全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Comparison of User-Directed and Automatic Mapping of the Planned Isocenter to Treatment Space for Prostate IGRT

DOI: 10.1155/2013/892152

Full-Text   Cite this paper   Add to My Lib

Abstract:

Image-guided radiotherapy (IGRT), adaptive radiotherapy (ART), and online reoptimization rely on accurate mapping of the radiation beam isocenter(s) from planning to treatment space. This mapping involves rigid and/or nonrigid registration of planning (pCT) and intratreatment (tCT) CT images. The purpose of this study was to retrospectively compare a fully automatic approach, including a non-rigid step, against a user-directed rigid method implemented in a clinical IGRT protocol for prostate cancer. Isocenters resulting from automatic and clinical mappings were compared to reference isocenters carefully determined in each tCT. Comparison was based on displacements from the reference isocenters and prostate dose-volume histograms (DVHs). Ten patients with a total of 243?tCTs were investigated. Fully automatic registration was found to be as accurate as the clinical protocol but more precise for all patients. The average of the unsigned and offsets and the standard deviations (σ) of the signed offsets computed over all images were (avg. ±??σ?(mm)): 1.1 ± 1.4, 1.8 ± 2.3, 2.5 ± 3.5 for the clinical protocol and 0.6 ± 0.8, 1.1 ± 1.5 and 1.1 ± 1.4 for the automatic method. No failures or outliers from automatic mapping were observed, while 8 outliers occurred for the clinical protocol. 1. Introduction Image-guided radiotherapy (IGRT) [1], off-line adaptive radiotherapy (ART) [2], and online reoptimization [3] involve pretreatment imaging, taken here to be CT imaging. A procedure held in common by all three methods is registration of the planning (pCT) and treatment (tCT) images to map the planned isocenter to treatment space. Accuracy and precision of this step are important for delivering an accumulated dose distribution that closely matches the treatment plan. Mapping methods involve at least rigid registration. Ideally a nonrigid step would be included to account for differences in organ shape between planning and treatment times (Figure 1). The composite of the rigid, and possibly nonrigid, matrices is then used to map the planned isocenter to the tCT. Figure 1: (a) Axial slice from the pCT showing planning prostate (white) and isocenter (black). (b) Corresponding slice from the tCT showing the prostate (black) segmented by automatic nonrigid model deformation. The rigidly mapped isocenter comes from translating the planning prostate (dim white) to the tCT. The nonrigidly mapped isocenter comes from applying the deformation matrix resulting from autosegmentation to the planned isocenter. Quantitative evaluation of isocenter mapping methods is muddled by

