 ± 1.20 and 0. 57 ± 0.26 vs. 3.83 ±2.13 and0.59 ± 0.24vs. 0.29± 0.23 and0.016 ±0.001, respectively, with a significant difference （F =7.62,P =0. 01 ; F = 10. 34, P =0. 005）. The SUVmax and SUV values of 125I implant group were significantly lower than empty seed implant group and control group and were significantly lower than before treatment. Before treatment, tumor necrosis rate of three groups were not significantly different. Immunohistochemical staining found the TK1 positive staining index of three groups were respectively（64. 25 ± 1.71 ） % , （62. 25 ± 2.22） % and （38.25 ± 1.71 ） % with statistically significant difference （F =233.67, P 〈 0. 001 ）. The TK1 positive staining index of 125I implant group was significantly lower than empty seed implant group and control group. The SUVmax values had some positive correlation with TK1 positive staining index （ r = 0. 85,P = 0. 001 ）. Conclusions is F-FDG Micro-PET/CT may be use