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<article xmlns:xlink="http://www.w3.org/1999/xlink">
  <front>
    <journal-meta />
    <article-meta>
      <title-group>
        <article-title>Assessment of in vivo dosimetry measurements in electron-based radiotherapy from a statistical perspective⋆</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <string-name>Aleksandra Kłos-Witkowska</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Vasyl Martsenyuk</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <aff id="aff0">
          <label>0</label>
          <institution>University of Bielsko-Biala</institution>
          ,
          <addr-line>Willowa St. 2, Bielsko-Biala, 43-300</addr-line>
          ,
          <country country="PL">Poland</country>
        </aff>
      </contrib-group>
      <pub-date>
        <year>2026</year>
      </pub-date>
      <abstract>
        <p>The following paper presents the results of a statistical analysis of dosimeter and in vivo measurements in electron beam radiotherapy of cancer. The main principles of radiotherapy are described and the differences resulting from the discrepancy between the planned and received doses are summarised. The analysis was performed for electron beams with energies of 9.12 and 15 MeV. The studies showed good agreement between the planned doses and those administered to patients; in a few cases, the discrepancies exceeded 5%. The main source of these discrepancies was an inaccurate treatment planning system and the method of attaching detectors to the patient's skin, which, due to the anatomical shape of the therapeutic area, prevented very precise placement of the detector in the radiation field.</p>
      </abstract>
      <kwd-group>
        <kwd>eol&gt;radiotherapy</kwd>
        <kwd>electron beams</kwd>
        <kwd>statistical analysis</kwd>
        <kwd>patients</kwd>
        <kwd>energy 1</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec id="sec-1">
      <title>1. Introduction</title>
      <p>
        One of the basic methods of treating cancer patients is radiotherapy [
        <xref ref-type="bibr" rid="ref1 ref2 ref3">1-3</xref>
        ], which is a treatment
using ionising radiation that exploits the sensitivity of individual tissues and tumours to radiation.
The therapeutic dose of radiation is designed to damage the tumour and inhibit the ability of cells
to reproduce without seriously damaging healthy tissue [
        <xref ref-type="bibr" rid="ref4 ref5 ref6">4-6</xref>
        ].
      </p>
      <p>
        The basic condition for the effectiveness of radiotherapy in cancer treatment is ensuring that
the dose administered matches the planned dose. For various reasons, such as malfunctioning of
the therapeutic device, insufficient precision of the treatment planning system, human error, and
instability of the patient's position during the irradiation session, the discrepancy between the
administered dose and the planned dose can reach several percent [
        <xref ref-type="bibr" rid="ref10 ref7 ref8 ref9">7-10</xref>
        ]. The standards applicable
in radiotherapy, contained in the so-called dosimetry protocols, allow for the possibility of
discrepancies, but their maximum value is strictly defined. According to the recommendations of
the International Agency for Radiological Units and Measurements, the differences between the
planned and delivered doses should not exceed 5%. Some authors even postulate that in order to
maintain a high level of treatment, these differences should not exceed 3.5%. Failure to comply with
the above recommendations results in a sharp decrease in the probability of cure and the risk of
cancer recurrence [
        <xref ref-type="bibr" rid="ref11 ref12 ref13">11-13</xref>
        ]. It is estimated that a 1% change in the absorbed dose relative to the
planned dose reduces the probability of cure by approximately 3%. Direct in vivo measurements are
an excellent test of the accuracy of dose delivery to the patient, as they also make it possible to
determine the causes of errors and correct them[
        <xref ref-type="bibr" rid="ref14 ref15 ref16">14-16</xref>
        ].
