Mulshine J L, Carrasquillo J A, Weinstein J N, Keenan A M, Reynolds J C, Herdt J, Bunn P A, Sausville E, Eddy J, Cotelingam J D
National Cancer Institute, NCI-Navy Medical Oncology Branch, Naval Hospital, Bethesda, MD 20814.
Cancer Res. 1991 Jan 15;51(2):688-95.
Direct intralymphatic administration of radiolabeled monoclonal antibody in targeting antigen-bearing lymphoma cells in regional lymph nodes of patients with cutaneous T-cell lymphoma was evaluated. Seven consecutive patients undergoing staging lymphangiography received intralymphatic infusions of 111In-T101 to evaluate lymph node involvement. This procedure was accomplished without significant complication. The 111In-T101 rapidly distributed throughout the regional lymphatic compartment and passed into the systemic circulation. Tumor-bearing sites in the inguinal-femoral lymph nodes retained from 0.42 to 4.8% of the injected dose of radiolabeled antibody. Three patients were upstaged to Stage IVA based on tumor involvement found after radiolymphoscintigraphy-directed biopsy of groin lymph nodes, selected because of intense radioactivity by gamma camera imaging. Compared with previously reported s.c. antibody administration, there was a marked reduction in the radioactive exposure of normal tissues at the injection sites in the lower extremities. Direct intralymphatic delivery of 111In-T101 appears to be a feasible, efficient method for delivering therapeutic doses of radiolabeled antibody.
对皮肤T细胞淋巴瘤患者局部淋巴结中携带抗原的淋巴瘤细胞进行靶向治疗时,评估了放射性标记单克隆抗体的直接淋巴管内给药。连续7例接受分期淋巴管造影的患者接受了111In-T101的淋巴管内输注,以评估淋巴结受累情况。该操作未出现明显并发症。111In-T101迅速分布于局部淋巴腔,并进入体循环。腹股沟-股淋巴结中的肿瘤部位保留了注射剂量放射性标记抗体的0.42%至4.8%。3例患者因腹股沟淋巴结放射性淋巴闪烁造影引导活检后发现肿瘤受累而被上调至IVA期,这些淋巴结因γ相机成像显示放射性强而被选中。与先前报道的皮下抗体给药相比,下肢注射部位正常组织的放射性暴露明显减少。111In-T101的直接淋巴管内给药似乎是一种可行、有效的方法,可用于递送治疗剂量的放射性标记抗体。