Proton Therapy Center, Sapporo Teishinkai Hospital, Sapporo, Hokkaido, Japan.
Department of Radiology, Hyogo Ion Beam Medical Center, Tatsuno, Hyogo, Japan.
Cancer Med. 2017 Oct;6(10):2234-2243. doi: 10.1002/cam4.1159. Epub 2017 Sep 6.
The aim of this retrospective study was to report long-term clinical outcomes in patients treated with proton therapy (PT) for localized prostate cancer. Between 2001 and 2014, 1375 consecutive patients were treated with PT. Patients were classified into prognostic risk groups based on the National Comprehensive Cancer Network criteria. Freedom from biochemical relapse (FFBR), cancer-specific survival (CSS) and incidence of late gastrointestinal (GI)/genitourinary (GU) toxicities were calculated. Multivariate analysis was performed to identify clinical prognostic factors for FFBR and late toxicities. The median follow-up period was 70 months (range, 4-145 months). In total, 99% of patients received 74 Gy (relative biologic effectiveness [RBE]); 56% of patients received neoadjuvant androgen deprivation therapy. For the low-, intermediate-, high-, and very high-risk groups, 5-year FFBR was 99% (95% confidence intervals [CI], 96-100%), 91% (95% CI, 88-93%), 86% (95% CI, 82-89%), and 66% (95% CI, 53-76%), respectively, and 5-year CSS was 100% (95% CI, 100-100%), 100% (95% CI, 100-100%) , 99% (95% CI, 97-100%), and 95% (95% CI, 94-98%), respectively. Patient age, T classification, Gleason score, prostate-specific antigen, and percentage of positive cores were significant prognostic factors for FFBR. Grade 2 or higher GI and GU toxicities were 3.9% and 2.0%. Patient age was a prognostic factor for both late GI and GU toxicities. This study represents the largest cohort of patients treated with PT for localized prostate cancer, with the longest follow-up to date. Our results demonstrate that the biochemical control of PT is favorable particularly for high- and very high-risk patients with lower late genitourinary toxicity and indicates the necessity of considering patient age in the treatment protocols.
本回顾性研究旨在报告接受质子治疗(PT)局部前列腺癌患者的长期临床结果。2001 年至 2014 年间,共治疗了 1375 例连续患者。根据国家综合癌症网络标准,患者被分为预后风险组。计算生化无复发生存率(FFBR)、癌症特异性生存率(CSS)和晚期胃肠道(GI)/泌尿生殖系统(GU)毒性的发生率。进行多变量分析以确定 FFBR 和晚期毒性的临床预后因素。中位随访时间为 70 个月(范围,4-145 个月)。总的来说,99%的患者接受了 74Gy(相对生物效应[RBE]);56%的患者接受了新辅助雄激素剥夺治疗。对于低、中、高和极高风险组,5 年 FFBR 分别为 99%(95%CI,96-100%)、91%(95%CI,88-93%)、86%(95%CI,82-89%)和 66%(95%CI,53-76%),5 年 CSS 分别为 100%(95%CI,100-100%)、100%(95%CI,100-100%)、99%(95%CI,97-100%)和 95%(95%CI,94-98%)。患者年龄、T 分类、Gleason 评分、前列腺特异性抗原和阳性核心百分比是 FFBR 的显著预后因素。2 级或更高级别的 GI 和 GU 毒性分别为 3.9%和 2.0%。患者年龄是晚期 GI 和 GU 毒性的预后因素。本研究代表了迄今为止接受 PT 治疗局部前列腺癌患者中最大的队列,随访时间最长。我们的结果表明,PT 的生化控制尤其对高风险和极高风险患者有利,晚期泌尿生殖系统毒性较低,并表明在治疗方案中需要考虑患者年龄。