Lu-177 PSMA I&T治疗前列腺癌治疗反应、治疗毒性和生存结果

E. Acar, Burak Sönmezer, E. Derebek, R. Bekiş, O. Ozdoğan, G. Kaya
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引用次数: 0

摘要

目的:本研究旨在评估接受Lu-177 PSMA治疗的去势抵抗性转移性前列腺癌患者的血清PSA反应、Ga-68 PSMA PET/CT反应、血液学/肾病毒性和生存结果。方法:回顾性分析57例经Lu-177 PSMA I&T治疗的患者资料,平均年龄68岁。根据不良事件通用毒性标准v5.0确定对治疗的二次毒性。Kaplan Meier法用于生存和无进展生存分析。结果:40%的患者在第一个治疗周期后血清PSA值下降>25%。75%的患者血清PSA值稳定/下降。57例患者中有2例出现3级贫血,没有一例出现3级白细胞减少或血小板减少。57例患者中有1例出现短暂性肾毒性。治疗8个周期后,未见血液学和肾学毒性,血清PSA值下降97%。所有患者的平均生存时间为11.6个月,血清PSA应答患者的平均生存时间为17.2个月。无进展生存期平均为9.9个月。结论:在75%的进展患者中,通过单周期治疗提供稳定或退化的疾病,尽管治疗提高了生存期,这是治疗成功的一个指标。患者血液和肾脏毒性发生率低(接受8个周期的患者中没有一例)表明该治疗是可靠的。治疗后血清PSA反应的患者生存时间更长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lu-177 PSMA I&T Therapy for Prostate Cancer; Treatment Response, Treatment Toxicity, and Survival Results
Purpose: This study aims to evaluate the serum PSA response, Ga-68 PSMA PET/CT response, hematological/nephrological toxicity and survival results of patients with castration-resistant metastatic prostate cancer who are receiving Lu-177 PSMA therapy. Methods: The data of 57 patients with a mean age of 68 years who were treated with Lu-177 PSMA I&T were retrospectively reviewed. Secondary toxicity to treatment was determined using the criteria of the Common Toxicity Criteria for Adverse Events v5.0. The Kaplan Meier method was used for survival and progression-free survival analysis. Results: Forty percent of patients’ serum PSA values’ showed >25% regression after the first cycle of treatment. Serum PSA values were stable/ regressed in 75% of the patients. While 2/57 patients showed grade 3 anemia, none showed grade 3 leukopenia or thrombocytopenia. One of 57 patient showed transient nephrotoxicity. Hematological and nephrological toxicity were not observed after treatment of eight cycles, and the serum PSA values of the patients were decreased by 97%. The mean survival time was 11.6 months in all patients, and 17.2 months in patients with serum PSA response. Progression-free survival was an average of 9.9 months. Conclusion: Providing a stable or regressed disease via single cycle treatment in 75% of patients with progression despite the treatments improving survival is an indicator of the success of the therapy. The low rate of hematological and nephrological toxicity in patients (none of the patients that received eight cycles) suggests that the treatment is reliable. Survival was longer in patients with serum PSA response after treatment.
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