Variation of the relative biological effectiveness with fractionation in proton therapy: Analysis of prostate cancer response

Author:

Pardo‐Montero Juan12,Pombar Miguel2,Gómez‐Caamaño Antonio3,Giordanengo Simona4,González‐Crespo Isabel15

Affiliation:

1. Group of Medical Physics and Biomathematics Instituto de Investigación Sanitaria de Santiago (IDIS) Santiago de Compostela Spain

2. Department of Medical Physics Complexo Hospitalario Universitario de Santiago de Compostela Santiago de Compostela Spain

3. Department of Radiation Oncology Complexo Hospitalario Universitario de Santiago de Compostela Santiago de Compostela Spain

4. Istituto Nazionale di Fisica Nucleare‐Torino Section Torino Italy

5. Department of Applied Mathematics Universidade de Santiago de Compostela Santiago de Compostela Spain

Abstract

AbstractBackgroundIn treatment planning for proton therapy a constant Relative Biological Effectiveness (RBE) of 1.1 is used, disregarding variations with linear energy transfer, clinical endpoint, or fractionation.PurposeTo present a methodology to analyze the variation of RBE with fractionation from clinical data of tumor control probability (TCP) and to apply it to study the response of prostate cancer to proton therapy.Methods and materialsWe analyzed the dependence of the RBE on the dose per fraction by using the LQ model and the Poisson TCP formalism. Clinical tumor control probabilities for prostate cancer (low and intermediate risk) treated with photon and proton therapy for conventional fractionation (2 Gy(RBE)×37 fractions), moderate hypofractionation (3 Gy(RBE)×20 fractions) and hypofractionation (7.25 Gy(RBE)×5 fractions) were obtained from the literature and analyzed aiming at obtaining the RBE and its dependence on the dose per fraction.ResultsThe theoretical analysis of the dependence of the RBE on the dose per fraction showed three distinct regions with RBE monotonically decreasing, increasing or staying constant with the dose per fraction, depending on the change of (α, β) values between photon and proton irradiation (the equilibrium point being at pp) = XX)(αXp)). An analysis of the clinical data showed RBE values that decline with increasing dose per fraction: for low risk RBE≈1.124, 1.119, and 1.102 for 1.82 Gy, 2.73 Gy and 6.59 Gy per fraction (physical proton doses), respectively; for intermediate risk RBE≈1.119 and 1.102 for 1.82 Gy and 6.59 Gy per fraction (physical proton doses), respectively. These values are nonetheless very close to the nominal 1.1 value.ConclusionsIn this study, we have presented a methodology to analyze the RBE for different fractionations, and we used it to study clinical data for prostate cancer and evaluate the RBE versus dose per fraction. The analysis shows a monotonically decreasing RBE with increasing dose per fraction, which is expected from the LQ formalism and the changes in (α, β) values between photon and proton irradiation. However, the calculations in this study have to be considered with care as they may be biased by limitations in the modeling assumptions and/or by the clinical data set used for the analysis.

Funder

Instituto de Salud Carlos III

Ministerio de Ciencia e Innovación

Publisher

Wiley

Subject

General Medicine

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