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Rates of PSMA PET Staging and Positivity in Newly Diagnosed Prostate Cancer in a National Health Care System
The Journal of Nuclear Medicine ( IF 9.1 ) Pub Date : 2025-01-01 , DOI: 10.2967/jnumed.124.268555
Sean R. Miller, Rachel Tucker Gonzalez, William C. Jackson, Megan E.V. Caram, Phoebe A. Tsao, Kristian Stensland, Yashesh Shah, Daniel Wale, Ka Kit Wong, Benjamin L. Viglianti, David Elliott, Tanner Caverly, Timothy P. Hofer, Sameer Saini, Michael D. Green, Matthew Schipper, Robert T. Dess, Alex K. Bryant

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. Methods: 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 (n = 657 low to intermediate risk) with staging PSMA PET reports available. Results: 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. Conclusion: 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.



中文翻译:


国家医疗保健系统中新诊断前列腺癌的 PSMA PET 分期和阳性率



前列腺特异性膜抗原 (PSMA) PET 于 2020 年被美国食品和药物管理局批准用于新诊断的前列腺癌的分期,但采用率和实际阳性率尚不清楚。我们表征了接受 PSMA PET 分期的患者,并在一个大型全国队列中描述了阳性发现。方法:我们从 2020 年 6 月至 2023 年 8 月在国家退伍军人健康管理局确定了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均来自电子病历数据。为了评估阳性结果,我们回顾了 1,994 名患者 (n = 657 名低至中度风险),并提供了分期 PSMA PET 报告。结果:在 31,838 名新诊断的前列腺癌患者中,4,538 名 (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 月高危或极高危患者的约 70%。在常规影像学检查为 N0/M0 的患者中,PSMA PET 阳性率 (N1 或 M1) 为良好中等风险 5.9%,不良中等风险 8.2%,高风险 14%,极高风险 34%。结论:在退伍军人健康管理局,新诊断前列腺癌的 PSMA PET 分期迅速增加。在这个大型中等风险队列中,阳性率低于 10%。这些数据证实了 PSMA PET 分期在高危疾病中的实用性,并表明需要更多的研究来改进中危疾病的患者选择。

更新日期:2025-01-04
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