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首页> 外文期刊>Journal of Contemporary Brachytherapy >Focal low-dose-rate prostate brachytherapy for low- and intermediate-risk prostate cancer
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Focal low-dose-rate prostate brachytherapy for low- and intermediate-risk prostate cancer

机译:局灶性低剂量率前列腺脱落放疗,用于低和中等风险前列腺癌

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Purpose To prospectively investigate the efficacy and feasibility of focal low-dose-rate (LDR) prostate brachytherapy for low- and intermediate-risk prostate cancer. Material and methods Between October 2014 and May 2019, nineteen low- and intermediate-risk prostate cancer patients who presented with abnormality on both diffusion-weighted and T2-weighted magnetic resonance imaging (MRI) underwent focal LDR brachytherapy at our institution. Focal gross tumor volume (F-GTV) was delineated on transrectal ultrasound, based on abnormality seen on fused T2-weighted MRI. F-GTV was expanded by 5 mm, as a safety margin, to create focal clinical target volume (F-CTV). Prescribed dose to F-CTV was 145 Gy. Biochemical recurrence (BCR) was determined using Phoenix criterion (prostate specific antigen nadir 2 ng/ml). Pre- and post-implant dosimetry data were compared using non-parametric Wilcoxon’s rank sum test. Treatment-related toxicities were evaluated using common terminology criteria for adverse events. Results Mean F-CTV D 90% was significantly lower in the post-implant evaluation than in intraoperative planning (p = 0.004). On post-implant dosimetry, the mean D 90% for F-GTV and mean V100% for the entire prostate were 222 Gy and 35%, respectively. Median follow-up time for all patients was 31 months. BCR occurred in one patient after 23 months. Kaplan-Meier 2-year BCR-free rate was 92.9% (95% confidence interval [CI]: 79.4-100%). No patients had grade 1 or greater gastrointestinal toxicity. Three patients who were taking ?-blockers to treat benign prostatic hyperplasia (present before brachytherapy), experienced no treatment-related genitourinary toxicities. Two patients suffered from temporary grade 2 urinary frequency. None of the remaining patients experienced grade 2 or higher genitourinary toxicity. Conclusions Focal LDR prostate brachytherapy appears acceptable for MRI-based index tumors, with a low cumulative incidence of BCR. Such brachytherapy might offer a feasible minimally invasive therapeutic option for localized prostate cancer.
机译:目的要预期探讨局灶性低剂量率(LDR)前列腺近级术治疗的疗效和可行性,用于低和中等风险前列腺癌。 2014年10月至2019年5月的材料和方法,19个低于和中间风险的前列腺癌患者,其在漫反应和T2加权磁共振成像(MRI)接受局灶性LDR近距离放射治疗的异常。基于熔融T2加权MRI的异常,局灶性肿瘤体积(F-GTV)在癌症超声中描绘。 F-GTV以5毫米为安全裕度扩展,以产生局灶性临床目标体积(F-CTV)。对F-CTV的规定剂量为145 Gy。使用凤凰标准(前列腺特异性抗原Nadir 2ng / ml)测定生物化学复发(BCR)。使用非参数威尔科逊度的秩和比较比较和植入后的剂量测定数据。使用普通术语标准对不良事件进行评估治疗相关的毒性。结果在植入后评价中,F-CTV D 90%显着较低,而不是术中规划(P = 0.004)。在植入后剂量测定中,F-GTV的平均值90%,整个前列腺的平均V100%分别为222倍,35%。所有患者的中位后续时间为31个月。 BCR在23个月后在一名患者发生。 Kaplan-Meier 2年的BCR-Free率为92.9%(95%置信区间[CI]:79.4-100%)。没有患者的1级或更大的胃肠道毒性。服用的三名患者? - 伯克洛斯治疗良性前列腺增生(在近距离放射治疗之前存在),没有治疗相关的泌尿病毒性。两名患者患有临时2级尿频。剩下的患者均没有经历2级或更高的泌尿族毒性。结论基于MRI的指数肿瘤似乎可接受的焦点LDR前列腺近距离放射治疗,BCR的累积发病率低。这种近距离放射治疗可能为局部前列腺癌提供可行的微创治疗选择。

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