Zelefsky M J, Aschkenasy E, Kelsen S, Leibel S A
Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Int J Radiat Oncol Biol Phys. 1997 Sep 1;39(2):327-33. doi: 10.1016/s0360-3016(97)00056-4.
Three-dimensional conformal radiotherapy (3D-CRT) has been associated with a reduction in acute and late toxicity among patients treated for localized prostatic cancer. The purpose of this study is to assess the acute and late toxicity of 3D-CRT delivered to patients in the postprostatectomy setting and to analyze which factors predict for durable biochemical control in this group of patients.
Between 1988 and 1994, 42 patients were treated after prostatectomy with three-dimensional conformal radiotherapy. The median time from prostatectomy to radiotherapy was 11 months. Indications for treatment included a rising serum PSA level in 28 patients (65%) and positive surgical margins without a rising PSA level in 14 (35%). Twenty-five patients (60%) had pathologic stage T3 disease, and 32 (74%) had tumor at or close to the surgical margins. The median dose was 64.8 Gy, and the median follow-up time was 2 years.
3D-CRT in the postprostatectomy setting was well tolerated. Three patients (7%) experienced Grade II acute genitourinary toxicity and nine patients (21%) experienced Grade II acute gastrointestinal toxicity during treatment. No patient experienced Grade III or higher acute morbidity. The 2-year actuarial risk for Grade II late genitourinary and gastrointestinal late complications were 5 and 9%, respectively. In patients with existing incontinence, the incidence of worsening stress incontinence 6 months after treatment was 17%, which resolved within 12 months to its preradiotherapy level in four of six cases (66%). The overall 2-year postirradiation PSA relapse-free survival rate was 53%. The 2-year PSA relapse-free survival was 66% for patients with undetectable PSA levels in the immediate postoperative period compared to 26% for those with detectable levels of PSA after surgery (p < 0.006). Furthermore, for patients with preradiotherapy PSA levels of < or = 1.0 ng/ml, the 2-year PSA relapse-free survival was 74% compared to 17% of those with preradiotherapy PSA levels of > 1.0 ng/ml (p < 0.002). The resection margin status, presence of seminal vesicle involvement, Gleason score, and the preprostatectomy PSA level did not impact on PSA relapse-free survival. A Cox proportional hazards regression analysis demonstrated that a preradiotherapy PSA value of > 1 ng/ml (p < 0.002) was the most important covariate predicting for a rising PSA after radiotherapy.
After prostatectomy, three-dimensional conformal radiotherapy is associated with minimal treatment-related morbidity. Patients with postprostatectomy, preradiotherapy PSA levels < or = 1.0 ng/ml, and those patients who had undetectable PSA levels in the immediate postoperative period are more likely to benefit from local adjuvant therapy.
三维适形放疗(3D - CRT)已使局限性前列腺癌患者的急性和晚期毒性反应有所降低。本研究旨在评估前列腺切除术后接受3D - CRT治疗患者的急性和晚期毒性反应,并分析哪些因素可预测该组患者持久的生化控制情况。
1988年至1994年间,42例患者在前列腺切除术后接受了三维适形放疗。从前列腺切除到放疗的中位时间为11个月。治疗指征包括28例(65%)患者血清PSA水平升高,14例(35%)手术切缘阳性但PSA水平未升高。25例(60%)患者为病理分期T3期疾病,32例(74%)患者肿瘤位于手术切缘处或接近手术切缘。中位剂量为64.8 Gy,中位随访时间为2年。
前列腺切除术后进行3D - CRT耐受性良好。3例(7%)患者在治疗期间出现II级急性泌尿生殖系统毒性反应,9例(21%)患者出现II级急性胃肠道毒性反应。无患者出现III级或更高级别的急性并发症。II级晚期泌尿生殖系统和胃肠道晚期并发症的2年精算风险分别为5%和9%。对于已有尿失禁的患者,治疗后6个月压力性尿失禁加重的发生率为17%,6例中有4例(66%)在12个月内恢复至放疗前水平。放疗后2年总的PSA无复发生存率为53%。术后即刻PSA水平不可检测患者的2年PSA无复发生存率为66%,而术后PSA水平可检测患者的该生存率为26%(p < 0.006)。此外,放疗前PSA水平≤1.0 ng/ml的患者,2年PSA无复发生存率为74%,而放疗前PSA水平>1.0 ng/ml的患者该生存率为17%(p < 0.002)。手术切缘状态、精囊受累情况、Gleason评分以及前列腺切除术前PSA水平均不影响PSA无复发生存率。Cox比例风险回归分析表明,放疗前PSA值>1 ng/ml(p < 0.002)是预测放疗后PSA升高的最重要协变量。
前列腺切除术后,三维适形放疗相关的治疗相关发病率极低。前列腺切除术后、放疗前PSA水平≤1.0 ng/ml以及术后即刻PSA水平不可检测的患者更可能从局部辅助治疗中获益。