Intraarterial Administration of Peptide Receptor Radionuclide Therapy in Patients with Advanced Meningioma: Initial Safety and Efficacy

Adriana Amerein, Christoph Maurer, Malte Kircher, Alexander Gäble, Anne Krebold, Andreas Rinscheid, Oliver Viering, Christian H. Pfob, Ralph A. Bundschuh, Lars Behrens, Arthur JAT Braat, Ansgar Berlis, Constantin Lapa
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Abstract

Peptide receptor radionuclide therapy (PRRT) is a treatment option for patients with advanced meningioma. Recently, intraarterial application of the radiolabeled somatostatin receptor agonists has been introduced as an alternative to standard intravenous administration. In this study, we assessed the safety and efficacy of intraarterial PRRT in patients with advanced, progressive meningioma. Methods: Patients with advanced, progressive meningioma underwent intraarterial PRRT with [177Lu]Lu-HA-DOTATATE. The safety of PRRT was evaluated according to the Common Terminology Criteria for Adverse Events version 5.0. Treatment response was assessed according to the proposed Response Assessment in Neuro-Oncology criteria for meningiomas and somatostatin receptor–directed PET/CT. Results: Thirteen patients (8 women, 5 men; mean age, 65 ± 13 y) with advanced meningioma underwent 1–4 cycles (median, 4 cycles) of intraarterial PRRT with [177Lu]Lu-HA-DOTATATE (mean activity per cycle, 7,428 ± 237 MBq; range, 6,000–7,700 MBq). Treatment was well tolerated with mainly grade 1–2 hematologic toxicity. Ten of 13 patients showed radiologic disease control at follow-up after therapy (1/10 complete remission, 1/10 partial remission, 8/10 stable disease), and 9 of 13 patients showed good control of clinical symptoms. Conclusion: Intraarterial PRRT in patients with advanced meningioma is feasible and safe. It may result in improved radiologic and clinical disease control compared with intravenous PRRT. Further research to validate these initial findings and to investigate long-term outcomes is highly warranted.

肽受体放射性核素疗法在晚期脑膜瘤患者中的动脉内给药:初步安全性和有效性
肽受体放射性核素疗法(PRRT)是晚期脑膜瘤患者的一种治疗选择。最近,放射性标记的体生长抑素受体激动剂被引入动脉内应用,作为标准静脉给药的替代方法。在这项研究中,我们评估了动脉内 PRRT 对晚期进展期脑膜瘤患者的安全性和有效性。方法晚期进展期脑膜瘤患者接受了[177Lu]Lu-HA-DOTATATE动脉内PRRT治疗。根据不良事件通用术语标准 5.0 版评估了 PRRT 的安全性。治疗反应根据脑膜瘤和体生长激素受体导向 PET/CT 神经肿瘤学反应评估标准进行评估。结果:13名晚期脑膜瘤患者(8名女性,5名男性;平均年龄为65 ± 13岁)接受了1-4个周期(中位数为4个周期)的[177Lu]Lu-HA-DOTATATE动脉内PRRT治疗(每个周期的平均活性为7,428 ± 237 MBq;范围为6,000-7,700 MBq)。治疗耐受性良好,主要存在 1-2 级血液学毒性。在治疗后的随访中,13 名患者中有 10 人的放射性疾病得到控制(1/10 完全缓解,1/10 部分缓解,8/10 病情稳定),13 名患者中有 9 人的临床症状得到良好控制。结论是对晚期脑膜瘤患者进行动脉内PRRT治疗是可行且安全的。与静脉 PRRT 相比,动脉内 PRRT 可改善放射学和临床疾病控制。我们非常有必要开展进一步的研究,以验证这些初步发现并调查长期疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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