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在晚期难治性脑膜瘤中肽受体放射性核素治疗:长期随访的疗效和毒性。

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

机构信息

Nuclear Medicine and Radiometabolic Units, IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori", Meldola, Italy.

Osteoncology and Rare Tumor Center, IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori", Meldola, Italy;

出版信息

J Nucl Med. 2024 Sep 3;65(9):1409-1415. doi: 10.2967/jnumed.123.266956.

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 Ga-DOTA-octreotide and peptide receptor radionuclide therapy (PRRT) with Y/Lu-DOTA-octreotide are currently possible options within experimental protocols or as compassionate use in small patient groups. From October 2009 to October 2021, 42 meningioma patients with radiologic recurrence after standard therapies were treated with Y-DOTATOC (dosage of 1.1 or 5.5 GBq) or with Lu-DOTATATE (dosage of 3.7 or 5.5 GBq) in a mean of 4 cycles. All patients showed intense uptake at diagnostic Ga-DOTATOC PET/CT or in an In-octreotide scan. Of 42 patients treated, 5 patients received Y-DOTATOC with a cumulative activity of 11.1 GBq and 37 patients received Lu-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 Lu-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. 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.

摘要

手术后和放疗后的脑膜瘤复发需要特别关注,因为缺乏积极的三线治疗方法。生长抑素受体通常在脑膜瘤的细胞膜上过度表达,这为放射性核素治疗方法开辟了道路。目前,使用 Ga-DOTA-octreotide 进行诊断,并使用 Y/Lu-DOTA-octreotide 进行肽受体放射性核素治疗(PRRT),这是在实验方案中的可行选择,或者在小患者组中作为同情使用。

从 2009 年 10 月到 2021 年 10 月,42 例接受标准治疗后影像学复发的脑膜瘤患者接受了 Y-DOTATOC(剂量为 1.1 或 5.5GBq)或 Lu-DOTATATE(剂量为 3.7 或 5.5GBq)治疗,平均 4 个周期。所有患者在诊断性 Ga-DOTATOC PET/CT 或 In-octreotide 扫描中均显示强烈摄取。

在接受治疗的 42 例患者中,5 例患者接受了 Y-DOTATOC 治疗,累积活度为 11.1GBq,37 例患者接受了 Lu-DOTATATE 治疗,累积活度为 22GBq。疾病控制率为 57%。中位随访 63 个月时,中位无进展生存期为 16 个月,中位总生存期为 36 个月。6 例患者接受了 Lu-PRRT 再治疗,中位活度为 13GBq,平均 5 个周期。在 75.8 个月的随访中,中位无进展生存期和总生存期分别为 6.5 和 17 个月。只有 1 例患者因 3 级血小板毒性而停止治疗。1 例接受再治疗的患者出现短暂的 2 级中性粒细胞减少症。

在过度表达生长抑素受体 2 的晚期脑膜瘤患者中,PRRT 具有活性且耐受性良好,疾病控制率为 57%。此外,PRRT 可能代表一种潜在的再治疗选择。需要进一步的研究,也可以与其他治疗方法联合进行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4367/11372258/5c5767034ff5/jnumed.123.266956absf1.jpg

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