Gawne Peter J, Bryant Helen E, DuBois Steven G, George Sally L, Gray Juliet, Knox Leona, Matchett Kyle B, Peet Connie, Vallis Katherine A, Wallace Hugh J, Wan Simon, Gaze Mark N
Centre for Cancer Biomarkers and Biotherapeutics, Barts Cancer Institute, Queen Mary, University of London, London, United Kingdom.
UCL Cancer Institute, University College London, London, United Kingdom.
J Nucl Med. 2025 Apr 1;66(4):490-496. doi: 10.2967/jnumed.124.269121.
Despite improvements in neuroblastoma treatment, survival figures lag behind those of many other childhood malignancies. New treatments, and better use of existing treatments, are essential to reduce mortality. Neuroblastoma expresses several molecular targets for radionuclide imaging and therapy, of which the most widely exploited is the norepinephrine transporter. [I]metaiodobenzylguanidine (MIBG) imaging and [I]MIBG treatment, which target this physiologic pathway, have been in clinical practice for 40 y. Although therapy outcomes have been favorable, [I]MIBG use has not yet been optimized. Somatostatin receptors and the disialoganglioside are alternative targets, but their use remains experimental. The charity Children's Cancer Research Fund organized a workshop bringing together a broad range of scientists including radiochemists, radiobiologists, radiation physicists, clinical researchers including pediatric oncologists and nuclear medicine physicians, and patient advocates from the United Kingdom, United States, and continental Europe to share their experiences with molecular imaging and radiotherapy of neuroblastoma and discuss potential ways of improving treatment outcomes and access. These include development of alternative vectors targeting somatostatin receptors and disialoganglioside, isotopes such as α-particle and Auger electron emitters with different radiation characteristics, and combinations with external-beam radiotherapy, immunotherapy, and DNA damage repair inhibitors. Barriers to progress discussed included the unpredictable radioisotope supply, production of novel radiopharmaceuticals, lack of data regarding which are the best combination therapies, and insufficient clinical facilities. The aim was to stimulate the development and assessment of more effective treatments.
尽管神经母细胞瘤的治疗有所改善,但其生存率仍落后于许多其他儿童恶性肿瘤。新的治疗方法以及对现有治疗方法的更好应用对于降低死亡率至关重要。神经母细胞瘤表达了几种用于放射性核素成像和治疗的分子靶点,其中应用最广泛的是去甲肾上腺素转运体。[I]间碘苄胍(MIBG)成像和[I]MIBG治疗靶向这一生理途径,已在临床实践中应用了40年。尽管治疗效果良好,但MIBG的使用尚未得到优化。生长抑素受体和双唾液酸神经节苷脂是替代靶点,但它们的应用仍处于实验阶段。慈善机构儿童癌症研究基金会组织了一次研讨会,汇聚了包括放射化学家、放射生物学家、放射物理学家在内的广泛科学家群体,以及包括儿科肿瘤学家和核医学医师在内的临床研究人员,还有来自英国、美国和欧洲大陆的患者权益倡导者,以分享他们在神经母细胞瘤分子成像和放射治疗方面的经验,并讨论改善治疗效果和可及性的潜在方法。这些方法包括开发靶向生长抑素受体和双唾液酸神经节苷脂的替代载体、具有不同辐射特性的同位素如α粒子和俄歇电子发射体,以及与外照射放疗、免疫疗法和DNA损伤修复抑制剂的联合应用。讨论的进展障碍包括不可预测的放射性同位素供应、新型放射性药物的生产、缺乏关于最佳联合治疗方案的数据以及临床设施不足。目的是促进更有效治疗方法的开发和评估。