Translational Prostate Cancer Group, Department of Oncology, Hutchinson MRC Research Centre, University of Cambridge, Hills Road, Cambridge CB2 0XZ, UK.
J Cancer Res Clin Oncol. 2011 Feb;137(2):235-41. doi: 10.1007/s00432-010-0877-9.
Primary androgen deprivation therapy (PADT) is an important treatment modality for men with localized or locally advanced prostate cancer and without bone metastasis. There is, however, a lack of data on the biochemical relapse (BR) outcomes in these patients. Here, we studied the outcome of a contemporary series of men treated by PADT and investigated predictive risk factors for BR.
One hundred and fifty-five patients treated by PADT formed the initial study cohort, and BR outcomes in this group were reviewed. The outcomes of men with bone scan negative disease were specifically analysed. The predictive value of a panel of clinical risk factors for BR was evaluated using univariate and multivariate analysis. The results were further validated in a separate cohort of patients without bone metastasis from a second institution (n = 84).
Median follow-up was 70 months. In the first study cohort, 109/155 men (70%) had bone scan negative disease. In these patients, only 45% developed BR during the follow-up period with only 28% relapsing within 5 years of initiating PADT. Key-independent factors predicting BR were a high PSA nadir (p = 0.001) and a shorter time to nadir (p < 0.001). A nadir of ≤0.1 ng/ml and time to nadir of >24 months specifically identified men with a very good outcome from PADT. In a second-independent cohort, very similar overall and 5-year BR rates were observed in men without bone metastasis (39 and 35%, respectively). PSA nadir thresholds identified in the first cohort were again able to define a good prognostic group in this re-test cohort (p = 0.005 and p = 0.01, respectively).
Men treated by PADT and without bone metastasis can have very durable responses to PADT with the majority remaining BR free at 5 years. PSA nadir and time to nadir are key predictors of a good outcome in this group.
主要雄激素剥夺疗法(PADT)是治疗局部或局部晚期前列腺癌且无骨转移男性的重要治疗方式。然而,目前缺乏关于这些患者生化复发(BR)结局的数据。在此,我们研究了接受 PADT 治疗的一组当代男性患者的结局,并探讨了 BR 的预测风险因素。
155 例接受 PADT 治疗的患者组成了初始研究队列,对该组患者的 BR 结局进行了回顾性分析。特别分析了骨扫描阴性疾病患者的结果。使用单因素和多因素分析评估了一组临床风险因素对 BR 的预测价值。结果在来自第二家机构的无骨转移患者的另一组患者中进一步验证(n = 84)。
中位随访时间为 70 个月。在第一个研究队列中,155 例患者中有 109 例(70%)骨扫描阴性疾病。在这些患者中,只有 45%在随访期间发生 BR,只有 28%在开始 PADT 后 5 年内复发。预测 BR 的独立关键因素是 PSA 最低值(p = 0.001)和达到最低值的时间(p < 0.001)。PSA 最低值≤0.1ng/ml 和达到最低值的时间>24 个月可明确识别出 PADT 预后良好的患者。在第二个独立队列中,无骨转移的男性患者的总 BR 率和 5 年 BR 率非常相似(分别为 39%和 35%)。在第一个队列中确定的 PSA 最低值阈值再次能够在该重新测试队列中定义预后良好的组(p = 0.005 和 p = 0.01)。
接受 PADT 治疗且无骨转移的男性患者对 PADT 可产生非常持久的反应,大多数患者在 5 年内仍无 BR。PSA 最低值和达到最低值的时间是该组患者良好结局的关键预测因素。