Peptide Receptor Radionuclide Therapy in Advanced Refractory Meningiomas: Efficacy and Toxicity in a Long Follow-up.

Stefano Severi, Ilaria Grassi, Alberto Bongiovanni, Silvia Nicolini, Irene Marini, Donatella Arpa, Nicoletta Ranallo, Irene Azzali, Valentina Di Iorio, Anna Sarnelli, Monti Manuela, Elena Amadori, Lucia Fabbri, Daniela Bartolini, Luigino Tosatto, Francesco Di Meco, Lorena Gurrieri, Nada Riva, Luana Calabro, Federica Matteucci, Giovanni Paganelli, Maddalena Sansovini
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Abstract

Recurrence of meningiomas after surgery and radiotherapy deserves specific attention because of the lack of active third-line therapies. Somatostatin receptors are usually overexpressed on the cell membrane of meningiomas, and this has led the way to a radionuclide theranostic approach. Diagnoses with 68Ga-DOTA-octreotide and peptide receptor radionuclide therapy (PRRT) with 90Y/177Lu-DOTA-octreotide are currently possible options within experimental protocols or as compassionate use in small patient groups. Methods: From October 2009 to October 2021, 42 meningioma patients with radiologic recurrence after standard therapies were treated with 90Y-DOTATOC (dosage of 1.1 or 5.5 GBq) or with 177Lu-DOTATATE (dosage of 3.7 or 5.5 GBq) in a mean of 4 cycles. All patients showed intense uptake at diagnostic 68Ga-DOTATOC PET/CT or in an 111In-octreotide scan. Results: Of 42 patients treated, 5 patients received 90Y-DOTATOC with a cumulative activity of 11.1 GBq and 37 patients received 177Lu-DOTATATE with a cumulative activity of 22 GBq. The disease control rate was 57%. With a median follow-up of 63 mo, median progression-free survival was 16 mo, and median overall survival was 36 mo. Retreatment 177Lu-PRRT was performed in 6 patients with an administered median activity of 13 GBq in a mean of 5 cycles. With a 75.8-mo follow-up, median progression-free survival and overall survival were 6.5 and 17 mo, respectively. Only 1 patient discontinued the treatment because of grade 3 platelet toxicity. A rapidly transient grade 2 neutropenia was recorded in 1 retreated patient. Conclusion: PRRT in patients with advanced meningiomas overexpressing somatostatin receptor 2 was active and well tolerated, showing a 57% disease control rate. Furthermore, PRRT could represent a potential retreatment option. Further studies, also in combination with other treatments, are warranted.

肽受体放射性核素治疗晚期难治性脑膜瘤:长期随访的疗效和毒性。
由于缺乏有效的三线疗法,脑膜瘤手术和放疗后的复发值得特别关注。脑膜瘤细胞膜上的体生长抑素受体通常会过度表达,这导致了放射性核素治疗方法的出现。使用68Ga-DOTA-octreotide进行诊断和使用90Y/177Lu-DOTA-octreotide进行肽受体放射性核素治疗(PRRT),是目前实验方案中可能的选择,或在小患者群体中作为同情性使用。方法:2009年10月至2021年10月,42名接受标准疗法后出现放射复发的脑膜瘤患者接受了90Y-DOTATOC(剂量为1.1或5.5 GBq)或177Lu-DOTATATE(剂量为3.7或5.5 GBq)治疗,平均4个周期。所有患者在诊断性68Ga-DOTATOC PET/CT或111In-奥曲肽扫描中均显示出强摄取。结果:在接受治疗的42名患者中,5名患者接受了累积活性为11.1 GBq的90Y-DOTATOC,37名患者接受了累积活性为22 GBq的177Lu-DOTATATE。疾病控制率为 57%。中位随访时间为63个月,中位无进展生存期为16个月,中位总生存期为36个月。6名患者接受了177Lu-PRRT再治疗,平均5个周期的中位活性为13 GBq。随访 75.8 个月,中位无进展生存期和总生存期分别为 6.5 个月和 17 个月。只有一名患者因血小板毒性达到 3 级而中断治疗。1名接受治疗的患者出现了快速短暂的2级中性粒细胞减少症。结论对过度表达体生长抑素受体2的晚期脑膜瘤患者进行PRRT治疗,效果活跃且耐受性良好,疾病控制率达57%。此外,PRRT还是一种潜在的再治疗方案。与其他治疗方法相结合的进一步研究仍有必要。
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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