Recent advances in photonic dosimeters for medical radiation therapy
James ARCHER, Enbang LI
Recent advances in photonic dosimeters for medical radiation therapy
Radiation therapy, which uses X-rays to destroy or injure cancer cells, has become one of the most important modalities to treat the primary cancer or advanced cancer. High resolution, water equivalent and passive X-ray dosimeters are highly desirable for developing quality assurance (QA) systems for novel cancer therapy like microbeam radiation therapy (MRT) which is currently under development. Here we present the latest developments of high spatial resolution scintillator based photonic dosimeters, and their applications to clinical external radiation beam therapies: specifically high energy linear accelerator (LINAC) photon beams and low energy synchrotron photon beams. We have developed optical fiber dosimeters with spatial resolutions ranging from 50 to 500 mm and tested them with LINAC beams and synchrotron microbeams. For LINAC beams, the fiber-optic probes were exposed to a 6 MV, 10 cm by 10 cm X-ray field and, the beam profiles as well as the depth dose profiles were measured at a source-to-surface distance (SSD) of 100 cm. We have also demonstrated the possibility for temporally separating Cherenkov light from the pulsed LINAC scintillation signals. Using the 50 mm fiber probes, we have successfully resolved the microstructures of the microbeams generated by the imaging and medical beamline (IMBL) at the Australian Synchrotron and measured the peak-to-valley dose ratios (PVDRs). In this paper, we summarize the results we have achieved so far, and discuss the possible solutions to the issues and challenges we have faced, also highlight the future work to further enhance the performances of the photonic dosimeters.
fiber-optic dosimetry / scintillators / X-ray / Cherenkov radiation / cancer therapy / microbeam radiation therapy (MRT)
[1] |
Leo W R. Techniques for Nuclear and Particle Physics. Berlin Heidelberg: Springer, 1994
|
[2] |
Čerenkov P A. Visible radiation produced by electrons moving in a medium with velocities exceeding that of light. Physical Review, 1937, 52(4): 378–379
CrossRef
Google scholar
|
[3] |
O’Keeffe S, McCarthy D, Woulfe P, Grattan M W D, Hounsell A R, Sporea D, Mihai L, Vata I, Leen G, Lewis E. A review of recent advances in optical fibre sensors for in vivo dosimetry during radiotherapy. The British Journal of Radiology, 2015, 88(1050): 20140702
CrossRef
Pubmed
Google scholar
|
[4] |
Aberle C, Elagin A, Frisch H J, Wetstein M, Winslow L. Measuring directionality in double-beta decay and neutrino interactions with kiloton-scale scintillation detectors. Journal of Instrumentation, 2014, 9: P06012
|
[5] |
Rusby D R, Brenner C M, Armstrong C, Wilson L A, Clarke R, Alejo A, Ahmed H, Butler N M H, Haddock D, Higginson A, McClymont A, Mirfayzi S R, Murphy C, Notley M, Oliver P, Allott R, Hernandez-Gomez C, Kar S, McKenna P, Neely D. Pulsed X-ray imaging of high-density objects using a ten picosecond high-intensity laser driver. In: Proceedings of Emerging Imaging & Sensing Technologies. 2016, 9992: 99920E
|
[6] |
Deas R M, Wilson L A, Rusby D, Alejo A, Allott R, Black P P, Black S E, Borghesi M, Brenner C M, Bryant J, Clarke R J, Collier J C, Edwards B, Foster P, Greenhalgh J, Hernandez-Gomez C, Kar S, Lockley D, Moss R M, Najmudin Z, Pattathil R, Symes D, Whittle M D, Wood J C, McKenna P, Neely D. A laser driven pulsed X-ray backscatter technique for enhanced penetrative imaging. Journal of X-Ray Science and Technology, 2015, 23(6): 791–797
CrossRef
Pubmed
Google scholar
|
[7] |
Beddar A S, Mackie T R, Attix F H. Water-equivalent plastic scintillation detectors for high-energy beam dosimetry: 1. physical characteristics and theoretical considerations. Physics in Medicine & Biology, 1992, 37(10): 1883–1900
|
[8] |
Beddar A S, Mackie T R, Attix F H. Water-equivalent plastic scintillation detectors for high-energy beam dosimetry: 2. properties and measurements. Physics in Medicine & Biology, 1992, 37(10): 1901–1913
|
[9] |
Beaulieu L, Beddar S. Review of plastic and liquid scintillation dosimetry for photon, electron, and proton therapy. Physics in Medicine & Biology, 2016, 61(20): R305
|
[10] |
Shaffer T M, Pratt E C, Grimm J. Utilizing the power of Cerenkov light with nanotechnology. Nature Nanotechnology, 2017, 12(2): 106
|
[11] |
Andreozzi J M, Zhang R, Gladstone D J, Williams B B, Glaser A K, Pogue B W, Jarvis L A. Cherenkov imaging method for rapid optimization of clinical treatment geometry in total skin electron beam therapy. Medical Physics, 2016, 43(2): 993–1002
|
[12] |
Vukolov A V, Novokshonov A I, Potylitsyn A P, Uglov S R. Electron beam diagnostics tool based on Cherenkov radiation in optical fibers. Journal of Physics Conference Series, 2016, 732 (1): 012011
|
[13] |
