Department of Radiation Oncology, Winship Cancer Institute, Emory University, Atlanta GA.
Department of Biostatistics and Bioinformatics, Emory University, Atlanta GA.
Brachytherapy. 2021 Nov-Dec;20(6):1130-1138. doi: 10.1016/j.brachy.2021.07.005. Epub 2021 Aug 18.
Addition of a brachytherapy boost to external beam radiation therapy (EBRT) reduces prostate cancer (PCa) recurrence at the expense of genitourinary (GU) toxicity. Whether brachytherapy boost technique, specifically low-dose-rate (LDR-BT) versus high-dose-rate (HDR-BT), impacts treatment-related toxicity is unclear.
Between 2012-2018, 106 men with intermediate/high risk PCa underwent EBRT (37.5-45 Gy in 1.8-2.5 Gy/fraction) plus brachytherapy boost, either with LDR-BT (110 Gy I-125 or 100 Gy Pd-103; n = 51) or HDR-BT (15 Gy x1 Ir-192; n = 55). Patient-reported outcomes (PRO) were assessed by International Prostate Symptom Score (IPSS) and Expanded Prostate Cancer Index Composite (EPIC-CP) surveys at 3-6-month intervals for up to three years following treatment, with higher scores indicating more severe toxicity. Provider-reported GU and gastrointestinal (GI) toxicity was graded per CTCAE v5.0 at each follow-up. Linear mixed models comparing PROs between LDR-BT versus HDR-BT were fitted. Stepwise multivariable analysis (MVA) was performed to account for age, gland size, androgen deprivation therapy use, and alpha-blocker medication use. Incidence rates of grade 2+ GU/GI toxicity was compared using Fisher's exact test.
Use of LDR-BT was associated with greater change in IPSS (p=0.003) and EPIC-CP urinary irritative score (p = 0.002) compared with HDR-BT, but effect size diminished over time (LDR-BT versus HDR-BT: baseline to 6-/24-month mean IPSS change, +6.4/+1.4 versus +2.7/-3.0, respectively; mean EPIC-CP irritative/obstructive change, +2.5/+0.1 versus +0.9/+0.1, respectively). Results remained significant on MVA. Post-treatment grade 2+ GU toxicity was significantly higher in the LDR-BT group (67.5% versus 42.9% for LDR-BT and HDR-BT, respectively; p <0.001). There were no differences between groups in incontinence, bowel function, and erectile function, or grade 2+ GI toxicity.
Compared with LDR-BT, HDR-BT was associated with lower acute patient- and provider-reported GU toxicity.
在外部束放射治疗(EBRT)中增加近距离放射治疗(BT)会降低前列腺癌(PCa)的复发率,但会增加泌尿生殖系统(GU)毒性。BT 增强技术,特别是低剂量率(LDR-BT)与高剂量率(HDR-BT),是否会影响治疗相关毒性尚不清楚。
2012 年至 2018 年,106 名患有中/高危 PCa 的男性接受了 EBRT(37.5-45 Gy,1.8-2.5 Gy/分数)加 BT 增强,分别采用 LDR-BT(110 Gy I-125 或 100 Gy Pd-103;n=51)或 HDR-BT(15 Gy x1 Ir-192;n=55)。通过国际前列腺症状评分(IPSS)和前列腺癌指数综合量表(EPIC-CP)调查,在治疗后 3-6 个月的时间内,以 3-6 个月的间隔评估患者报告的结果(PRO),得分越高表示毒性越严重。按照 CTCAE v5.0 在每次随访时对 GU 和胃肠道(GI)毒性进行分级。使用线性混合模型比较 LDR-BT 与 HDR-BT 之间的 PRO。采用逐步多变量分析(MVA)来考虑年龄、腺体大小、雄激素剥夺治疗的使用以及 α 阻滞剂的使用。使用 Fisher 精确检验比较 2+GU/GI 毒性的发生率。
与 HDR-BT 相比,LDR-BT 与 IPSS(p=0.003)和 EPIC-CP 尿激惹评分(p=0.002)的变化更大,但随着时间的推移,影响会减小(LDR-BT 与 HDR-BT:从基线到 6/24 个月的平均 IPSS 变化,分别为+6.4/+1.4 与+2.7/-3.0;平均 EPIC-CP 刺激/梗阻变化,分别为+2.5/+0.1 与+0.9/+0.1)。在 MVA 中结果仍然显著。LDR-BT 组治疗后 2+GU 毒性明显更高(LDR-BT 和 HDR-BT 组分别为 67.5%和 42.9%;p<0.001)。两组之间在尿失禁、肠道功能和勃起功能或 2+GI 毒性方面无差异。
与 LDR-BT 相比,HDR-BT 与较低的急性患者和提供者报告的 GU 毒性相关。