Cohen Michael S, Triaca Veronica, Billmeyer Brian, Hanley Robert S, Girshovich Lyubov, Shuster Todd, Oberfield Richard A, Zinman Leonard
Department of Urology, Lahey Clinic Medical Center, Burlington, Massachusetts, USA.
J Urol. 2008 Feb;179(2):536-41; discussion 541. doi: 10.1016/j.juro.2007.09.068.
We evaluated the efficacy of a combined chemoradiation therapy protocol for the primary treatment of primary invasive carcinoma of the male urethra.
From January 1991 to December 2006, 18 patients with invasive carcinoma of the male urethra referred to our institution were treated with a chemoradiation therapy protocol, consisting of 2 cycles of 5-fluorouracil (1,000 mg/m(2)) on days 1 to 4 and days 29 to 32, and mitomycin-C (10 mg/m(2)) on days 1 and 29 with concurrent external beam radiation therapy (45 to 55 Gy in 25 fractions during 5 weeks) to the genitalia, perineum, and inguinal and external iliac lymph nodes. Kaplan-Meier curves were constructed to assess overall, disease specific and disease-free survival.
The stage and node distribution was T2N0 in 2 patients (11%), T3N0 in 8 (44%), T4N0 in 2 (11%), TXN1 in 1(6%) and TXN2 in 5 (28%). The most prevalent histology was moderately (7 of 18 patients or 39%) or poorly (10 of 18 or 56%) differentiated squamous cell carcinoma (17 of 18 or 95%). Overall 83% (15 of 18) of the patients had a complete response to the primary chemoradiation therapy protocol, and the 5-year overall and disease specific survival rates were 60% and 83%, respectively. Five-year disease-free survival rates after chemoradiation therapy and after chemoradiation therapy with salvage surgery were 54% and 72%, respectively. The 3 nonresponders died of disease after undergoing salvage surgery and 5 of the 15 complete responders (30%) had recurrence. Complex urethral reconstruction was required in 3 of 10 patients (30%) who had prolonged disease-free survival.
The chemoradiation therapy protocol is an alternative primary treatment modality for invasive urethral carcinoma. It enables an unprecedented potential for organ preservation.
我们评估了一种联合放化疗方案用于男性尿道原发性浸润癌初始治疗的疗效。
1991年1月至2006年12月,18例转诊至我院的男性尿道浸润癌患者接受了放化疗方案治疗,该方案包括两个周期的5-氟尿嘧啶(1000mg/m²),分别在第1至4天和第29至32天使用,丝裂霉素-C(10mg/m²)在第1天和第29天使用,同时对生殖器、会阴、腹股沟和髂外淋巴结进行外照射放疗(5周内25次分割,剂量为45至55Gy)。构建Kaplan-Meier曲线以评估总生存率、疾病特异性生存率和无病生存率。
分期和淋巴结分布情况为:2例(11%)为T2N0,8例(44%)为T3N0,2例(11%)为T4N0,1例(6%)为TXN1,5例(28%)为TXN2。最常见的组织学类型为中分化(18例中的7例,即39%)或低分化(18例中的10例,即56%)鳞状细胞癌(18例中的17例,即95%)。总体而言,83%(18例中的15例)的患者对初始放化疗方案有完全反应,5年总生存率和疾病特异性生存率分别为60%和83%。放化疗后及放化疗联合挽救性手术后的5年无病生存率分别为54%和72%。3例无反应者在接受挽救性手术后死于疾病,15例完全反应者中有5例(30%)复发。10例无病生存期延长的患者中有3例(30%)需要进行复杂的尿道重建。
放化疗方案是浸润性尿道癌的一种替代初始治疗方式。它为器官保留带来了前所未有的潜力。