225Ac-Prostate-Specific Membrane Antigen Therapy for Castration-Resistant Prostate Cancer

医学 前列腺癌 不利影响 内科学 前列腺特异性抗原 泌尿科 肿瘤科 谷氨酸羧肽酶Ⅱ 统计显著性 前列腺 阉割 癌症 激素
作者
Yasemin Şanlı,Serkan Kuyumcu,Duygu Has Şimşek,Fikret Büyükkaya,Caner Civan,Emine Göknur Işık,Zeynep Gözde Özkan,Mert Başaran,Öner Şanlı
出处
期刊:Clinical Nuclear Medicine [Ovid Technologies (Wolters Kluwer)]
卷期号:46 (12): 943-951 被引量:14
标识
DOI:10.1097/rlu.0000000000003925
摘要

Purpose Prostate-specific membrane antigen (PSMA)–targeted therapies are among the current promising treatments. We present our preliminary results on the use of 225 Ac-PSMA therapy in patients with metastatic castration-resistant prostate cancer as a single center. Methods Twelve advanced stage metastatic castration-resistant prostate cancer patients who received 225 Ac-PSMA therapy were recruited in this retrospective study. Patients were treated with 225 Ac-PSMA therapy every 8 weeks, and prostate-specific antigen (PSA) response was analyzed. Meanwhile, overall survival (OS) and progression-free survival (PFS) were estimated. Hematological and nonhematological adverse effects were recorded before and at 8 weeks after the last treatment cycle. Results In total, 25 cycles of 225 Ac-PSMA were administered to 12 patients. The pretreatment median PSA level was 129 ng/mL. After the first cycle of therapy, any PSA response was observed in 9 of 12 patients, whereas 6 of them had biochemical response of >50%. Four of 12 patients reached the best PSA response after the first treatment cycle, whereas 3 patients after the second and 2 patients after the third cycle. The median PFS and OS were 4 and 10 months, respectively. For patients with any PSA response after the first cycle, OS was found to be higher despite without any statistical significance (10 vs 4 months; P = 0.301) when compared with the nonresponsive group. No significant difference was encountered in terms of adverse effect in the pretreatment and posttreatment era. Conclusions Our preliminary results are encouraging, especially patients who had PSA response after the first cycle of 225 Ac-PSMA therapy.
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