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Measurement of peripheral dose to the pelvic region and the associated risk for cancer development after breast intraoperative electron radiation therapy

机译:乳腺术中电子放射治疗后骨盆区外周期剂量的测量和癌症发育的相关风险

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This study aimed to measure the received dose to the pelvic region of patients during breast intraoperative electron radiation therapy (IOERT). Furthermore, we compared the findings with those of external beam radiation therapy. Finally, secondary ovarian and uterus cancer risks following breast IOERT were estimated. In the current study, the received dose to the pelvic surface of 18 female patients during breast IOERT boosts were measured by thermo-luminescent dosimeter (TLD-100) chips. All patients were treated with 12 Gy given in a single fraction. To estimate the dose to the ovary and uterus of the patients, conversion coefficients for depth from the surface dose were obtained in a Rando phantom. Given the received dose to the pelvic region of the patients, secondary ovarian and uterus cancer risks following breast IOERT were estimated. The received doses to the ovary and uterus surface of the patients were 0.260 +/- 0.155 mGy to 31.460 +/- 6.020 mGy and 0.485 +/- 0.122 mGy to 22.387 +/- 15.476 mGy, respectively. Corresponding intra-pelvic (ovary and uterus) regional doses were 0.012 +/- 0.007 mGy to 1.479 +/- 0.283 mGy and 0.027 +/- 0.001 mGy to 1.164 +/- 0.805 mGy, respectively. Findings demonstrated that the ratio of the received dose by the pelvic surface to the regional dose during breast IOERT was much less than external beam radiation therapy. The mean of the secondary cancer risks for the ovary in 8 and 10 MeV electron beam energies were 135.722 +/- 117.331 x 10(-6) and 69.958 +/- 28.072 x 10(-6), and for the uterus were 17.342 +/- 10.583 x 10(-6) and 2.971 +/- 3.604 x 10(-6), respectively. According to our findings, the use of breast IOERT in pregnant patients can be considered as a safe radiotherapeutic technique, because the received dose to the fetus was lower than 50 mGy. Furthermore, IOERT can efficiently reduce the unnecessary dose to the pelvic region and lowers the risk of secondary ovarian and uterus cancer following breast irradiation.
机译:本研究旨在在乳房术中电子放射治疗(IOERT)期间测量患者骨盆区域的接受剂量。此外,我们与外部光束放射治疗的结果进行了比较。最后,估计乳腺IOERT后的继发性卵巢和子宫癌症风险。在目前的研究中,通过热发光剂量计(TLD-100)芯片测量乳腺IOERT升压期间18例女性患者骨盆表面的接受剂量。所有患者均在单一级分中含有12种。为了估算患者的卵巢和子宫的剂量,在RANDO Phantom中获得了从表面剂量的深度的转化系数。鉴于患者的骨盆区接受剂量,估计乳腺IOERT后的继发性卵巢和子宫癌风险。患者的卵巢和子宫表面的接受剂量分别为0.260 +/- 0.155 mgy至31.460 +/- 6.020 mgy,分别为0.485 +/- 0.122 mgy至22.387 +/-15.476 mgy。相应的骨盆内(卵巢和子宫)区域剂量分别为0.012 +/- 0.283 MGY和0.027 +/- 0.001 mgy,分别为1.164 +/- 0.805 mgy。结果证明,骨盆表面接受剂量与乳房IOERT期间的区域剂量的比率远低于外部光束放射治疗。 8和10MeV电子束能量为卵巢的二次癌症风险的平均值为135.722 +/- 117.31×10(-6)和69.958 +/- 28.072 x 10(-6),并且对于子宫为17.342 + / - 10.583 x 10(-6)和2.971 +/- 3.604 x 10(-6)。根据我们的研究结果,在怀孕患者中使用乳房IOERT可以被视为一种安全的放射治疗技术,因为胎儿的接受剂量低于50毫米。此外,IOERT可以有效地降低骨盆区域的不必要剂量,并降低乳房照射后继发卵巢和子宫癌症的风险。

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