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. 2022 Mar 3;36(2):1013–1017. doi: 10.21873/invivo.12795

Clinical Application Study of Semi-cylindrical Beam Spoiler for Radiation Treatment of Early-stage Glottic Cancer Patients

DONG HYEOK CHOI 1, SO HYUN AHN 2,#, WOO SANG AHN 3,#, SEONG SOO SHIN 3, JIN SUNG KIM 2
PMCID: PMC8931932  PMID: 35241564

Abstract

Background/Aim: The purpose of this study was to determine whether a semi-cylindrical beam spoiler (sCBS) developed herein effectively increases the skin dose in patients with early-stage glottic cancer.

Patients and Methods: We measured the surface doses for 26 patients who used the sCBS during treatment of early-stage glottic cancer through a parallel-opposed lateral two-field 6 MV photon beam. Measurements were performed by attaching optically stimulated luminescent dosimeters to the left, right, anterior (in-field), inferior, and superior (out-field) sides of the patient.

Results: The measured results were 81.8±2.1% (left), 81.0±1.7% (right), and 76.8±2.7% (anterior) in the in-field region compared to prescription doses, with 5.7±1.7% (superior) and 2.7±0.7% (inferior) in the out-field region.

Conclusion: sCBS can deliver a suitably ideal surface dose for treatment of early-stage glottic cancer.

Keywords: Beam spoiler, glottic cancer, photon beam, surface dose, radiotherapy, optically stimulated luminescent dosimeter


Several studies have reported that the average 5-year overall survival rate for T1 glottic cancer is 85-95% (1-4). Thus, the survival rate for patients with early-stage glottic cancer is high; however, there are factors that affect local control, such as fraction size, biologically effective dose (BED) of a tumor, and inclusion/exclusion of the anterior commissure; many studies have been conducted and reported on these factors (5-9). Kitani et al. evaluated prognostic factors in patients who received definitive radiation therapy from 1999 to 2011 and confirmed that the anterior commissure involvement was an important factor affecting local control (5). Lim et al. analyzed local failure in 222 patients with T1-2N0 squamous-cell carcinoma of the glottis larynx who received definitive radiation therapy (RT) from 1981 to 2010 (6).

Therefore, during RT, it is necessary to ensure that the prescribed dose is sufficiently delivered to the entire lesion, including the anterior commissure located at a shallow depth. As noted in our previous work, bolus or beam spoilers for total body irradiation (TBI) can be considered as suitable options, but they are imperfect solutions owing to several shortcomings. In general, a bolus is used to increase the dose delivered to the skin area by compensating for insufficient electron balance when using megavolt treatment beams. However, since the head and neck regions have many curvatures due to anatomical characteristics, if a typical bolus is used, it may not be in close contact with the target area, and an air layer may be formed. On anatomically curved surfaces, air gaps are likely to occur between the bolus and skin, resulting in an underdose owing to the unexpected air gap. Butson et al. reported that an underdose of up to 6% may occur in the skin region from a 1 cm air gap (10). In addition, there may be difficulties in securing reproducibility during treatments that are repeated daily. The beam spoiler for TBI cannot be positioned close to the skin because of its structural characteristics; since the treatment for glottic cancer uses two bilateral beams, it may be cumbersome to move the beam spoiler for each field, and the position reproducibility with the beam spoiler may be poor.

Hence, we developed a dedicated beam spoiler for head and neck irradiation, called a semi-cylindrical beam spoiler (sCBS), to overcome these concerns and studied the percent depth dose (PDD) measurement and phantom treatment plan (11). Then, we applied this beam spoiler to actual patient treatments and measured the skin doses to check for accurate delivery of the prescribed dosage. The reason for using the device in actual treatment is that unlike a phantom, the body weight of a patient may change over the course of the treatment, and there may be daily variations in the setup. Since the treatment is 2D in nature and does not use image guided radiation therapy (IGRT), the reproducibility was confirmed through in vivo dosimetry.

Patients and Methods

Semi-cylindrical beam spoiler (sCBS). We used an sCBS for early-stage glottic cancer RT along with a parallel-opposed lateral two-field 6 MV photon beam. The sCBS was made of polymethylmethacrylate (PMMA, density: 1.18 g/cm3) and had an inner radius of 18 cm and a thickness of 0.5 cm with respect to the semi-cylindrical shape (11).

Patients. A total of 26 early-stage glottic cancer patients who were treated with the sCBS from February 2012 to March 2016 were enrolled in this study. The details regarding the patients are summarized in Table I. All patients were treated with two-opposing, bilateral beams using a Varian Clinac iX (Varian Medical Systems, Palo Alto, CA, USA). In addition, the sCBS was applied to the patients during computed tomography (CT) simulation and treatment. Figure 1 shows the CT images of a patient with the sCBS. The source-to-surface distance (SSD) was set to 100 cm, and the dose rate and field size were set to 500 MU/s and 10×10 cm2, respectively. The 6 MV photon beam was then used to deliver the prescribed dose of 200 cGy.

