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在一个国家医疗保健系统中,新诊断前列腺癌患者的PSMA PET分期率及阳性率

Rates of PSMA PET Staging and Positivity in Newly Diagnosed Prostate Cancer in a National Health Care System.

作者信息

Miller Sean R, Gonzalez Rachel Tucker, Jackson William C, Caram Megan E V, Tsao Phoebe A, Stensland Kristian, Shah Yashesh, Wale Daniel, Wong Ka Kit, Viglianti Benjamin L, Elliott David, Caverly Tanner, Hofer Timothy P, Saini Sameer, Green Michael D, Schipper Matthew, Dess Robert T, Bryant Alex K

机构信息

Department of Radiation Oncology, Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, Michigan.

Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.

出版信息

J Nucl Med. 2025 Jan 3;66(1):75-83. doi: 10.2967/jnumed.124.268555.

Abstract

Prostate-specific membrane antigen (PSMA) PET was approved by the U.S. Food and Drug Administration in 2020 for the staging of newly diagnosed prostate cancer, yet rates of adoption and real-world positivity rates are unknown. We characterized patients undergoing PSMA PET staging and describe positive findings in a large national cohort. We identified all newly diagnosed prostate cancer patients in the national Veterans Health Administration from June 2020 to August 2023. Demographics, staging imaging reports, and cancer-related information were obtained from electronic medical record data. To assess positive findings, we chart-reviewed 1,994 patients ( = 657 low to intermediate risk) with staging PSMA PET reports available. Among 31,838 patients with newly diagnosed prostate cancer, 4,538 (14%) underwent PSMA staging. Use of PSMA staging increased rapidly from near 0 in early 2021 to approximately 70% of patients with high- or very-high-risk disease by August 2023. Among patients who were N0/M0 by conventional imaging, PSMA PET positivity rates (N1 or M1) were 5.9% for favorable intermediate risk, 8.2% for unfavorable intermediate risk, 14% for high risk, and 34% for very high risk. PSMA PET staging for newly diagnosed prostate cancer increased rapidly in the Veterans Health Administration. Positivity rates were less than 10% in this large intermediate-risk cohort. These data confirm the utility of PSMA PET staging in high-risk disease and suggest that additional study is needed to refine patient selection in intermediate-risk disease.

摘要

前列腺特异性膜抗原(PSMA)正电子发射断层扫描(PET)于2020年获得美国食品药品监督管理局批准,用于新诊断前列腺癌的分期,但采用率和实际阳性率尚不清楚。我们对接受PSMA PET分期的患者进行了特征分析,并描述了一个大型国家队列中的阳性发现。我们在国家退伍军人健康管理局中识别出2020年6月至2023年8月期间所有新诊断的前列腺癌患者。人口统计学、分期影像学报告和癌症相关信息从电子病历数据中获取。为了评估阳性发现,我们对1994例(其中657例为低至中风险)有分期PSMA PET报告的患者进行了图表回顾。在31838例新诊断的前列腺癌患者中,4538例(14%)接受了PSMA分期。PSMA分期的使用从2021年初的接近0迅速增加到2023年8月时高危或极高危疾病患者的约70%。在传统影像学检查为N0/M0的患者中,PSMA PET阳性率(N1或M1)在有利中风险患者中为5.9%,在不利中风险患者中为8.2%,在高风险患者中为14%,在极高风险患者中为34%。在退伍军人健康管理局中,新诊断前列腺癌的PSMA PET分期迅速增加。在这个大型中风险队列中,阳性率低于10%。这些数据证实了PSMA PET分期在高危疾病中的效用,并表明需要进一步研究以优化中风险疾病患者的选择。

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