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首页> 外文期刊>Radiotherapy and oncology: Journal of the European Society for Therapeutic Radiology and Oncology >Applicability of the linear-quadratic formalism for modeling local tumor control probability in high dose per fraction stereotactic body radiotherapy for early stage non-small cell lung cancer
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Applicability of the linear-quadratic formalism for modeling local tumor control probability in high dose per fraction stereotactic body radiotherapy for early stage non-small cell lung cancer

机译:线性二次方程式在早期非小细胞肺癌高剂量每级立体定向放疗中模拟局部肿瘤控制概率的适用性

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摘要

Background and purpose To compare the linear-quadratic (LQ) and the LQ-L formalism (linear cell survival curve beyond a threshold dose dT) for modeling local tumor control probability (TCP) in stereotactic body radiotherapy (SBRT) for stage I non-small cell lung cancer (NSCLC). Materials and methods This study is based on 395 patients from 13 German and Austrian centers treated with SBRT for stage I NSCLC. The median number of SBRT fractions was 3 (range 1-8) and median single fraction dose was 12.5 Gy (2.9-33 Gy); dose was prescribed to the median 65% PTV encompassing isodose (60-100%). Assuming an α/β-value of 10 Gy, we modeled TCP as a sigmoid-shaped function of the biologically effective dose (BED). Models were compared using maximum likelihood ratio tests as well as Bayes factors (BFs). Results There was strong evidence for a dose-response relationship in the total patient cohort (BFs 20), which was lacking in single-fraction SBRT (BFs 3). Using the PTV encompassing dose or maximum (isocentric) dose, our data indicated a LQ-L transition dose (dT) at 11 Gy (68% CI 8-14 Gy) or 22 Gy (14-42 Gy), respectively. However, the fit of the LQ-L models was not significantly better than a fit without the dT parameter (p = 0.07, BF = 2.1 and p = 0.86, BF = 0.8, respectively). Generally, isocentric doses resulted in much better dose-response relationships than PTV encompassing doses (BFs 20). Conclusion Our data suggest accurate modeling of local tumor control in fractionated SBRT for stage I NSCLC with the traditional LQ formalism.
机译:背景与目的为了比较I阶段非立体定向放疗(SBRT)中的局部肿瘤控制概率(TCP),比较线性二次方程式(LQ)和LQ-L形式主义(线性细胞存活曲线超过阈值剂量dT)。小细胞肺癌(NSCLC)。材料和方法本研究基于来自13个德国和奥地利中心的395例接受SBRT治疗的I期非小细胞肺癌患者。 SBRT分数的中位数为3(范围为1-8),单分数的中位数为12.5 Gy(2.9-33 Gy);处方剂量应设定为中位数65%的PTV,包括等剂量(60-100%)。假设α/β值为10 Gy,我们将TCP建模为生物有效剂量(BED)的S形函数。使用最大似然比检验以及贝叶斯因子(BF)比较了模型。结果有强有力的证据表明整个患者队列(BFs> 20)中存在剂量反应关系,而单次SBRT(BFs <3)则缺乏。使用包含剂量或最大(等中心点)剂量的PTV,我们的数据表明LQ-L过渡剂量(dT)分别为11 Gy(68%CI 8-14 Gy)或22 Gy(14-42 Gy)。但是,LQ-L模型的拟合并不比没有dT参数的拟合好得多(分别为p = 0.07,BF = 2.1和p = 0.86,BF = 0.8)。通常,等中心剂量比PTV包含剂量(BF> 20)产生更好的剂量反应关系。结论我们的数据表明,采用传统的LQ形式对I期NSCLC分级SBRT中局部肿瘤控制进行准确建模。

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