The biological effectiveness of intermittent irradiation as a function of overall treatment time: Development of correction factors for linac-based stereotactic radiotherapy

Stanley H Benedict, Peck Sun Lin, Robert D. Zwicker, David T. Huang, Rupert K A Schmidt-Ullrich

Research output: Contribution to journalArticle

60 Citations (Scopus)

Abstract

Purpose: Continuous irradiation of relatively short duration as administered in gamma-ray stereotactic radiosurgery (SRS) is biologically not equivalent to the more protracted intermittent exposures during accelerator- based radiosurgery with multiple arcs. Accelerator-based SRS and fractionated stereotactic radiotherapy (SRT) is currently performed with a high degree of variability in equipment and techniques resulting in highly variable treatment delivery times. The present work is designed to quantify the effects of radiation delivery times on biological effectiveness. For this, the intermittent radiation delivery schemes, typical for linac-based SRS/SRT, have been simulated in vitro to derive biological correction factors. Methods and Materials: The experiments were carried out using U-87MG human glioma cells in suspension at 37°C irradiated with 6 MV X-rays to clinically relevant doses ranging from 6 to 18 Gy, delivered over total irradiation times from 16 min to 3 h. The resulting cell survival data was used to calculate dose correction factors to compensate for wide variations in dose delivery times. Results: At each total dose level, cell survival increased with increasing total irradiation time. The increase in survival was more pronounced at higher dose levels. At a total dose of 12 Gy, cell survival increased by a factor of 4.7 when irradiation time was increased from 16 to 112 min. Dose correction factors were calculated to allow biologically equivalent irradiations over the range of exposure times. Cells irradiated with corrected total doses of 11.5 Gy delivered incrementally in 16 min up to 13.3 Gy in 112 min were found to exhibit the same survival within the experimental limits of accuracy. Conclusions: For a given total dose, variations in dose delivery time typical of SRS/SRT techniques will result in significant changes in cell survival. In the dose range studied, an isoeffect dose correction factor of 2 to 3 cGy/min was shown to compensate for the change in delivery time for U-87 MG human glioma cells in vitro.

Original languageEnglish (US)
Pages (from-to)765-769
Number of pages5
JournalInternational Journal of Radiation Oncology Biology Physics
Volume37
Issue number4
DOIs
StatePublished - Mar 1 1997
Externally publishedYes

Fingerprint

radiation therapy
Radiotherapy
Radiosurgery
dosage
irradiation
delivery
Cell Survival
Therapeutics
Glioma
Stereotaxic Techniques
accelerators
Survival
Gamma Rays
Radiation Effects
Biological Factors
Suspensions
radiation
cells
X-Rays
Radiation

Keywords

  • Stereotactic radiosurgery
  • Stereotactic radiotherapy
  • U-87 MG

ASJC Scopus subject areas

  • Oncology
  • Radiology Nuclear Medicine and imaging
  • Radiation

Cite this

The biological effectiveness of intermittent irradiation as a function of overall treatment time : Development of correction factors for linac-based stereotactic radiotherapy. / Benedict, Stanley H; Lin, Peck Sun; Zwicker, Robert D.; Huang, David T.; Schmidt-Ullrich, Rupert K A.

In: International Journal of Radiation Oncology Biology Physics, Vol. 37, No. 4, 01.03.1997, p. 765-769.

Research output: Contribution to journalArticle

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abstract = "Purpose: Continuous irradiation of relatively short duration as administered in gamma-ray stereotactic radiosurgery (SRS) is biologically not equivalent to the more protracted intermittent exposures during accelerator- based radiosurgery with multiple arcs. Accelerator-based SRS and fractionated stereotactic radiotherapy (SRT) is currently performed with a high degree of variability in equipment and techniques resulting in highly variable treatment delivery times. The present work is designed to quantify the effects of radiation delivery times on biological effectiveness. For this, the intermittent radiation delivery schemes, typical for linac-based SRS/SRT, have been simulated in vitro to derive biological correction factors. Methods and Materials: The experiments were carried out using U-87MG human glioma cells in suspension at 37°C irradiated with 6 MV X-rays to clinically relevant doses ranging from 6 to 18 Gy, delivered over total irradiation times from 16 min to 3 h. The resulting cell survival data was used to calculate dose correction factors to compensate for wide variations in dose delivery times. Results: At each total dose level, cell survival increased with increasing total irradiation time. The increase in survival was more pronounced at higher dose levels. At a total dose of 12 Gy, cell survival increased by a factor of 4.7 when irradiation time was increased from 16 to 112 min. Dose correction factors were calculated to allow biologically equivalent irradiations over the range of exposure times. Cells irradiated with corrected total doses of 11.5 Gy delivered incrementally in 16 min up to 13.3 Gy in 112 min were found to exhibit the same survival within the experimental limits of accuracy. Conclusions: For a given total dose, variations in dose delivery time typical of SRS/SRT techniques will result in significant changes in cell survival. In the dose range studied, an isoeffect dose correction factor of 2 to 3 cGy/min was shown to compensate for the change in delivery time for U-87 MG human glioma cells in vitro.",
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