Beyer D C, Priestley J B
Arizona Oncology Services, Phoenix 85013, USA.
Int J Radiat Oncol Biol Phys. 1997 Feb 1;37(3):559-63. doi: 10.1016/s0360-3016(96)00609-8.
To assess the 5-year clinical and biochemical results of ultrasound-guided permanent 125I brachytherapy in early adenocarcinoma of the prostate. Biochemical disease-free survival (BDFS) is reported, using PSA follow-up and is compared to the surgical and radiation therapy literature.
From December 1988 through December 1993, ultrasound-guided brachytherapy was preplanned with 125I and delivered 160 Gy as the sole treatment in 499 patients. All were clinically staged as T1 or T2 node-negative adenocarcinoma of the prostate. Within the first year, 10 patients were lost to follow-up and have been excluded from further study. The remaining 489 patients form the basis of this report. Clinical status and prostate specific antigen (PSA) values were systematically recorded before and after treatment.
With a median follow-up of 35 months (3-70), the actuarial clinical local control is 83%. Both stage and grade are shown to predict for this endpoint. Actuarial biochemical disease-free survival (BDFS) is also correlated with stage, grade, and PSA at presentation. Biochemical disease-free survival at 5 years is 94% for T1, 70% for unilateral T2, and 34% for T2c tumors. Grade is also predictive, ranging from 85% in low-grade tumors to 30% in high-grade tumors. In a multivariate analysis, the pretreatment PSA is most highly correlated (p < 0.0001) with BDFS, local control, and clinical disease-free survival. Patients with a normal pretreatment PSA enjoyed 93% BDFS, while those presenting with PSA > 10 had a BDFS of 40%. Complications have been few, with severe urinary urgency or dysuria in 4% and both incontinence and proctitis seen in 1%.
While biochemical disease-free survival reports in the literature are immature and have short follow-up, our data compares favorably with studies following radical prostatectomy or radiation therapy. Further follow-up of this cohort is required. The complication rate is low and patient acceptance excellent. Permanent implantation of 125I as the sole treatment for early prostate adenocarcinoma is a viable alternative for patients with early-stage and low- to moderate-grade cancers. The PSA provides significant prognostic information and aids in case selection. Better management options are needed for high grade and bilateral tumors.
评估超声引导下永久性¹²⁵I近距离放射治疗早期前列腺腺癌的5年临床和生化结果。报告生化无病生存率(BDFS),采用前列腺特异性抗原(PSA)随访,并与手术和放射治疗的文献进行比较。
1988年12月至1993年12月,对499例患者预先计划采用¹²⁵I进行超声引导下近距离放射治疗,作为唯一治疗方式给予160Gy剂量。所有患者临床分期均为前列腺T1或T2期且淋巴结阴性腺癌。在第一年,10例患者失访,被排除在进一步研究之外。其余489例患者构成本报告的基础。系统记录治疗前后的临床状况和前列腺特异性抗原(PSA)值。
中位随访35个月(3 - 70个月),精算临床局部控制率为83%。分期和分级均显示可预测该终点。精算生化无病生存率(BDFS)也与分期、分级以及初始PSA相关。T1期肿瘤5年生化无病生存率为94%,单侧T2期为70%,T2c期为34%。分级也具有预测性,低级别肿瘤为85%,高级别肿瘤为30%。多因素分析显示,治疗前PSA与BDFS、局部控制和临床无病生存率相关性最高(p < 0.0001)。治疗前PSA正常的患者BDFS为93%,而PSA > 10的患者BDFS为40%。并发症较少,4%的患者出现严重尿急或尿痛,1%的患者出现尿失禁和直肠炎。
虽然文献中的生化无病生存率报告尚不成熟且随访时间短,但我们的数据与前列腺癌根治术或放射治疗的研究相比具有优势。需要对该队列进行进一步随访。并发症发生率低,患者接受度良好。永久性植入¹²⁵I作为早期前列腺腺癌的唯一治疗方法,对于早期以及低至中度分级癌症患者是一种可行的选择。PSA提供了重要的预后信息并有助于病例选择。对于高级别和双侧肿瘤需要更好的管理方案。