Extension of the ML-EM algorithm for dose estimation using PET in proton therapy: application to an inhomogeneous target

被引:5
|
作者
Masuda, Takamitsu [1 ]
Nishio, Teiji [1 ]
Sano, Akira [1 ,2 ]
Karasawa, Kumiko [3 ]
机构
[1] Tokyo Womens Med Univ, Grad Sch Med, Dept Med Phys, Shinjuku Ku, 8-1 Kawadacho, Tokyo 1628666, Japan
[2] Mizuho Informat & Res Inst Inc, Chiyoda Ku, 2-3 Kanda Nishikicho, Tokyo 1018443, Japan
[3] Tokyo Womens Med Univ, Sch Med, Dept Radiat Oncol, Shinjuku Ku, 8-1 Kawadacho, Tokyo 1628666, Japan
来源
PHYSICS IN MEDICINE AND BIOLOGY | 2020年 / 65卷 / 18期
关键词
proton therapy; PET imaging; dose estimation; range verification; filtering; ML-EM algorithm; POSITRON-EMISSION-TOMOGRAPHY; IN-BEAM; IMAGE-RECONSTRUCTION; RING OPENPET; VERIFICATION; DELIVERY; WASHOUT; BODY;
D O I
10.1088/1361-6560/ab98cf
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Positron emission tomography (PET) has been used forin vivotreatment verification, mainly for range verification, in proton therapy. Evaluating the direct dose from PET measurements remains challenging; however, it is highly desirable from a clinical perspective. In this study, a method for estimating the dose distribution from the positron emitter distributions was developed using the maximum likelihood expectation maximization algorithm. The 1D spatial relationship between positron emitter distributions and a dose distribution in an inhomogeneous target was inputted into the system matrix based on a filter framework. In contrast, spatial resolution of the PET system and total variation regularization (as prior knowledge for dose distribution) were considered in the 3D image-space. The dose estimation was demonstrated using Monte Carlo simulated PET activity distributions with substantial noise in a head and neck phantom. This mimicked the single field irradiation of the spread-out Bragg peak beams at clinical dose levels. Besides the simple implementation of the algorithm, this strategy achieved a high-speed calculation (30 s for a 3D dose estimation) and accurate dose and range estimations (less than 10% and 2 mm errors at 1-sigma values, respectively). The proposed method could be key for using PET forin vivodose monitoring.
引用
收藏
页数:15
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