Megavoltage x-ray skin dose variation with an angle using grid carbon fibre couch tops

It is well known that a skin dose from high-energy x-ray radiation varies with the angle of beam incidence or the presence of a radiotherapy linear accelerator couch top material. This note investigates changes produced to the skin dose from a Varian carbon fibre grid couch top at differing angles of incidence for 6 MV x-rays as is often the case clinically. Results have shown that the skin dose can easily be measured using an EBT Gafchromic film whereby the delivered skin dose can be quantified to a high level of spatial resolution, not easily achieved with other skin dose detectors. Results have shown a significant increase in the skin dose specifically at the point of a cross-sectional carbon fibre grid. Values in % of the skin dose increased from approximately 27% (an open area within a 10 cm x 10 cm field) up to 55% (same field size) at the centre of the carbon fibre mesh strip (0 degrees incidence). This is compared to 19% of the skin dose for an open field of a 10 cm x 10 cm beam without the couch material present. At larger angles similar effects occur with values changing from 52% to 75% (60 degrees , 10 cm x 10 cm) in the open area and under the grid, respectively. This produces a wave effect for the skin dose. The average skin dose magnitude increases with the angle of incidence of the beam, ranging from 37.5% to 66% from 0 degrees to 60 degrees (10 x 10 cm), respectively. The symmetric wave nature of the skin dose profile skews to deliver an increased dose on the posterior side of the carbon fibre grid as the angle of incidence increases. Simulated fractional dose delivery on a phantom has shown that over 30 fractions the wave nature of the delivered skin dose is minimized due to the random nature of most patient positioning on the treatment couch. However, some variations are still present as the ratio of the open to grid area is approximately 4:1 and the dose spread is not necessarily completely averaged during a typical fractionated radiotherapy treatment. As such, if the treatment type results in a more rigorously positioned patient on the treatment couch, the wave nature of skin dose delivery may need to be taken into account.     

Elekta Infinity直线加速器治疗床对放疗剂量的影响

目的:研究Elekta Infinity直线加速器治疗床在常用X射线能量下对放疗剂量的影响。方法:将圆柱体模体分别置于碳纤维主治疗床、延长板以及治疗床与延长板衔接处正中,旋转机架,分别让6和10 MV高能X射线穿过治疗床,利用指形电离室测量固体水中间的绝对剂量,得出不同角度下的剂量分布,并计算治疗床对X射线的衰减因子。结果:治疗床与延长板衔接处在120°和240°两个机架角处的剂量衰减因子在6和10 MV两种治疗模式下分别达到了36.02%和36.01%以及30.46%和30.63%,而当机架角为140°~220°时,衔接处与主治疗床的剂量衰减因子相近,在6与10 MV能量下的剂量衰减因子平均值及标准差分别为2.56%±0.49%和2.14%±0.39%以及2.55%±0.48%和1.95%±0.41%,机架角由180°增大或减小时两处的剂量衰减均呈上升趋势,二者均在120°和240°附近达到最大;6和10 MV两种能量下延长板在该角度区间的剂量衰减因子平均值及标准差分别为1.55%±0.24%和1.07%±0.25%,并在115°和245°附近达到最大值,剂量衰减因子分别为4.08%和3.97%以及3.20%和3.34%。结论:后斜野主体部分在主治疗床与衔接处对剂量的衰减低于3%,在延长板处对剂量的衰减小于2%,但在120°和240°附近以及115°和245°附近3处位置的剂量衰减会达到最大,需在计划系统中考虑床的影响;此外,主治疗床与延长板衔接处在120°和240°附近对剂量的衰减急剧增大,不适合作为治疗区域,在治疗病人时需注意避免将靶区移到该区域。     

The effect of gantry angle on megavoltage photon beam attenuation by a carbon fiber couch insert

