J Vet Sci.  2018 Jul;19(4):550-556. 10.4142/jvs.2018.19.4.550.

Kilovoltage radiotherapy for companion animals: dosimetric comparison of 300 kV, 450 kV, and 6 MV X-ray beams

Affiliations
  • 1Department of Bio-Convergence Engineering, Korea University, Seoul 02841, Korea. radioyoon@korea.ac.kr
  • 2Department of Radiation Oncology, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul 03722, Korea. jinsung.k@gmail.com
  • 3Korea Animal Cancer Center, Seoul 01684, Korea.
  • 4Department of Radiation Oncology, Kyung Hee University Hospital at Gangdong, Seoul 05278, Korea.

Abstract

Radiotherapy for the treatment of cancer in companion animals is currently administered by using megavoltage X-ray machines. Because these machines are expensive, most animal hospitals do not perform radiotherapy. This study evaluated the ability of relatively inexpensive kilovoltage X-ray machines to treat companion animals. A simulation study based on a commercial treatment-planning system was performed for tumors of the brain (non-infectious meningoencephalitis), nasal cavity (malignant nasal tumors), forefoot (malignant muscular tumors), and abdomen (malignant intestinal tumors). The results of kilovoltage (300 kV and 450 kV) and megavoltage (6 MV) X-ray beams were compared. Whereas the 300 kV and 6 MV X-ray beams provided optimal radiation dose homogeneity and conformity, respectively, for brain tumors, the 6 MV X-rays provided optimal homogeneity and radiation conformity for nasal cavity, forefoot, and abdominal tumors. Although megavoltage X-ray beams provided better radiation dose distribution in most treated animals, the differences between megavoltage and kilovoltage X-ray beams were relatively small. The similar therapeutic effects of the kilovoltage and 6 MV X-ray beams suggest that kilovoltage X-ray beams may be effective alternatives to megavoltage X-ray beams in treating cancers in companion animals.

Keyword

X-ray; companion animals; radiation therapy

MeSH Terms

Abdomen
Animals
Brain
Brain Neoplasms
Friends*
Hospitals, Animal
Humans
Nasal Cavity
Pets*
Radiotherapy*
Therapeutic Uses
Therapeutic Uses

Figure

  • Fig. 1 Percentage depth doses (PDD) of 300 kV, 450 kV, and 6 MV X-ray beams at field sizes of (A) 3 cm × 3 cm, (B) 6 cm × 6 cm, (C) 10 cm × 10 cm, (D) 15 cm × 15 cm, and (E) 20 cm × 20 cm.

  • Fig. 2 Percent isodose distributions in nasal tumors (non-infectious meningoencephalitis or necrotizing meningoencephalitis). (A and B) Axial (A) and sagittal (B) views using a 300 kV X-ray beam; (C and D) axial and sagittal (D) views using a 450 kV X-ray beam; and (E and F) axial (E) and sagittal (F) views using a 6 MV X-ray beam. Colored scale bars indicate isodose levels normalized to the prescribed dose.

  • Fig. 3 Percent isodose distributions in forefoot tumors (malignant muscular tumor or anaplastic rhabdomyosarcoma). (A and B) Axial (A) and sagittal (B) views using a 300 kV X-ray beam; (C and D) axial (C) and sagittal (D) views using a 450 kV X-ray beam; and (E and F) axial (E) and sagittal (F) views using a 6 MV X-ray beam. Colored scale bars indicate isodose levels normalized to the prescribed dose.

  • Fig. 4 Dose-volume histogram results for nasal tumors (malignant nasal tumor or transitional cell sarcoma) from the 300 kV, 450 kV, and 6 MV X-ray beams. Results are shown for (A) the planning target volume of the tumor, as well as for the (B) body, (C) brain, (D) left eye, (E) right eye, (F) left lens, and (G) right lens.

  • Fig. 5 Dose-volume histogram results for brain tumors (non-infectious meningoencephalitis or necrotizing meningoencephalitis) from the 300 kV, 450 kV, and 6 MV X-ray beams. Results are shown for (A) the planning target volume of the tumor, as well as for the (B) body, (C) oral cavity, (D) brain, (E) left eye, (F) right eye, (G) left lens, and (H) right lens.