Boer S F D, Beddar A S, Rawlinson J A. Optical filtering and spectral measurements of radiation-induced light in plastic scintillation dosimetry. Physics in Medicine & Biology, 1993, 38(7): 945–958
|
[14] |
Clift M A, Sutton R A, Webb D V. Dealing with Cerenkov radiation generated in organic scintillator dosimeters by bremsstrahlung beams. Physics in Medicine & Biology, 2000, 45(5): 1165–1182
|
[15] |
Archambault L, Therriault-Proulx F, Beddar S, Beaulieu L. A mathematical formalism for hyperspectral, multipoint plastic scintillation detectors. Physics in Medicine & Biology, 2012, 57 (21): 7133–7145
|
[16] |
Therriault-Proulx F, Archambault L, Beaulieu L, Beddar S. Development of a novel multi-point plastic scintillation detector with a single optical transmission line for radiation dose measurement. Physics in Medicine & Biology, 2012, 57(21): 7147–7159
|
[17] |
Clift M A, Johnston P N, Webb D V. A temporal method of avoiding the Cerenkov radiation generated in organic scintillator dosimeters by pulsed mega-voltage electron and photon beams. Physics in Medicine & Biology, 2002, 47(8): 1421–1433
|
[18] |
Justus B L, Falkenstein P, Huston A L, Plazas M C, Ning H, Miller R W. Gated fiber-optic-coupled detector for in vivo real-time radiation dosimetry. Applied Optics, 2004, 43(8): 1663–1668
CrossRef
Pubmed
Google scholar
|
[19] |
Bouchet A, Lemasson B, Christen T, Potez M, Rome C, Coquery N, Le Clec'h C, Moisan A, Brauer-Krisch E, Leduc G, Remy C, Laissue J A, Barbier E L, Brun E, Serduc R. Synchrotron microbeam radiation therapy induces hypoxia in intracerebral gliosarcoma but not in the normal brain. Radiotherapy and Oncology, 2013, 108(1): 143–148
|
[20] |
Crosbie J C, Anderson R L, Rothkamm K, Restall C M, Cann L, Ruwanpura S, Meachem S, Yagi N, Svalbe I, Lewis R A, Williams B R, Rogers P A. Tumor cell response to synchrotron microbeam radiation therapy differs markedly from cells in normal tissues. International Journal of Radiation Oncology, Biology, Physics, 2010, 77(3): 886–894
|
[21] |
Regnard P, Le Duc G, Brauer-Krisch E, Clair C, Kusak A, Dallery D,
CrossRef
Google scholar
|
[22] |
Serduc R, Vérant P, Vial J C, Farion R, Rocas L, Rémy C, Fadlallah T, Brauer E, Bravin A, Laissue J, Blattmann H, van der Sanden B. In vivo two-photon microscopy study of short-term effects of microbeam irradiation on normal mouse brain microvasculature. International Journal of Radiation Oncology, Biology, Physics, 2006, 64(5): 1519–1527
CrossRef
Pubmed
Google scholar
|
[23] |
Smyth L M L, Senthi S, Crosbie J C, Rogers P A W. The normal tissue effects of microbeam radiotherapy: what do we know, and what do we need to know to plan a human clinical trial? International Journal of Radiation Biology, 2016, 92(6): 302–311
CrossRef
Pubmed
Google scholar
|
[24] |
Cornelius I, Guatelli S, Fournier P, Crosbie J C, Sanchez Del Rio M, Bräuer-Krisch E, Rosenfeld A, Lerch M. Benchmarking and validation of a Geant4-SHADOW Monte Carlo simulation for dose calculations in microbeam radiation therapy. Journal of Synchrotron Radiation, 2014, 21(3): 518–528
CrossRef
Pubmed
Google scholar
|
[25] |
Fournier P, Cornelius I, Donzelli M, Requardt H, Nemoz C, Petasecca M, Bräuer-Krisch E, Rosenfeld A, Lerch M. X-Tream quality assurance in synchrotron X-ray microbeam radiation therapy. Journal of Synchrotron Radiation, 2016, 23(5): 1180–1190
CrossRef
Pubmed
Google scholar
|
[26] |
Fournier P, Cornelius I, Dipuglia A, Cameron M, Davis J A, Cullen A, Petasecca M, Rosenfeld A B, Brauer-Krisch E, Häusermann D, Stevenson A W, Perevertaylo V, Lerch M L F. X-Tream dosimetry of highly brilliant X-ray microbeams in the MRT hutch of the Australian Synchrotron. Radiation Measurements, 2017 doi: 10.1016/j.radmeas.2017.01.011
|
[27] |
Lerch M L F, Dipuglia A, Cameron M, Fournier P, Davis J, Petasecca M, CorneliusI, Perevertaylo V, RosenfeldA B. New 3D silicon detectors for dosimetry in Microbeam Radiation Therapy. Journal of Physics Conference Series, 2017, 777(1): 012009
|
[28] |
Belley M D, Stanton I N, Hadsell M, Ger R, Langloss B W, Lu J, Zhou O, Chang S X, Therien M J, Yoshizumi T T. Fiber-optic detector for real time dosimetry of a micro-planar X-ray beam. Medical Physics, 2015, 42(4): 1966–1972
CrossRef
Pubmed
Google scholar
|
[29] |
Archer J, Li E, Petasecca M, Lerch M, Rosenfeld A, Carolan M. High-resolution fiber-optic dosimeters for microbeam radiation therapy. Medical Physics, 2017, 44(5): 1965–1968
CrossRef
Pubmed
Google scholar
|
[30] |
Archer J, Madden L, Li E, Carolan M, Petasecca M, Metcalfe P, Rosenfeld A. Temporally separating Cherenkov radiation in a scintillator probe exposed to a pulsed X-ray beam. Physica Medica, 2017, 42: 185–188
CrossRef
Google scholar
|
[31] |
Archer J, Li E, Petasecca M, Dipuglia A, Cameron M, Stevenson A, Hall C, Hausermann D, Rosenfeld A, Lerch M. X-ray microbeam measurements with a high resolution scintillator fibre-optic dosimeter. Scientific Reports, 2017, 7(1): 12450
CrossRef
Pubmed
Google scholar
|
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