The use of rigid carbon fiber couch inserts in radiotherapy treatment couches is a well-established method of reducing patient set-up errors associated with couch sag. Several published studies have described such inserts as radiotranslucent with negligible attenuation of the radiation field. Most of these studies were conducted with the radiation field normally incident on the couch and there appears to be no evidence in the literature of the effect of the gantry angle on the extent of beam attenuation by the carbon fiber insert alone during external beam radiotherapy. In this study we examined the magnitude of this effect over a range of posterior oblique gantry angles using a cylindrical solid water phantom containing an ionization chamber placed isocentrically. It was found that a 6 MV photon beam, field size 10 x 5 cm, was attenuated significantly as the gantry angle approached the plane of the couch, from 2% at normal incidence and reaching 9% attenuation at angle of incidence 70 degrees. This could have serious implications regarding dose to the treatment volume for treatments requiring posterior oblique angles of incidence with a possible correction factor necessary in monitor unit calculations.     

Measurement of skin dose variations produced by a silicon-based protective dressing in radiotherapy

Variations in skin dose caused by a silicon-based burn dressing used in radiotherapy during treatment have been investigated. Measurement of these variations in skin dose has been achieved using thermoluminescent dosimeters (TLDs) and Gafchromic film. For a 6 MV x-ray beam results have shown that an approximately 0.4 mm thick silicon mesh dressing increases the average surface dose by approximately 12.5% to 14% of the maximum and average dose at 1 mm depth and by 4% to 6% of the maximum for field sizes ranging from 5 cm x 5 cm up to 40 cm x 40 cm at 100 cm source to surface distance (SSD). The radiation effective thickness of the silicon dressing was calculated to be 0.5 mm +/- 0.05 mm water equivalent. TLDs of various thicknesses provide point-dose assessment and Gafchromic film can provide a detailed two-dimensional dose map with a high spatial resolution. Results have shown that a large variation in skin dose is delivered under the dressing depending on the amount of material directly above it as defined by the silicon mesh outline.     

A Monte Carlo model of the Varian IGRT couch top for RapidArc QA

The objectives of this study are to evaluate the effect of couch attenuation on quality assurance (QA) results and to present a couch top model for Monte Carlo (MC) dose calculation for RapidArc treatments. The IGRT couch top is modelled in Eclipse as a thin skin of higher density material with a homogeneous fill of foam of lower density and attenuation. The IGRT couch structure consists of two longitudinal sections referred to as thick and thin. The Hounsfield Unit (HU) characterization of the couch structure was determined using a cylindrical phantom by comparing ion chamber measurements with the dose predicted by the treatment planning system (TPS). The optimal set of HU for the inside of the couch and the surface shell was found to be respectively -960 and -700 HU in agreement with Vanetti et al (2009 Phys. Med. Biol. 54 N157-66). For each plan, the final dose calculation was performed with the thin, thick and without the couch top. Dose differences up to 2.6% were observed with TPS calculated doses not including the couch and up to 3.4% with MC not including the couch and were found to be treatment specific. A MC couch top model was created based on the TPS geometrical model. The carbon fibre couch top skin was modelled using carbon graphite; the density was adjusted until good agreement with experimental data was observed, while the density of the foam inside was kept constant. The accuracy of the couch top model was evaluated by comparison with ion chamber measurements and TPS calculated dose combined with a 3D gamma analysis. Similar to the TPS case, a single graphite density can be used for both the thin and thick MC couch top models. Results showed good agreement with ion chamber measurements (within 1.2%) and with TPS (within 1%). For each plan, over 95% of the points passed the 3D gamma test.     

Verification of cell irradiation dose deposition using a radiochromic film

We describe a technique for the MTT assay that irradiates all cells at once by a combination of couch movement and a step-and-shoot irradiation technique on a linear accelerator with 6 MV and 18 MV photon beams. In two experimental setups, we obtained maximum to minimum dose ranges of 10 for the constant MU/bin (monitor units per bin) setup and 20 for the variable MU/bin technique. The irradiation technique described is dose rate independent and it can be used on any teletherapy irradiation machine. We also employed radiochromic film dosimetry to verify dose delivered in each of the wells within the dish. It is shown that for the lowest doses, relative dose variation within wells reaches a value of 6%. We also demonstrated that the radiochromic film positioned below the 96-well plate does not underestimate dose deposited within each compartment by more than 2% due to the vertical dose gradient.     