      </p>
      <p>The aim of this study is to statistically analyse the results obtained by applying in vivo
symmetry in radiotherapy of tumours with electron beams. In vivo dosimetry is performed using
EDE semiconductor detectors. The paper presents a histogram of percentage differences between
the planned dose and the dose administered to the patient. The statistical analysis covers 209 cases,
and the data comes from one of the hospitals in Silesia, Poland.</p>
      <sec id="sec-1-1">
        <title>1.1. Interaction of electrons with the environment</title>
        <p>Electrons are particles with an electric charge. As they pass through an environment, they transfer
their energy to it. The manner in which energy is transferred depends on the energy of the
electrons and the atomic number of the environment. The energy of electrons is lost as a result of
collisions with atoms in the environment (excitation and ionisation) and as a result of deceleration
in the environment. In the case of deceleration, part of the electron's energy is converted into
bremsstrahlung (electromagnetic radiation), which is observed especially when the environment
has a high atomic number. The total loss of electron energy dE over a distance dl in the
environment is the sum of the energy losses transferred to ionisation and bremsstrahlung, which
can be written as follows:
dE
dl</p>
        <p>dE dE
=( ) +( )</p>
        <p>dl jon dl prom</p>
        <p>For a given environment, the value of energy loss dE of electrons along the path dl is called the
linear damping capacity and is denoted by S(E). The linear damping capacity is a function of
electron energy, which can be written as:
dE</p>
        <p>=S ( E )
dl</p>
        <p>If we take into account that an electron loses its energy in an environment with a density of ɋ,
we can divide the linear braking capacity by the density of the environment. The result is a
quantity called the mass braking capacity, denoted by S(E)/ ɋ. Taking into account the energy
dissipation by the electron, we can write:</p>
        <p>S ( E )
ɋ</p>
        <p>S ( E )</p>
        <p>) +(
ɋ jon</p>
        <p>S ( E )</p>
        <p>)
ɋ
prom</p>
        <p>From the point of view of the use of electrons in radiotherapy, the loss of electron energy due to
ionisation of the environment is significant. The absorption of energy by the environment is, by
definition, the dose. By definition, the dose range of electrons used in radiotherapy is between 4
MeV and 25 MeV. Electron beams used in radiotherapy are currently produced mainly in linear
electron accelerators.</p>
      </sec>
      <sec id="sec-1-2">
        <title>1.2. From physical phenomena to biological effects</title>
        <p>As the electrons in the beam pass through matter, they interact with the atoms of the medium
through various processes: inelastic collisions with atomic electrons leading to excitation or
ionisation of the medium atoms, inelastic collisions with the nucleus resulting in bremsstrahlung,
elastic collisions with medium atoms, and elastic collisions with the nucleus. In an inelastic
collision, the electron loses part of its kinetic energy, which is transferred to the electron of the
medium atom, causing excitation or ionisation of the atom, or is converted into bremsstrahlung. In
an elastic collision, the energy of the electron is distributed among the particles involved in the
collision in such a way that the sum of the kinetic energy of the interacting particles before and
after the collision is the same.</p>
        <p>In biological tissue or water, as well as in other media with a low atomic number, electrons lose
their kinetic energy mainly through the ionisation of atoms. The loss of kinetic energy by the beam
electron continues until the electron reaches thermal energy and is captured by the atoms of the
medium. At the same time, the atom knocked out of the atom as a result of ionisation, the so-called
secondary electron, can cause further ionisation if its kinetic energy is sufficiently high. The
primary process in the chain of changes producing a specific biological effect is the ionisation of
atoms in the body's cells. Ionisation can disrupt the functionally important chemical structure of
the cell and initiate chemical reactions that disrupt cell function. Of particular importance here is
the phenomenon of water radiolysis initiated by ionisation, which results in the formation of
radicals with high chemical activity and strong biological effects. Radicals cause further chemical
reactions that ultimately contribute to the inhibition of enzymatic activity, disruption of protein
synthesis and carbohydrate metabolism, and ultimately cause the destruction of the cell's biological
system.</p>
      </sec>
      <sec id="sec-1-3">
        <title>1.3. Input Dose measurement</title>
