Department of Nuclear Medicine, Royal Free Hospital, London, NW3 2QG, UK.
Eur J Nucl Med Mol Imaging. 2010 May;37(5):904-12. doi: 10.1007/s00259-009-1326-3. Epub 2009 Dec 17.
The aim of this analysis was to evaluate the response to standard activity of (131)I-meta-iodobenzylguanidine (MIBG) in patients with disseminated neuroendocrine tumours (NETs), comparing overall survival of patients with symptomatic response, tumour size (as assessed by CT) and relevant plasma tumour markers.
A retrospective review of patients who had undergone (131)I-MIBG treatment between March 2001 and December 2006 was carried out. The administered activity of (131)I-MIBG was 5.5 GBq (NETs) and 7 GBq (phaeochromocytoma). Three cycles of treatment were planned with an interval of 10-12 weeks. A pre-therapy scan with (123)I-MIBG was performed to ascertain appropriate biodistribution.
Thirty-eight patients were identified. Only two patients developed significant bone marrow suppression. Symptomatic response: data were available in 37 of 38 patients: 15 patients had improved symptoms, 19 had no improvement in symptoms and 3 were asymptomatic. In those with a symptomatic response, the median overall survival was 58 months vs no response of 20.0 months (p = 0.001). CT response: in those with stable disease, the median overall survival was 58 months compared with progressive disease of 16.0 months. The difference between these groups was significant (p = 0.006). Hormonal response: this was available in only 20 of 38 patients. The median overall survival was the same for patients that had increased hormone levels and patients that had stable/decreased hormone levels (48 months).
Standard activity (131)I-MIBG is well tolerated. Symptomatic response to treatment is a significant predictor of overall survival. Whilst CT response also appears to predict survival, hormonal levels do not appear to correlate with survival.
本分析旨在评估标准活性(131)I-间碘苄胍(MIBG)在广泛分布的神经内分泌肿瘤(NET)患者中的反应,比较有症状反应、肿瘤大小(通过 CT 评估)和相关血浆肿瘤标志物的患者的总生存率。
对 2001 年 3 月至 2006 年 12 月期间接受(131)I-MIBG 治疗的患者进行了回顾性审查。(131)I-MIBG 的给予剂量为 5.5GBq(NET)和 7GBq(嗜铬细胞瘤)。计划进行三个周期的治疗,间隔 10-12 周。进行(123)I-MIBG 前治疗扫描以确定适当的生物分布。
确定了 38 名患者。只有两名患者出现明显骨髓抑制。症状反应:38 名患者中的 37 名有数据:15 名患者症状改善,19 名患者症状无改善,3 名患者无症状。在有症状反应的患者中,中位总生存率为 58 个月,无反应者为 20.0 个月(p=0.001)。CT 反应:在稳定疾病的患者中,中位总生存率为 58 个月,而进展性疾病为 16.0 个月。这些组之间的差异具有统计学意义(p=0.006)。激素反应:只有 38 名患者中的 20 名有数据。激素水平升高和激素水平稳定/降低的患者的中位总生存率相同(48 个月)。
标准活性(131)I-MIBG 耐受良好。对治疗的症状反应是总生存率的重要预测指标。虽然 CT 反应似乎也预测生存,但激素水平似乎与生存无关。