Miszczyk Marcin, Rembak-Szynkiewicz Justyna, Magrowski Łukasz, Stawiski Konrad, Namysł-Kaletka Agnieszka, Napieralska Aleksandra, Kraszkiewicz Małgorzata, Woźniak Grzegorz, Stąpór-Fudzińska Małgorzata, Głowacki Grzegorz, Pradere Benjamin, Laukhtina Ekaterina, Rajwa Paweł, Majewski Wojciech
IIIrd Radiotherapy and Chemotherapy Department, Maria Skłodowska-Curie National Research Institute of Oncology, 44-102 Gliwice, Poland.
Radiology Department, Maria Skłodowska-Curie National Research Institute of Oncology, 44-102 Gliwice, Poland.
Cancers (Basel). 2022 Mar 23;14(7):1613. doi: 10.3390/cancers14071613.
Prostate Imaging-Reporting and Data System (PI-RADS) has been widely implemented as a diagnostic tool for significant prostate cancer (PCa); less is known about its prognostic value, especially in the setting of primary radiotherapy. We aimed to analyze the association between PI-RADS v. 2.1 classification and risk of metastases, based on a group of 152 patients treated with ultra-hypofractionated stereotactic CyberKnife radiotherapy for localized low or intermediate risk-group prostate cancer. We found that all distant failures (n = 5) occurred in patients diagnosed with a PI-RADS score of 5, and axial measurements of the target lesion were associated with the risk of developing metastases (p < 0.001). The best risk stratification model (based on a combination of greatest dimension, the product of multiplication of PI-RADS target lesion axial measurements, and age) achieved a c-index of 0.903 (bootstrap-validated bias-corrected 95% CI: 0.848−0.901). This creates a hypothesis that PI-RADS 5 and the size of the target lesion are important prognostic factors in early-stage PCa patients and should be considered as an adverse prognostic measure for patients undergoing early treatment such as radiation or focal therapy.
前列腺影像报告和数据系统(PI-RADS)已被广泛用作诊断显著前列腺癌(PCa)的工具;但其预后价值却鲜为人知,尤其是在原发性放疗的情况下。我们旨在基于一组152例接受超分割立体定向射波刀放疗的局限性低危或中危组前列腺癌患者,分析PI-RADS v. 2.1分类与转移风险之间的关联。我们发现,所有远处转移(n = 5)均发生在PI-RADS评分为5的患者中,并且靶病变的轴向测量值与发生转移的风险相关(p < 0.001)。最佳风险分层模型(基于最大直径、PI-RADS靶病变轴向测量值的乘积以及年龄的组合)的c指数为0.903(自展验证偏差校正95%置信区间:0.848 - 0.901)。这提出了一个假设,即PI-RADS 5和靶病变大小是早期PCa患者的重要预后因素,对于接受放疗或聚焦治疗等早期治疗的患者应将其视为不良预后指标。