Total body irradiation techniques and dosimetry.

Irradiation techniques and dosimetric methods used for total body irradiation (TBI) performed at Institut Gustave Roussy (Villejuif) are presented. TBI are performed in a 5,6 MV X-ray beam produced by a linear accelerator Neptune. The patient, lying laterally on a couch at 4.20 m from the target, is irradiated by a horizontal beam with a mean nominal dose rate at the abdomen mid-plane of about 9 cGy per minute. The procedure used for TBI consists of three parts in order to deliver 8 Gy in the whole body except for lungs which are protected with a lead screen during a part of irradiation and receive a dose of 4 Gy. We have preferred using "in vivo" measurements methods rather than calculations to determine the doses at different points of the patients. Two kinds of detectors are placed on the patient's skin all along the total body irradiation : two sets of five Therados semi conductors probes permit to control the irradiation and lithium fluoride thermoluminescent dosimeters are used like reference detectors. The dosimetric results obtained during the TBI performed at IGR are discussed.     

Monte Carlo simulation of a dynamic MLC based on a multiple source model.

Detailed knowledge of the characteristics of the radiation field shaped by a multileaf collimator (MLC) is essential in intensity modulated radiotherapy (IMRT). A previously developed multiple source model (MSM) for a 6 MV beam was extended to a 15 MV beam and supplemented with an accurate model of an 80-leaf dynamic MLC. Using the supplemented MSM and the MC code GEANT, lateral dose distributions were calculated in a water phantom and a portal water phantom. A field which is normally used for the validation of the step and shoot technique and a field from a realistic IMRT treatment plan delivered with dynamic MLC are investigated. To assess possible spectral changes caused by the modulation of beam intensity by an MLC, the energy spectra in five portal planes were calculated for moving slits of different widths. The extension of the MSM to 15 MV was validated by analysing energy fluences, depth doses and dose profiles. In addition, the MC-calculated primary energy spectrum was verified with an energy spectrum which was reconstructed from transmission measurements. MC-calculated dose profiles using the MSM for the step and shoot case and for the dynamic MLC case are in very good agreement with the measured data from film dosimetry. The investigation of a 13 cm wide field shows an increase in mean photon energy of up to 16% for the 0.25 cm slit compared to the open beam for 6 MV and of up to 6% for 15 MV, respectively. In conclusion, the MSM supplemented with the dynamic MLC has proven to be a powerful tool for investigational and benchmarking purposes or even for dose calculations in IMRT.     

Two-dimensional measurement of photon beam attenuation by the treatment couch and immobilization devices using an electronic portal imaging device

In our institution, an individualized dosimetric quality assurance protocol for intensity modulated radiotherapy (IMRT) is being implemented. This protocol includes dosimetric measurements with a fluoroscopic electronic portal imaging device (EPID) for all IMRT fields while the patient is being irradiated. For some of the first patients enrolled in this protocol, significant beam attenuation by (carbon fiber) components of the treatment couch was observed. To study this beam attenuation in two-dimensional, EPID images were also acquired in absence of the patient, both with and without treatment couch and immobilization devices, as positioned during treatment. For treatments of head and neck cancer patients with a 6 MV photon beam, attenuation of up to 15% was detected. These findings led to the development of new tools and procedures for planning and treatment delivery to avoid underdosages in the tumor.     

