Monitor units are not predictive of neutron dose for high-energy IMRT
© Hälg et al.; licensee BioMed Central Ltd. 2012
Received: 19 April 2012
Accepted: 2 August 2012
Published: 10 August 2012
Due to the substantial increase in beam-on time of high energy intensity-modulated radiotherapy (>10 MV) techniques to deliver the same target dose compared to conventional treatment techniques, an increased dose of scatter radiation, including neutrons, is delivered to the patient. As a consequence, an increase in second malignancies may be expected in the future with the application of intensity-modulated radiotherapy. It is commonly assumed that the neutron dose equivalent scales with the number of monitor units.
Measurements of neutron dose equivalent were performed for an open and an intensity-modulated field at four positions: inside and outside of the treatment field at 0.2 cm and 15 cm depth, respectively.
It was shown that the neutron dose equivalent, which a patient receives during an intensity-modulated radiotherapy treatment, does not scale with the ratio of applied monitor units relative to an open field irradiation. Outside the treatment volume at larger depth 35% less neutron dose equivalent is delivered than expected.
The predicted increase of second cancer induction rates from intensity-modulated treatment techniques can be overestimated when the neutron dose is simply scaled with monitor units.
With the application of new radiation treatment modalities such as intensity-modulated radiotherapy (IMRT) or intensity-modulated arc-therapy, increased tumor control probabilities are anticipated. However, with the application of these treatment techniques also a larger number of secondary cancers is expected. Some scientists believe that we will see an increase in second malignancies due to the substantial increase in beam-on time of IMRT techniques to deliver the same target dose compared to conventional treatment techniques [1, 2]. A consequence of the extended beam-on time is an increased dose of scatter radiation, including neutrons, which affects the whole patient. The neutrons could lead to a considerable contribution to the integral dose, in particular, since neutrons have a large quality factor and thus even a small physical dose can result in substantial biological effects.
Most measurements and estimates of neutron dose equivalent from radiotherapy treatments found in literature are usually given in operational dose quantities, which represent effective dose and thus a person risk. A compilation of current literature is listed in the review article by Xu et al. . It should be noted that the neutron dose is only one contribution to integral dose and person risk. Others are for example dose contributions from scattered photons, leakage radiation, products from inelastic nuclear reactions and imaging modalities.
In this report neutron detectors were used, which were calibrated to measure local neutron dose equivalent, at different depths in a solid water phantom in- and outside of the primary radiation field for an open and intensity-modulated radiation field.
The neutron dose measurements were performed with a detector system consisting of a PADC (poly(allyl diglycol carbonate)) track etch detector (Thermo Fisher Scientific Inc., Waltham MA, USA) with 2 mm thick radiators (polyethylene and polyethylene with lithium) on both sides. The detectors were provided and read-out by the Division for Radiation Safety and Security of the Paul Scherrer Institut (PSI) [4, 5].
A linear accelerator (Varian Medical System, Palo Alto CA, USA) was used to produce a photon radiation beam with a nominal energy of 16 MV, having a tissue phantom ratio TPR20,10 at 20 cm/10 cm depth of 0.760. Two irradiation techniques have been used. The first field was an open radiation field delivering 75 monitor units (MU) and a total dose of 0.592 Gy in 15 cm depth. The field size of 10 x 10 cm2 was defined by the jaws and the multileaf collimator (MLC) was retracted. The second radiation field was intensity-modulated, with a 2.32 cm sweeping MLC gap of 10 cm lateral dimension. With the IMRT field the same dose was delivered as with the open field, but with 225 monitor units. The jaws were positioned to form a 10 x 10 cm2 field. The MU-ratio between IMRT and open field was three. Since the sensitivity of the PADC detectors is optimal in a limited dose range, the detectors at the different positions were irradiated with different doses. For the measurement position D1, the radiation field was applied two times, for the positions D2 and D3 six times and for D4 120 times.
The detector output given in tracks per area was first calibrated into personal dose equivalent Hp(10). For this purpose, a subset of the PADC detectors from the measurement batch was mounted on an ISO water slab phantom and irradiated with neutrons from an 241Am-Be neutron source. The dose at the detector position was determined with a Berthold LB6411 neutron dose rate meter calibrated at the Physikalisch-Technische Bundesanstalt in Braunschweig, Germany , which is used as a secondary standard at PSI. The resulting calibration factor for the used batch of PADC detectors was 16.39 · 10-3 mSv cm2 ±36% (one standard deviation).
