Carrasquillo J A, Abrams P G, Schroff R W, Reynolds J C, Woodhouse C S, Morgan A C, Keenan A M, Foon K A, Perentesis P, Marshall S
Nuclear Medicine Department, National Institutes of Health, Bethesda, Maryland 20892.
J Nucl Med. 1988 Jan;29(1):39-47.
Eleven patients with metastatic melanoma underwent serial gamma camera imaging and biodistribution measurements after i.v. injection of escalating doses of [111In]9.2.27, an antimelanoma murine monoclonal antibody. Patients received a fixed dose of 1 mg of [111In]9.2.27, with no additional 9.2.27 (five patients), or co-infused with 49 mg (five patients) or 99 mg (one patient) of unlabeled, unconjugated 9.2.27. Higher doses resulted in prolonged blood-pool retention, less uptake in spleen and bone marrow, and appeared to have a positive effect in improving tumor imaging. A dose of 1 mg of 9.2.27 permitted detection of tumors in two of five patients and two of ten lesions, while with greater than or equal to 50 mg, tumors were detected in all patients and in 24 of 32 lesions. Human gamma globulin injected prior to administration of [111In]9.2.27 failed to block the prominent liver, spleen, and bone marrow uptake. No toxicity was observed. These results indicate the feasibility of imaging metastatic melanoma with [111In]9.2.27 and suggest that antibody dose may be a critical determinant of biodistribution and tumor uptake.
11例转移性黑色素瘤患者在静脉注射递增剂量的抗黑色素瘤鼠单克隆抗体[111In]9.2.27后,接受了系列γ相机成像和生物分布测量。患者接受固定剂量1mg的[111In]9.2.27,其中5例患者未额外注射9.2.27,5例患者同时输注49mg未标记、未偶联的9.2.27,1例患者同时输注99mg。更高剂量导致血池滞留时间延长,脾脏和骨髓摄取减少,且似乎对改善肿瘤成像有积极作用。1mg剂量的9.2.27能在5例患者中的2例以及10个病灶中的2个检测到肿瘤,而剂量大于或等于50mg时,所有患者均能检测到肿瘤,32个病灶中的24个也能被检测到。在注射[111In]9.2.27之前注射人γ球蛋白未能阻断肝脏、脾脏和骨髓的显著摄取。未观察到毒性。这些结果表明用[111In]9.2.27对转移性黑色素瘤进行成像的可行性,并提示抗体剂量可能是生物分布和肿瘤摄取的关键决定因素。