Deger Serdar, Boehmer Dirk, Roigas Jan, Schink Tania, Wernecke Klaus Dieter, Wiegel Thomas, Hinkelbein Wolfgang, Budach Volker, Loening Stefan A
Department of Urology, Charité Campus Mitte, Charité -- University Medicine Berlin, Berlin, Germany.
Eur Urol. 2005 Apr;47(4):441-8. doi: 10.1016/j.eururo.2004.11.014. Epub 2005 Jan 18.
To evaluate the outcome of high dose rate (HDR) brachytherapy with iridium 192 (Ir(192)) and 3D conformal external beam radiotherapy in patients with localized prostate cancer.
A total of 442 patients with localized prostate cancer underwent combined radiotherapy with interstitial brachytherapy with Ir(192) and 3D conformal external beam radiotherapy between December 1992 and March 2001. Patients underwent laparoscopic pelvic lymph node dissection to exclude patients with lymphatic involvement. Iridium 192 was delivered twice with a one-week interval in afterloading technique. 247 patients (56%) had clinical T3 disease and 128 patients (29%) had an initial PSA of more than 20 ng/ml. Progression was defined as biochemical failure according to ASTRO criteria. Patients were divided according to pretreatment variables that independently affected prostate-specific antigen (PSA) relapse-free survival in three risk groups. Low risk was defined as cT1c-cT2 and G1-G2 and PSA<10 ng/ml (n=94). Intermediate risk included patients with cT1c-cT2 and G1-G2 and PSA between 10 and 20 ng/ml (n=53). High risk group patients were cT3 or G3 or PSA>20 ng/ml (n=295).
Median follow-up was 5 years. Late grade 3-4 complications according to RTOG/EORTC criteria occurred in 50 patients (11%). The initial PSA value decreased from median 11.8 ng/ml to 0.98 ng/ml 12 months after treatment, to 0.3 ng/ml after 60 months and to 0.1 ng/ml 10 years after therapy. 53% of the patients (n=235) reached a PSA nadir of 0.5 ng/ml. 66 patients (15%) had a local recurrence, 54 (12%) developed systemic disease and 12 (3%) had both local and systemic failure. The progression free survival rate was 65% at 5-year follow-up. Five-year progression free survival was 81% in the low risk group, 65% in the intermediate risk group and 59% in the high risk group. Five-year overall survival was 87% and 5-year disease specific survival 94%. Initial PSA value, risk group and age were significantly related to progression free survival.
Combined HDR brachytherapy with Iridium 192 is an alternative treatment option for patients with localized prostate cancer. Initial PSA value, risk group, and age are important prognostic factors for progression free survival.
评估高剂量率(HDR)铱192(Ir(192))近距离放射治疗联合三维适形外照射放疗在局限性前列腺癌患者中的治疗效果。
1992年12月至2001年3月期间,共有442例局限性前列腺癌患者接受了Ir(192)组织间近距离放射治疗联合三维适形外照射放疗。患者接受腹腔镜盆腔淋巴结清扫以排除有淋巴结转移的患者。采用后装技术,铱192分两次给药,间隔1周。247例(56%)患者有临床T3期疾病,128例(29%)患者初始前列腺特异性抗原(PSA)大于20 ng/ml。根据美国放射肿瘤学会(ASTRO)标准,疾病进展定义为生化失败。根据独立影响前列腺特异性抗原(PSA)无复发生存的治疗前变量,将患者分为三个风险组。低风险定义为cT1c - cT2期、G1 - G2级且PSA<10 ng/ml(n = 94)。中风险包括cT1c - cT2期、G1 - G2级且PSA在10至20 ng/ml之间的患者(n = 53)。高风险组患者为cT3期或G3级或PSA>20 ng/ml(n = 295)。
中位随访时间为5年。根据美国放射肿瘤学协作组(RTOG)/欧洲癌症研究与治疗组织(EORTC)标准,50例患者(11%)出现3 - 4级晚期并发症。治疗后12个月时,初始PSA值从中位11.8 ng/ml降至0.98 ng/ml,60个月后降至0.3 ng/ml,治疗10年后降至0.1 ng/ml。53%的患者(n = 235)PSA最低点达到0.5 ng/ml。66例患者(15%)出现局部复发,54例(12%)发生全身转移,12例(3%)既有局部又有全身转移。5年随访时无进展生存率为65%。低风险组5年无进展生存率为81%,中风险组为65%,高风险组为59%。5年总生存率为87%,5年疾病特异性生存率为94%。初始PSA值、风险组和年龄与无进展生存率显著相关。
铱192高剂量率近距离放射治疗联合外照射放疗是局限性前列腺癌患者的一种替代治疗选择。初始PSA值、风险组和年龄是无进展生存率的重要预后因素。