Calibration factors for converting tracks per cm 2 into neutron dose equivalent in mSv for the different positions in the phantom
Depth in cm
Neutron dose HP(10) (Am-Be)/(tracks per cm2) in mSv cm2
Neutron dose equivalent H (16 MV photons)/HP(10) (Am-Be)
16.39 · 10-3
16.39 · 10-3
The measurement series were performed once for the open field and twice for the IMRT field, leading to three and six measurement values per location, respectively. The average value of the measurements at each location was used to report the results.
Neutron dose equivalent in mSv per treatment Gy measured at different depths for an open field and an intensity-modulated field
Depth in cm
Neutron dose equivalent in mSv/Gy for an open field
Neutron dose equivalent in mSv/Gy for an IMRT field
The uncertainty of the calibration and readout of the PADC detectors was estimated by the standard deviation of the readout of two subsets of the detector batch which were used as background detectors or have been irradiated with neutrons from the 241Am-Be source for the absolute calibration. It was calculated to be σ = 36%. This was verified by the statistical deviations of the minimum or maximum readout to the mean value of the three repeated measurements at each measurement position, which were in the range of −17% to +30% with an average of less than 10%. The error of the mean was calculated using the Student’s t-distribution ΔD = t · σ/√n = 27% with n = 3 and a corresponding t = 1.32. The total uncertainty was then calculated by error propagation for the ratios of the open and the intensity-modulated field doses. The overall uncertainty of the dose ratios was 39%.
In addition to the detector batch variation of 36% an uncertainty of 17% comes from three sources. One source of around 5% comes from the spectral difference of the calibration conditions (neutrons from an Am-Be source) and the open photon radiotherapy beam. Another source of around 15% comes from the spectral change with depth in the phantom. Both of these uncertainties apply more or less in a similar way to the open and the MLC field and were therefore not considered for the error estimate of the dose ratios. The residual uncertainty of maximal 7% comes from the differences in fluence between the open and the MLC field which was not accounted for, as it is much smaller than the 36% batch uncertainty.
An IMRT treatment delivers more monitor units than a conventional irradiation due to the realization of the intensity modulation. As a consequence, beam-on time is longer for the same delivered dose. Commonly it is assumed that neutron dose equivalent scales with the number of applied monitor units for a radiotherapy treatment irrespectively of the used treatment technique [1, 2]. The measurements presented in this report indicate that this may only be true for superficial tissues outside of the treatment field. Deeper lying tissues outside the treatment volume receive around 35% less neutron dose equivalent than expected (three times expected and around two times observed). In the treated volume the dose reduction is even more pronounced with a 45% reduction at the surface and a 65% reduction in larger depth. However, it should be noted here that the irradiated volume is in general much smaller than the body volume which receives only scatter dose. Therefore, if it is assumed that cancer induction is a function of dose and irradiated volume, the neutron dose reduction in the irradiated volume might not have a large impact. In addition the neutron dose equivalent must be viewed always in relation to the primary dose distribution, which is several orders of magnitude larger in the treated volume.
A possible explanation for the measured difference in scaling of the neutron dose with applied monitor units for open and intensity-modulated fields could be the interplay between neutron production and neutron shielding of the multileaf collimator when used in IMRT. Kry et al.  found in Monte Carlo simulations of neutron production in a Varian linear accelerator head that the MLC can act as a neutron absorber where the primary photon beam is shielded by the jaws. Zanini et al.  did a Monte Carlo study on the photoneutron fields of a Varian linear accelerator operating at a nominal energy of 18 MV. They determined neutron spectra at different locations (inside and outside of the primary field) for different collimation settings. The spectra simulated in that study at 3 cm (as in-field) and 15 cm (as out-of-field) laterally from the isocenter were used to estimate the expected readout of the PADC detectors used in this work. For this purpose the spectra were convolved with the energy dependent detector response function of the PADC detectors determined by PSI [4, 5, 9]. The absolute neutron fluence per cm2 per Gy obtained by Zanini et al. for the static MLC field was multiplied by a factor of three to account for the elongated beam-on time for intensity modulation. The calculated PADC response includes not only the spectral change, but also effects like for example the absorption of neutrons by the MLC. The simulated detector response yielded a neutron dose ratio of 2.4 for the in-field spectrum and 2.0 for the out-of-field spectrum at the surface. These values are in agreement with the measurements of this study. In the work by Zanini et al. it was also shown that for equal field sizes the amount of neutron production in the MLC is smaller than in the jaws.
