Hoefnagel C A, Taal B G, Sivro F, Boot H, Valdes Olmos R A
Department of Nuclear Medicine, The Netherlands Cancer Institute, Amsterdam.
Nucl Med Commun. 2000 Aug;21(8):755-61. doi: 10.1097/00006231-200008000-00009.
Iodine-131 metaiodobenzylguanidine (131I-MIBG) has been used with success for the palliation of symptomatic, metastatic carcinoid tumours. However, only 70% of cases are MIBG-avid and tumour uptake is not always sufficient for therapy. At The Netherlands Cancer Institute 34 carcinoid patients with no or insufficient uptake were treated with escalating doses of unlabelled ('cold') MIBG. No objective remissions were recorded, but a palliative effect (i.e. subjective disappearance of symptoms and/or reduction of medication by more than 50%) was observed in 60% of cases (mean duration 4.5 months). In 24 of the patients undergoing therapy with 'cold' MIBG, total body scintigraphy using 37 MBq 131I-MIBG was performed before and after infusion of 'cold' MIBG. The biodistribution of 131I-MIBG and its tumour to non-tumour ratios were compared. After 'cold' MIBG the 131I-MIBG uptake in the salivary glands was suppressed in all patients, myocardial uptake in 21, and uptake in normal liver tissue in 14. Pulmonary uptake was increased in 13 patients. More importantly, the tumour to non-tumour (T/NT) ratios improved in 17 of the 24 cases (by 7.8-111.4% at 24 h). Of the initial six patients demonstrating a significant increase in the T/NT ratio, five have subsequently received combined treatment of 7.4 GBq 131I-MIBG following the administration of 'cold' MIBG (both by 4 h intravenous infusion), resulting in a good palliative response in four of them. These patients had previously been excluded from therapy with 131I-MIBG only. It is concluded that the administration of unlabelled MIBG may not only provide palliation to patients with carcinoid tumours, but may also alter the biodistribution of MIBG, enabling 131I-MIBG therapy to be used in cases not qualifying for this treatment due to insufficient tumour uptake.
碘-131间碘苄胍(131I-MIBG)已成功用于缓解有症状的转移性类癌肿瘤。然而,只有70%的病例对MIBG摄取阳性,且肿瘤摄取量并不总是足以进行治疗。在荷兰癌症研究所,34例对MIBG摄取阴性或摄取不足的类癌患者接受了递增剂量的未标记(“冷”)MIBG治疗。未记录到客观缓解情况,但60%的病例观察到了姑息效果(即症状主观消失和/或药物用量减少超过50%)(平均持续时间4.5个月)。在24例接受“冷”MIBG治疗的患者中,在输注“冷”MIBG前后使用37 MBq 131I-MIBG进行了全身闪烁扫描。比较了131I-MIBG的生物分布及其肿瘤与非肿瘤的比值。给予“冷”MIBG后,所有患者唾液腺中131I-MIBG的摄取均受到抑制,21例患者心肌摄取受到抑制,14例患者正常肝组织摄取受到抑制。13例患者肺部摄取增加。更重要的是,24例中的17例(24小时时)肿瘤与非肿瘤(T/NT)比值得到改善(提高了7.8 - 111.4%)。最初显示T/NT比值显著增加的6例患者中,有5例随后在给予“冷”MIBG(均通过4小时静脉输注)后接受了7.4 GBq 131I-MIBG的联合治疗,其中4例获得了良好的姑息反应。这些患者此前仅因肿瘤摄取不足而被排除在131I-MIBG治疗之外。结论是,给予未标记的MIBG不仅可为类癌肿瘤患者提供姑息治疗,还可能改变MIBG的生物分布,使131I-MIBG治疗能够用于因肿瘤摄取不足而不符合该治疗条件的病例。