Department of Radiation Oncology, RWTH Aachen University, Pauwelsstrasse 30, 52072, Aachen, Germany.
Department of Urology, RWTH Aachen University, Pauwelsstrasse 30, 52072, Aachen, Germany.
Radiat Oncol. 2017 Jun 14;12(1):98. doi: 10.1186/s13014-017-0837-5.
The aim of this study was to evaluate the long-term prognostic significance of rising PSA levels, particularly focussing on overall survival.
Two hundred ninety-five patients with localized prostate cancer were either treated with low-dose-rate (LDR) brachytherapy with I-125 seeds as monotherapy (n = 94; 145Gy), high-dose-rate (HDR) brachytherapy with Ir-192 as a boost to external beam RT (n = 66; 50.4Gy in 1.8Gy fractions EBRT + 18Gy in 9Gy fractions HDR) or EBRT alone (70.2Gy in 1.8Gy fractions; n = 135). "PSA bounce" was defined as an increase of at least 0.2 ng/ml followed by spontaneous return to pre-bounce level or lower, biochemical failure was defined according to the Phoenix definition.
Median follow-up after the end of radiotherapy was 108 months. A PSA bounce showed to be a significant factor for biochemical control (BC) and overall survival (OS) after ten years (BC10 of 83% with bounce vs. 34% without, p < 0.01; OS10 of 82% with bounce vs. 59% without bounce, p < 0.01). The occurrence of a bounce, a high nadir and the therapy modality (LDR-BT vs. EBRT and HDR-BT + EBRT vs. EBRT) proved to be independent factors for PSA recurrence in multivariate Cox regression analysis. A bounce was detected significantly earlier than a PSA recurrence (median 20 months vs. 32 months after RT; p < 0.01; median PSA doubling time 5.5 vs. 5.0 months, not significant). PSA doubling time was prognostically significant in case of PSA recurrence (OS10 of 72% vs. 36% with PSA doubling time ˃ 5 months vs. ≤ 5 months; p < 0.01).
Rising PSA levels within the first two years can usually be classified as a benign PSA bounce, with favourable recurrence-free and overall survival rates. PSA doubling time is an important predictor for overall survival following the diagnosis of a recurrence.
本研究旨在评估 PSA 水平升高的长期预后意义,特别是关注总生存率。
295 例局限性前列腺癌患者分别接受低剂量率(LDR)近距离放射治疗(I-125 种子作为单药治疗,n=94;145Gy)、高剂量率(HDR)近距离放射治疗(Ir-192 作为外照射放疗的加量治疗,n=66;EBRT 50.4Gy,1.8Gy 分数;HDR 18Gy,9Gy 分数)或单独外照射放疗(EBRT,n=135;70.2Gy,1.8Gy 分数)。“PSA 反弹”定义为至少增加 0.2ng/ml,随后自发恢复至反弹前水平或更低,生化失败根据凤凰定义定义。
放疗结束后中位随访时间为 108 个月。PSA 反弹是生化控制(BC)和总生存率(OS)十年后的显著因素(BC10 为 83%有反弹,34%无反弹,p<0.01;OS10 为 82%有反弹,59%无反弹,p<0.01)。反弹的发生、最低值和治疗方式(LDR-BT 与 EBRT 和 HDR-BT+EBRT 与 EBRT)在多变量 Cox 回归分析中被证明是 PSA 复发的独立因素。反弹的发生明显早于 PSA 复发(放疗后中位时间为 20 个月 vs. 32 个月,p<0.01;中位 PSA 倍增时间为 5.5 个月 vs. 5.0 个月,无显著差异)。在 PSA 复发的情况下,PSA 倍增时间具有预后意义(OS10 为 72%有 PSA 倍增时间>5 个月 vs. 36%有 PSA 倍增时间≤5 个月,p<0.01)。
前两年内 PSA 水平升高通常可归类为良性 PSA 反弹,具有良好的无复发和总生存率。PSA 倍增时间是诊断复发后总生存率的重要预测指标。