        <p>The input dose is defined as the dose in the radiation beam axis at a depth of dmax, where it
reaches its maximum value. The input dose is one of the basic pieces of information in treatment
planning. In radiotherapy, the entrance dose is determined on the basis of the efficiency of the
therapeutic device, i.e. the dose measured for specific geometric parameters (distance:
sourceskin(SSD), size of the irradiated field (S)). Factors such as the accuracy of determining the efficiency
of the device, the correct operation of the systems used to determine the distance d and the
irradiation field, the correct positioning of the patient on the treatment table, the stability of the
patient's position during therapy, and the correct selection of the irradiation time are reflected in
the value of the entrance dose. Direct measurement of this dose during the irradiation session
allows us to determine whether the administered input dose is equal to the planned dose and, in
the event of a discrepancy, to identify its causes. If systematic errors are found, we add the
possibility of eliminating the error in all subsequently treated patients. On the other hand, the
detection of a random error makes it possible to correct the value of the administered dose for a
given patient in subsequent irradiation sessions. The measurement of the input dose in vivo is
performed by attaching a detector to the patient's skin in the axis of the radiation beam.</p>
        <p>In order to determine the input dose based on the detector reading, appropriate calibration and
correction factors for semiconductor detectors must first be determined in phantom measurements
in relation to the ionisation chamber dose measurement. The patient's entrance dose (Dkom) can be
expressed as the product of the readings of the detector placed on the skin in the radiation beam
axis (Rwej) and the calibration factor (Fwej).</p>
        <p>Dkom= F wej Rwej</p>
        <p>The calibration factor may depend on the size of the irradiation field S, the distance from the
source to the irradiated surface SSD, the angle (α) between the line perpendicular to the detector
base and the beam axis, and the temperature (t) of the detector.</p>
        <p>F wej= F wej ( S , SSD , α , t )</p>
      </sec>
      <sec id="sec-1-4">
        <title>1.4. Input Dose measurement</title>
        <p>The output dose (Dwyj) is defined as the dose value in the radiation beam axis at a distance dmax
measured from the beam exit point from the irradiated area. The output dose in a patient can be
determined based on the reading of a detector placed on the skin in the beam axis on the side of the
exit from the irradiation area (Rwyj). This procedure requires the prior determination of
appropriate calibration and correction factors (Fwyj). These coefficients are determined on the basis
of phantom measurements.</p>
        <p>Dwyj= F wyj Rwyj</p>
        <p>As with the input dose, this coefficient for a given SSD is a function of several parameters:
phantom thickness d, irradiation field size S, angle α between the beam axis and the line
perpendicular to the detector base, and temperature t. For a given phantom thickness d</p>
        <p>F wej= F wej ( d , SSD , α , t )</p>
      </sec>
    </sec>
    <sec id="sec-2">
      <title>2. Material and methods</title>
      <p>The in vivo dosimetry measurement were out with the use of the EDE-5 semiconductors diodes.
The detectors were linked to the DPD-510 electrometer (Scanditronix). The 0.6 cm3 cylindrical
ionization chamber (type NE 2571) and the tissue equivalent phantom composed of slabs with the
are of 30cmx30cm were used for the calibration of applied detectors. The measurement were
performed for patients with the cancer of the lung, chest and neck region. Total number of
measurement 208. Patients were irradiated with the 9,12,15,18,22, MEV electron beams, generated
by biomedical accelerator Clinac Varian 2300 C/D. Detectors were positioned on the surface of the
body at the centre of irradiated field. Results are shown on the histrograms of percentage
differences between the planed dose and received one.</p>
    </sec>
    <sec id="sec-3">
      <title>3. Results</title>
      <p>A key issue in cancer radiotherapy is the development of a method that allows the input dose
during irradiation to be determined with high accuracy (in vivo dosimetry).</p>
      <p>This method allows for high accuracy in determining the doses administered to patients. Thanks
to in vivo dosimetry, discrepancies between the planned dose and the dose administered to the
patient can be verified during subsequent radiotherapy sessions. The graph below shows the results
of a study conducted on a group of 14 patients with laryngeal cancer. Some patients were
irradiated several times. Graph 1 was created for 50 doses and shows the percentage differences
