Faculty of Medicine, Department of Medical Oncology, Ege University, Izmir, Turkey.
Faculty of Medicine, Department of Medical Oncology, Kocaeli University, Kocaeli, Turkey.
Int J Cancer. 2024 Feb 15;154(4):692-700. doi: 10.1002/ijc.34749. Epub 2023 Oct 11.
Metastatic castration-resistant prostate cancer (mCRPC) remains a challenging condition to treat despite recent advancements. This retrospective study aimed to assess the activity and tolerability of Lutetium-177 (Lu-177) PSMA-617 radioligand therapy (RLT) in mCRPC patients across multiple cancer centers in Turkey. The study included 165 patients who received at least one cycle of Lu-177 PSMA-617 RLT, with the majority having bone metastases and undergone prior treatments. Prostate-specific antigen (PSA) levels were assessed before each treatment cycle, and the biochemical response was evaluated in accordance with the Prostate Cancer Work Group 3 Criteria. The PSA decline of ≥50% was classified as a response, while an increase of ≥25% in PSA levels was indicative of progressive disease. Neither response nor progression was considered as stable disease. The Lu-177 PSMA-617 RLT led to a significant PSA response, with 50.6% of patients achieving a >50% decrease in PSA levels. Median overall survival (OS) and progression-free survival were 13.5 and 8.2 months, respectively. Patients receiving Lu-177 PSMA-617 RLT in combination with androgen receptor pathway inhibitors (ARPIs) had a higher OS compared to those receiving Lu-177 PSMA-617 RLT alone (18.2 vs 12.3 months, P = .265). The treatment was generally well-tolerated, with manageable side effects such as anemia and thrombocytopenia. This study provides real-world evidence supporting the effectiveness and safety of Lu-177 PSMA-617 RLT in mCRPC patients, particularly when used in combination with ARPIs. These findings contribute to the growing body of evidence on the potential benefits of PSMA-targeted therapies in advanced prostate cancer.
转移性去势抵抗性前列腺癌(mCRPC)尽管最近取得了进展,但仍然是一种难以治疗的疾病。本回顾性研究旨在评估镥-177(Lu-177)PSMA-617 放射性配体疗法(RLT)在土耳其多家癌症中心的 mCRPC 患者中的疗效和耐受性。该研究纳入了 165 名至少接受过一个周期 Lu-177 PSMA-617 RLT 治疗的患者,其中大多数患者有骨转移且接受过前期治疗。在每个治疗周期前评估前列腺特异性抗原(PSA)水平,并根据前列腺癌工作组 3 标准评估生化反应。PSA 下降≥50%定义为有反应,PSA 水平升高≥25%则提示疾病进展。无反应或无进展均被认为是疾病稳定。Lu-177 PSMA-617 RLT 导致 PSA 显著下降,50.6%的患者 PSA 水平下降≥50%。中位总生存期(OS)和无进展生存期分别为 13.5 个月和 8.2 个月。与单独接受 Lu-177 PSMA-617 RLT 治疗的患者相比,同时接受 Lu-177 PSMA-617 RLT 和雄激素受体通路抑制剂(ARPI)治疗的患者 OS 更高(18.2 个月 vs 12.3 个月,P=0.265)。该治疗总体耐受性良好,副作用可管理,如贫血和血小板减少症。本研究提供了真实世界证据,支持 Lu-177 PSMA-617 RLT 在 mCRPC 患者中的有效性和安全性,尤其是与 ARPI 联合使用时。这些发现为 PSMA 靶向治疗在晚期前列腺癌中的潜在益处提供了更多的证据。