The neutron spectra simulated in the study by Zanini et al. show a slight shift towards lower energies for the field using the MLC when compared to the open field. This shift lowers also the mean energy, which could be responsible for the change of the ratio between the open field and the intensity-modulated field with depth in the phantom seen in this study, as the moderation of neutrons is energy dependent. Dedicated Monte Carlo simulations would be necessary to assess this in detail.
The findings of this study indicate that the number of applied monitor units during a radiotherapy treatment alone is not predictive for the neutron dose equivalent the patient receives. Outside the treatment volume in larger depth 35% less neutron dose equivalent was delivered than expected for a MU scaling of a factor of three to deliver the same dose to the target for IMRT compared to the open field. As a consequence, the predicted increase of second cancer induction rates from intensity-modulated treatment techniques at large photon beam energies might have been overestimated. The neutron dose to the patient is dependent on several parameters, such as the type and material of the multileaf collimator and the photon energy, which were not investigated in this work and should be included in further studies.
- Followill D, Geis P, Boyer A: Estimates of whole-body dose equivalent produced by beam intensity-modulated conformal therapy. Int J Radiat Oncol Biol Phys 1997,1(3):667-672. Erratum in Int J Radiat Oncol Biol Phys 1997,1;39(3):783View ArticleGoogle Scholar
- Hall EJ, Wuu CS: Radiation-induced second cancers: the impact of 3D-CRT and IMRT. Int J Radiat Oncol Biol Phys 2003, 56: 83-88. 10.1016/S0360-3016(03)00073-7View ArticlePubMedGoogle Scholar
- Xu XG, Bednarz B, Paganetti H: A review of dosimetry studies on external-beam radiation treatment with respect to second cancer induction. Phys Med Biol 2008, 53: R193-R241. 10.1088/0031-9155/53/13/R01PubMed CentralView ArticlePubMedGoogle Scholar
- Fiechtner A, Wernli C: Neutronendosimetrie mit CR-39-Detektoren und AUTOSCAN 60. Anwendung bei PSI-Beschleunigerspektren, Technical Report TM-23-97-10. Paul Scherrer Institut, Villigen, Switzerland; 1998.Google Scholar
- Fiechtner A, Wernli C: Individual neutron monitoring with CR-39 detectors at an accelerator centre. Radiat Prot Dosim 1999, 85: 35-38. 10.1093/oxfordjournals.rpd.a032869View ArticleGoogle Scholar
- Hoedlmoser H, Schuler C, Butterweck G, Chetelat N, Mayer S: Characterization of the 241Am-Be neutron source of the PSI Calibration Laboratory. Technical Report TM-96-11-02, Paul Scherrer Institut, Villigen, Switzerland; 2011.Google Scholar
- Kry SF, Titt U, Followill D, Pönisch F, Vassiliev ON, White RA, Stovall M, Salehpour M: A Monte Carlo model for out-of-field dose calculation from high-energy photon therapy. Med Phys 2007, 34: 3489-3499. 10.1118/1.2756940View ArticlePubMedGoogle Scholar
- Hälg RA, Besserer J, Boschung M, Mayer S, Clasie B, Kry SF, Schneider U: Field calibration of PADC track etch detectors for local neutron dosimetry in man using different radiation qualities. Nucl Inst Meth A 2012.Google Scholar
- Fiechtner A: Messung von thermischen Neutronen mit CR-39-Detektoren. Paul Scherrer Institut, Villigen, Switzerland; 2005. Technical Report TM-96-05-03Google Scholar
- Kry SF, Howell RM, Titt U, Salehpour M, Mohan R, Vassiliev ON: Energy spectra, sources, and shielding considerations for neutrons generated by a flattening filter-free Clinac. Med Phys 2008, 35: 1906-1911. 10.1118/1.2905029View ArticlePubMedGoogle Scholar
- Zanini A, Durisi E, Fasolo F, Ongaro C, Visca L, Nastasi U, Burn KW, Scielzo G, Adler JO, Annand JRM, Rosner G: Monte Carlo simulation of the photoneutron field in linac radiotherapy treatments with different collimation systems. Phys Med Biol 2004, 49: 571-582. 10.1088/0031-9155/49/4/008View ArticlePubMedGoogle Scholar
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