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방사선 치료 시 조사야 내에 위치할 수 있는 이물질이 체표선량에 미치는 영향
홍채선,김경태,주상규,김종식,박영환,Hong, Chae-Seon,Kim, Kyung-Tae,Ju, Sang-Gyu,Kim, Jong-Sik,Park, Young-Hwan 대한방사선치료학회 2002 大韓放射線治療技術學會誌 Vol.14 No.1
Purpose : In radiotherapy, various materials are used to located in treatment field unintentionally. It increases the dose delivered to the skin by interactions of the X-ray within the materials and occurs unwanted skin reaction.(due to the dose build-up effect) This aim of the this study is to measure the increase in skin dose when 13 materials are located in treatment field. Methods : Photon beam measurements were made using an plane-parallel chamber (Markus, PTW-Freiburg) in a polystyrene phantom. skin dose were measured using various overlaying 13 materials. a fixed geometry of a $10{\times}10cm$ field, a SSD=100cm and photon energy 4MV on Varian CLINAC 600C accelerator were used for all measurements. Results : There is an increase in skin dose for all materials($16.4{\sim}160.1\%$). As a percentage of maximum dose, the lowest skin dose were measured for the underwear with silk($43.2\%$) and the highest were measured for the 100m1 fluid-bag($96.6\%$) Conclusion : There is a significant increase in skin dose with 13 materials in the treatment field. a significant increase in skin dose can occur which could produce unwanted skin reaction. considerations for placement of 13 materials to be outside the treatment field whenever possible should be used to keep skin dose to a minimum level.
변형 근치적 유방절제술 후 방사선치료에서 볼루스 적용횟수에 대한 고찰
홍채선,김종식,김영곤,박영환,Hong, Chae-Seon,Kim, Jong-Sik,Kim, Young-Kon,Park, Young-Hwan 대한방사선치료학회 2006 대한방사선치료학회지 Vol.18 No.2
Purpose: Post-mastectomy radiotherapy (PMR) is known to decrease loco-regional recurrence. Adequate skin and dermal dose are achieved by adding bolus. The more difficult clinical issue is determining the necessary number of bolus treatment, given the limits of normal skin tolerance. The aim of this study is to evaluate the necessary number of bolus treatment after PMR in patients with breast cancer. Materials and Methods: Four female breast cancer patients were included in the study. The median age was 53 years(range, $38{\sim}74$), tumor were left sided in 2 patients and right sided in 2patients. All patients were treated with postoperative radiotherapy after MRM. Radiotherapy was delivered to the chest wall (C.W) and supraclavicular lymph nodes (SCL) using 4 MV X-ray. The total dose was 50 Gy, in 2 Gy fractions (with 5 times a week). CT was peformed for treatment planning, treatment planning was peformed using $ADAC-Pinnacles^3$ (Phillips, USA) for all patients without and with bolus. Bolus treatment plans were generated using image tool (0.5 cm of thickness and 6 cm of width). Dose distribution was analyzed and the increased skin dose rate in the build-up region was computed and the skin dose using TLD-100 chips (Harshaw, USA) was measured. Results: No significant difference was found in dose distribution without and with bolus; C.W coverage was $95{\sim}100%$ of the prescribed dose in both. But, there was remarkable difference in the skin dose to the scar. The skin dose to the scar without and with bolus were $100{\sim}105%\;and\;50{\sim}75%$. The increased skin dose rates in the build-up region for Pt. 1, Pt. 2. Pt. 3 and Pt. 4 were 23.3%, 35.6%, 34.9%, and 41.7%. The results of measured skin dose using TLD-100 chips in the cases without and with bolus were 209.3 cGy and 161.1 cGy, 200 cGy and 150.2 cGy, 211.4 cGy and 160.5 cGy, 198.6 cGy and 155.5 cGy for Pt. 1, Pt. 2, Pt. 3, and Pt. 4. Conclusion: It was concludes through this analysis that the adequate number of bolus treatments is 50-60% of the treatment program. Further, clinical trial is needed to evaluate the benefit and toxicity associated with the use of bolus in PMR.
