Division of Radiological Sciences, Department of Nuclear Medicine and Molecular Imaging, Singapore General Hospital, Singapore, Singapore.
Radiological Sciences Academic Clinical Program, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.
Asia Pac J Clin Oncol. 2024 Oct;20(5):572-581. doi: 10.1111/ajco.13944. Epub 2023 Mar 31.
Lutetium-177 (Lu-177) prostate-specific membrane antigen radioligand therapy (PSMA-RLT) is a promising therapy for metastatic castration-resistant prostate cancer (mCRPC), but there is limited data of its efficacy and safety in Asian population. We aim to explore the clinical outcomes of Lu-177 PSMA-RLT in this population.
We evaluated 84 patients with progressive mCRPC receiving Lu-177 PSMA-RLT between 9 May 2018 and 21 February 2022. Lu-177-PSMA-I&T was administered at 6-8-week intervals. Primary end point was overall survival (OS), and secondary end points included prostate-specific antigen (PSA) progression-free survival (PFS), PSA response rate, clinical response, toxicity assessment, and prognostic indicators.
The median OS and PSA PFS were 12.2 and 5.2 months, respectively. PSA decline of ≥50% was observed in 51.8% of patients. Patients achieving PSA response had longer median OS (15.0 vs. 9.5 months, p = .03) and PSA PFS (6.5 vs. 2.9 months, p < .001). Pain score improvement was seen in 19 out of 34 patients. A hematotoxicity of ≥grade 3 was observed in 13 out of 78 patients. Multivariable analyses showed that PSA velocity, alkaline phosphatase, hemoglobin (Hb), and the number of treatment cycles were independent prognostic indicators for OS. The retrospective design was the main limitation of the study.
Our study demonstrated a similar safety and efficacy of Lu-177 PSMA-RLT in Asian mCRPC patients compared to the existing literature. A PSA decline ≥50% was associated with longer OS and PSA PFS. Several prognostic indicators for patient outcomes were also identified.
镥-177(Lu-177)前列腺特异性膜抗原放射性配体治疗(PSMA-RLT)是治疗转移性去势抵抗性前列腺癌(mCRPC)的一种有前途的方法,但在亚洲人群中的疗效和安全性数据有限。我们旨在探讨该人群中 Lu-177 PSMA-RLT 的临床疗效。
我们评估了 84 例于 2018 年 5 月 9 日至 2022 年 2 月 21 日期间接受 Lu-177 PSMA-RLT 治疗的进展性 mCRPC 患者。Lu-177-PSMA-I&T 每 6-8 周给药一次。主要终点为总生存期(OS),次要终点包括前列腺特异性抗原(PSA)无进展生存期(PFS)、PSA 缓解率、临床反应、毒性评估和预后指标。
中位 OS 和 PSA PFS 分别为 12.2 和 5.2 个月。51.8%的患者出现 PSA 下降≥50%。PSA 缓解的患者具有更长的中位 OS(15.0 与 9.5 个月,p=0.03)和 PSA PFS(6.5 与 2.9 个月,p<0.001)。34 例患者中有 19 例疼痛评分改善。78 例患者中有 13 例出现≥3 级血液毒性。多变量分析显示,PSA 速度、碱性磷酸酶、血红蛋白(Hb)和治疗周期数是 OS 的独立预后因素。本研究的主要局限性是回顾性设计。
与现有文献相比,我们的研究表明 Lu-177 PSMA-RLT 在亚洲 mCRPC 患者中的安全性和疗效相似。PSA 下降≥50%与更长的 OS 和 PSA PFS 相关。还确定了几个预测患者结局的预后指标。