Horwitz E M, Hanlon A L, Pinover W H, Hanks G E
Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Int J Radiat Oncol Biol Phys. 1998 Jun 1;41(3):519-23. doi: 10.1016/s0360-3016(98)00095-9.
We reviewed our institution's experience treating patients with nonpalpable PSA-detected prostate cancer with three-dimensional conformal radiation therapy (3DCRT) to determine prognostic factors that predict for biochemical-free survival (bNED) control and present the bNED control rates.
Between May 1, 1990 and November 30, 1994, 160 patients with nonpalpable PSA-detected prostate cancer received 3DCRT at Fox Chase Cancer Center (median total dose 73 Gy; range: 67-78 Gy). bNED failure was defined as three consecutive increases in posttreatment PSA after achieving a nadir. bNED failure was recorded as the time midway between the nadir and the first consecutive rising PSA. Five-year actuarial rates of bNED control were calculated for pretreatment PSA (0-9.9 vs. 10-19.9 vs. > or = 20 ng/ml), Gleason score (2-6 vs. 7-10), treatment field size (prostate vs. small pelvis), age (<65 vs. > or = 65), and dose (< or = 73 vs. >73 Gy) using Kaplan-Meier methods and compared using the Log rank test. The Cox model was used to multivariately establish independent predictors based on significant univariate factors. Median follow-up was 39 months (range: 2-84 months).
The 5-year actuarial rate of bNED control was 86% for the entire group of patients. The Cox Proportional Hazards model demonstrated that pretreatment PSA was an independent predictor of bNED control. Treatment field size was marginally predictive. There was no difference in bNED control when patients were stratified by the number of lobes positive for disease. Statistically different rates of bNED control were seen when the patients with nonpalpable disease were univariately compared to T2b and T2c patients. Three patients experienced Grade 3-4 genitourinary (GU) toxicity and 3 patients experienced Grade 3-4 gastrointestinal (GI) toxicity.
Patients with nonpalpable PSA-detected prostate cancer can be effectively treated with 3DCRT with minimal morbidity and high rates of bNED control at 5 years. Pretreatment PSA level is an independent predictor of bNED control.
我们回顾了本机构采用三维适形放疗(3DCRT)治疗经PSA检测出的不可触及前列腺癌患者的经验,以确定预测无生化复发生存(bNED)控制的预后因素,并呈现bNED控制率。
1990年5月1日至1994年11月30日期间,160例经PSA检测出的不可触及前列腺癌患者在福克斯蔡斯癌症中心接受了3DCRT(中位总剂量73 Gy;范围:67 - 78 Gy)。bNED失败定义为达到最低点后治疗后PSA连续三次升高。bNED失败记录为最低点与首次连续升高的PSA之间的中间时间。采用Kaplan - Meier方法计算治疗前PSA(0 - 9.9 vs. 10 - 19.9 vs.≥20 ng/ml)、Gleason评分(2 - 6 vs. 7 - 10)、治疗野大小(前列腺 vs. 小骨盆)、年龄(<65 vs.≥65)和剂量(≤73 vs.>73 Gy)的5年bNED控制精算率,并使用对数秩检验进行比较。Cox模型用于基于显著的单因素因素多变量建立独立预测因子。中位随访时间为39个月(范围:2 - 84个月)。
整个患者组的5年bNED控制精算率为86%。Cox比例风险模型表明,治疗前PSA是bNED控制的独立预测因子。治疗野大小有一定的预测性。根据疾病阳性叶的数量对患者进行分层时,bNED控制无差异。将不可触及疾病患者与T2b和T2c患者进行单因素比较时,观察到bNED控制率在统计学上有差异。3例患者出现3 - 4级泌尿生殖系统(GU)毒性,3例患者出现3 - 4级胃肠道(GI)毒性。
经PSA检测出的不可触及前列腺癌患者可以通过3DCRT有效治疗,发病率最低,5年bNED控制率高。治疗前PSA水平是bNED控制的独立预测因子。