Fossati Nicola, Karnes R Jeffrey, Cozzarini Cesare, Fiorino Claudio, Gandaglia Giorgio, Joniau Steven, Boorjian Stephen A, Goldner Gregor, Hinkelbein Wolfgang, Haustermans Karin, Tombal Bertrand, Shariat Shahrokh, Karakiewicz Pierre I, Montorsi Francesco, Van Poppel Hein, Wiegel Thomas, Briganti Alberto
Division of Oncology/Unit of Urology, URI, IRCCS Ospedale San Raffaele, Milan, Italy.
Department of Urology, Mayo Clinic, Rochester, MN, USA.
Eur Urol. 2016 Apr;69(4):728-733. doi: 10.1016/j.eururo.2015.10.009. Epub 2015 Oct 21.
Early salvage radiation therapy (eSRT) represents a treatment option for patients who experience a prostate-specific antigen (PSA) rise after radical prostatectomy (RP); however, the optimal PSA level for eSRT administration is still unclear.
To test the impact of PSA level on cancer control after eSRT according to pathologic tumour characteristics.
DESIGN, SETTING, AND PARTICIPANTS: The study included 716 node-negative patients with undetectable postoperative PSA who experienced a PSA rise after RP. All patients received eSRT, defined as local radiation to the prostate and seminal vesicle bed, delivered at PSA ≤ 0.5 ng/ml. Biochemical recurrence (BCR) after eSRT was defined as two consecutive PSA values ≥ 0.2 ng/ml.
Multivariable Cox regression analysis tested the association between pre-eSRT PSA level and BCR after eSRT. Covariates consisted of pathologic stage (pT2 vs pT3a vs pT3b or higher), pathologic Gleason score (≤ 6, 7, or ≥ 8), and surgical margin status (negative vs positive). We tested an interaction with PSA level and baseline pathologic risk for the hypothesis that BCR-free survival differed by pre-eSRT PSA level. Three pathologic risk factors were identified: pathologic stage pT3b or higher, pathologic Gleason score ≥ 8, and negative surgical margins.
Median follow-up among patients who did not experience BCR after eSRT was 57 mo (interquartile range: 27-105). At 5 yr after eSRT, BCR-free survival rate was 82% (95% confidence interval [CI], 78-85). At multivariable Cox regression analysis, pre-eSRT PSA level was significantly associated with BCR after eSRT (hazard ratio: 4.89; 95% CI, 1.40-22.9; p < 0.0001). When patients were stratified according to the number of risk factors at final pathology, patients with at least two pathologic risk factors showed an increased risk of 5-yr BCR as high as 10% per 0.1 ng/ml of PSA level compared with only 1.5% in patients with one or no pathologic risk factors.
In this retrospective study, cancer control after eSRT greatly depended on pretreatment PSA. The absolute PSA level had a different prognostic value depending on the pathologic characteristics of the tumour. In patients with more adverse pathologic features, eSRT conferred better cancer control when administered at the very first sign of PSA rise. Conversely, the benefit of eSRT was less evident in men with favourable disease at RP.
In this retrospective study, cancer control after early salvage radiation therapy (eSRT) was influenced by pretreatment prostate-specific antigen (PSA) level. This effect was highest in men with at least two of the following pathologic features: pT3b/pT4 disease, pathologic Gleason score ≥ 8, and negative surgical margins. In these patients, eSRT conferred better cancer control when administered at the very first sign of PSA rise.
早期挽救性放射治疗(eSRT)是根治性前列腺切除术(RP)后前列腺特异性抗原(PSA)升高患者的一种治疗选择;然而,eSRT治疗的最佳PSA水平仍不明确。
根据病理肿瘤特征,测试PSA水平对eSRT后癌症控制的影响。
设计、设置和参与者:该研究纳入了716例术后PSA检测不到的淋巴结阴性患者,这些患者在RP后PSA升高。所有患者均接受eSRT,定义为对前列腺和精囊床进行局部放疗,在PSA≤0.5 ng/ml时进行。eSRT后的生化复发(BCR)定义为连续两次PSA值≥0.2 ng/ml。
多变量Cox回归分析测试了eSRT前PSA水平与eSRT后BCR之间的关联。协变量包括病理分期(pT2与pT3a与pT3b或更高)、病理Gleason评分(≤6、7或≥8)和手术切缘状态(阴性与阳性)。我们测试了PSA水平与基线病理风险的相互作用,以验证无BCR生存期是否因eSRT前PSA水平而异的假设。确定了三个病理风险因素:病理分期pT3b或更高、病理Gleason评分≥8和手术切缘阴性。
eSRT后未发生BCR的患者中位随访时间为57个月(四分位间距:27 - 105)。eSRT后5年,无BCR生存率为82%(95%置信区间[CI],78 - 85)。在多变量Cox回归分析中,eSRT前PSA水平与eSRT后BCR显著相关(风险比:4.89;95%CI,1.40 - 22.9;p < 0.0001)。当根据最终病理的风险因素数量对患者进行分层时,与有一个或无病理风险因素的患者相比,至少有两个病理风险因素的患者5年BCR风险每0.1 ng/ml PSA水平增加高达10%,而前者仅为1.5%。
在这项回顾性研究中,eSRT后的癌症控制很大程度上取决于治疗前的PSA。根据肿瘤的病理特征,绝对PSA水平具有不同的预后价值。在具有更不利病理特征的患者中,在PSA升高的最初迹象出现时给予eSRT可实现更好的癌症控制。相反,在RP时疾病情况良好的男性中,eSRT的益处不太明显。
在这项回顾性研究中,早期挽救性放射治疗(eSRT)后的癌症控制受治疗前前列腺特异性抗原(PSA)水平影响。在具有以下至少两种病理特征的男性中这种影响最大:pT3b/pT4疾病、病理Gleason评分≥8和手术切缘阴性。在这些患者中,在PSA升高的最初迹象出现时给予eSRT可实现更好的癌症控制。