Villalba Silvia Rodríguez, Denia Paula Monasor, Pérez-Calatayud Maria Jose, Sancho Jose Richart, Pérez-Calatayud Jose, Escrivá Antonio Fuster, Tendero Pedro Torrus, Ortega Manuel Santos
Radiotherapy Department, Hospital Clínica Benidorm, Benidorm, Alicante, Spain.
Radiotherapy Department, Fundación IVO Valencia, València, Spain.
J Contemp Brachytherapy. 2021 Apr;13(2):135-144. doi: 10.5114/jcb.2021.105280. Epub 2021 Apr 14.
To compare brachytherapy (BT) boost of low-dose-rate (LDR) and high-dose-rate (HDR) techniques in patients diagnosed with intermediate-risk prostate cancer.
Between January 2005 and February 2018, 142 patients (50 LDR and 92 HDR) with intermediate-risk prostate cancer were treated with a BT boost, and retrospectively analyzed. Prescribed dose was 45 Gy with external beam radiotherapy (EBRT) plus 100-108 Gy with LDR-BT, and 60 Gy with EBRT plus one fraction of 10 Gy with HDR-BT. 99% of patients received androgen deprivation therapy (ADT) for 6 months. Primary endpoint was to compare LDR and HDR boosts in terms of biochemical progression-free survival (bPFS). Secondary endpoint, after re-classifying patients into "favorable" and "unfavorable" sub-groups, was to analyze differences with a similar treatment intensity.
Median overall follow-up for the total cohort was 66.5 months (range, 16-185 months). There were no significant differences in bPFS, overall survival, cause specific survival, local failure, lymph node failure, or distant failure when LDR or HDR was employed. bPFS at 90 months was 100% for favorable, and 89% and 85% for unfavorable patients at 60 months and 90 months, respectively (log-rank test, = 0.017). The crude incidence of genitourinary acute and chronic toxicity grade 3 was 0.7% and 4%, respectively. Twelve patients (8%) had chronic rectal hemorrhage grade 2, in whom argon was applied (4 LDR and 8 HDR).
Combined treatment is an excellent therapeutic option in patients with intermediate-risk prostate carcinoma, with similar results in both LDR and HDR approaches and very low toxicities. Importantly, the current literature has indicated that unfavorable-risk patients belong to a different category, and should be treated as patients with high-risk factors. Therefore, the stratification and identification of both risk groups is extremely relevant.
比较低剂量率(LDR)和高剂量率(HDR)近距离放射治疗(BT)对中度风险前列腺癌患者的增敏效果。
回顾性分析2005年1月至2018年2月间接受BT增敏治疗的142例中度风险前列腺癌患者(50例LDR和92例HDR)。外照射放疗(EBRT)的处方剂量为45 Gy,LDR-BT为100 - 108 Gy,EBRT为60 Gy加HDR-BT单剂量10 Gy。99%的患者接受了6个月的雄激素剥夺治疗(ADT)。主要终点是比较LDR和HDR增敏在生化无进展生存期(bPFS)方面的差异。次要终点是将患者重新分类为“有利”和“不利”亚组后,分析相似治疗强度下的差异。
整个队列的中位总随访时间为66.5个月(范围16 - 185个月)。采用LDR或HDR时,bPFS、总生存期、病因特异性生存期、局部失败、淋巴结失败或远处失败均无显著差异。有利患者90个月时的bPFS为100%,不利患者60个月和90个月时分别为89%和85%(对数秩检验,P = 0.017)。泌尿生殖系统急性和慢性3级毒性的粗发生率分别为0.7%和4%。12例患者(8%)出现2级慢性直肠出血,其中4例LDR和8例HDR患者接受了氩气治疗。
联合治疗是中度风险前列腺癌患者的一种优秀治疗选择,LDR和HDR方法效果相似且毒性极低。重要的是,目前的文献表明,不利风险患者属于不同类别,应作为高危因素患者进行治疗。因此,对这两个风险组的分层和识别极为重要。