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@ARTICLE{Niebuhr:168316,
author = {N. I. Niebuhr$^*$ and M. Splinter$^*$ and T. Bostel$^*$ and
J. Seco$^*$ and C. M. Hentschke and R. O. Floca$^*$ and J.
Hörner-Rieber$^*$ and M. Alber and P. Huber$^*$ and N. H.
Nicolay$^*$ and A. Pfaffenberger$^*$},
title = {{B}iologically consistent dose accumulation using daily
patient imaging.},
journal = {Radiation oncology},
volume = {16},
number = {1},
issn = {1748-717X},
address = {London},
publisher = {BioMed Central},
reportid = {DKFZ-2021-00826},
pages = {65},
year = {2021},
note = {#EA:E040#LA:E040#},
abstract = {This work addresses a basic inconsistency in the way dose
is accumulated in radiotherapy when predicting the
biological effect based on the linear quadratic model (LQM).
To overcome this inconsistency, we introduce and evaluate
the concept of the total biological dose, bEQDd.Daily
computed tomography imaging of nine patients treated for
prostate carcinoma with intensity-modulated radiotherapy was
used to compute the delivered deformed dose on the basis of
deformable image registration (DIR). We compared
conventional dose accumulation (DA) with the newly
introduced bEQDd, a new method of accumulating biological
dose that considers each fraction dose and tissue
radiobiology. We investigated the impact of the applied
fractionation scheme (conventional/hypofractionated),
uncertainties induced by the DIR and by the assigned
α/β-value.bEQDd was systematically higher than the
conventionally accumulated dose with difference hot spots of
3.3-4.9 Gy detected in six out of nine patients in regions
of high dose gradient in the bladder and rectum. For
hypofractionation, differences are up to 8.4 Gy. The
difference amplitude was found to be in a similar range to
worst-case uncertainties induced by DIR and was higher than
that induced by α/β.Using bEQDd for dose accumulation
overcomes a potential systematic inaccuracy in biological
effect prediction based on accumulated dose. Highest impact
is found for serial-type late responding organs at risk in
dose gradient regions and for hypofractionation. Although
hot spot differences are in the order of several Gray, in
dose-volume parameters there is little difference compared
with using conventional or biological DA. However, when
local dose information is used, e.g. dose surface maps,
difference hot spots can potentially change outcomes of
dose-response modelling and adaptive treatment strategies.},
keywords = {Delivered dose (Other) / Dose accumulation (Other) / Image
guidance (Other) / Linear quadratic model (Other) / Normal
tissue response (Other) / Radiobiology (Other)},
cin = {E040 / E050 / E041 / E230 / E055},
ddc = {610},
cid = {I:(DE-He78)E040-20160331 / I:(DE-He78)E050-20160331 /
I:(DE-He78)E041-20160331 / I:(DE-He78)E230-20160331 /
I:(DE-He78)E055-20160331},
pnm = {315 - Bildgebung und Radioonkologie (POF4-315)},
pid = {G:(DE-HGF)POF4-315},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:33823885},
doi = {10.1186/s13014-021-01789-3},
url = {https://inrepo02.dkfz.de/record/168316},
}