Large Pendulous Breast 환자의 방사선 치료에 있어서 엎드린 자세의 유용성 평가
홍채선,주상규,박주영,Hong, Chae-Seon,Ju, Sang-Gyu,Park, Ju-Young 대한방사선치료학회 2008 대한방사선치료학회지 Vol.20 No.1
Purpose: To evaluate dosimetry results of three different techniques for whole breast irradiation after conservative surgery of large pendulous breast patient. Materials and Methods: Planning computed tomography (CT) scans for three techniques were performed on a GE Hi-speed advantage CT scanner in the supine (SP), supine with breast supporting Device (SD) and prone position on a custom prone mattress (PP). Computed tomography images were acquired at 5 mm thickness. The clinical target volumes (CTV), ipsilateral lung and heart were delineated to evaluate the dose statistic, and all techniques were planned with the tangential photon beams (Pinnacle$^3$, Philips Medical System, USA). The prescribed dose was 50 Gy delivered in 25 fractions. To evaluate the dose coverage for CTV, we analysed percent volume of CTV receiving minimum of 95%, 100%, 105%, and 110% of prescription dose ($V_{95}$, $V_{100}$, $V_{105}$, and $V_{110}$) and minimal dose covering 95% ($D_{95}$) of CTV. The dosimetric comparison for heart and ipsilateral lung was analysed using the minimal dose covering 5% of each organs ($D_5$) and the volume that received >18 Gy for the heart and >20 Gy for the ipsilateral lung. Results: Target volume coverage ($V_{95}$ and $V_{100}$) was not significantly different for all technique. The V105 was lower for PP (1.2% vs. 4.4% for SP, 11.1% for SD). Minimal dose covering 95% ($D_{95}$) of target was 47.5 Gy, 47.7 Gy and 48 Gy for SP, SD and PP. The volume of ipsilateral lung received >20 Gy was 21.7%, 11.6% and 4.9% for SP, SD and PP. The volume of heart received >18 Gy was 17.0%, 16.1% and 9.8% for SP, SD and PP. Conclusion: Prone positioning of patient for large pendulous breast irradiation enables improving dose uniformity with minimal heart and lung doses.
세기조절방사선치료의 환자별 정도관리를 위한 2차원적 선량계의 유용성 평가
홍채선(Chae Seon Hong),임종수(Jongsoo Lim),주상규(Sang Gyu Ju),신은혁(Eunhyuk Shin),한영이(Youngyih Han),안용찬(Yong Chan Ahn) 대한방사선종양학회 2009 Radiation Oncology Journal Vol.27 No.2
목 적: 세기조절방사선치료에 있어서 치료 전 환자별 정도관리(QA)에 사용하는 EDR2 필름과 2차원 이온전리함배열(MatriXX), 그리고 전자포탈영상장치(EPID)에 대해 절대선량계와 상대선량계로서의 정확도와 효율성을 평가했다.대상 및 방법: 6 MV X-선을 이용하여 두 가지 유형(기준 조사면, 오차 평가 조사면)의 세기조절 조사면을 설계하고 EDR2 필름, MatriXX, EPID를 사용하여 절대선량과 상대적 선량분포를 비교, 분석했다. 세 시스템의 절대선량 정확성을 평가하기 위해 세 시스템의 선량 측정값과 전리함 측정값을 비교했고, 상대적 선량분포 평가를 위해 기준 조사면과 의도적으로 MLC leaf 위치를 변형시킨 오차 평가 조사면에서 감마(γ)값과 조사면 수직 프로파일을 분석했다. 또한, 환자별 QA 전 과정을 수행하는데 소요되는 시간을 측정하여 시스템에 따른 업무 부하를 비교했다.결 과: EDR2 필름, MatriXX, 그리고 EPID의 절대선량 측정값과 전리함 측정값을 비교한 결과 EPID는 1%, MatriXX는 2%, EDR2 필름은 3% 이내의 오차 측정 정확도를 보였다. EDR2 필름과 EPID는 허용기준 3%/3 mm와 2%/2 mm 모두에서 감마값이 1을 초과하는 화소(γ%>1)가 전체 화소의 2% 이내였다. 