Peripheral dose measurements for 6 and 18 MV photon beams on a linear accelerator with multileaf collimator

Peripheral dose (PD) to critical structures outside treatment volume is of clinical importance. The aim of the current study was to estimate PD on a linear accelerator equipped with multileaf collimator (MLC). Dose measurements were carried out using an ionization chamber embedded in a water phantom for 6 and 18 MV photon beams. PD values were acquired for field sizes from 5 x 5 to 20 x 20 cm2 in increments of 5 cm at distances up to 24 cm from the field edge. Dose data were obtained at two collimator orientations where the measurement points are shielded by MLC and jaws. The variation of PD with the source to skin distance (SSD), depth, and lateral displacement of the measurement point was evaluated. To examine the dependence of PD upon the tissue thickness at the entrance point of the beam, scattered dose was measured using thermoluminescent dosemeters placed on three anthropomorphic phantoms simulating 5- and 10-year-old children and an average adult patient. PD from 6 MV photons varied from 0.13% to 6.75% of the central-axis maximum dose depending upon the collimator orientation, extent of irradiated area, and distance from the treatment field. The corresponding dose range from 18 MV x rays was 0.09% to 5.61%. The variation of PD with depth and with lateral displacements up to 80% of the field dimension was very small. The scattered dose from both photon beams increased with the increase of SSD or tissue thickness along beam axis. The presented dosimetric data set allows the estimation of scattered dose outside the primary beam.     

Feasibility study of multi-pass respiratory-gated helical tomotherapy of a moving target via binary MLC closure

Gated radiotherapy of lung lesions is particularly complex for helical tomotherapy, due to the simultaneous motions of its three subsystems (gantry, couch and collimator). We propose a new way to implement gating for helical tomotherapy, namely multi-pass respiratory gating. In this method, gating is achieved by delivering only the beam projections that occur within a respiratory gating window, while blocking the rest of the beam projections by fully closing all collimator leaves. Due to the continuous couch motion, the planned beam projections must be delivered over multiple passes of radiation deliveries. After each pass, the patient couch is reset to its starting position, and the treatment recommences at a different phase of tumour motion to 'fill in' the previously blocked beam projections. The gating process may be repeated until the plan dose is delivered (full gating), or halted after a certain number of passes, with the entire remaining dose delivered in a final pass without gating (partial gating). The feasibility of the full gating approach was first tested for sinusoidal target motion, through experimental measurements with film and computer simulation. The optimal gating parameters for full and partial gating methods were then determined for various fractionation schemes through computer simulation, using a patient respiratory waveform. For sinusoidal motion, the PTV dose deviations of -29 to 5% observed without gating were reduced to range from -1 to 3% for a single fraction, with a 4 pass full gating. For a patient waveform, partial gating required fewer passes than full gating for all fractionation schemes. For a single fraction, the maximum allowed residual motion was only 4 mm, requiring large numbers of passes for both full (12) and partial (7 + 1) gating methods. The number of required passes decreased significantly for 3 and 30 fractions, allowing residual motion up to 7 mm. Overall, the multi-pass gating technique was shown to be a promising way to reduce the impact of lung tumour motion during helical tomotherapy.     

Dose delivered from Varian's CBCT to patients receiving IMRT for prostate cancer

With the increased use of cone beam CT (CBCT) for daily patient setup, the accumulated dose from CBCT may be significantly higher than that from simulation CT or portal imaging. The objective of this work is to measure the dose from daily pelvic scans with fixed technical settings and collimations. CBCT scans were acquired in half-fan mode using a half bowtie and x-rays were delivered in pulsed-fluoro mode. The skin doses for seven prostate patients were measured on an IRB-approved protocol. TLD capsules were placed on the patient's skin at the central axis of three beams: AP, left lateral (Lt Lat) and right lateral (Rt Lat). To avoid the ring artefacts centred in the prostate, the treatment couch was dropped 3 cm from the patient's tattoo (central axis). The measured AP skin doses ranged 3-6 cGy for 20-33 cm separation. The larger the patient size the less the AP skin dose. Lateral doses did not change much with patient size. The Lt Lat dose was approximately 4.0 cGy, which was approximately 40% higher than the Rt Lat dose of approximately 2.6 cGy. To verify this dose asymmetry, surface doses on an IMRT QA phantom (oval shaped, 30 cm x 20 cm) were measured at the same three sites using TLD capsules with 3 cm table-drop. The dose asymmetry was due to: (1) kV source rotation which always starts from the patient's Lt Lat and ends at Lt Lat. Gantry rotation gets much slower near the end of rotation but dose rate stays constant and (2) 370 degrees scan rotation (10 degrees scan overlap on the Lt Lat side). In vivo doses were measured inside a Rando pelvic heterogeneous phantom using TLDs. The left hip (femoral head and neck) received the highest doses of approximately 10-11 cGy while the right hip received approximately 6-7 cGy. The surface and in vivo doses were also measured for phantoms at the central-axis setup. The difference was less than approximately 12% to the table-drop setup.     

