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. Author manuscript; available in PMC: 2023 Oct 7.
Published in final edited form as: Radiother Oncol. 2023 Jul 25;187:109819. doi: 10.1016/j.radonc.2023.109819

Erratum to “A systematic analysis of the particle irradiation data ensemble in the key of the microdosimetric kinetic model: Should clonogenic data be used for clinical relative biological effectiveness?” [Radiother. Oncol. 185 (2023) 109730]

Daniel Suárez-García a, Miguel Antonio Cortés-Giraldo a, Alejandro Bertolet b,*
PMCID: PMC10557462  NIHMSID: NIHMS1926275  PMID: 37499618

The Publisher would like to point out that an error was introduced into Fig. 3 during the typesetting of this paper, whereby the error bands were cut off in a straight line at the bottom where there should have been a curve.

Fig. 3.

Fig. 3.

Comparison of the experimental relative biological effectiveness measured in in-vitro experiments from the PIDE database (black triangle, blue point and green cross for protons, alphas and carbons ions, respectively), calculated using the assumption rd = 320 nm (blue dotted line) (see main text for details) and using rd values calculated in this work (orange solid line), all of them as a function of yD. Panels (a) and (b) show the RBE for the endpoint of 10% of surviving cells (RBE10); panels (c) and (d) show the RBE for the endpoint of 50% of surviving cells (RBE50); and panels (e) and (f) show RBE in the very low dose limit, i.e., the quotient RBEα = α*/α0. The left panels show results for V79 cell line, and the right panels show the results for HSG cell line. The purple band over the green line show RBE calculated using the percentile 25 and percentile 75 of domain radius distribution (see Table 2). RMSE calculated for the different subplots are (a) 0.88–0.92, (b) 0.61–0.50, (c) 1.33–1.37, (d) 0.84–0.67, (e) 3.17–3.38, and (f) 1.12–0.88, for rd = 320 nm and rd calculated, respectively.

Fig. 3 as it should have appeared is below

The Publisher apologises for this error.

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