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Megavoltage cone beam CT near surface dose measurements: potential implications for breast radiotherapy.

机译:兆伏锥束CT近表面剂量测量:对乳房放射治疗的潜在影响。

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PURPOSE: Cone beam computed tomography (CBCT) is fast becoming standard on modern linear accelerators. CBCT increases the dose to regions within and outside the treatment field, potentially increasing secondary cancer induction and toxicity. This study quantified megavoltage (MV) CBCT skin dose and compared it to skin dose delivered during standard tangential breast radiotherapy. METHOD: Dosimetry was performed both in- and out-of-field using thermoluminescent dosimeters (TLDs) and a metal-oxide-semiconductor-field-effect-transistor (MOSFET) detector specifically designed for skin dosimetry; these were placed superficially on a female anthropomorphic phantom. RESULTS: The skin dose from a single treatment fraction ranged from 0.5 to 1.4 Gy on the ipsilateral breast, 0.031-0.18 Gy on the contralateral breast, and 0-0.02 Gy in the head and pelvic region. An 8 MU MV CBCT delivered a skin dose that ranged from 0.02 to 0.05 Gy in the chest region and was less than 0.01 Gy in the head and pelvis regions. One MV CBCT per fraction was found to increase the out-of-field skin dose from both the CBCT and the treatment fields by approximately 20%. The imaging dose as a percentage of treatment doses in the ipsilateral breast region was 3% for both dosimeters. CONCLUSION: Imaging increases the skin dose to regions outside the treatment field particularly regions immediately adjacent the target volume. This small extra dose to the breasts should be considered when developing clinical protocols and assessing dose for clinical trials.
机译:目的:锥束计算机断层扫描(CBCT)正在迅速成为现代线性加速器的标准配置。 CBCT增加了治疗区域内外的剂量,可能会增加继发性癌症的诱导和毒性。这项研究量化了兆伏(MV)CBCT皮肤剂量,并将其与标准切线乳房放射治疗期间递送的皮肤剂量进行了比较。方法:使用热发光剂量计(TLD)和专为皮肤剂量学设计的金属氧化物半导体场效应晶体管(MOSFET)检测器在场内和场外进行剂量测定;这些被放置在女性拟人化模型的表面上。结果:单次治疗的皮肤剂量在同侧乳房上为0.5至1.4 Gy,对侧乳房为0.031-0.18 Gy,在头部和骨盆区域为0-0.02 Gy。 8 MU MV CBCT在胸部区域的皮肤剂量范围为0.02至0.05 Gy,而在头部和骨盆区域的皮肤剂量小于0.01 Gy。发现每级分一个MV CBCT可使CBCT和治疗场的野外皮肤剂量增加约20%。对于两个剂量计,在同侧乳房区域中成像剂量占治疗剂量的百分比为3%。结论:成像增加了皮肤剂量到治疗区域之外的区域,特别是紧邻目标体积的区域。在制定临床方案并评估临床试验剂量时,应考虑给乳房带来的少量额外剂量。

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