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醋酸盐-前列腺特异性膜抗原用于治疗转移性去势抵抗性前列腺癌:一项系统评价和荟萃分析。

[Ac]Ac-PSMA for the treatment of metastatic castration-resistant prostate cancer: A systematic review and meta-analysis.

作者信息

Garo Maria Luisa, Ovčariček Petra Petranović, Fanti Stefano, Giovanella Luca

机构信息

Biostatistic Unit, Mathsly Research, Rome, Italy.

Oncology and Nuclear Medicine, University Hospital Center Sestre Milosrdnice, Zagreb, Croatia.

出版信息

Eur J Clin Invest. 2025 May;55(5):e14358. doi: 10.1111/eci.14358. Epub 2024 Nov 18.

Abstract

BACKGROUND

Approximately 10%-20% of prostate cancers progress to metastatic and castration-resistant forms (mCRPC). Radioligand (RLT) therapy with [Lu]Lu-prostate-specific membrane antigen (PSMA) is an approved treatment for metastasized mCRPC. Moreover, Actinium-225 (Ac), an alpha-emitter isotope, has also been used to label PSMA and, recently, to treat mCRPC patients with encouraging results. However, robust clinical data on [Ac]Ac-PSMA therapy and its comparison with [Lu]Lu-PSMA are still limited. Our aim was to evaluate the role of [Ac]Ac-PSMA in treating mCRPC and compare it with conventional [Lu]Lu-PSMA therapy.

METHODS

A systematic search was performed in PubMed, Web of Science, Scopus and the Cochrane Register of Controlled Trials from June 2023 to January 2024. This work was conducted in accordance with PRISMA guidelines.

RESULTS

After screening and study selection according to PRISMA guidelines, 11 studies were included, 9 of which focused on [Ac]Ac-PSMA only and two on tandem therapy ([Ac]Ac-PSMA/[Lu]Lu-PSMA). Overall, the pooled proportion of PSA decline in patients was .85 (95% CI: .79-.91, p < .001); patients pretreated with [Lu]Lu-PSMA achieved a pooled proportion of PSA decline of .90 (95% CI: .82-.97, p < .001). In patients treated with tandem therapy, PSA decline was observed in approximately 90% of them, while PSA response rates above 50% ranged from 53.3% to 65%. Xerostomia was the most frequently reported side effect, along with anaemia, thrombocytopenia and nephrotoxicity.

CONCLUSIONS

Overall, the main results of our study showed that [Ac]Ac-PSMA-617 had a significant therapeutic effect on mCRPC with an acceptable toxicity level. The latter, however, appears greater than with [Lu]Lu-PSMA-617. In future studies, an adequate analysis of the incidence of side effects associated with [Ac]Ac-PSMA should be performed to evaluate the role of cumulative toxicity of earlier treatments and the higher frailty of heavily pretreated patients.

摘要

背景

约10%-20%的前列腺癌会进展为转移性去势抵抗性前列腺癌(mCRPC)。用[镥]镥-前列腺特异性膜抗原(PSMA)进行放射性配体治疗(RLT)是一种已获批准的转移性mCRPC治疗方法。此外,α发射体同位素锕-225(Ac)也已用于标记PSMA,最近还用于治疗mCRPC患者,取得了令人鼓舞的结果。然而,关于[锕]锕-PSMA治疗及其与[镥]镥-PSMA比较的有力临床数据仍然有限。我们的目的是评估[锕]锕-PSMA在治疗mCRPC中的作用,并将其与传统的[镥]镥-PSMA治疗进行比较。

方法

于2023年6月至2024年1月在PubMed、科学网、Scopus和Cochrane对照试验注册库中进行了系统检索。这项工作是按照PRISMA指南进行的。

结果

根据PRISMA指南进行筛选和研究选择后,纳入了11项研究,其中9项仅关注[锕]锕-PSMA,2项关注联合治疗([锕]锕-PSMA/[镥]镥-PSMA)。总体而言,患者前列腺特异抗原(PSA)下降的合并比例为0.85(95%置信区间:0.79-0.91,p<0.001);接受过[镥]镥-PSMA预处理的患者PSA下降的合并比例为0.90(95%置信区间:0.82-0.97,p<0.001)。在接受联合治疗的患者中,约90%观察到PSA下降,而PSA缓解率高于50%的范围为53.3%至65%。口干是最常报告的副作用,还有贫血、血小板减少和肾毒性。

结论

总体而言,我们研究的主要结果表明,[锕]锕-PSMA-617对mCRPC有显著治疗效果,毒性水平可接受。然而,后者的毒性似乎比[镥]镥-PSMA-617更大。在未来的研究中,应充分分析与[锕]锕-PSMA相关的副作用发生率,以评估早期治疗累积毒性的作用以及多次预处理患者更高的虚弱程度。

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