Kuusk Teele, Pulliainen Kristiina, Vaarala Markku H
Division of Operative Care and Medical Research Center Oulu, Oulu University Hospital, 90220 Oulu, Finland.
Mol Clin Oncol. 2017 Mar;6(3):428-432. doi: 10.3892/mco.2017.1156. Epub 2017 Feb 6.
Patients who undergo early androgen-deprivation therapy for prostate cancer may eventually develop castration-resistant prostate cancer. However, no optimal treatment for non-metastasized castration-resistant prostate cancer has yet been established. In the present retrospective, single-institutional study, the radiotherapy (RT) outcomes were evaluated in patients who underwent androgen-deprivation therapy for non-metastatic prostate cancer and subsequently developed castration-resistant disease. Following a thorough chart review, the data of 21 patients with castration-resistant prostate cancer who were treated between 2000 and 2010 with external beam radiation therapy (EBRT) at a prostate radiation dose of >45 Gy were evaluated. Of the 21 patients, 16 (76%) developed biochemical recurrence after RT, with a mean time to biochemical recurrence of 17 months. A total of 18 patients succumbed to the disease during follow-up, with a mean survival of 3 years after RT. A radiation dose of >66 Gy was associated with a longer time to biochemical recurrence after RT (P=0.011) and a longer survival, compared with a dose of ≤66 Gy (P=0.028). The mean overall survival time after RT was 42 months and did not depend on the primary hormonal treatment. Prostate-specific survival time was negatively associated with the Gleason score at diagnosis. The prostate-specific antigen (PSA) concentration prior to RT was a prognostic factor for biochemical recurrence of prostate cancer after RT, as well as for prostate cancer-specific survival. Finally, the multivariate analysis revealed that age, PSA concentration prior to RT and a high Gleason score were independent prognostic factors for prostate cancer-specific survival. Overall, our study findings demonstrated that disease progression was common after EBRT for castration-resistant prostate cancer and that survival was limited. However, young patients and those with low-risk disease at the time of diagnosis may benefit from RT.
接受前列腺癌早期雄激素剥夺治疗的患者最终可能会发展为去势抵抗性前列腺癌。然而,对于非转移性去势抵抗性前列腺癌,尚未确立最佳治疗方法。在本项回顾性单机构研究中,对接受雄激素剥夺治疗的非转移性前列腺癌患者随后发展为去势抵抗性疾病后接受放射治疗(RT)的结果进行了评估。在全面查阅病历后,对2000年至2010年间在前列腺放疗剂量>45 Gy下接受外照射放疗(EBRT)治疗的21例去势抵抗性前列腺癌患者的数据进行了评估。21例患者中,16例(76%)在放疗后出现生化复发,生化复发的平均时间为17个月。共有18例患者在随访期间死于该疾病,放疗后的平均生存期为3年。与剂量≤66 Gy相比,剂量>66 Gy与放疗后更长的生化复发时间相关(P=0.011)和更长的生存期(P=0.028)。放疗后的平均总生存时间为42个月,且不依赖于初始激素治疗。前列腺特异性生存时间与诊断时的Gleason评分呈负相关。放疗前的前列腺特异性抗原(PSA)浓度是前列腺癌放疗后生化复发以及前列腺癌特异性生存的预后因素。最后,多变量分析显示年龄、放疗前的PSA浓度和高Gleason评分是前列腺癌特异性生存的独立预后因素。总体而言,我们的研究结果表明,去势抵抗性前列腺癌患者接受EBRT后疾病进展常见且生存期有限。然而,年轻患者以及诊断时疾病风险较低的患者可能从放疗中获益。