面膜及床单对皮肤剂量的影响

目的：观测面膜和治疗床床单对皮肤剂量的影响。方法：我们用DPD510多通道剂量监测仪及其配套的EDD2型半导体探头分别在水箱上及在患者治疗中对皮肤剂量进行了测定。结果：在水箱上测定结果显示面膜增加8.4%左右，双层床单影响4.8%，双层床单加网格状治疗床板影响14.7%。患者身上实测的结果显示面膜使皮肤剂量增加了4.5%。结论：使用面膜及床单增加了皮肤剂量，临床上需注意这一问题。     

Comparison of build-up dose between Elekta and Varian linear accelerators for high-energy photon beams using radiochromic film and clinical implications for IMRT head and neck treatments

Skin toxicity has been reported for IMRT of head and neck cancer. The purpose of this study was to investigate the dose in the build-up region delivered by a 6 MV treatment plan for which important skin toxicity was observed. We also investigated if the different designs of the treatment head of an Elekta and a Varian linear accelerator, especially the lower position of the Varian multi-leaf collimator, give rise to different build-up doses. For regular square open beams, the build-up dose along the central beam axis is higher for the Varian machine than for the Elekta machine, both for 6 MV and 18 MV. At the Elekta machine at 18 MV, the superficial dose of a diamond shaped 10 x 10 cm2 field is 3.6% lower than the superficial dose of a regular 10 x 10 cm2 field. This effect is not seen at 6 MV. At the Varian machine, the superficial dose of the diamond shaped field is respectively 3.5 and 14.2% higher than the superficial dose of the regular 10 x 10 cm2 field for 6 MV and 18 MV. Despite the differences measured in build-up dose for single beams between the Elekta and the Varian linear accelerator, there were no measurable differences in superficial dose when a typical IMRT dose plan of 6 MV for a head and neck tumour is executed at the two machines.     

碳素纤维床CT值对头部肿瘤放疗计划剂量分布的影响

目的:定量分析碳素纤维床CT值对头部肿瘤放疗计划剂量分布的影响。方法:在Varian Eclipse 13.6计划系统中建立9种不同CT值的碳素纤维床和均匀圆柱水模体模型,并将圆柱水模体放置于碳素纤维床中间,在10 cm[×]10 cm射野下,采用6 MV X射线机架在0°~180°之间以10°为间隔行等中心照射,计算不同CT值的碳素纤维床的吸收剂量差异系数。选取头部肿瘤患者15例,以Eclipse计划系统提供的默认CT值碳素纤维床为基础,设计放疗计划,并将该计划保存为模板计划。随后将模板计划移植至其余8种不同CT值的碳素纤维床图像中,不进行通量优化,重新计算剂量分布。记录9种不同CT值碳素纤维床计划的D2%、D50%、D98%、CI、HI以及GI。结果:在-700 HU至-300 HU内,随着Panel Surface CT值的增加,吸收剂量差异系数逐渐减小;在-1 000 HU至-900 HU内,随着Panel Interior CT值的增加,吸收剂量差异系数逐渐增大。默认CT值的碳素纤维床计划与其他8种碳素纤维床计划的D2%、D50%、D98%,以及GI差异具有统计意义（P<0.05）,而HI则无统计学差异（P>0.05）。结论:物理师在设计放疗计划时,应根据实测治疗床的CT值构建碳素纤维床模型。     

Build-up and surface dose measurements on phantoms using micro-MOSFET in 6 and 10 MV x-ray beams and comparisons with Monte Carlo calculations

