Charbonnel B, Chatal J F, Brendel A J, Lanehche B, Lumbroso J, Marchandise X, Mornex R, Schlumberger M, Wemeau J L
Services d'Endocrinologie et de Médecine Nucléaire, Nantes.
Ann Endocrinol (Paris). 1988;49(4-5):344-7.
Twelve patients (2 with only bone metastases, 3 with only soft tissues metastases and 7 with bone and soft tissues metastases) were treated with 131-I-MIBG (specific activity: 20 mCi/mg), 100 to 200 mCi every 3-6 months. A dosimetric study was carried out before each administration. The follow-up ranged from 6 to 24 months and the number of doses ranged from 1 to 8, with 1.85-9 GBq per administration and a cumulative activity of 1.85-62. 2 GBq according to patients. The cumulative absorbed activity ranged from 850 to 9700 cGy. The following side effects were observed: a bone marrow hypoplasia (1 patient) and a transient increase in catecholamines (3 patients). The treatment was successful in 7 patients (3 with soft tissue metastases, 3 with bone and soft tissue metastases and one with bone metastases). This success consisted in clinical improvement and a decrease greater than 50% of hormonal values in the 7 patients and a decrease greater than 50% of tumoral masses in only 3 patients. No complete remission was obtained at this stage of the study. The disease recurred in 1 patient after a year of partial remission. There was no clear-cut relation between the number of doses and the results. This study shows that 131-I-MIBG can give encouraging though limited results.
12例患者(2例仅有骨转移,3例仅有软组织转移,7例有骨和软组织转移)接受了131-I-MIBG治疗(比活度:20mCi/mg),每3 - 6个月给予100至200mCi。每次给药前进行剂量测定研究。随访时间为6至24个月,给药次数为1至8次,每次给药剂量为1.85 - 9GBq,根据患者情况累积活度为1.85 - 62.2GBq。累积吸收活度范围为850至9700cGy。观察到以下副作用:1例骨髓发育不全和3例儿茶酚胺短暂升高。7例患者治疗成功(3例软组织转移、3例骨和软组织转移以及1例骨转移)。成功表现为7例患者临床症状改善且激素值下降超过50%,仅3例患者肿瘤肿块缩小超过50%。在本研究阶段未获得完全缓解。1例患者在部分缓解1年后疾病复发。给药次数与结果之间无明确关系。本研究表明,131-I-MIBG虽能取得令人鼓舞的结果,但效果有限。