Monte Carlo role in radiobiological modelling of radiotherapy outcomes

被引:76
作者
El Naqa, Issam [1 ]
Pater, Piotr [1 ]
Seuntjens, Jan [1 ]
机构
[1] McGill Univ, Dept Oncol, Med Phys Unit, Montreal, PQ, Canada
关键词
TUMOR-CONTROL PROBABILITY; SYSTEMS RADIATION BIOLOGY; NORMAL TISSUE-RESPONSE; TRACK STRUCTURE CODE; DOSE-VOLUME; LUNG-CANCER; DNA-DAMAGE; ACCELERATED REPOPULATION; ACUTE ESOPHAGITIS; ELECTRON TRACKS;
D O I
10.1088/0031-9155/57/11/R75
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Radiobiological models are essential components of modern radiotherapy. They are increasingly applied to optimize and evaluate the quality of different treatment planning modalities. They are frequently used in designing new radiotherapy clinical trials by estimating the expected therapeutic ratio of new protocols. In radiobiology, the therapeutic ratio is estimated from the expected gain in tumour control probability (TCP) to the risk of normal tissue complication probability (NTCP). However, estimates of TCP/NTCP are currently based on the deterministic and simplistic linear-quadratic formalism with limited prediction power when applied prospectively. Given the complex and stochastic nature of the physical, chemical and biological interactions associated with spatial and temporal radiation induced effects in living tissues, it is conjectured that methods based on Monte Carlo (MC) analysis may provide better estimates of TCP/NTCP for radiotherapy treatment planning and trial design. Indeed, over the past few decades, methods based on MC have demonstrated superior performance for accurate simulation of radiation transport, tumour growth and particle track structures; however, successful application of modelling radiobiological response and outcomes in radiotherapy is still hampered with several challenges. In this review, we provide an overview of some of the main techniques used in radiobiological modelling for radiotherapy, with focus on the MC role as a promising computational vehicle. We highlight the current challenges, issues and future potentials of the MC approach towards a comprehensive systems-based framework in radiobiological modelling for radiotherapy.
引用
收藏
页码:R75 / R97
页数:23
相关论文
共 125 条
[51]   Stochastic Simulation of DNA Double-Strand Break Repair by Non-homologous End Joining Based on Track Structure Calculations [J].
Friedland, Werner ;
Jacob, Peter ;
Kundrat, Pavel .
RADIATION RESEARCH, 2010, 173 (05) :677-688
[52]   Study of prognostic predictors for non-small cell lung cancer [J].
Fu, XL ;
Zhu, XZ ;
Shi, DR ;
Xiu, LZ ;
Wang, LJ ;
Zhao, S ;
Qian, H ;
Lu, HF ;
Xiang, YB ;
Jiang, GL .
LUNG CANCER, 1999, 23 (02) :143-152
[53]  
Giaccia, 2006, RADIOBIOLOGY RADIOLO, VVol 6
[54]   INITIAL EVENTS IN THE CELLULAR EFFECTS OF IONIZING-RADIATIONS - CLUSTERED DAMAGE IN DNA [J].
GOODHEAD, DT .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1994, 65 (01) :7-17
[55]   Prediction of normal tissue response and individualization of doses in radiotherapy [J].
Guirado, D ;
de Almodóvar, JMR .
PHYSICS IN MEDICINE AND BIOLOGY, 2003, 48 (19) :3213-3223
[56]   Use of artificial neural networks to predict biological outcomes for patients receiving radical radiotherapy of the prostate [J].
Gulliford, SL ;
Webb, S ;
Rowbottom, CG ;
Corne, DW ;
Dearnaley, DP .
RADIOTHERAPY AND ONCOLOGY, 2004, 71 (01) :3-12
[57]  
Hall E.J., 2018, Radiobiology for the Radiologist, V8th ed.
[58]  
Halperin EC, 2008, PEREZ BRADYS PRINCIP
[59]   Monte Carlo radiotherapy simulations of accelerated repopulation and reoxygenation for hypoxic head and neck cancer [J].
Harriss-Phillips, W. M. ;
Bezak, E. ;
Yeoh, E. K. .
BRITISH JOURNAL OF RADIOLOGY, 2011, 84 (1006) :903-918
[60]   Clinical, dosimetric, and location-related factors to predict local control in non-small cell lung cancer [J].
Hope, AJ ;
Lindsay, PE ;
El Naqa, I ;
Bradley, JD ;
Vivic, M ;
Deasy, JO .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2005, 63 (02) :S231-S231