Experience of rescue therapy with [177Lu]Lu-rhPSMA-10.1 in patients with primary or acquired resistance to [177Lu]Lu-PSMA-I&T.

IF 8.6 1区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING European Journal of Nuclear Medicine and Molecular Imaging Pub Date : 2024-11-04 DOI:10.1007/s00259-024-06959-5
Alexander Gäble, Alexander Dierks, Andreas Rinscheid, Marianne Patt, Georgine Wienand, Christian H Pfob, Malte Kircher, Kazuhito Fukushima, Ana Antić Nikolić, Johanna S Enke, Tilman Janzen, Julie Steinestel, Hildegard Kempter, Martin Trepel, Dorothea Weckermann, Constantin Lapa, Ralph A Bundschuh
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Abstract

Purpose: Radioligand therapy is an increasingly important option for the treatment of metastatic castrate-resistant prostate cancer (mCRPC). Radiohybrid ligands targeting prostate-specific membrane antigen (PSMA) are a novel group of theranostic radioligand therapy agents for which higher tumour absorbed radiation doses have been demonstrated compared to established PSMA ligands. Here, we report data from ten patients who were treated within a compassionate use program with the radiohybrid PSMA-ligand [177Lu]Lu-rhPSMA-10.1 after experiencing disease progression under treatment with [177Lu]Lu-PSMA-I&T.

Methods: Ten patients with advanced PSMA-positive prostate cancer who showed progression under treatment with [177Lu]Lu-PSMA-I&T received up to three cycles of rescue therapy with [177Lu]Lu-rhPSMA-10.1 (7.4-8.1 GBq per cycle). Efficacy (PSA response according to PCWG3 and RECIP) and overall survival were evaluated. Adverse events were recorded from first application.

Results: Despite progression with [177Lu]Lu-PSMA-I&T, after the first cycle of [177Lu]Lu-rhPSMA-10.1 rescue therapy, five patients (50%) showed a decrease in serum PSA level. In imaging, three of the ten patients (30%) showed a partial radiologic response. Four of the five patients with a decrease of serum PSA under [177Lu]Lu-rhPSMA-10.1 had initially responded to treatment with [177Lu]Lu-PSMA-I&T but had become resistant. However, the remaining patient had shown continuous disease progression during [177Lu]Lu-PSMA-I&T therapy but showed an immediate response to [177Lu]Lu-rhPSMA-10.1. The additional treatment with [177Lu]Lu-rhPSMA-10.1 was generally well tolerated by all patients.

Conclusions: Patients showing tumour progression while receiving [177Lu]Lu-PSMA-I&T radioligand therapy may benefit from rescue therapy with the novel radiohybrid PSMA ligand, [177Lu]Lu-rhPSMA-10.1. Higher tumour absorbed radiation doses with [177Lu]Lu-rhPSMA-10.1 may overcome primary and acquired radiation resistance.

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使用[177Lu]Lu-rhPSMA-10.1对[177Lu]Lu-PSMA-I&T原发性或获得性耐药性患者进行抢救性治疗的经验。
目的:放射性配体疗法是治疗转移性难治性前列腺癌(mCRPC)的一种日益重要的选择。以前列腺特异性膜抗原(PSMA)为靶点的放射性杂化配体是一组新型治疗放射配体疗法药物,与已有的PSMA配体相比,它的肿瘤吸收辐射剂量更高。在此,我们报告了十位患者的数据,他们在接受[177Lu]Lu-PSMA-I&T治疗后出现疾病进展,在一项同情使用计划中接受了放射性混合PSMA配体[177Lu]Lu-rhPSMA-10.1的治疗:10名PSMA阳性的晚期前列腺癌患者在接受[177Lu]Lu-PSMA-I&T治疗后病情出现进展,接受了最多三个周期的[177Lu]Lu-rhPSMA-10.1(每个周期7.4-8.1 GBq)抢救治疗。对疗效(根据 PCWG3 和 RECIP 的 PSA 反应)和总生存期进行了评估。从首次应用开始记录不良事件:尽管[177Lu]Lu-PSMA-I&T治疗出现了进展,但在[177Lu]Lu-rhPSMA-10.1救援治疗的第一个周期后,五名患者(50%)的血清PSA水平出现了下降。在影像学方面,10 名患者中有 3 名(30%)出现了部分放射学反应。在接受[177Lu]Lu-rhPSMA-10.1治疗后血清PSA下降的五名患者中,有四名最初对[177Lu]Lu-PSMA-I&T治疗有反应,但后来出现了耐药性。然而,另一名患者在接受[177Lu]Lu-PSMA-I&T治疗期间疾病持续进展,但对[177Lu]Lu-rhPSMA-10.1立即产生了反应。所有患者都能很好地耐受[177Lu]Lu-rhPSMA-10.1的额外治疗:结论:在接受[177Lu]Lu-PSMA-I&T放射性配体治疗期间出现肿瘤进展的患者可能会从新型放射性杂交PSMA配体[177Lu]Lu-rhPSMA-10.1的挽救治疗中获益。使用[177Lu]Lu-rhPSMA-10.1可使肿瘤吸收更高的放射剂量,从而克服原发性和获得性放射抗性。
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来源期刊
CiteScore
15.60
自引率
9.90%
发文量
392
审稿时长
3 months
期刊介绍: The European Journal of Nuclear Medicine and Molecular Imaging serves as a platform for the exchange of clinical and scientific information within nuclear medicine and related professions. It welcomes international submissions from professionals involved in the functional, metabolic, and molecular investigation of diseases. The journal's coverage spans physics, dosimetry, radiation biology, radiochemistry, and pharmacy, providing high-quality peer review by experts in the field. Known for highly cited and downloaded articles, it ensures global visibility for research work and is part of the EJNMMI journal family.
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