DuBois S G, Matthay K K
Department of Pediatrics, UCSF School of Medicine, San Francisco, CA, USA.
Q J Nucl Med Mol Imaging. 2013 Mar;57(1):53-65.
Neuroblastoma is an aggressive childhood cancer, with a propensity for early widespread metastasis. Approximately 90% of tumors accumulate the norepinephrine analogue metaiodobenzylguanidine (MIBG) avidly, allowing the use of radiolabeled MIBG for targeted imaging and radiotherapy. After preclinical studies demonstrated activity of 131I-MIBG in models of neuroblastoma, clinical development of this agent ensued. Early clinical trials of 131I-MIBG in patients with relapsed or refractory neuroblastoma defined the toxicity profile of this agent, with myelosuppression as the main dose-limiting toxicity. Subsequent trials defined the activity of 131I-MIBG, with response rates of 20-40% in patients with relapsed or refractory disease. More recent clinical trials have tested 131I-MIBG in combination with chemotherapy or as a component of myeloablative therapies. Given the documented activity of 131I-MIBG, future studies will need to evaluate the impact of radiation sensitizers on this activity and define the role of this agent in treating patients with newly diagnosed high-risk neuroblastoma.
神经母细胞瘤是一种侵袭性儿童癌症,易于早期广泛转移。约90%的肿瘤大量摄取去甲肾上腺素类似物间碘苄胍(MIBG),这使得放射性标记的MIBG可用于靶向成像和放射治疗。临床前研究证明131I-MIBG在神经母细胞瘤模型中有活性后,该药物进入了临床开发阶段。131I-MIBG在复发或难治性神经母细胞瘤患者中的早期临床试验确定了该药物的毒性特征,骨髓抑制是主要的剂量限制性毒性。随后的试验确定了131I-MIBG的活性,复发或难治性疾病患者的缓解率为20%-40%。最近的临床试验对131I-MIBG与化疗联合使用或作为清髓性治疗的组成部分进行了测试。鉴于131I-MIBG已证实的活性,未来的研究需要评估辐射增敏剂对该活性的影响,并确定该药物在治疗新诊断的高危神经母细胞瘤患者中的作用。