Fang Breanna, McGeachy Philip, Husain Siraj, Meyer Tyler, Thind Kundan, Martell Kevin
Department of Oncology, University of Calgary, Calgary, Alberta, Canada.
Henry Ford Health System, Detroit, Michigan, United States.
J Contemp Brachytherapy. 2024 Apr;16(2):111-120. doi: 10.5114/jcb.2024.139278. Epub 2024 Apr 30.
Isolated intra-prostatic recurrence of prostate adenocarcinoma after definitive radiotherapy presents a challenging clinical scenario. Salvage options require specialized expertise and pose risks of harm. This study aimed to present the acute toxicity results from using salvage high-dose-rate brachytherapy (sHDR-BT) as treatment in locally recurrent prostate cancer cases.
Seventeen consecutive patients treated with sHDR-BT between 2019 and 2022 were evaluated retrospectively. Eligible patients had to have received curative intent prostate radiotherapy previously, and showed evidence of new biochemical failure. Evaluation with American Urological Association (AUA) and Common Terminology Criteria for Adverse Events (CTCAE) symptom assessments were performed for each case.
The median (inter-quartile range) age prior to salvage treatment was 68 (66-74) years. The median post-sHDR-BT follow-up time was 20 (13-24) months. At baseline prior to sHDR-BT, 8 (47%) patients had significant lower urinary tract symptoms. The median AUA score prior to sHDR-BT was 7 (3-18). Three (18%) patients reported irregular bowel function and 2 (12%) reported hematochezia prior to sHDR-BT. One-month post-treatment, the median AUA score was 13 (8-21, = 0.21). Using CTCAE scoring, there were no cases of grade 2+ bowel or rectal toxicity, and no cases of grade 3+ urinary toxicity. Reported grade 2 urinary toxicities included 10 (59%) cases of bladder spasms, 2 (12%) cases of incontinence, 1 (6%) urinary obstruction, and 4 (24%) reports of urinary urgency. All these adverse events were temporary.
This study adds to the existing literature by demonstrating that the acute toxicity profile of sHDR-BT is acceptable even without intra-operative magnetic resonance (MR) guidance or image registration. Further study is ongoing to determine long-term efficacy and toxicity of treatment.
前列腺癌根治性放疗后孤立性前列腺内复发是一种具有挑战性的临床情况。挽救性治疗方案需要专业技能且存在造成伤害的风险。本研究旨在呈现采用挽救性高剂量率近距离放疗(sHDR - BT)治疗局部复发性前列腺癌病例的急性毒性结果。
回顾性评估了2019年至2022年间连续接受sHDR - BT治疗的17例患者。符合条件的患者必须先前接受过根治性前列腺放疗,且有新的生化失败证据。对每个病例进行美国泌尿外科学会(AUA)和不良事件通用术语标准(CTCAE)症状评估。
挽救性治疗前的中位(四分位间距)年龄为68(66 - 74)岁。sHDR - BT后的中位随访时间为20(13 - 24)个月。在sHDR - BT前的基线时,8例(47%)患者有明显的下尿路症状。sHDR - BT前的中位AUA评分为7(3 - 18)。3例(18%)患者报告肠道功能不规则,2例(12%)在sHDR - BT前报告有便血。治疗后1个月,中位AUA评分为13(8 - 21,P = 0.21)。使用CTCAE评分,无2级以上肠道或直肠毒性病例,也无3级以上泌尿毒性病例。报告的2级泌尿毒性包括10例(59%)膀胱痉挛、2例(12%)尿失禁、1例(6%)尿路梗阻和4例(24%)尿急报告。所有这些不良事件都是暂时的。
本研究通过证明即使没有术中磁共振(MR)引导或图像配准,sHDR - BT的急性毒性特征也是可接受的,从而为现有文献增添了内容。正在进行进一步研究以确定治疗的长期疗效和毒性。