Nakai Yasushi, Tanaka Nobumichi, Asakawa Isao, Morizawa Yosuske, Yamaki Kaori, Hori Shunta, Gotoh Daisuke, Miyake Makito, Torimoto Kazumasa, Hasegawa Masatoshi, Fujimoto Kiyohide
Department of Urology, Nara Medical University, Kashihara, Nara, Japan.
Department of Urology, Nara Medical University, Kashihara, Nara, Japan.
Brachytherapy. 2022 Sep-Oct;21(5):626-634. doi: 10.1016/j.brachy.2022.04.008. Epub 2022 May 27.
To evaluate late genitourinary (GU) and gastrointestinal (GI) toxicities and radiation-induced second primary cancers (RISPCs) in patients who received low-dose-rate brachytherapy (LDR-BT) with or without external beam radiotherapy for prostate cancer.
This retrospective study included 897 consecutive patients who received LDR-BT between July 2004 and July 2015 in our institution. Adverse events and the incidence of second primary cancers were evaluated at 1, 3, 6, 12, 18, 24, 30, 36, 48, 54, and 60 mo after LDR-BT and then once a year. Related factors to ≥grade 2 (G2) toxicity were evaluated using the Cox proportional-hazards model.
The median follow-up time was 85.2 (interquartile range: 66.8-111.3) mo. The cumulative incidence rates of ≥G2 GU toxicity at 5 and 10 yrs after LDR-BT were 11.2% and 14.7%, respectively. The International Prostate Symptom Score before LDR-BT (continuous) (hazard ratio [HR]: 1.03), no neoadjuvant androgen deprivation therapy (HR: 1.69), and combination external beam radiotherapy (HR: 3.30) were risk factors related to the incidence of ≥G2 GU toxicity. The cumulative incidence rates of ≥G2 GI toxicity at 5 and 10 yrs after LDR-BT were 3.3% and 3.3%, respectively. Age (continuous) (HR: 1.09), body mass index (continuous) (HR: 0.87), and rectum V100 (continuous) (HR: 1.64) were risk factors related to ≥G2 GI toxicity. A total of 12 (1.3%) patients developed metachronous RISPCs (bladder cancer: 9; rectal cancer: 3).
The incidence rates of late GU and GI toxicities and RISPCs after LDR-BT were low.
评估接受低剂量率近距离放射治疗(LDR-BT)联合或不联合外照射放疗的前列腺癌患者的晚期泌尿生殖系统(GU)和胃肠道(GI)毒性以及放射诱发的第二原发性癌症(RISPCs)。
这项回顾性研究纳入了2004年7月至2015年7月在本机构接受LDR-BT的897例连续患者。在LDR-BT后1、3、6、12、18、24、30、36、48、54和60个月评估不良事件和第二原发性癌症的发生率,之后每年评估一次。使用Cox比例风险模型评估与≥2级(G2)毒性相关的因素。
中位随访时间为85.2(四分位间距:66.8-111.3)个月。LDR-BT后5年和10年≥G2 GU毒性的累积发生率分别为11.2%和14.7%。LDR-BT前的国际前列腺症状评分(连续变量)(风险比[HR]:1.03)、未接受新辅助雄激素剥夺治疗(HR:1.69)以及联合外照射放疗(HR:3.30)是与≥G2 GU毒性发生率相关的危险因素。LDR-BT后5年和10年≥G2 GI毒性的累积发生率分别为3.3%和3.3%。年龄(连续变量)(HR:1.09)、体重指数(连续变量)(HR:0.87)和直肠V100(连续变量)(HR:1.64)是与≥G2 GI毒性相关的危险因素。共有12例(1.3%)患者发生异时性RISPCs(膀胱癌:9例;直肠癌:3例)。
LDR-BT后晚期GU和GI毒性以及RISPCs的发生率较低。