4.6 Article

The minimal FLASH sparing effect needed to compensate the increase of radiobiological damage due to hypofractionation for late-reacting tissues

Journal

MEDICAL PHYSICS
Volume 49, Issue 12, Pages 7672-7682

Publisher

WILEY
DOI: 10.1002/mp.15911

Keywords

BED; FLASH effect; hypofractionation; LQ model; LQ-L model

Funding

  1. ISREC Foundation
  2. Fondation pour le soutien de la recherche et du developpement de l'oncologie (FSRDO)

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In this study, we developed a formalism based on the LQ and LQ-L models to quantify the minimal NT sparing needed to compensate for the reduction in protection caused by hypofractionation. We predicted if a net NT sparing benefit is expected for hypofractionated UHDR treatments compared to normofractionated CONV treatments.
Purpose Normal tissue (NT) sparing by ultra-high dose rate (UHDR) irradiations compared to conventional dose rate (CONV) irradiations while being isotoxic to the tumor has been termed FLASH effect and has been observed when large doses per fraction (d greater than or similar to 5 Gy) have been delivered. Since hypofractionated treatment schedules are known to increase toxicities of late-reacting tissues compared to normofractionated schedules for many clinical scenarios at CONV dose rates, we developed a formalism based on the biologically effective dose (BED) to assess the minimum magnitude of the FLASH effect needed to compensate the loss of late-reacting NT sparing when reducing the number of fractions compared to a normofractionated CONV treatment schedule while remaining isoeffective to the tumor. Methods By requiring the same BED for the tumor, we derived the break-even NT sparing weighting factor W-BE for the linear-quadratic (LQ) and LQ-linear (LQ-L) models for an NT region irradiated at a relative dose r (relative to the prescribed dose per fraction d to the tumor). W-BE was evaluated numerically for multiple values of d and r, and for different tumor and NT alpha/beta-ratios. W-BE was compared against currently available experimental data on the magnitude of the NT sparing provided by the FLASH effect for single fraction doses. Results For many clinically relevant scenarios, W-BE decreases steeply initially for d > 2 Gy for late-reacting tissues with (alpha/beta)(NT) approximate to 3 Gy, implying that a significant NT sparing by the FLASH effect (between 15% and 30%) is required to counteract the increased radiobiological damage experienced by late-reacting NT for hypofractionated treatments with d alpha/beta-ratios for tumor and late-reacting NT of (alpha/beta)(T) = 10 Gy and (alpha/beta)(NT) = 3 Gy, respectively, most currently available experimental evidence about the magnitude of NT sparing by the FLASH effect suggests no net NT sparing benefit for hypofractionated FLASH radiotherapy (RT) in the high-dose region when compared with W-BE. Instead, clinical indications with more similar alpha/beta-ratios of the tumor and dose-limiting NT toxicities [i.e., (alpha/beta)(T) approximate to (alpha/beta)(NT)], such as prostate treatments, are generally less penalized by hypofractionated treatments and need consequently smaller magnitudes of NT sparing by the FLASH effect to achieve a net benefit. For strongly hypofractionated treatments (>10-15 Gy/fraction), the LQ-L model predicts, unlike the LQ model, a larger W-BE suggesting a possible benefit of strongly hypofractionated FLASH RT, even for generic alpha/beta-ratios of (alpha/beta)(T) = 10 Gy and (alpha/beta)(NT) = 3 Gy. However, knowledge on the isoeffect scaling for high doses per fraction (greater than or similar to 10 Gy/fraction) and its modeling is currently limited and impedes accurate and reliable predictions for such strongly hypofractionated treatments. Conclusions We developed a formalism that quantifies the minimal NT sparing by the FLASH effect needed to compensate for hypofractionation, based on the LQ and LQ-L models. For a given hypofractionated UHDR treatment scenario and magnitude of the FLASH effect, the formalism predicts if a net NT sparing benefit is expected compared to a respective normofractionated CONV treatment.

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