Preclinical and First-in-Human Study of Carbonic Anhydrase IX-Targeting Theranostic Pair, [68Ga]Ga/[177Lu]Lu-NYM096, in Clear Cell Renal Cell Carcinoma.

Jingnan Wang,Xinchun Yan,Meixi Liu,Xueqian Yang,Guoyang Zheng,Xiaoyuan Li,Yuejuan Cheng,Chunmei Bai,Yushi Zhang,Wenjia Zhu,Li Huo
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Abstract

Small-molecule PET tracers targeting carbonic anhydrase IX (CAIX) have recently been developed for patients with clear cell renal cell carcinoma (ccRCC). Here, we report the preclinical results and first-in-human study of a CAIX-targeting theranostic pair, [68Ga]Ga/[177Lu]Lu-NYM096, for patients with metastatic ccRCC, aiming to assess its safety, tolerability, dosimetry, and preliminary efficacy. Methods: The in vivo biodistribution of [68Ga]Ga-NYM096 was evaluated in mice bearing OS-RC-2 xenografts. The therapeutic efficacy of [177Lu]Lu-NYM096 was assessed with a dose escalating from 8.1 to 74 MBq. Patients with metastatic ccRCC who had disease progression after standard therapy were prospectively enrolled. Serial whole-body [68Ga]Ga-NYM096 PET/CT scans were performed to evaluate biodistribution and dosimetry. Patients with positive CAIX expression entered the therapeutic phase and received [177Lu]Lu-NYM096 following a standard 3-plus-3 dose escalation design that started from 1.85 GBq. Serial whole-body planar imaging was performed after the first therapy cycle. Safety, dosimetry, and preliminary efficacy were evaluated. Results: High tumor accumulation of [68Ga]Ga/[177Lu]Lu-NYM096 was observed in OS-RC-2 xenograft tumor models. Moreover, [177Lu]Lu-NYM096 was well tolerated and demonstrated a significant dose-dependent tumor suppression effect. In the 2 patients, [68Ga]Ga-NYM096 demonstrated excellent tumor uptake, with an SUVmax of 330.0 at 1 h postinjection. Subsequent [177Lu]Lu-NYM096 treatment demonstrated no evidence of nephrotoxicity, hepatotoxicity, or pancreatic toxicity. Patient 1 experienced grade 1 gastric side effects and anemia, whereas patient 2 developed grade 3 radiation-induced gastritis. Follow-up [68Ga]Ga-NYM096 PET/CT evaluations showed evidence of tumor response to [177Lu]Lu-NYM096 treatment. Conclusion: This is early evidence that the CAIX-targeting theranostic pair [68Ga]Ga/[177Lu]Lu-NYM096 is feasible, offering a strategy for patients with end-stage ccRCC. The gastric toxicity proposes a significant challenge for CAIX-targeting radiopharmaceutical therapy.
碳酸酐酶ix靶向治疗对[68Ga]Ga/[177Lu]Lu-NYM096在透明细胞肾细胞癌中的临床前和首次人体研究。
靶向碳酸酐酶IX (CAIX)的小分子PET示踪剂最近被开发用于透明细胞肾细胞癌(ccRCC)患者。在这里,我们报告了一种以caix为靶点的治疗组合[68Ga]Ga/[177Lu]Lu-NYM096用于转移性ccRCC患者的临床前结果和首次人体研究,旨在评估其安全性、耐受性、剂量学和初步疗效。方法:测定[68Ga]Ga-NYM096在OS-RC-2移植小鼠体内的生物分布。评估[177Lu]Lu-NYM096的治疗效果,剂量从8.1 MBq递增到74 MBq。在标准治疗后出现疾病进展的转移性ccRCC患者被前瞻性纳入研究。连续进行全身[68Ga]Ga-NYM096 PET/CT扫描以评估生物分布和剂量学。CAIX阳性表达的患者进入治疗期,按照从1.85 GBq开始的标准3 + 3剂量递增设计接受[177Lu]Lu-NYM096。第一个治疗周期后进行连续全身平面成像。安全性、剂量学和初步疗效进行了评估。结果:在OS-RC-2异种移植瘤模型中观察到[68Ga]Ga/[177Lu]Lu-NYM096的高肿瘤蓄积。此外,[177Lu]Lu-NYM096耐受性良好,并表现出明显的剂量依赖性肿瘤抑制作用。在2例患者中,[68Ga]Ga-NYM096表现出良好的肿瘤摄取,注射后1小时SUVmax为330.0。随后的[177Lu]Lu-NYM096治疗未显示肾毒性、肝毒性或胰腺毒性。患者1出现了1级胃副作用和贫血,而患者2出现了3级放射性胃炎。随访[68Ga]Ga-NYM096 PET/CT评价显示肿瘤对[177Lu]Lu-NYM096治疗有反应。结论:早期证据表明,以cax为靶点的治疗组合[68Ga]Ga/[177Lu]Lu-NYM096是可行的,为终末期ccRCC患者提供了一种治疗策略。胃毒性对靶向cax的放射性药物治疗提出了重大挑战。
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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