그러나 MatriXX의 경우 3%/3 mm에서는 1% 이내의 오차를 보였으나 2%/2 mm를 적용한 10×20 cm2와 10×10 cm2에서는 각각 5.94%와 4.95%로 증가했다. 세 시스템으로부터 얻은 오차 평가 조사면의 선량 분포를 치료계획 장치로부터 얻은 기준 조사면과 중첩하여 감마 분석한 결과, 3%/3 mm에서 EDR2 필름이 ?4 mm의 MLC leaf 오차 식별이 가능했고 EPID는 ?3 mm 오차를 감지했다. 2%/2 mm의 경우, EDR2 필름과 EPID에서 각각 ?3 mm와 ?2 mm의 오차 식별이 가능했다. 그러나 MatriXX의 경우 경계가 불분명해 오차 구분이 어려웠다. 환자별 QA 전 과정을 수행하는데 소요되는 시간은 EDR2 필름이 약 110분, MatriXX가 약 80분, EPID가 약 55분이었다. 결 론: 본 연구는 IMRT의 치료 전 환자별 QA를 위한 EDR2 필름, MatriXX, 그리고 EPID의 측정 정확도와 효율성을 분석했다. EDR2 필름과 EPID는 선량 측정 정확도가 우수했으며, MatriXX는 측정 시간이 짧았다. 본 연구 결과는 임상에서 효율적인 IMRT QA 시스템을 구축하는데 좋은 자료가 될 것으로 생각한다. Purpose: To compare the accuracy and efficacy of EDR2 film, a 2D ionization chamber array (MatriXX) and an amorphous silicon electronic portal imaging device (EPID) in the pre-treatment QA of IMRT. Materials and Methods: Fluence patterns, shaped as a wedge with 10 steps (segments) by a multi-leaf collimator (MLC), of reference and test IMRT fields were measured using EDR2 film, the MatriXX, and EPID. Test fields were designed to simulate leaf positioning errors. The absolute dose at a point in each step of the reference fields was measured in a water phantom with an ionization chamber and was compared to the dose obtained with the use of EDR2 film, the MatriXX and EPID. For qualitative analysis, all measured fluence patterns of both reference and test fields were compared with calculated dose maps from a radiation treatmentplanning system (Pinnacle, Philips, USA) using profiles and γ evaluation with 3%/3 mm and 2%/2 mm criteria. By measurement of the time to perform QA, we compared the workload of EDR2 film, the MatriXX and EPID. Results: The percent absolute dose difference between the measured and ionization chamber dose was within 1% for the EPID, 2% for the MatriXX and 3% for EDR2 film. The percentage of pixels with γ%>1 for the 3%/3 mm and 2%/2 mm criteria was within 2% for use of both EDR2 film and the EPID. However, differences for the use of the MatriXX were seen with a maximum difference as great as 5.94% with the 2%/2 mm criteria. For the test fields, EDR2 film and EPID could detect leaf-positioning errors on the order of ?3 mm and ?2 mm, respectively. However it was difficult to differentiate leaf-positioning errors with the MatriXX due to its poor resolution. The approximate time to perform QA was 110 minutes for the use of EDR2 film, 80 minutes for the use of the MatriXX and approximately 55 minutes for the use of the EPID. Conclusion: This study has evaluated the accuracy and efficacy of EDR2 film, the MatriXX and EPID in the pre-treatment verification of IMRT. EDR2 film and the EPID showed better erformance for accuracy, while the use of the MatriXX significantly reduced measurement and analysis times. We propose practical and useful methods to establish an effective QA system in a clinical environment.