Table I. Characteristics of the 26 glottic cancer patients: sex, age, location, grade, stage, ECOG performance, and commissure involvement for each patient.

graphic file with name in_vivo-36-1014-i0001.jpg

M: Male.

Figure 1. Computed tomography simulation of a patient with a semicylindrical beam spoiler applied: (A) cross-sectional view; (B) front view.

Figure 1

Measurements. As shown in Figure 2, optically stimulated luminescent dosimeters (OSLDs) were attached to the left side, right side, anterior (in-field) direction, inferior direction, and superior (out-field) direction to measure the surface dose. The number of measurements performed was 1-5 fractions per patient, and the ratio of surface dose according to the prescribed dose was obtained. Our study was based on at least three in vivo measurements per patient. However, if repeated measurements were impossible owing to the conditions of the treatment room, only one or two in vivo measurements were obtained. Furthermore, if the in vivo results measured thrice had large deviations, up to five measurements were performed.

Figure 2. Optically stimulated luminescent dosimeters attached to a patient with a semi-cylindrical beam spoiler applied: (A) front view; (B) side view.

Figure 2

Results

Table II shows the surface dose for each patient and ratio of surface dose per prescribed dose (200 cGy). The average in-field surface doses obtained were 163.7±4.1 (81.8±2.1%), 162.2±3.4 (81.0±1.7%), and 153.5±5.3 (76.8±2.7%) cGy for the left side, right side, and anterior direction, respectively. The outfield measurement results were 5.7±1.7 (2.8±1.7%) and 2.7±1.5 (1.4±0.7%) cGy in the superior and inferior directions, respectively. The average measured deviation by fraction was 2.2%, and the largest deviation was 8.2%.

Table II. Surface dose to the patients as measured through optically stimulated luminescent dosimeters: left, right, and anterior surface doses measured in the in-field condition, and external dose on the superior and inferior regions as measured in the out-field condition and ratio of received to prescribed dose.

graphic file with name in_vivo-36-1015-i0001.jpg

Discussion

We conducted a study to evaluate the basic dose characteristics, such as PDD, using the previously developed sCBS with a phantom (11). From the results of the previous phantom study, it was confirmed that when the sCBS was applied, a dose of about 85.13% of the prescribed dose entered the skin. From the measured results in patients in this study, it was confirmed that the expected build-up effect was adequately exhibited, with 81.8% and 81.0% delivered doses for the left and right sides, respectively.

In principle, we decided to measure more than three fractions to increase the reliability of the measurements. However, there were patients from whom measurements could not be obtained owing to their treatment times, therefore, only one or two measurements were recorded. In addition, there were patients from whom four or five measurements were obtained owing to large differences in the first three measurements. As shown in Table II, it is observed that there is a deviation of up to 8.2% during repeated measurements, which is attributed to patient movements during the treatment, weight variations, or changes in the measurement positions.

As shown in the results, the measured result from the anterior direction is lower than those from the left and right sides, which is attributed to underestimations due to the influence of angular dependence because the angle between the active window of the OSLDs and beam incident direction is 90˚ (12-14). The sCBS developed exclusively for head and neck treatments in this study need not be moved from one field to the next during treatment, does not need customization for each patient, and has the advantage of a simple setup. However, if IMRT or VMAT treatments are performed, the beam spoiler’s positional reproducibility must be more precise than that available at present through IGRT because IMRT is more sensitive to positional accuracy by transmitting beams using small beamlets using multi leaf collimator (MLC) (15-19).

Conclusion

This study explored the clinical application and usefulness of the sCBS through evaluation of the surface dose accumulation characteristics during treatment for early-stage glottic cancer. The sCBS provides improved build-up to the beam, thereby providing increased skin protection and helping deliver a sufficient percentage of the prescribed dose. In addition, it is very convenient for clinical use in the field, with a simple installation method. Therefore, we confirm that the sCBS is a useful tool for early-stage glottic cancer RT.

Conflicts of Interest

The Authors declare no conflicts of interest in relation to this study.

Authors’ Contributions

Conceptualization: DHC and WSA; methodology: WSA and SA; data curation: WSA; formal analysis: DHC; funding acquisition: WSA and SA, DHC and WSA; supervision: WSA and SA; validation: JSK and SSS; visualization: JSK and SSS; writing-original draft: DHC and SA; writing-review and editing: WSA, DHC, and SA.

Acknowledgements

This research was supported by the Nuclear Safety Research Program through the Korea Foundation of Nuclear Safety (KoFONS) using financial resources granted by the Nuclear Safety and Security Commission (NSSC) of the Republic of Korea (No. 2003013), National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (No. 2019R1A2C108912912), Basic Science Research Program through the National Research Foundation of Korea (NRF) grant funded by the Ministry of Education (Nos. 2018R1D1A1B07050217 and 2021R1I1A1A01057995), and Medical Research Promotion Program through the Gangneung Asan Hospital funded by the Asan Foundation (No. 2021IC003).

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