Sisson J C, Shapiro B, Beierwaltes W H, Glowniak J V, Nakajo M, Mangner T J, Carey J E, Swanson D P, Copp J E, Satterlee W G
J Nucl Med. 1984 Feb;25(2):197-206.
Apart from relieving effects of secreted catecholamines, treatments of malignant pheochromocytoma have achieved little success. When the radiopharmaceutical, meta-[131I] iodobenzylguanidine (I-131 MIBG ), was found to concentrate in some malignant pheochromocytomas, we calculated that this agent could impart therapeutic doses of radiation to these tumors. We therefore treated five patients with two to four doses of I-131 MIBG prepared in high specific activity, 8-11 Ci/mmol. Individual doses were given at 3- to 10-mo intervals and in 97- to 197-mCi amounts. Two patients exhibited subjective and objective benefits. Their tumors declined in size (to 28% and 30% of original volumes) and in hormone secretion (to 50% or less of baseline rates). The other three patients manifested few symptoms before treatment and showed few or no objective improvement afterward. The tumors of the patients who responded to I-131 MIBG (a) appeared to be more rapidly growing, (b) received more cumulative rads, and (c) were more predominantly in soft tissues (in contrast to bone) than those in the patients who obtained little benefit. No toxic effects were encountered during the treatments, and only minor and temporary untoward responses were seen later.
除了分泌的儿茶酚胺的缓解作用外,恶性嗜铬细胞瘤的治疗几乎没有取得成功。当发现放射性药物间位-[¹³¹I]碘苄胍(I-131 MIBG)在一些恶性嗜铬细胞瘤中浓聚时,我们计算出这种药物可以给这些肿瘤给予治疗剂量的辐射。因此,我们用高比活度(8-11 Ci/mmol)制备的两到四剂I-131 MIBG治疗了5名患者。个体剂量以3至10个月的间隔给予,剂量为97至197 mCi。两名患者表现出主观和客观上的益处。他们的肿瘤大小缩小(至原始体积的28%和30%),激素分泌减少(至基线水平的50%或更低)。另外三名患者在治疗前症状很少,治疗后几乎没有或没有客观改善。对I-131 MIBG有反应的患者的肿瘤(a)似乎生长更快,(b)接受的累积拉德更多,(c)与获益很少的患者相比,更多地主要位于软组织(与骨骼相比)。治疗期间未遇到毒性作用,之后仅出现轻微和暂时的不良反应。