Onishi Masahiro, Kawamura Hidemasa, Murata Kazutoshi, Inoue Tatsuro, Murata Hiroto, Takakusagi Yosuke, Okonogi Noriyuki, Ohkubo Yu, Okamoto Masahiko, Kaminuma Takuya, Sekihara Tetsuo, Nakano Takashi, Ohno Tatsuya
Oncology Center, Hidaka Hospital, Takasaki 370-0001, Japan.
Department of Radiation Oncology, Gunma University Graduate School of Medicine, Maebashi 371-8511, Japan.
Cancers (Basel). 2021 Jul 31;13(15):3868. doi: 10.3390/cancers13153868.
This study aimed to evaluate clinical outcomes and the toxicity of intensity-modulated radiation therapy with simultaneous integrated boost (SIB-IMRT) combined with androgen-deprivation therapy for clinically node-positive (cN1) prostate cancer. We retrospectively analyzed 97 patients with cN1 prostate cancer who received SIB-IMRT between June 2008 and October 2017 at our hospital. The prescribed dosages delivered to the prostate and seminal vesicle, elective node area, and residual lymph nodes were 69, 54, and 60 Gy in 30 fractions, respectively. Kaplan-Meier analysis was used to determine 5-year biochemical relapse-free survival (bRFS), relapse-free survival (RFS), overall survival (OS), and prostate cancer-specific survival (PCSS). Toxicity was evaluated using the Common Terminology Criteria for Adverse Events ver. 4.0. Over a median follow-up duration of 60 months, the 5-year bRFS, RFS, OS, and PCSS were 85.1%, 88.1%, 92.7% and 95.0%, respectively. Acute Grade 2 genito-urinary (GU) and gastro-intestinal (GI) toxicities were observed in 10.2% and 2.1%, respectively, with no grade ≥3 toxicities being detected. The cumulative incidence rates of 5-year Grade ≥2 late GU and GI toxicities were 4.7% and 7.4%, respectively, with no Grade 4 toxicities being detected. SIB-IMRT for cN1 prostate cancer demonstrated favorable 5-year outcomes with low incidences of toxicity.
本研究旨在评估调强放疗同步整合加量(SIB-IMRT)联合雄激素剥夺治疗对临床淋巴结阳性(cN1)前列腺癌的临床疗效及毒性。我们回顾性分析了2008年6月至2017年10月在我院接受SIB-IMRT的97例cN1前列腺癌患者。前列腺、精囊、选择性淋巴结区域和残留淋巴结的处方剂量分别为69 Gy、54 Gy和60 Gy,分30次给予。采用Kaplan-Meier分析确定5年生化无复发生存率(bRFS)、无复发生存率(RFS)、总生存率(OS)和前列腺癌特异性生存率(PCSS)。使用《不良事件通用术语标准》第4.0版评估毒性。中位随访时间为60个月,5年bRFS、RFS、OS和PCSS分别为85.1%、88.1%、92.7%和95.0%。急性2级泌尿生殖系统(GU)和胃肠道(GI)毒性分别在10.2%和2.1%的患者中观察到,未检测到≥3级毒性。5年≥2级晚期GU和GI毒性的累积发生率分别为4.7%和7.4%,未检测到4级毒性。cN1前列腺癌的SIB-IMRT显示出良好的5年疗效,毒性发生率低。