Major P, Wang T Q, Ishida M, Unger M, Rosenthall L
McGill Cancer Centre, McGill University, Montreal, PQ, Canada.
Eur J Nucl Med. 1989;15(10):655-60. doi: 10.1007/BF00251679.
The localization of 111In-labelled MA5 monoclonal antibody, reactive with a breast tumor associated antigen, was studied in 17 patients. MA5 was selected because 1) it reacts with greater than 95% of primary and metastatic lesions, 2) the recognized antigen is present on the cell surface in vivo and 3) MA5 gives excellent localization in human breast tumor xenografts. Each patient received 2 mg antibody labeled with 5 mCi 111In and in some cases, 3 mg or 18 mg unlabeled carrier antibody. No serious allergic reactions were noted. There was a large uptake in the liver, less significant uptake in the spleen and bone, and minimal accumulation in the bowel. Bone lesions, primary tumors, soft tissue recurrences and lung metastases larger than 3 cm diameter were imaged, while only 1 lesion smaller than 3 cm was detected. Non specific accumulation of tracer was noted at the site of a port-a-cath, in a hematoma, in fibrocystic lesions, and at sites of previous radiation treatment. Extensive fibrosis and poor vascularization characteristic of breast tumors may explain in part the limited sensitivity of the imaging.
对17例患者研究了与乳腺肿瘤相关抗原发生反应的铟-111标记的MA5单克隆抗体的定位情况。选择MA5是因为:1)它与超过95%的原发性和转移性病变发生反应;2)所识别的抗原在体内存在于细胞表面;3)MA5在人乳腺肿瘤异种移植中定位良好。每位患者接受2mg用5mCi铟-111标记的抗体,在某些情况下还接受3mg或18mg未标记的载体抗体。未观察到严重的过敏反应。肝脏摄取量大,脾脏和骨骼摄取量较小,肠道积聚极少。对直径大于3cm的骨病变、原发性肿瘤、软组织复发和肺转移灶进行了成像,而仅检测到1个小于3cm的病变。在输液港部位、血肿内、纤维囊性病变以及既往放疗部位观察到示踪剂的非特异性积聚。乳腺肿瘤广泛的纤维化和血管化不良特征可能部分解释了成像敏感性有限的原因。