Shepherd J H, Granowska M, Britton K E, Mather S, Epenetos A A, Ward B G, Slevin M
Br J Obstet Gynaecol. 1987 Feb;94(2):160-7. doi: 10.1111/j.1471-0528.1987.tb02344.x.
A tumour-associated radiolabelled monoclonal antibody (HMFG 2) was used to investigate 51 patients who were referred with a pelvic mass and suspected ovarian cancer or recurrent disease. The day before operation the 123I-labelled antibody was injected and the patients then underwent radioimmunoscintigraphy immediately and again 4 and 22 h after the injection. An exploratory laparotomy with appropriate surgery was then performed and the tumours were staged. Tumours were positively imaged 3 min-22 h after injection in all the patients with ovarian cancer, with a mean 0.6% of the injected antibody taken up by the tumour. The presence of HMFG antigen on the tumour was confirmed by immunoperoxidase staining of the surgically-removed tissues. Of the 51 patients, 39 proved to have ovarian cancer. The accuracy of diagnosis and detection of primary and metastatic malignant disease was 95% when correlating pre-operative radioimmune scan findings and laparotomy findings. The procedure is minimally invasive, apparently without side-effects and offers information for tumour detection as an adjunct or alternative to existing methods.
一种肿瘤相关放射性标记单克隆抗体(HMFG 2)被用于研究51例因盆腔肿块就诊且怀疑患有卵巢癌或复发性疾病的患者。手术前一天注射123I标记的抗体,然后患者立即接受放射免疫闪烁扫描,并在注射后4小时和22小时再次进行扫描。随后进行了 exploratory laparotomy(此处可能有误,应为“剖腹探查术”)及适当的手术,并对肿瘤进行分期。在所有卵巢癌患者中,注射后3分钟至22小时肿瘤均呈阳性显像,肿瘤摄取的注射抗体平均为0.6%。通过对手术切除组织进行免疫过氧化物酶染色,证实肿瘤上存在HMFG抗原。51例患者中,39例被证实患有卵巢癌。将术前放射免疫扫描结果与剖腹探查结果相关联时,原发性和转移性恶性疾病的诊断及检测准确率为95%。该程序微创,显然无副作用,并为肿瘤检测提供信息,可作为现有方法的辅助手段或替代方法。