This work is intended to investigate the application and accuracy of micro-MOSFET for superficial dose measurement under clinically used MV x-ray beams. Dose response of micro-MOSFET in the build-up region and on surface under MV x-ray beams were measured and compared to Monte Carlo calculations. First, percentage-depth-doses were measured with micro-MOSFET under 6 and 10 MV beams of normal incidence onto a flat solid water phantom. Micro-MOSFET data were compared with the measurements from a parallel plate ionization chamber and Monte Carlo dose calculation in the build-up region. Then, percentage-depth-doses were measured for oblique beams at 0 degrees-80 degrees onto the flat solid water phantom with micro-MOSFET placed at depths of 2 cm, 1 cm, and 2 mm below the surface. Measurements were compared to Monte Carlo calculations under these settings. Finally, measurements were performed with micro-MOSFET embedded in the first 1 mm layer of bolus placed on a flat phantom and a curved phantom of semi-cylindrical shape. Results were compared to superficial dose calculated from Monte Carlo for a 2 mm thin layer that extends from the surface to a depth of 2 mm. Results were (1) Comparison of measurements with MC calculation in the build-up region showed that micro-MOSFET has a water-equivalence thickness (WET) of 0.87 mm for 6 MV beam and 0.99 mm for 10 MV beam from the flat side, and a WET of 0.72 mm for 6 MV beam and 0.76 mm for 10 MV beam from the epoxy side. (2) For normal beam incidences, percentage depth dose agree within 3%-5% among micro-MOSFET measurements, parallel-plate ionization chamber measurements, and MC calculations. (3) For oblique incidence on the flat phantom with micro-MOSFET placed at depths of 2 cm, 1 cm, and 2 mm, measurements were consistent with MC calculations within a typical uncertainty of 3%-5%. (4) For oblique incidence on the flat phantom and a curved-surface phantom, measurements with micro-MOSFET placed at 1.0 mm agrees with the MC calculation within 6%, including uncertainties of micro-MOSFET measurements of 2%-3% (1 standard deviation), MOSFET angular dependence of 3.0%-3.5%, and 1%-2% systematical error due to phantom setup geometry asymmetry. Micro-MOSFET can be used for skin dose measurements in 6 and 10 MV beams with an estimated accuracy of +/- 6%.     

测量治疗床、SBRT体架及DAVID系统造成的剂量衰减

目的:通过测量6 MV的X线经过治疗床、SBRT体架和DAVID系统后的剂量衰减,为计划设计时的剂量补偿提供参考数据。方法:加速器与固体水之间无任何器材,源皮距(SDD)为100 cm,出束照射100 MU,利用电离室测量固体水下深度5 cm的剂量,作为基准剂量。同样条件下测量治疗床、SBRT体架和DAVID系统以不同组合在水下深度5 cm的剂量。结果:射线穿过治疗床剂量衰减了3.08%,经过治疗床和SBRT体架衰减了13.10%,经过治疗床、SBRT体架和DAVID系统衰减了13.10%,经过治疗床和DAVID系统衰减了10.88%,经过DAVID系统衰减8.07%。结论:在没有安装DAVID系统时,只有经过治疗床和SBRT体架的射线需要进行剂量补偿。安装了DAVID系统时,所有的射线束都需要计算DAVID系统对射线的衰减,经过治疗床和SBRT体架的射线还需要计算这两个器材对剂量的衰减。不同情况下衰减比例不同,需要补偿的剂量也不同。     

Surface dosimetry for oblique tangential photon beams: a Monte Carlo simulation study