연속촬영 전자조사 문 영상을 이용한 오프라인 기반 치료 중 내부 장기 움직임 확인 시스템의 개발
주상규,홍채선,허웅,김민규,한영이,신은혁,신정석,김진성,박희철,안성환,임도훈,최두호,Ju, Sang-Gyu,Hong, Chae-Seon,Huh, Woong,Kim, Min-Kyu,Han, Young-Yih,Shin, Eun-Hyuk,Shin, Jung-Suk,Kim, Jing-Sung,Park, Hee-Chul,Ahn, Sung-Hwan,Lim, Do-Ho 한국의학물리학회 2012 의학물리 Vol.23 No.2
방사선치료 중 내부 장기의 움직임을 확인하고 이를 보정하는 것은 움직이는 종양에 정확히 방사선을 조사하는데 매우 중요한 역할을 한다. 실제 치료 중 획득한 연속촬영 전자조사 문(cine EPID) 영상을 이용해 치료 중 내부 장기 움직임을 추적하는 오프라인 기반 분석 시스템(IMVS, Internal-organ Motion Verification System using cine EPID)을 개발하였고 모형을 이용하여 개발된 시스템의 정확도와 유용성을 평가했다. IMVS는 cine EPID영상을 이용한 내부 장기 움직임 추적을 위해 내부 표지자를 이용한 유형 정합 알고리즘을 이용했다. 시스템의 성능평가를 위해 폐와 폐 종양을 묘사한 인체 모형과 이를 상하(SI, superior-inferior)방향으로 직선 운동시키는 구동 장치와 제어 프로그램을 고안했다. 모형을 4초 주기로 2 cm 직선 운동 시키면서 10 MV X선으로 3.3 fps, 6.6 fps속도로 cine EPID 영상($1,024{\times}768$ 해상도)를 획득했다. 획득된 cine EPID 영상은 IMVS를 이용하여 표적의 움직임을 추적하고 기존 외부 표지자를 이용한 비디오 영상 기반 추적시스템(RPM, Real-time Position Management, Varian, USA)으로부터 얻은 결과와 비교했다. 정량적 평가를 위해 두 시스템으로부터 움직임의 평균 주기(Peak-To-Peak), 진폭과 패턴(RMS, Root Mean Square)을 측정하여 비교했다. RPM과 IMVS로 측정한 폐 종양 모형의 움직임 주기는 각각 $3.95{\pm}0.02$ (RPM), $3.98{\pm}0.11$ (IMVS 3.3 fps), $4.005{\pm}0.001$ (IMVS 6.6 fps) 초로 실제움직임 주기인 4초와 잘 일치했다. IMVS로 획득한 모형 내부장기의 평균 움직임 진폭은 3.3 fps에서 $1.85{\pm}0.02$ cm, 6.6 fps에서 $1.94{\pm}0.02$ cm으로 실제 진폭 2 cm에 비해 각각 0.15 cm (오차 7.5%) 및 0.06 cm (오차 3%)의 차를 보였다. 움직임 신호의 일치성 평가를 위해 측정한 RMS는 0.1044 (IMVS 3.3 fps), 0.0480 (IMVS 6.6 fps)로 계획된 신호와 잘 일치 했다. cine EPID 영상을 이용하여 내부 표지자의 움직임을 추적하는 IMVS는 모형 실험에서 내부 장기의 움직임을 3% 오차 내에서 확인 가능했다. IMVS는 치료 중 내부장기 움직임을 측정하고 이를 사차원 방사선 치료계획과 비교하여 오차를 보정하는데 기여할 것으로 생각된다. Verification of internal organ motion during treatment and its feedback is essential to accurate dose delivery to the moving target. We developed an offline based internal organ motion verification system (IMVS) using cine EPID images and evaluated its accuracy and availability through phantom study. For verification of organ motion using live cine EPID images, a pattern matching algorithm using an internal surrogate, which is very distinguishable and represents organ motion in the treatment field, like diaphragm, was employed in the self-developed analysis software. For the system performance test, we developed a linear motion phantom, which consists of a human body shaped phantom with a fake tumor in the lung, linear motion cart, and control software. The phantom was operated with a motion of 2 cm at 4 sec per cycle and cine EPID images were obtained at a rate of 3.3 and 6.6 frames per sec (2 MU/frame) with $1,024{\times}768$ pixel counts in a linear accelerator (10 MVX). Organ motion of the target was tracked using self-developed analysis software. Results were compared with planned data of the motion phantom and data from the video image based tracking system (RPM, Varian, USA) using an external surrogate in order to evaluate its accuracy. For quantitative analysis, we analyzed correlation between two data sets in terms of average cycle (peak to peak), amplitude, and pattern (RMS, root mean square) of motion. Averages for the cycle of motion from IMVS and RPM system were $3.98{\pm}0.11$ (IMVS 3.3 fps), $4.005{\pm}0.001$ (IMVS 6.6 fps), and $3.95{\pm}0.02$ (RPM), respectively, and showed good agreement on real value (4 sec/cycle). Average of the amplitude of motion tracked by our system showed $1.85{\pm}0.02$ cm (3.3 fps) and $1.94{\pm}0.02$ cm (6.6 fps) as showed a slightly different value, 0.15 (7.5% error) and 0.06 (3% error) cm, respectively, compared with the actual value (2 cm), due to time resolution for image acquisition. In analysis of pattern of motion, the value of the RMS from the cine EPID image in 3.3 fps (0.1044) grew slightly compared with data from 6.6 fps (0.0480). The organ motion verification system using sequential cine EPID images with an internal surrogate showed good representation of its motion within 3% error in a preliminary phantom study. The system can be implemented for clinical purposes, which include organ motion verification during treatment, compared with 4D treatment planning data, and its feedback for accurate dose delivery to the moving target.
