Momma Tetsuo, Saito Shiro, Toya Kazuhito, Yorozu Atsunori, Dokiya Takushi, Murai Masaru
Department of Urology, National Hospital Organization Tokyo Medical Center, and Department of Radiation Oncology, Saitama Medical College, Japan.
Int J Urol. 2006 Mar;13(3):218-23. doi: 10.1111/j.1442-2042.2006.01266.x.
To report the 3-year treatment results of definitive irradiation by using a temporary interstitial implant with low-dose rate iridium-192 with or without external beam radiotherapy in the treatment of localized prostate cancer.
One-hundred and forty-three patients with pathologically defined prostate carcinoma were treated from December 1997 to April 2003. The patients were classified into a low-risk group (T2, PSA<or=20 ng/mL and Gleason score<or=6) or a high-risk group (T3, PSA>20 ng/mL or Gleason score>or=7). Low-risk patients were treated with low-dose-rate iridium brachytherapy as monotherapy delivering 70 Gy. High-risk patients were treated with the combination of brachytherapy and external beam radiotherapy delivering 40 Gy and 36 Gy, respectively. Kaplan-Meier estimates of prostate-specific antigen (PSA) progression-free survival rate were analysed. To assess the treatment quality in different periods, PSA progression-free survival rates in late era (year of 2000 and after) and in early era (before 2000) were compared. Morbidity was graded according to the Radiation Therapy Oncology Group grading scale.
One hundred and nineteen patients were analysed, of which 86 patients underwent monotherapy with an iridium implant, and 33 were treated with the combination of external beam radiotherapy. Twenty-four patients were excluded from the analysis because the classification of risk group did not suit the criteria. The total (n=119) PSA progression-free survival rate at 3 years was 80.3%. The PSA progression-free survival rate at 3 years for the monotherapy group (n=86) and the combination therapy group (n=33) were 78.2% and 86.9%, respectively. There were 23 patients who were followed for more than 36 to 63 months, and, during this period, only 1 patient who received the monotherapy was diagnosed as PSA failure at 50 months. The 3-year PSA progression-free survival rate of monotherapy in late era was significantly higher than that in early era; however, no significant difference was seen in the combination treatment. Morbidity for the combination treatment was low; however, for the monotherapy, three patients developed severe rectal ulcers, and colostomies were made.
The PSA progression-free survival rate after low-dose rate iridium-192 brachytherapy with or without external beam radiotherapy can be satisfactory and longer follow up is necessary to compare the efficacy of other treatments.
报告使用低剂量率铱-192临时组织间植入联合或不联合外照射放疗对局限性前列腺癌进行根治性放疗的3年治疗结果。
1997年12月至2003年4月期间,对143例经病理确诊的前列腺癌患者进行了治疗。患者被分为低风险组(T2,前列腺特异性抗原[PSA]≤20 ng/mL且Gleason评分≤6)或高风险组(T3,PSA>20 ng/mL或Gleason评分≥7)。低风险患者接受低剂量率铱近距离放疗作为单一疗法,给予70 Gy。高风险患者接受近距离放疗与外照射放疗联合治疗,分别给予40 Gy和36 Gy。分析前列腺特异性抗原(PSA)无进展生存率的Kaplan-Meier估计值。为评估不同时期的治疗质量,比较了晚期(2000年及以后)和早期(2000年以前)的PSA无进展生存率。根据放射肿瘤学组的分级标准对并发症进行分级。
对119例患者进行了分析,其中86例患者接受了铱植入单一疗法,33例患者接受了外照射放疗联合治疗。24例患者因风险组分类不符合标准而被排除在分析之外。119例患者3年时的总PSA无进展生存率为80.3%。单一疗法组(n = 86)和联合治疗组(n = 33)3年时的PSA无进展生存率分别为78.2%和86.9%。有23例患者随访超过36至63个月,在此期间,单一疗法组仅有1例患者在50个月时被诊断为PSA失败。晚期单一疗法的3年PSA无进展生存率显著高于早期;然而,联合治疗组未见显著差异。联合治疗的并发症发生率较低;然而,单一疗法组有3例患者出现严重直肠溃疡并进行了结肠造口术。
低剂量率铱-192近距离放疗联合或不联合外照射放疗后的PSA无进展生存率可能令人满意,需要更长时间的随访来比较其他治疗方法的疗效。