Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Mol Imaging Biol. 2012 Apr;14(2):237-44. doi: 10.1007/s11307-011-0491-5.
The objective of this study is to evaluate the therapeutic response to a novel monoclonal antibody targeting human extracellular matrix metalloproteinase inducer (EMMPRIN) in combination with gemcitabine in a pancreatic-tumor xenograft murine model by sequential 2-deoxy-2-[18F]fluoro-D-glucose ((18)F-FDG) positron emission tomography/computed tomgraphy (PET/CT) imaging.
Four groups of SCID mice bearing orthotopic pancreatic tumor xenografts were injected with phosphate-buffered saline, gemcitabine (120 mg/kg BW), anti-EMMPRIN antibody (0.2 mg), or combination, respectively, twice weekly for 2 weeks, while (18)F-FDG PET/CT imaging was performed weekly for 3 weeks. Changes in mean standardized uptake value (SUV(mean)) of (18)F-FDG and volume of tumors were determined.
The tumor SUV(mean) change in the group receiving combination therapy was significantly lower than those of the other groups. Tumor-volume changes of groups treated with anti-EMMPRIN monotherapy or combined therapy were significantly lower than that of the control group.
These data provide support for clinical studies of anti-EMMPRIN therapy with gemcitabine for pancreatic cancer treatment.
本研究旨在通过连续的 2-脱氧-2-[18F]氟-D-葡萄糖 ((18)F-FDG) 正电子发射断层扫描/计算机断层扫描 (PET/CT) 成像,评估靶向人细胞外基质金属蛋白酶诱导因子 (EMMPRIN) 的新型单克隆抗体与吉西他滨联合用于胰腺肿瘤异种移植小鼠模型的治疗反应。
将四组荷有原位胰腺肿瘤异种移植的 SCID 小鼠分别注射磷酸盐缓冲液、吉西他滨 (120mg/kg BW)、抗 EMMPRIN 抗体 (0.2mg) 或联合用药,每周两次,共 2 周,同时每周进行 (18)F-FDG PET/CT 成像,共 3 周。确定 (18)F-FDG 的平均标准化摄取值 (SUV(mean)) 和肿瘤体积的变化。
联合治疗组的肿瘤 SUV(mean)变化明显低于其他组。接受抗 EMMPRIN 单药治疗或联合治疗的组的肿瘤体积变化明显低于对照组。
这些数据为抗 EMMPRIN 联合吉西他滨治疗胰腺癌的临床研究提供了支持。