References

[1]  W. Y. Song, B. Schaly, G. Bauman, J. J. Battista, and J. van Dyk, “Evaluation of image-guided radiation therapy (IGRT) technologies and their impact on the outcomes of hypofractionated prostate cancer treatments: a radiobiologic analysis,” International Journal of Radiation Oncology, Biology, Physics, vol. 64, no. 1, pp. 289–300, 2006.
[2]  D. Yan, D. Lockman, D. Brabbins, L. Tyburski, and A. Martinez, “An off-line strategy for constructing a patient-specific planning target volume in adaptive treatment process for prostate cancer,” International Journal of Radiation Oncology Biology Physics, vol. 48, no. 1, pp. 289–302, 2000.
[3]  D. Schulze, J. Liang, D. Yan, and T. Zhang, “Comparison of various online IGRT strategies: the benefits of online treatment plan re-optimization,” Radiotherapy and Oncology, vol. 90, no. 3, pp. 367–376, 2009.
[4]  P. Jannin, J. M. Fitzpatrick, D. J. Hawkes, X. Pennec, R. Shahidi, and M. W. Vannier, “Validation of medical image processing in image-guided therapy,” IEEE Transactions on Medical Imaging, vol. 21, no. 12, pp. 1445–1449, 2002.
[5]  J. R. Wong, Z. Gao, M. Uematsu et al., “Interfractional prostate shifts: review of 1870 computed tomography (CT) scans obtained during image-guided radiotherapy using CT-on-rails for the treatment of prostate cancer,” International Journal of Radiation Oncology, Biology, Physics, vol. 72, no. 5, pp. 1396–1401, 2008.
[6]  E. G. A. Aird and J. Conway, “CT simulation for radiotherapy treatment planning,” British Journal of Radiology, vol. 75, no. 900, pp. 937–949, 2002.
[7]  S. Sailer, E. L. Chaney, J. G. Rosenman, G. W. Sherouse, and J. E. Tepper, “Three dimensional treatment planning at the University of North Carolina at Chapel Hill,” Seminars in Radiation Oncology, vol. 2, pp. 267–273, 1992.
[8]  S. X. Chang, T. J. Cullip, J. G. Rosenman, P. H. Halvorsen, and J. E. Tepper, “Dose optimization via index-dose gradient minimization,” Medical Physics, vol. 29, no. 6, pp. 1130–1146, 2002.
[9]  S. M. Pizer, P. T. Fletcher, S. Joshi et al., “A method and software for segmentation of anatomic object ensembles by deformable m-reps,” Medical Physics, vol. 32, no. 5, pp. 1335–1345, 2005.
[10]  S. M. Pizer, R. E. Broadhurst, J. Y. Jeong et al., “Intra-patient anatomic statistical models for adaptive radiotherapy,” in Proceedings of the Medical Image Computing and Computer-Assisted Intervention Workshop (MICCAI '06), A. Frangi and H. Delingette, Eds., pp. 43–46, Copenhagen, Denmark, October 2006, From Statistical Atlases to Personalized Models: Understanding Complex Diseases in Populations and Individuals.
[11]  D. Merck, G. Tracton, R. Saboo et al., “Training models of anatomic shape variability,” Medical Physics, vol. 35, no. 8, pp. 3584–3596, 2008.
[12]  L. E. Court and L. Dong, “Automatic registration of the prostate for computed-tomography-guided radiotherapy,” Medical Physics, vol. 30, no. 10, pp. 2750–2757, 2003.
[13]  M. Smitsmans, J. Wolthaus, X. Artignan et al., “Automatic localization of the prostate for on-line or off-line image-guided radiotherapy,” International Journal of Radiation Oncology, Biology, Physics, vol. 60, no. 2, pp. 623–635, 2004.
[14]  F. Maes, D. Vandermeulen, and P. Suetens, “Comparative evaluation of multiresolution optimization strategies for multimodality image registration by maximization of mutual information,” Medical Image Analysis, vol. 3, no. 4, pp. 373–386, 1999.
[15]  K. Siddiqi and S. Pizer, Eds., Medial Representations: Mathematics, Algorithms and Applications, vol. 37, chapter 8, Springer, Berlin, Germany, 2008.
[16]  M. J. Murphy, F. J. Salguero, J. V. Siebers, D. Staub, and C. Vaman, “A method to estimate the effect of deformable image registration uncertainties on daily dose mapping,” Medical Physics, vol. 39, no. 2, pp. 573–580, 2012.
[17]  R. E. Broadhurst, J. Stough, S. M. Pizer, and E. L. Chaney, “A statistical appearance model based on intensity quantiles,” in Proceedings of the 3rd IEEE International Symposium on Biomedical Imaging, pp. 422–425, April 2006.
[18]  S. Frantz, K. Rohr, and H. Stiehl, “Localization of 3D anatomical point landmarks in 3D tomographic images using deformable models. Medical image computing and computer-assisted intervention,” in Medical Image Computing and Computer-Assisted Intervention, vol. 1935 of Lecture Notes in Computer Science, pp. 492–501, 2000.
[19]  A. Niemierko and M. Goitein, “The influence of the size of the grid used for dose calculation on the accuracy of dose estimation,” Medical Physics, vol. 16, no. 2, pp. 239–247, 1989.
[20]  J. F. Dempsey, H. E. Romeijn, J. G. Li, D. A. Low, and J. R. Palta, “A Fourier analysis of the dose grid resolution required for accurate IMRT fluence map optimization,” Medical Physics, vol. 32, no. 2, pp. 380–388, 2005.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133