Department of Radiation Oncology, Cooper University Hospital, Camden, NJ, USA.
Int J Radiat Oncol Biol Phys. 2012 Apr 1;82(5):1949-56. doi: 10.1016/j.ijrobp.2011.04.005. Epub 2011 Jul 15.
Men with Gleason score (GS) 8-10 prostate cancer (PCa) are assumed to have a high risk of micrometastatic disease at presentation. However, local failure is also a major problem. We sought to establish the importance of more aggressive local radiotherapy (RT) to ≥80 Gy.
There were 226 men treated consecutively with RT ± ADT from 1988 to 2002 for GS 8-10 PCa. Conventional, three-dimensional conformal or intensity-modulated (IM) RT was used. Radiation dose was divided into three groups: (1) <75 Gy (n = 50); (2) 75-79.9 Gy (n = 60); or (3) ≥80 Gy (n = 116). The endpoints examined included biochemical failure (BF; nadir + 2 definition), distant metastasis (DM), cause-specific mortality, and overall mortality (OM).
Median follow-up was 66, 71, and 58 months for Groups 1, 2, and 3. On Fine and Gray's competing risk regression analysis, significant predictors of reduced BF were RT dose ≥80 Gy (p = 0.011) and androgen deprivation therapy duration ≥24 months (p = 0.033). In a similar model of DM, only RT dose ≥80 Gy was significant (p = 0.007). On Cox regression analysis, significant predictors of reduced OM were RT dose ≥80 Gy (p = 0.035) and T category (T3/4 vs. T1, p = 0.041). Dose was not a significant determinant of cause-specific mortality. Results for RT dose were similar in a model with RT dose and ADT duration as continuous variables.
The results indicate that RT dose escalation to ≥80 Gy is associated with lower risks of BF, DM, and OM in men with GS 8-10 PCa, independently of androgen deprivation therapy.
患有 Gleason 评分(GS)8-10 前列腺癌(PCa)的男性被认为在发病时存在微转移疾病的高风险。然而,局部失败也是一个主要问题。我们试图确定更积极的局部放射治疗(RT)至≥80Gy 的重要性。
1988 年至 2002 年,连续有 226 名男性接受 RT±ADT 治疗,GS 8-10PCa。使用常规、三维适形或强度调制(IM)RT。辐射剂量分为三组:(1)<75Gy(n=50);(2)75-79.9Gy(n=60);或(3)≥80Gy(n=116)。检查的终点包括生化失败(BF;最低点+2 定义)、远处转移(DM)、特异性死亡率和总死亡率(OM)。
第 1、2 和 3 组的中位随访时间分别为 66、71 和 58 个月。在 Fine 和 Gray 的竞争风险回归分析中,降低 BF 的显著预测因素是 RT 剂量≥80Gy(p=0.011)和雄激素剥夺治疗持续时间≥24 个月(p=0.033)。在 DM 的类似模型中,只有 RT 剂量≥80Gy 是显著的(p=0.007)。在 Cox 回归分析中,降低 OM 的显著预测因素是 RT 剂量≥80Gy(p=0.035)和 T 分期(T3/4 与 T1,p=0.041)。剂量不是特异性死亡率的显著决定因素。在 RT 剂量和 ADT 持续时间作为连续变量的模型中,RT 剂量的结果相似。
结果表明,在 GS 8-10PCa 男性中,RT 剂量升级至≥80Gy 与降低 BF、DM 和 OM 的风险相关,独立于雄激素剥夺治疗。