Stone Nelson N, Stock Richard G, Unger Pam
Department of Urology, Mount Sinai School of Medicine, New York, New York, USA.
J Urol. 2005 Mar;173(3):803-7. doi: 10.1097/01.ju.0000152558.63996.29.
We determined the 10-year biochemical and local control results for I prostate brachytherapy in men followed a minimum of 4 years.
A total of 279 men with T1-T2 prostate cancer with a minimum followup of 4 years were implanted with I from 1990 to 1998 using the real-time technique. Patients were treated with the implant alone (215 or 72.5%) or with the implant and 6 months of hormone therapy (64 or 27.6%). Of the men 185 (66.3%) agreed to ultrasound guided biopsy (6 to 12 cores) a minimum of 2 years after implantation. All patients with increasing prostate specific antigen (PSA), evidence of local recurrence or a prior positive biopsy underwent repeat biopsy yearly until biopsy became negative or there was clear evidence of biochemical (PSA) progression. The radiation dose delivered to 90% of the gland (D90) was determined 30 days after implantation by computerized tomography based dosimetry. Biochemical failure was defined as 3 consecutive PSA increases. Survival curves were calculated by the Kaplan-Meier method. Cross tabulations were tested by Pearson chi-square analysis. The effect of multiple variables was tested by the log rank test (Cox regression).
Median patient age was 67 years (range 42 to 82) and median followup was 6 years (range 4 to 12). Of the patients 49 (17.6%) experienced failure, for a 10-year freedom from failure (FFF) rate of 78%. Univariate analysis for 10-year FFF demonstrated that initial PSA (p = 0.001), stage (p = 0.002), risk group (p <0.001), hormone therapy (p = 0.013) and D90 (p <0.001) were significant. Multivariate analysis demonstrated that D90 (p <0.001) and risk group (p = 0.013) were the only significant variables. The RR of PSA failure was 3.0 (95% CI 2.0 to 4.4, p <0.001) and 5.6 (95% CI 3.1 to 10, p <0.001) for doses below 140 and 120 Gy, respectively. Of the 185 patients 166 (90%) had a negative post-implantation prostate biopsy. FFF was 85% vs 21% in those with a positive biopsy (p <0.001). Patients with a D90 of at least 140 Gy had a positive biopsy rate of 4.8% compared to 20.5% in those with a lower dose (p <0.001). The RR for positive biopsy at doses less than 140 and 120 Gy was 2.6 (95% CI 1.6 to 4.4, p = 0.002) and 4.3 (95% CI 2.3 to 8.1, p <0.001), respectively.
These data demonstrate high biochemical and local control in men with T1-T2 prostate cancer treated with I brachytherapy. The delivered radiation dose and risk category are important predictors of success. Patients receiving a dose of at least 140 Gy have a 90% chance of biochemical FFF and a 95.2% likelihood of local control.
我们确定了接受前列腺近距离放射治疗的男性患者至少随访4年后的10年生化及局部控制结果。
1990年至1998年期间,共有279例T1 - T2期前列腺癌男性患者采用实时技术植入碘-125,这些患者的最短随访时间为4年。患者单独接受植入治疗(215例,占72.5%)或接受植入治疗并联合6个月激素治疗(64例,占27.6%)。其中185例(66.3%)男性患者在植入后至少2年同意接受超声引导下活检(6至12针)。所有前列腺特异性抗原(PSA)升高、有局部复发证据或之前活检呈阳性的患者每年接受重复活检,直至活检结果转为阴性或有明确的生化(PSA)进展证据。植入后30天通过基于计算机断层扫描的剂量测定法确定给予前列腺90%体积的辐射剂量(D90)。生化失败定义为PSA连续3次升高。采用Kaplan - Meier法计算生存曲线。交叉表采用Pearson卡方分析进行检验。通过对数秩检验(Cox回归)检验多个变量的影响。
患者的中位年龄为67岁(范围42至82岁),中位随访时间为6年(范围4至12年)。49例(17.6%)患者出现失败,10年无失败率(FFF)为78%。对10年FFF的单因素分析表明,初始PSA(p = 0.001)、分期(p = 0.002)、风险组(p <0.001)、激素治疗(p = 0.013)和D90(p <0.001)具有显著意义。多因素分析表明,D90(p <0.001)和风险组(p = 0.013)是仅有的显著变量。对于剂量低于140 Gy和120 Gy的患者,PSA失败的相对风险分别为3.0(95%可信区间2.0至4.4,p <0.001)和5.6(95%可信区间3.1至10,p <0.001)。在185例患者中,166例(90%)植入后前列腺活检结果为阴性。活检阳性患者的FFF为21%,而活检阴性患者为85%(p <0.001)。D90至少为140 Gy的患者活检阳性率为4.8%,而较低剂量组为20.5%(p <0.001)。剂量低于140 Gy和120 Gy时活检阳性的相对风险分别为2.6(95%可信区间1.6至4.4,p = 0.002)和4.3(95%可信区间2.3至8.1,p <0.001)。
这些数据表明,接受碘-125近距离放射治疗的T1 - T2期前列腺癌男性患者具有较高的生化及局部控制率。给予的辐射剂量和风险类别是成功的重要预测因素。接受至少140 Gy剂量的患者生化FFF的概率为90%,局部控制的可能性为95.2%。