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线性二次放射生物学模型中参数的敏感性分析

Sensitivity analysis of parameters in linear-quadratic radiobiologic modeling.

作者信息

Fowler Jack F

机构信息

Department of Human Oncology, School of Medicine, University of Wisconsin, Madison, WI, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2009 Apr 1;73(5):1532-7. doi: 10.1016/j.ijrobp.2008.11.039.

Abstract

PURPOSE

Radiobiologic modeling is increasingly used to estimate the effects of altered treatment plans, especially for dose escalation. The present article shows how much the linear-quadratic (LQ) (calculated biologically equivalent dose [BED] varies when individual parameters of the LQ formula are varied by +/-20% and by 1%.

METHODS

Equivalent total doses (EQD2 = normalized total doses (NTD) in 2-Gy fractions for tumor control, acute mucosal reactions, and late complications were calculated using the linear- quadratic formula with overall time: BED = nd (1 + d/ [alpha/beta]) - log(e)2 (T - Tk) / alphaTp, where BED is BED = total dose x relative effectiveness (RE = nd (1 + d/ [alpha/beta]). Each of the five biologic parameters in turn was altered by +/-10%, and the altered EQD2s tabulated; the difference was finally divided by 20. EQD2 or NTD is obtained by dividing BED by the RE for 2-Gy fractions, using the appropriate alpha/beta ratio.

RESULTS

Variations in tumor and acute mucosal EQD ranged from 0.1% to 0.45% per 1% change in each parameter for conventional schedules, the largest variation being caused by overall time. Variations in "late" EQD were 0.4% to 0.6% per 1% change in the only biologic parameter, the alpha/beta ratio. For stereotactic body radiotherapy schedules, variations were larger, up to 0.6 to 0.9 for tumor and 1.6% to 1.9% for late, per 1% change in parameter.

CONCLUSIONS

Robustness occurs similar to that of equivalent uniform dose (EUD), for the same reasons. Total dose, dose per fraction, and dose-rate cause their major effects, as well known.

摘要

目的

放射生物学建模越来越多地用于估计改变治疗计划的效果,尤其是剂量递增的情况。本文展示了当线性二次(LQ)公式的各个参数变化±20%和1%时,计算得到的生物等效剂量(BED)会有多大变化。

方法

使用线性二次公式并结合总时间来计算肿瘤控制、急性黏膜反应和晚期并发症的等效总剂量(EQD2 = 2 Gy分次照射的归一化总剂量(NTD)):BED = nd(1 + d/[α/β]) - log(e)2(T - Tk)/αTp,其中BED = 总剂量×相对生物效应(RE = nd(1 + d/[α/β]))。依次将五个生物学参数中的每一个改变±10%,并将改变后的EQD2制成表格;最后将差值除以20。EQD2或NTD通过使用适当的α/β比值,将BED除以2 Gy分次照射的RE来获得。

结果

对于传统放疗方案,每个参数每变化1%,肿瘤和急性黏膜EQD的变化范围为0.1%至0.45%,其中总时间引起的变化最大。在唯一的生物学参数α/β比值每变化1%时,“晚期”EQD变化为0.4%至0.6%。对于立体定向体部放疗方案,参数每变化1%,肿瘤的变化更大,高达0.6%至0.9%,晚期变化为1.6%至1.9%。

结论

出于相同原因,其稳健性与等效均匀剂量(EUD)相似。总剂量、分次剂量和剂量率如大家所知会产生主要影响。

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