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首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >High-dose-rate brachytherapy as monotherapy delivered in two fractions within one day for favorable/intermediate-risk prostate cancer: Preliminary toxicity data
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High-dose-rate brachytherapy as monotherapy delivered in two fractions within one day for favorable/intermediate-risk prostate cancer: Preliminary toxicity data

机译:高剂量率近距离放射疗法作为单一疗法,可在一天之内分两部分送给有利/中度风险的前列腺癌:初步毒性数据

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摘要

Purpose: To report the toxicity profile of high-dose-rate (HDR)-brachytherapy (BT) as monotherapy in a Human Investigation Committee-approved study consisting of a single implant and two fractions (12 Gy × 2) for a total dose of 24 Gy, delivered within 1 day. The dose was subsequently increased to 27 Gy (13.5 Gy × 2) delivered in 1 day. We report the acute and early chronic genitourinary and gastrointestinal toxicity. Methods and Materials: A total of 173 patients were treated between December 2005 and July 2010. However, only the first 100 were part of the IRB-approved study and out of these, only 94 had a minimal follow-up of 6 months, representing the study population for this preliminary report. All patients had clinical Stage T2b or less (American Joint Committee on Cancer, 5th edition), Gleason score 6-7 (3+4), and prostate-specific antigen level of ≤12 ng/mL. Ultrasound-guided HDR-BT with real-time dosimetry was used. The prescription dose was 24 Gy for the first 50 patients and 27 Gy thereafter. The dosimetric goals and constraints were the same for the two dose groups. Toxicity was scored using the National Cancer Institute Common Terminology Criteria for Adverse Events, version 3. The highest toxicity scores encountered at any point during follow-up are reported. Results: The median follow-up was 17 months (range, 6-40.5). Most patients had Grade 0-1 acute toxicity. The Grade 2 acute genitourinary toxicity was mainly frequency/urgency (13%), dysuria (5%), hematuria, and dribbling/hesitancy (2%). None of the patients required a Foley catheter at any time; however, 8% of the patients experienced transient Grade 1 diarrhea. No other acute gastrointestinal toxicities were found. The most common chronic toxicity was Grade 2 urinary frequency/urgency in 16% of patients followed by dysuria in 4% of patients; 2 patients had Grade 2 rectal bleeding and 1 had Grade 4, requiring laser treatment. Conclusions: Favorable-risk prostate cancer patients treated with a single implant HDR-BT to 24-27 Gy in two fractions within 1 day have excellent tolerance with minimal acute and chronic toxicity. Longer follow-up is needed to confirm these encouraging early results.
机译:目的:在一项由人类研究委员会批准的研究中,报告高剂量率(HDR)-近距离放射疗法(BT)作为单一疗法的毒性概况,该研究包括一个植入物和两个部分(12 Gy×2),总剂量为24 Gy,在1天内交付。随后在1天内将剂量增加至27 Gy(13.5 Gy×2)。我们报告了急性和早期的慢性泌尿生殖系统和胃肠道毒性。方法和材料:2005年12月至2010年7月间共治疗173例患者。但是,只有前100例属于IRB批准的研究,其中只有94例的最低随访时间为6个月,代表此初步报告的研究人群。所有患者的临床分期为T2b或更低(美国癌症联合委员会,第5版),格里森评分为6-7(3 + 4),前列腺特异性抗原水平≤12ng / mL。使用具有实时剂量测定法的超声引导HDR-BT。前50名患者的处方剂量为24 Gy,此后为27 Gy。两个剂量组的剂量学目标和限制条件相同。使用国家癌症研究所不良事件通用术语标准(版本3)对毒性进行评分。据报道,随访期间在任何时候遇到的最高毒性评分。结果:中位随访时间为17个月(范围6-40.5)。大多数患者有0-1级急性毒性。 2级急性泌尿生殖系统毒性主要是频率/尿急(13%),排尿困难(5%),血尿和盘带/粘连性(2%)。没有患者在任何时候都需要Foley导管。但是,有8%的患者经历了短暂的1级腹泻。没有发现其他急性胃肠道毒性。最常见的慢性毒性是16%的患者出现2级尿频/尿急,其次是4%的患者出现排尿困难。 2例有2级直肠出血,1例为4级,需要激光治疗。结论:在一天之内用单一植入物HDR-BT分为24-27 Gy的两个分数治疗的有利风险前列腺癌患者具有优异的耐受性,急性和慢性毒性最小。需要更长的随访时间来确认这些令人鼓舞的早期结果。

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