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First report of transperineal polyethylene glycol hydrogel spacer use to curtail rectal radiation dose after permanent iodine-125 prostate brachytherapy

机译:永久性碘125前列腺近距离放射治疗后使用会阴聚乙二醇水凝胶垫片来减少直肠放射剂量的首次报道

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Purpose: To demonstrate the feasibility of transperineal polyethylene glycol (PEG) hydrogel insertion into anterior perirectal fat for reducing rectal radiation dose in patients with suboptimal rectal dosimetry after permanent iodine-125 prostate brachytherapy. Methods and Materials: Five patients with suboptimal rectal dosimetry after iodine-125 seed brachytherapy implant underwent a single transperineal injection of PEG hydrogel into the anterior perirectal fat under general anesthetic using transrectal ultrasound guidance. Prostate-rectum separation and rectal radiation dose before and after PEG hydrogel spacer insertion were measured. Toxicity because of spacer insertion was assessed at Days 0-1 and 4-6 weeks using National Cancer Institute Common Terminology Criteria for Adverse Events version 4.0. Results: All patients experienced a clinically significant reduction in the volume of rectum receiving greater than or equal to the prescription dose (RV100) on the postspacer postimplant dosimetry, compared with the prespacer postimplant dosimetry. Mean prostate-rectum separation that was achieved with the insertion of the spacer was 15.1 mm (±3.4). The mean difference in separation from before to after spacer insertion was 12.5 mm (±4.5). This was associated with a reduction in mean RV100 from 3.04 (±1.2) to 0.06 (±0.1) cc. Toxicities were limited to Grade 1 (National Cancer Institute Common Terminology Criteria for Adverse Events version 4.0) perineal pain and rectal discomfort (3/5 patients). There were no Grade 2 or greater toxicities reported after insertion of the spacer. Conclusions: PEG hydrogel is safe and effective at reducing rectal radiation dose in select patients with suboptimal rectal dosimetry after prostate seed brachytherapy.
机译:目的:证明在永久性碘125前列腺近距离放射治疗后,直肠剂量不理想的患者中,经直肠会阴聚乙二醇(PEG)水凝胶插入直肠前直肠脂肪中以减少直肠放射剂量的可行性。方法和材料:五名碘125粒子近距离放射治疗植入物后直肠剂量不足的患者,在全麻下行经直肠超声引导下,经会阴将PEG水凝胶单次经会阴注入PEG前凝胶。测量了插入PEG水凝胶垫片之前和之后的直肠-直肠分离和直肠放射剂量。使用美国国家癌症研究所不良事件通用术语标准4.0版在0-1天和4-6周评估由于间隔物插入引起的毒性。结果:与前间隔物后植入物剂量测定法相比,所有患者在植入后间隔物剂量测定法上接受大于或等于处方剂量(RV100)的直肠体积均有临床显着减少。插入垫片可实现的平均前列腺直肠直肠分离为15.1 mm(±3.4)。垫片插入之前与之后的平均分离距离为12.5 mm(±4.5)。这与平均RV100从3.04(±1.2)cc降低到0.06(±0.1)cc有关。毒性仅限于1级(国家癌症研究所不良事件通用术语标准,版本4.0)会阴部疼痛和直肠不适(3/5例)。插入间隔物后没有报告2级或更高的毒性。结论:PEG水凝胶可安全有效地降低前列腺种子近距离放射治疗后部分直肠剂量不足的部分患者的直肠放射剂量。

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