Ultra-low dose rate brachytherapy (uLDR-BT) in treatment of patients with unfavorable intermediate-risk group prostate cancer - retrospective analysis.

IF 1.2 Q4 ONCOLOGY Reports of Practical Oncology and Radiotherapy Pub Date : 2024-12-04 eCollection Date: 2024-01-01 DOI:10.5603/rpor.103135
Adam Kluska, Artur Chyrek, Wojciech Maria Burchardt, Marcin Włodarczyk, Grzegorz Bielęda, Adam Chicheł
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Abstract

Background: Treatment with sole ultra-low dose rate brachytherapy (uLDR-BT) for unfavorable intermediate risk factor (IUR) group prostate cancer patients is not recommended by guidelines due to the lack of strong evidence of its effectiveness. However, there were numerous patients treated with good results with this method in older trials. Purpose of this work was to retrospectively asses effectiveness of uLDR-BT in IUR group treated in our department.

Materials and methods: We performed retrospective analysis of 39 IUR prostate cancer patients treated in our department with uLDR-BT between 2015-2019. All Patients had confirmed prostate cancer in biopsy and had local staging assessed with digital rectal examination and either transrectal ultrasound (TRUS) or magnetic resonance imaging (MRI) before treatment. Treatment was performed using 125I seeds, and the dose prescribed to the clinical target volume was 145 Gy. After treatment, all patients were followed in our outpatient ambulatory one month after the procedure and every 3-6 months later on. Toxicity was assessed using the International Prostate Symptom Score (IPSS) and Radiation Therapy Oncology Group (RTOG) scales.

Results: The median follow-up was 56,3 months [interquartile range (IQR): 36.9-73.4]. The mean nadir prostate-specific antigen (PSA) was 0.20 ng/mL (range 0.001-1.7). The actuarial 5-year biochemical failure-free survival (BFFS) was 87.02%. There was no statistically significant difference in BFFS between groups with antigen deprivation therapy (ADT) and without (p = 0.439). Analysis also showed no impact on BFFS of each intermediate group risk factors: initial PSA (iPSA) (p = 0.595). Gleason (p = 0.671) and Tumor stage (p = 0.694). There were no statistically significant differences in BFFS depending on number of those factors (p = 0.330).

Conclusion: The uLDR-BT may be an effective option for selected IUR prostate cancer patients.

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超低剂量率近距离放疗(uLDR-BT)治疗不良中危组前列腺癌的回顾性分析。
背景:单纯超低剂量率近距离放疗(uLDR-BT)治疗不良中间危险因素(IUR)组前列腺癌患者,由于缺乏其有效性的有力证据,不被指南推荐。然而,在较早的试验中,有许多患者使用这种方法治疗效果良好。本研究的目的是回顾性评估uLDR-BT在我科治疗的IUR组中的效果。材料与方法:回顾性分析2015-2019年在我科应用uLDR-BT治疗的39例IUR前列腺癌患者。所有患者均经活检证实前列腺癌,并在治疗前通过直肠指检和经直肠超声(TRUS)或磁共振成像(MRI)评估局部分期。采用125I粒子治疗,临床靶体积剂量为145 Gy。治疗后,所有患者术后1个月及以后每3-6个月在门诊进行随访。使用国际前列腺症状评分(IPSS)和放射治疗肿瘤组(RTOG)量表评估毒性。结果:中位随访时间为56.3个月[四分位间距(IQR): 36.9-73.4]。平均最低前列腺特异性抗原(PSA)为0.20 ng/mL(范围0.001 ~ 1.7)。精算5年生化无失败生存率(BFFS)为87.02%。抗原剥夺治疗(ADT)组与未进行ADT治疗组的BFFS比较,差异无统计学意义(p = 0.439)。分析还显示,各中间组危险因素对闺蜜的初始PSA (iPSA)无影响(p = 0.595)。Gleason (p = 0.671)和肿瘤分期(p = 0.694)。这些因素的数量对闺蜜的影响没有统计学意义(p = 0.330)。结论:uLDR-BT可能是部分IUR前列腺癌患者的有效选择。
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来源期刊
CiteScore
2.80
自引率
8.30%
发文量
115
审稿时长
16 weeks
期刊介绍: Reports of Practical Oncology and Radiotherapy is an interdisciplinary bimonthly journal, publishing original contributions in clinical oncology and radiotherapy, as well as in radiotherapy physics, techniques and radiotherapy equipment. Reports of Practical Oncology and Radiotherapy is a journal of the Polish Society of Radiation Oncology, the Czech Society of Radiation Oncology, the Hungarian Society for Radiation Oncology, the Slovenian Society for Radiotherapy and Oncology, the Polish Study Group of Head and Neck Cancer, the Guild of Bulgarian Radiotherapists and the Greater Poland Cancer Centre, affiliated with the Spanish Society of Radiotherapy and Oncology, the Italian Association of Radiotherapy and the Portuguese Society of Radiotherapy - Oncology.
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