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Are doses to ICRU reference points valuable for predicting late rectal and bladder morbidity after definitive radiotherapy in uterine cervix cancer?

机译:ICRU参考点的剂量对预测子宫颈明确放疗后直肠和膀胱的晚期发病率是否有价值?

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AIMS AND BACKGROUND: To evaluate whether doses or dose rates at International Commission on Radiation Units (ICRU) reference points are of value for predicting risks of late rectal and bladder morbidity in patients with uterine cervical cancer who have undergone external beam radiotherapy and intracavitary irradiation. METHODS: Late rectal complications and late bladder complications were evaluated in 54 patients who were treated by external beam radiotherapy followed by intracavitary irradiation between January 1996 and December 1999. External beam radiotherapy was delivered in 1.8 Gy daily fractions to a whole pelvis dose of 50.4 Gy followed by intracavitary irradiation at total point A doses ranging from 75 Gy to 85 Gy. Intracavitary irradiation was performed with dose rates of 0.5-0.7 Gy/h to point A in most patients, but 8 patients were treated at a higher dose rate (0.83-1.15 Gy/h) to shorten the hospitalization period. Biologically effective doses for the reference points were calculated using alinear quadratic model. RESULTS: Grade 3 rectal and bladder morbidity by Radiation Therapy Oncology Group (RTOG) criteria developed in 4 patients (7.4%) and 1 (1.9%), respectively. An age of 60 years (P = 0.01) and a total dose to the rectal reference point of or =80 Gy (P = 0.03) were found to be correlated with a higher rate of rectal morbidity. Total dose ( or =80 Gy), dose rate ( or = 0.75 Gy/h), and biologically effective doses ( or =135 Gy3) at the bladder reference point were found to be significant factors for the development of late bladder morbidity. By multivariate analysis, age was identified as the only significant factor of late rectal complications, and biologically effective doses at the bladder reference point was the only significant factor of late bladder complications. CONCLUSIONS: RTOG grade 3 late rectal and bladder morbidity developed in respectively 7.4% and 1.9% of the patients. The significant risk factors for late rectal and bladder morbidity were old age and biologically effective doses at the bladder reference point, respectively.
机译:目的和背景:评估国际辐射单位委员会(ICRU)参考点的剂量或剂量率是否对预测接受外照射和腔内照射的宫颈癌患者晚期直肠和膀胱疾病的风险具有参考价值。方法:1996年1月至1999年12月,对54例接受外束放疗并腔内照射的患者的直肠晚期并发症和膀胱晚期并发症进行了评估。每天1.8 Gy的剂量进行外束放射治疗,总骨盆剂量为50.4 Gy然后在总点A剂量范围从75 Gy至85 Gy进行腔内照射。在大多数患者中,以0.5-0.7 Gy / h的剂量率对A点进行腔内照射,但以更高的剂量率(0.83-1.15 Gy / h)治疗了8例患者,以缩短住院时间。使用线性二次模型计算参考点的生物有效剂量。结果:根据放射治疗肿瘤学组(RTOG)的标准,分别有4例(7.4%)和1例(1.9%)的3级直肠和膀胱发病。发现年龄大于60岁(P = 0.01),并且直肠参考点的总剂量大于或等于80 Gy(P = 0.03)与较高的直肠发病率相关。发现总剂量(>或= 80 Gy),剂量率(>或= 0.75 Gy / h)和在膀胱参考点的生物学有效剂量(>或= 135 Gy3)是晚期膀胱发育的重要因素发病率。通过多变量分析,年龄被确定为直肠晚期并发症的唯一重要因素,而在膀胱参考点的生物学有效剂量是膀胱晚期并发症的唯一重要因素。结论:RTOG 3级晚期直肠和膀胱发病率分别为7.4%和1.9%。直肠和膀胱疾病晚期的重要危险因素分别是老年和膀胱参考点的生物学有效剂量。

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