Accelerated prompt gamma estimation for clinical proton therapy simulations

被引:13
|
作者
Huisman, Brent F. B. [1 ,2 ]
Letang, J. M. [1 ]
Testa, E. [2 ]
Sarrut, D. [1 ]
机构
[1] Univ Lyon 1, CREATIS, INSERM, CNRS,UMR5220,INSA Lyon,Ctr Leon Berard,U1206, Lyon, France
[2] Univ Lyon 1, IPNL, CNRS, IN2P3,UMR5822, Lyon, France
来源
PHYSICS IN MEDICINE AND BIOLOGY | 2016年 / 61卷 / 21期
关键词
prompt gamma; proton therapy; Monte Carlo; variance reduction techniques; RANGE VERIFICATION; RAY EMISSION; SLIT CAMERA; PET; DISTRIBUTIONS; PATIENT;
D O I
10.1088/0031-9155/61/21/7725
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
There is interest in the particle therapy community in using prompt gammas (PGs), a natural byproduct of particle treatment, for range verification and eventually dose control. However, PG production is a rare process and therefore estimation of PGs exiting a patient during a proton treatment plan executed by a Monte Carlo (MC) simulation converges slowly. Recently, different approaches to accelerating the estimation of PG yield have been presented. Sterpin et al (2015 Phys. Med. Biol. 60 4915-46) described a fast analytic method, which is still sensitive to heterogeneities. El Kanawati et al (2015 Phys. Med. Biol. 60 8067-86) described a variance reduction method (pgTLE) that accelerates the PG estimation by precomputing PG production probabilities as a function of energy and target materials, but has as a drawback that the proposed method is limited to analytical phantoms. We present a two-stage variance reduction method, named voxelized pgTLE (vpgTLE), that extends pgTLE to voxelized volumes. As a preliminary step, PG production probabilities are precomputed once and stored in a database. In stage 1, we simulate the interactions between the treatment plan and the patient CT with low statistic MC to obtain the spatial and spectral distribution of the PGs. As primary particles are propagated throughout the patient CT, the PG yields are computed in each voxel from the initial database, as a function of the current energy of the primary, the material in the voxel and the step length. The result is a voxelized image of PG yield, normalized to a single primary. The second stage uses this intermediate PG image as a source to generate and propagate the number of PGs throughout the rest of the scene geometry, e.g. into a detection device, corresponding to the number of primaries desired. We achieved a gain of around 10(3) for both a geometrical heterogeneous phantom and a complete patient CT treatment plan with respect to analog MC, at a convergence level of 2% relative uncertainty in the 90% yield region. The method agrees with reference analog MC simulations to within 10(-4), with negligible bias. Gains per voxel range from 10(2) to 10(4). The presented generic PG yield estimator is drop-in usable with any geometry and beam configuration. We showed a gain of three orders of magnitude compared to analog MC. With a large number of voxels and materials, memory consumption may be a concern and we discuss the consequences and possible tradeoffs. The method is available as part of Gate 7.2.
引用
收藏
页码:7725 / 7743
页数:19
相关论文
共 50 条
  • [1] Accelerated Prompt Gamma estimation for clinical Proton Therapy simulations
    Huisman, B. F. B.
    Letang, J. M.
    Testa, E.
    Sarrut, D.
    RADIOTHERAPY AND ONCOLOGY, 2016, 118 : S51 - S51
  • [2] Feasibility of Proton Range Estimation with Prompt Gamma Imaging in Proton Therapy of Lung Cancer: Monte Carlo Study
    Rohollahpour, Elham
    Ahangari, Hadi Taleshi
    JOURNAL OF MEDICAL PHYSICS, 2024, 49 (04) : 531 - 538
  • [3] Reducing the risk of proton therapy with prompt-gamma
    Patuleia Venancio, Jose Miguel
    PARTICLES AND NUCLEI INTERNATIONAL CONFERENCE 2021, PANIC2021, 2021,
  • [4] Prompt gamma detection for range verification in proton therapy
    Kurosawa, Shunsuke
    Kubo, Hidetoshi
    Ueno, Kazuki
    Kabuki, Shigeto
    Iwaki, Satoru
    Takahashi, Michiaki
    Taniue, Kojiro
    Higashi, Naoki
    Miuchi, Kentaro
    Tanimori, Toru
    Kim, Dogyun
    Kim, Jongwon
    CURRENT APPLIED PHYSICS, 2012, 12 (02) : 364 - 368
  • [5] Experimentally Optimizing Prompt Gamma Detection for Proton Therapy
    Moteabbed, M.
    Binns, P.
    Flanz, J.
    Paganetti, H.
    Riley, K.
    MEDICAL PHYSICS, 2010, 37 (06)
  • [6] Factors influencing the accuracy of beam range estimation in proton therapy using prompt gamma emission
    Janssen, F. M. F. C.
    Landry, G.
    Lopes, P. Cambraia
    Dedes, G.
    Smeets, J.
    Schaart, D. R.
    Parodi, K.
    Verhaegen, F.
    PHYSICS IN MEDICINE AND BIOLOGY, 2014, 59 (15): : 4427 - 4441
  • [7] Towards clinical application: Potential margin reduction in proton therapy with prompt-gamma imaging
    Bertschi, S.
    Berthold, J.
    Pietsch, J.
    Smeets, J.
    Janssens, G.
    Stuetzer, K.
    Richter, C.
    RADIOTHERAPY AND ONCOLOGY, 2023, 182 : S1586 - S1588
  • [8] Prompt Gamma Measurements for the Verification of Dose Deposition in Proton Therapy
    Kim, J.
    Kubo, H.
    Tanimori, T.
    MEDICAL PHYSICS, 2009, 36 (06)
  • [9] The optimization of prompt gamma based range estimation in proton therapy using Cramer-Rao theory
    Lens, E.
    Tolboom, E.
    Schaart, D.
    RADIOTHERAPY AND ONCOLOGY, 2019, 133 : S295 - S296
  • [10] First test of the prompt gamma ray timing method with heterogeneous targets at a clinical proton therapy facility
    Hueso-Gonzalez, Fernando
    Enghardt, Wolfgang
    Fiedler, Fine
    Golnik, Christian
    Janssens, Guillaume
    Petzoldt, Johannes
    Prieels, Damien
    Priegnitz, Marlen
    Roemer, Katja E.
    Smeets, Julien
    Stappen, Francois Vander
    Wagner, Andreas
    Pausch, Guntram
    PHYSICS IN MEDICINE AND BIOLOGY, 2015, 60 (16): : 6247 - 6272