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添加标准恩杂鲁胺药物对即将治疗失败的转移性去势抵抗性前列腺癌(mCRPC)患者对[镥]镥-PSMA-617放射性配体疗法的反应显示出协同作用——初步试验经验证据。

Addition of Standard Enzalutamide Medication Shows Synergistic Effects on Response to [Lu]Lu-PSMA-617 Radioligand Therapy in mCRPC Patients with Imminent Treatment Failure-Preliminary Evidence of Pilot Experience.

作者信息

Rosar Florian, Bader Hanna, Bartholomä Mark, Maus Stephan, Burgard Caroline, Linxweiler Johannes, Khreish Fadi, Ezziddin Samer

机构信息

Department of Nuclear Medicine, Saarland University Hospital, 66421 Homburg, Germany.

Department of Urology, Saarland University Hospital, 66421 Homburg, Germany.

出版信息

Cancers (Basel). 2022 May 29;14(11):2691. doi: 10.3390/cancers14112691.

DOI:10.3390/cancers14112691
PMID:35681671
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9179420/
Abstract

Well-received strong efficacy of prostate-specific membrane antigen (PSMA)-targeted radioligand therapy (RLT) does not prevent patients from either early or eventual disease progression under this treatment. In this study, we investigated co-medication with enzalutamide as a potential re-sensitizer for PSMA-RLT in patients with imminent treatment failure on standard Lu-based PSMA-RLT. Ten mCRPC patients who exhibited an insufficient response to conventional [Lu]Lu-PSMA-617 RLT received oral medication of enzalutamide 160 mg/d as an adjunct to continued PSMA-RLT. Prostate-specific antigen (PSA) and standard toxicity screening lab work-up were performed to assess the treatment efficacy and safety in these individuals. The mean PSA increase under PSMA-RLT before starting the re-sensitizing procedure was 22.4 ± 26.5%. After the introduction of enzalutamide medication, all patients experienced a PSA decrease, -43.4 ± 20.0% and -48.2 ± 39.0%, after one and two cycles of enzalutamide-augmented PSMA-RLT, respectively. A total of 70% of patients (7/10) experienced partial remission, with a median best PSA response of -62%. Moreover, 5/6 enzalutamide-naïve patients and 2/4 patients who had previously failed enzalutamide exhibited a partial remission. There was no relevant enzalutamide-induced toxicity observed in this small cohort. This pilot experience suggests the synergistic potential of adding enzalutamide to PSMA-RLT derived from the intra-individual comparison of Lu-based PSMA-RLT ± enzalutamide.

摘要

前列腺特异性膜抗原(PSMA)靶向放射性配体疗法(RLT)虽疗效显著且广受认可,但并不能阻止患者在此治疗过程中出现早期或最终的疾病进展。在本研究中,我们调查了使用恩杂鲁胺联合用药,作为标准的基于镥的PSMA-RLT治疗即将失败的患者中PSMA-RLT的潜在再敏化剂。10例对传统的[镥]镥-PSMA-617 RLT反应不足的转移性去势抵抗性前列腺癌(mCRPC)患者接受了每日160 mg恩杂鲁胺的口服药物治疗,作为持续PSMA-RLT的辅助治疗。进行前列腺特异性抗原(PSA)检测和标准毒性筛查实验室检查,以评估这些患者的治疗效果和安全性。在开始再敏化程序之前,PSMA-RLT治疗期间PSA的平均升高为22.4±26.5%。引入恩杂鲁胺药物治疗后,所有患者的PSA均下降,在恩杂鲁胺增强的PSMA-RLT治疗1个周期和2个周期后,分别下降了-43.4±20.0%和-48.2±39.0%。共有70%的患者(7/10)出现部分缓解,最佳PSA反应中位数为-62%。此外,6例未使用过恩杂鲁胺的患者中有5例,以及之前使用恩杂鲁胺治疗失败的4例患者中有2例出现部分缓解。在这个小队列中未观察到与恩杂鲁胺相关的毒性。这一初步经验表明,基于镥的PSMA-RLT±恩杂鲁胺的个体内比较显示,在PSMA-RLT中添加恩杂鲁胺具有协同潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9179420/e58d6794806d/cancers-14-02691-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9179420/ca2a1fa54ebf/cancers-14-02691-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9179420/9451752c3e9e/cancers-14-02691-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9179420/39925a58a226/cancers-14-02691-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9179420/e58d6794806d/cancers-14-02691-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9179420/ca2a1fa54ebf/cancers-14-02691-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9179420/9451752c3e9e/cancers-14-02691-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9179420/39925a58a226/cancers-14-02691-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f85/9179420/e58d6794806d/cancers-14-02691-g004.jpg

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Enzalutamide Enhances PSMA Expression of PSMA-Low Prostate Cancer.恩杂鲁胺增强低PSMA表达的前列腺癌的PSMA表达。
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Rapid Modulation of PSMA Expression by Androgen Deprivation: Serial Ga-PSMA-11 PET in Men with Hormone-Sensitive and Castrate-Resistant Prostate Cancer Commencing Androgen Blockade.雄激素剥夺快速调节 PSMA 表达:开始雄激素阻断的激素敏感和去势抵抗性前列腺癌男性的 Ga-PSMA-11 PET 系列检查。
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