177Lu-DOTATATE治疗进展性转移性嗜铬细胞瘤和副神经节瘤的II期研究:疗效、安全性和生物标志物的中期分析

IF 41.9 1区 医学 Q1 ONCOLOGY
Journal of Clinical Oncology Pub Date : 2025-10-01 Epub Date: 2025-08-19 DOI:10.1200/JCO-25-00791
Frank I Lin, Jaydira Del Rivero, Jorge A Carrasquillo, Abhishek Jha, Joy Zou, Inna Shamis, Sara Talvacchio, Baris Turkbey, Erich P Huang, Joanna Shih, Joanna Klubo-Gwiezdzinska, Esther Mena, Liza Lindenberg, Yating Teng, Freddy E Escorcia, Clara Chen, Peter Herscovitch, Corina Millo, Peter L Choyke, Karel Pacak
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引用次数: 0

摘要

目的:177Lu-DOTA(0)-Tyr(3)-octreotate (177Lu-DOTATATE)是一种靶向生长抑素受体(SSTR)的放射性药物,有望治疗转移性嗜铬细胞瘤/副神经节瘤(PPGLs),这是一种罕见的表达SSTR的肿瘤。方法:在这个两期Simon II期试验的第一阶段,36名在12个月内RECIST 1.1进展的PPGL患者被前瞻性地招募到两个遗传队列(琥珀酸脱氢酶[SDHx]-突变v明显散在,每个队列18人),并接受4个周期的177Lu-DOTATATE治疗。主要终点是6个月(从治疗开始)的无进展生存(PFS)率。次要终点包括安全性、总生存期(OS)、有效率、影像学/血清生物标志物和降压药减量。计算机断层扫描/磁共振成像(CT/ mri)和正电子发射断层扫描(PET)-CT (68Ga-DOTATATE和18f标记的氟脱氧葡萄糖)在2和4个周期后获得,然后每3个月(CT/ mri)至6个月(PET/CT)。收缩压(SBP)低于200 mmHg的患者在重症监护病房(ICU)接受治疗。结果:所有患者的6个月PFS率为0.861 (95% CI, 0.755 ~ 0.982), SDHx患者的6个月PFS率为0.72 (95% CI, 0.542 ~ 0.962),而散发性患者的6个月PFS率为1.00 (95% CI, 1.0 ~ 1.0),显著低于SDHx患者(P = 0.009)。中位PFS为19.9个月(12.9个月SDHx v 24.3个月散发性),中位OS为51.7个月(31.2个月SDHx v未达到散发性)。在完成177Lu-DOTATATE治疗后平均11.0个月达到最佳疗效。3+级儿茶酚胺释放综合征(CRS)的发生率为17%,这可能有利于提前进入ICU。血浆嗜铬粒蛋白A和去甲肾上腺素是最好的肿瘤标志物替代品,与68Ga-DOTATATE系列PET-CT扫描RECIST总和和肿瘤病变总摄取的变化具有良好的相关性。结论:177Lu-DOTATATE对进展性、转移性PPGL具有有效性和可接受的安全性。CRS可能会发生,但可以通过抗高血压药物的预处理来缓解,并且在适当的时候,在ICU加强静脉注射抗高血压药物的监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phase II Study of 177Lu-DOTATATE for Progressive Metastatic Pheochromocytomas and Paragangliomas: Interim Analysis of Efficacy, Safety, and Biomarkers.

Purpose: 177Lu-DOTA(0)-Tyr(3)-octreotate (177Lu-DOTATATE) is a somatostatin receptor (SSTR)-targeting radiopharmaceutical that shows promise for treating metastatic pheochromocytomas/paragangliomas (PPGLs), a rare SSTR-expressing tumor.

Methods: In the first stage of this two-stage Simon phase II trial, 36 PPGL patients with RECIST 1.1 progression within 12 months were prospectively recruited into two genetic cohorts (succinate dehydrogenase [SDHx]-mutated v apparent sporadic, 18 per cohort) and treated with four cycles of 177Lu-DOTATATE. The primary end point was progression-free survival (PFS) rate at 6 months (from initiation of treatment). Secondary end points included safety, overall survival (OS), response rate, imaging/serum biomarkers, and antihypertensive medication reduction. Computed tomography/magnetic resonance imaging (CT/MRIs) and positron emission tomography (PET)-CTs (68Ga-DOTATATE and 18F-labeled fluorodeoxyglucose) were obtained after two and four cycles, then every 3 (CT/MRIs) to 6 months (PET/CTs). Patients with systolic blood pressure (SBP) > 200 mmHg despite medical management were treated in the intensive care unit (ICU).

Results: Six-month PFS rate for all patients was 0.861 (95% CI, 0.755 to 0.982), which was significantly lower (P = .009) for SDHx at 0.72 (95% CI, 0.542 to 0.962) versus sporadic at 1.00 (95% CI, 1.0 to 1.0). Median PFS was 19.9 months (12.9 months SDHx v 24.3 months sporadic) and median OS was 51.7 months (31.2 months SDHx v not reached in sporadic). Best response was achieved on average 11.0 months after completing 177Lu-DOTATATE. A 17% incidence of grade 3+ catecholamine release syndrome (CRS) was noted, which may benefit from preemptive ICU admission. Plasma chromogranin A and normetanephrine were the best tumor-marker surrogates and correlated well with changes in RECIST sum and total tumor lesion uptake on serial 68Ga-DOTATATE PET-CT scans.

Conclusion: 177Lu-DOTATATE demonstrated effectiveness and acceptable safety profile for progressive, metastatic PPGL. CRS may occur but can be mitigated through pretreatment with antihypertensives, and, when appropriate, intensified monitoring in the ICU with intravenous antihypertensives.

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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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