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采用 177Lu-DOTATATE 的肽受体放射性核素疗法治疗无法手术或转移性副神经节瘤和嗜铬细胞瘤。

Treatment of inoperable or metastatic paragangliomas and pheochromocytomas with peptide receptor radionuclide therapy using 177Lu-DOTATATE.

机构信息

Department of Internal Medicine, Sector Endocrinology.

Department of Radiology & Nuclear Medicine, ENETS Centre of Excellence, Erasmus University Medical Center and Erasmus MC Cancer Institute, Rotterdam, Netherlands.

出版信息

Eur J Endocrinol. 2019 Jul;181(1):45-53. doi: 10.1530/EJE-18-0901.

Abstract

OBJECTIVES

Inoperable or metastatic paragangliomas (PGLs) and malignant pheochromocytomas (PCCs) are rare tumours with limited options for systemic treatment. Aim of this study was to assess the safety and efficacy of the radiolabelled somatostatin analogue (177LutetiumDOTA0-Tyr3)octreotate (177Lu-DOTATATE) for the treatment of PGLs and PCCs.

METHODS

Patients with histologically proven inoperable or malignant PGLs and PCCs treated with 177Lu-DOTATATE at our centre were retrospectively analysed. Patients were treated with up to four cycles of 177Lu-DOTATATE with an intended dose of 7.4 Gb per cycle. Response was assessed with use of RECIST 1.1.

RESULTS

Thirty patients were included: 17 with parasympathetic, 10 with sympathetic PGLs and 3 with PCCs. Grade 3/4 subacute haematotoxicity occurred in 6 (20%) of patients. A reversible subacute adverse event due to cardiac failure following possible catecholamine release occurred in two patients. Best tumour response was partial response in 7 (23%) and stable disease in 20 (67%), whereas 3 (10%) patients had progressive disease. In 20 patients with baseline disease progression, tumour control was observed in 17 (85%); the median progression-free survival was 91 months in patients with parasympathetic PGLs, 13 months in patients with sympathetic PGLs and 10 months in patients with metastatic PCCs.

CONCLUSION

This study suggests that PRRT with 177Lu-DOTATATE is a safe and effective treatment option for patients with inoperable or malignant PGL and PCC.

摘要

目的

无法手术或转移的副神经节瘤(PGL)和恶性嗜铬细胞瘤(PCC)是罕见的肿瘤,其全身治疗选择有限。本研究旨在评估放射性标记的生长抑素类似物(177 镥-DOTA0-酪氨酰 3)奥曲肽(177Lu-DOTATATE)治疗 PGL 和 PCC 的安全性和疗效。

方法

对在我们中心接受 177Lu-DOTATATE 治疗的经组织学证实的无法手术或恶性 PGL 和 PCC 患者进行回顾性分析。患者接受了多达四个周期的 177Lu-DOTATATE 治疗,每个周期的预期剂量为 7.4GB。使用 RECIST 1.1 评估反应。

结果

共纳入 30 例患者:17 例副交感神经 PGL、10 例交感神经 PGL 和 3 例 PCC。6 例(20%)患者出现 3/4 级亚急性血液毒性。2 例可能因儿茶酚胺释放而发生的心脏衰竭导致的可逆性亚急性不良事件。最佳肿瘤反应为部分缓解 7 例(23%),稳定疾病 20 例(67%),进展性疾病 3 例(10%)。在 20 例基线疾病进展的患者中,观察到肿瘤控制在 17 例(85%);副交感神经 PGL 患者的中位无进展生存期为 91 个月,交感神经 PGL 患者为 13 个月,转移性 PCC 患者为 10 个月。

结论

本研究表明,PRRT 用 177Lu-DOTATATE 是治疗无法手术或恶性 PGL 和 PCC 患者的安全有效治疗选择。

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