British Journal of Radiology (2006) 79, 71-75
© 2006 British Institute of Radiology
doi: 10.1259/bjr/50464795
Radiosurgical palliation of aggressive murine SCCVII squamous cell carcinomas using synchrotron-generated X-ray microbeams
M Miura, PhD
1
H Blattmann, PhD
2
E Bräuer-Krisch, BEng
3
A Bravin, PhD
3
A L Hanson, PhD
1
M M Nawrocky, BA
1
P L Micca, BS
1
D N Slatkin, MD
1,4 and
J A Laissue, MD
4
1 Medical Department, Brookhaven National Laboratory, Upton, NY 11973-5000, USA, 2 Niederwiesstrasse 13C, Untersiggenthal, Switzerland, 3 European Synchrotron Radiation Facility, 6 Rue Jules Horowitz, BP 220, Grenoble, France and 4 Pathologisches Institut der Universität Bern, Murtenstrasse 31, Bern, Switzerland

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Figure 1. Photograph of anaesthetized female C3H mouse bearing a leg squamous-cell carcinoma (SCCVII) carcinoma taped to Plexiglas® block, readied for microbeam radiosurgery (MBRS) at the European Synchrotron Radiation Facility (ESRF).
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Figure 2. A Plexiglas® polymethylmethacrylate block (thick black outline) served as a "saddle" for the mouse, viewed as it would be by an observer directly above it. The mouse was anaesthetized and placed prone on the block for its first tumour irradiation. In this figure, the outline of the mouse is represented by an ellipse. Two black dots represent its eyes. To avoid irradiating its left foreleg, the 150 mm long axis of the block was rotated 5° (about a vertical axis through the centre of the block) clockwise from the reference 0° microbeam direction. The microbeam array, symbolized by thin arrows, was propagated in a thin, wide, slightly divergent fan-beam, substantially in a horizontal plane, represented here as the plane of this page. The second irradiation was implemented after the block was rotated 95° clockwise from the 0° reference direction about the same vertical axis.
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Figure 3. Kaplan-Meier graphs of C3H mice bearing aggressive squamous-cell carcinoma (SCCVII) leg carcinomas irradiated with various radiation modalities. The on-centre distances for microbeam radiosurgery (MBRS)-irradiations were 200 µm. Mice euthanized due to foot/leg damage were not distinguished from those euthanized due to tumour overgrowth: (a) Survival graphs of mice bearing SCCVII carcinomas treated with seamless 25 Gy or 35 Gy skin-entrance doses of X-rays in comparison with unirradiated controls. (b) Survival graphs of similar mice in MBRS groups (16) with skin entrance doses of 442 Gy, 625 Gy, and 884 Gy at 35 µm and 442 at 70 µm beam width. "Al" designates a 16 mm-thick aluminium filter placed upstream from the collimator.
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Figure 4. Average relative tumour volumes of the various microbeam radiosurgery (MBRS)-irradiated and control mice. The lower tumour volumes noted in groups 3 to 6 relate to the fact that those tumours had regressed to relatively small or undetectable volumes when most of the mice had to be euthanized due to severe radiodermatitis of the inner thigh.
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Copyright © 2006 by the British Institute of Radiology.