between the input doses and the planned doses.</p>
      <p>12
10</p>
      <p>Analysis of the presented values (Fig 1) showed that the mean value of the distribution (ŚR) is
-9.1% and the standard deviation SD = 4%. Analysis of the causes of the distribution shift revealed a
systematic error resulting from the failure to take into account radiation absorption in the shield
support tray. Taking this fact into account leads to the dose distribution shown in Figure 2.</p>
      <p>It can be seen that the average value is ŚR=- 2.1%, SD=4%. The use of TLD detectors in in vivo
dosimetry has the disadvantage that the measurement results are obtained after some time. It is not
possible to correct any errors that may occur during the irradiation session. This disadvantage is
eliminated by semiconductor detectors. The method of direct dose measurement during the
irradiation session was implemented for EDE-5 semiconductor detectors using electron beams with
energies of 9, 12 15, 18, 22 MeV. Radiotherapy was administered to a group of 209 patients with
cancer in the neck, chest and lungs. The discrepancies between the dose administered to the patient
and the planned dose are presented in the form of a histogram 3</p>
      <p>9, 12 15, 18, 22 MeV</p>
      <p>An analysis of the above chart (Fig 3) shows that the average value of the distribution obtained
is 2.48%, with the extreme values of the percentage differences being -25% and 37%.</p>
      <p>Next, an analysis was performed for individual electron beam energies, and thus histogram 4
shows the percentage differences between the measured and planned doses for the 9 MeV electron
beam.</p>
      <p>9 MeV
-18 -14 -10 -8 -6 -4 -2 0 2 4 6 8 10 14 18 24 30</p>
      <p>Histogram 4 was created for 177 patients irradiated with a 9 MeV electron beam. The mean
value of the obtained distribution is 3.02%, with extreme percentage differences of -18% and 30%
and a standard deviation not exceeding 2%</p>
      <p>12 MeV
16
e 14
cen 12
rru 10
c
co 8
fo 6
y
cn 4
e
uq 2
e
rF 0
2,5</p>
      <p>2</p>
      <p>On Figure 5 the results of irradiation with a 12 MeV electron beam for 10 patients is presented.
The mean value of the obtained distribution is 0,5%, with extreme percentage differences of -6% and
6% and a standard deviation not exceeding 1%
2,5</p>
      <p>2
-25 -19 -16 -13 -10 -7 -6 -5 -4 -1
2
5
8</p>
      <p>Histogram 6 was created for 22 patients irradiated with a 15 MeV electron beam. The average
value of the distribution obtained is 1.47%, while the standard deviation is 0.51. Extreme percentage
differences are -25% and 38%.</p>
      <p>Hospital practice shows that radiotherapy with electron beams of 18 and 22 MeV energy is
performed extremely rarely, hence the number of cases collected for the following analysis is too
small and is not taken into account in the final summary.</p>
    </sec>
    <sec id="sec-4">
      <title>4. Summary and final conclusions</title>
      <p>Verification measurements of doses in patients based on in vivo symmetries indicate a high degree
of consistency between planned doses and doses administered to patients. Only in a few cases do
the discrepancies between the planned and administered doses significantly exceed 5%. In these
cases, a thorough analysis of the patient's irradiation process was performed. It was found that the
main source of the discrepancies was the treatment planning system, which automatically
calculates the dose for electron beams. The influence of other factors on the above-mentioned
differences was also analysed, such as the influence of the anatomical shape of the irradiated area,
the accuracy of SSD setting, and the like. It turned out that a significant factor contributing to the
overestimation of the intended dose was the fact that the directors were fixed in a few cases away
from the surface of the patient's body, which in turn meant that the detector was located at a
slightly shorter distance from the beam source than on the surface. It is extremely difficult to
accurately determine the extent of dose overestimation resulting from the director's fixation,
because while it is possible to accurately calculate the SSD correction value, it is difficult to
determine the effect of backward scatter reduction on the detector reading due to the absence of a
small layer of air between the detector fixation and the patient's skin. No significant human factor
influence was found (technicians' errors that may occur when positioning the patient on the
treatment table and setting the correct irradiation parameters, i.e. SSD distance, irradiation time,
etc.).</p>
    </sec>
    <sec id="sec-5">
      <title>Declaration on Generative AI</title>
      <p>The authors have not employed any Generative AI tools.</p>
    </sec>
  </body>
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