The effect of beam obliquity on the surface relative dose profiles for the tangential photon beams was studied. The 6 and 15 MV photon beams with 4 x 4 and 10 x 10 cm2 field sizes produced by a Varian 21 EX linear accelerator were used. Phase-space models of the photon beams were created using Monte Carlo simulations based on the EGSnrc code, and were verified using film measurements. The relative dose profiles in the phantom skin, at 2 mm depth from the surface of the half-phantom geometry, or HPG, were calculated for increasing gantry angles from 270 to 280 deg clockwise. Relative dose profiles of a full phantom enclosing the whole tangential beam (full phantom geometry, or FPG) were also calculated using Monte Carlo simulation as a control for comparison. The results showed that, although the relative dose profiles in the phantom skin did not change significantly with an oblique beam using a FPG, the surface relative depth dose was increased for the HPG. In the HPG, with 6 MV photon beams and field size = 10 x 10 cm2, when the beam angle, starting from 270 deg, was increased from 1 to 3 deg, the relative depth doses in the phantom skin were increased from 68% to 79% at 10 cm depth. This increase in dose was slightly larger than the dose from 15 MV photon beams with the same field size and beam angles, where the relative depth doses in phantom skin were increased from 81% to 87% at 10 cm depth. A parameter called the percent depth dose (PDD) ratio, defined as the relative depth dose from the HPG to the relative depth dose from the FPG at a given depth along the phantom skin, was used to evaluate the effect of the phantom-air interface. It is found that the PDD ratio increased significantly when the beam angle was changed from zero to 1-3 degrees. Moreover, the PDD ratio, for a given field size, experienced a greater increase for 6 MV than for 15 MV. For the same photon beam energy, the PDD ratio increased more with a 4 x 4 cm2 field compared to 10 x 10 cm2. The results in this study will be useful for physicists and dosimetrists to predict the surface relative dose variations when using clinical tangential-like photon beams in radiation therapy.     

有无均整器模式下臂架与准直器不同角度条件下的剂量学比较

目的:探讨臂架或准直器角度的改变对均整（FF）与非均整（FFF）两种模式的射线剂量的影响。方法:选用Versa HD直线加速器配备的6 MV/10 MV光子束FF/FFF模式4档能量在设定好九点位置的10 cm×10 cm标准射野内进行实验。首先,借助IMF等中心夹具将Mapcheck2固定于治疗机机头,并用Mapcheck2测量相同臂架与准直器角度条件下4种光子束输出的平面剂量值;其次,用Mapcheck2测量在相同臂架角度、不同准直器角度与相同准直器角度、不同臂架角度两种条件下4种光子束的中心轴剂量值;最后,固定准直器为0°,设立两组臂架对穿射野（0°与180°,90°与270°）。拆除Mapcheck2,采用固体水和FC65-G电离室建立一个测量模体来测量4种光子束在两组等中心对穿野的剂量。运用SPSS统计软件对该实验收集到的数据进行对比分析。结果:在相同臂架与准直器角度条件下,4种光子束辐照9个点的平面剂量之间均存在明显统计学差异（P6 MV FF =0.020, P6 MV FFF=0.017, P10 MV FF =0.030, P10 MV FFF=0.016）;而不同臂架角度或不同准直器角度条件下,4种能量光子束的中心轴点剂量值均无统计学差异。在0°与180°的对穿野,4种能量光子束的输出剂量存在统计学差异（P6 MV FF =0.001, P6 MV FFF=0.002, P10 MV FF =0.003, P10 MV FFF=0.001）,而在90°与270°的对穿野无统计学差异。结论:Versa HD直线加速器拥有优良的机械等中心性能。在实际工作时,臂架和准直器的旋转,均不影响光子束的中心轴剂量的准确输出。在FF模式下,射线能量越高,受治疗床影响越小;FFF模式射线由于射线质软,能量越高,更易受到治疗床的衰减作用,在实际中应引起重视。     

Dose delivery error detection by a computer-controlled linear accelerator

A commercial dual photon energy, computer-controlled linear accelerator has a complex collimation and beam delivery system. For accurate dose delivery, six separate motorized elements must be properly positioned for a given beam selection. Experimentally instituted misalignments of the primary electron scattering foils, the primary collimator, the flattening filter, the scattering foil carousel, and the backscatter shield or shutter produced significant dose delivery errors. The ability of the Mylar window monitor chamber to detect these errors was examined for x-ray beams. The fault detection system failed to interrupt dose delivery in a number of situations where the error in dose per monitor unit delivered ranged from -6% to +270% of the calibrated value.