Reference

1. Austin-Seymour MM, Chen GT, Castro JR, Saunders WM, Pitluck S, Woodruff KH, Kessler M. Dose volume histogram analysis of liver radiation tolerance. Int J Radiat Oncol Biol Phys. 1986; 12:31–35.
Article
2. Axlund TW, McGlasson ML, Smith AN. Surgery alone or in combination with radiation therapy for treatment of intracranial meningiomas in dogs: 31 cases (1989–2002). J Am Vet Med Assoc. 2002; 221:1597–1600.
Article
3. Berlato D, Schrempp D, Van Den Steen N, Murphy S. Radiotherapy in the management of localized mucocutaneous oral lymphoma in dogs: 14 cases. Vet Comp Oncol. 2012; 10:16–23.
Article
4. Blackwood L, Dobson J. Radiotherapy in small animal oncology. InPractice. 1998; 20:566–575.
Article
5. Buvat I, Lazaro D. Monte Carlo simulations in emission tomography and GATE: an overview. Nucl Instrum Methods Phys Res A. 2006; 569:323–329.
Article
6. Colvett K. The history of radiation oncology. South Med J. 2006; 99:1155–1156.
Article
7. DeBoer DJ, Turrel JM, Moore PF. Mycosis fungoides in a dog: demonstration of T-cell specificity and response to radiotherapy. J Am Anim Hosp Assoc. 1990; 26:566–572.
8. Dobson JM, Samuel S, Milstein H, Rogers K, Wood JL. Canine neoplasia in the UK: estimates of incidence rates from a population of insured dogs. J Small Anim Pract. 2002; 43:240–246.
Article
9. Dorn CR, Taylor DO, Schneider R, Hibbard HH, Klauber MR. Survey of animal neoplasms in Alameda and Contra Costa Counties, California. II. Cancer morbidity in dogs and cats from Alameda County. J Natl Cancer Inst. 1968; 40:307–331.
10. Drzymala RE, Mohan R, Brewster L, Chu J, Goitein M, Harms W, Urie M. Dose-volume histograms. Int J Radiat Oncol Biol Phys. 1991; 21:71–78.
Article
11. Gardner H, Fidel J, Haldorson G, Dernell W, Wheeler B. Canine oral fibrosarcomas: a retrospective analysis of 65 cases (1998–2010). Vet Comp Oncol. 2015; 13:40–47.
Article
12. Henry CJ, Brewer WG Jr, Tyler JW, Brawner WR, Henderson RA, Hankes GH, Royer N. Survival in dogs with nasal adenocarcinoma: 64 cases (1981–1995). J Vet Intern Med. 1998; 12:436–439.
Article
13. Hutson CA, Willauer CC, Walder EJ, Stone JL, Klein MK. Treatment of mandibular squamous cell carcinoma in cats by use of mandibulectomy and radiotherapy: seven cases (1987–1989). J Am Vet Med Assoc. 1992; 201:777–781.
14. International Commission on Radiation Units and Measurements. Prescribing, Recording, and Reporting Photon Beam Therapy. Bethesda: International Commission on Radiation Units and Measurements;1993.
15. International Commission on Radiation Units and Measurements. Prescribing, Recording, and Reporting Photon Beam Therapy. Bethesda: International Commission on Radiation Units and Measurements;1999.
16. Jan S, Benoit D, Becheva E, Carlier T, Cassol F, Descourt P, Frisson T, Grevillot L, Guigues L, Maigne L, Morel C, Perrot Y, Rehfeld N, Sarrut D, Schaart DR, Stute S, Pietrzyk U, Visvikis D, Zahra N, Buvat I. GATE V6: a major enhancement of the GATE simulation platform enabling modelling of CT and radiotherapy. Phys Med Biol. 2011; 56:881–901.
Article
17. Jung JY, Cho W, Kim MJ, Lee JW, Suh TS. Evaluation of beam modeling using collapsed cone convolution algorithm for dose calculation in radiation treatment planning system. Prog Med Phys. 2012; 23:188–198.
18. Jung JY, Cho W, Lee JW, Suh TS. The experimental verification of collapsed cone convolution algorithm for dose calculation in radiation treatment planning system. IFMBE Proc. 2013; 39:1211–1214.
Article
19. Khan FM, Gibbons JP. Khan's the Physics of Radiation Therapy. Philadelphia: Lippincott Williams & Wilkins;2014.
20. MacEwen EG. Spontaneous tumors in dogs and cats: models for the study of cancer biology and treatment. Cancer Metastasis Rev. 1990; 9:125–136.
Article
21. Mesbahi A, Zakariaee SS. Effect of anode angle on photon beam spectra and depth dose characteristics for X-RAD320 orthovoltage unit. Rep Pract Oncol Radiother. 2013; 18:148–152.
Article
22. Miceli A, Thierry R, Flisch A, Sennhauser U, Casali F, Simon M. Monte Carlo simulations of a high-resolution X-ray CT system for industrial applications. Nucl Instrum Methods Phys Res A. 2007; 583:313–323.
Article
23. Nolan MW, Kogan L, Griffin LR, Custis JT, Harmon JF, Biller BJ, Larue SM. Intensity-modulated and image-guided radiation therapy for treatment of genitourinary carcinomas in dogs. J Vet Intern Med. 2012; 26:987–995.
Article
24. Padikal TN, Deye JA. Electron contamination of a high-energy X-ray beam. Phys Med Biol. 1978; 23:1086–1092.
Article
25. Pang LY, Argyle DJ. Veterinary oncology: biology, big data and precision medicine. Vet J. 2016; 213:38–45.
Article
26. Poirier VJ, Bley CR, Roos M, Kaser-Hotz B. Efficacy of radiation therapy for the treatment of macroscopic canine oral soft tissue sarcoma. In Vivo. 2006; 20:415–419.
27. Schiffman JD, Breen M. Comparative oncology: what dogs and other species can teach us about humans with cancer. Philos Trans R Soc Lond B Biol Sci. 2015; 370:20140231.
Article
28. Shaw E, Kline R, Gillin M, Souhami L, Hirschfeld A, Dinapoli R, Martin L. Radiation Therapy Oncology Group: radiosurgery quality assurance guidelines. Int J Radiat Oncol Biol Phys. 1993; 27:1231–1239.
Article
29. Strulab D, Santin G, Lazaro D, Breton V, Morel C. GATE (geant4 application for tomographic emission): a PET/SPECT general-purpose simulation platform. Nucl Phys B Proc Suppl. 2003; 125:75–79.
Article
30. Thiam CO, Breton V, Donnarieix D, Habib B, Maigne L. Validation of a dose deposited by low-energy photons using GATE/GEANT4. Phys Med Biol. 2008; 53:3039–3055.
Article
31. Wu Q, Mohan R, Morris M, Lauve A, Schmidt-Ullrich R. Simultaneous integrated boost intensity-modulated radiotherapy for locally advanced head-and-neck squamous cell carcinomas. I: dosimetric results. Int J Radiat Oncol Biol Phys. 2003; 56:573–585.
Article
Full Text Links
  • JVS
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr