Epenetos A A, Shepherd J, Britton K E, Hawkins L, Nimmon C C, Taylor-Papadimitriou J, Durbin H, Malpas J S, Mather S, Granowska M
Cancer Detect Prev. 1984;7(1):45-9.
Monoclonal antibodies to epithelial cells, antigenic determinants labelled with I123 and I125, were administered to 10 immunodeficient mice bearing subcutaneous xenografts of human ovarian cancer. Radio scans of the body taken with a gamma camera at various time intervals demonstrated the presence of the cancer in all the mice. The smallest detectable tumor was approximately 1 mm in diameter. In a subsequent clinical study using 123I-labelled monoclonal antibodies in 10 patients with ovarian cancer, tumor detection was achieved in 8 patients, with tumor uptake of labelled antibody ranging between 0.2-2.6%. As a complementary method to existing forms of diagnosis, the targeting of monoclonal antibodies to ovarian cancer cells in vivo raises the hope of achieving early diagnosis in otherwise undetectable ovarian cancer, and provides encouragement to the concept of selective therapy in oncology.
将针对上皮细胞的单克隆抗体、用碘-123和碘-125标记的抗原决定簇注射给10只携带人卵巢癌皮下异种移植物的免疫缺陷小鼠。在不同时间间隔用伽马相机对小鼠进行全身放射性扫描,结果显示所有小鼠体内均存在癌症。可检测到的最小肿瘤直径约为1毫米。在随后一项针对10名卵巢癌患者使用碘-123标记单克隆抗体的临床研究中,8名患者实现了肿瘤检测,标记抗体在肿瘤中的摄取率在0.2%至2.6%之间。作为现有诊断形式的一种补充方法,体内单克隆抗体靶向卵巢癌细胞有望实现对原本无法检测到的卵巢癌进行早期诊断,并为肿瘤学中的选择性治疗概念提供了支持。