콘빔CT 촬영 시 mAs의 변화에 따른 피부선량과 영상 품질에 관한 평가
안종호,홍채선,김진만,장준영,Ahn, Jong-Ho,Hong, Chae-Seon,Kim, Jin-Man,Jang, Jun-Young 대한방사선치료학회 2008 대한방사선치료학회지 Vol.20 No.1
Purpose: Cone-beam CT using linear accelerator attached to on-board imager is a image guided therapy equipment. Because it is to check the patient's set-up error, correction, organ and target movement. but imaging dose should be cause of the secondary cancer when taking a image. The aim of this study is investigation of appropriate cone beam CT scan mode to compare and estimate the image quality and skin dose. Materials and Methods: Measurement by Thermoluminescence dosimeter (TLD-100, Harshaw) with using the Rando phantom are placed on each eight sites in seperately H&N, thoracic, abdominal section. each 4 methods of scan modes of are measured the for skin dose in three time. Subsequently, obtained average value. Following image quality QA protocol of equipment manufacturers using the catphan 504 phantom, image quality of each scan mode is compared and analyzed. Results: The results of the measured skin dose are described in here. The skin dose of Head & Neck are measured mode A: 8.96 cGy, mode B: 4.59 cGy, mode C: 3.46 cGy mode D: 1.76 cGy and thoracic mode A: 9.42 cGy, mode B: 4.58 cGy, mode C: 3.65 cGy, mode D: 1.85 cGy, and abdominal mode A: 9.97 cGy, mode B: 5.12 cGy, mode C: 4.03 cGy, mode D: 2.21 cGy. Approximately, dose of mode B are reduced 50%, mode C are reduced 60%, mode D are reduced 80% a point of reference dose of mode A. the results of analyzed HU reproducibility, low contrast resolution, spatial resolution (high contrast resolution), HU uniformity in evaluation item of image quality are within the tolerance value by recommended equipment manufacturer in all scan mode. Conclusion: Maintaining the image quality as well as reducing the image dose are very important in cone beam CT. In the result of this study, we are considered when to take mode A when interested in soft tissue. And we are considered to take mode D when interested in bone scan and we are considered to take mode B, C when standard scan. Increasing secondary cancer risk due to cone beam CT scan should be reduced by low mAs technique.
Total Scalp의 방사선 치료 시 Helmet Bolus 제작방법에 관한 연구
송용민,김종식,홍채선,주상규,박주영,박수연,Song, Yong-Min,Kim, Jong-Sik,Hong, Chae-Seon,Ju, Sang-Gyu,Park, Ju-Young,Park, Su-Yeon 대한방사선치료학회 2012 대한방사선치료학회지 Vol.24 No.1
목 적: Total Scalp의 방사선 치료 시 표면선량(surface dose)을 증가시키기 위해 조직보상체(bolus)를 사용한다. 이에 본 저자는 두피(scalp) 전체를 덮는 조직보상체로서 Bolx-II, paraffin wax, solid thermoplastic물질을 각각 적용한 Helmet bolus를 제작하여 유용성을 비교 평가해보고자 한다. 대상 및 방법: Rando 팬톰을 이용하여 두피 고정용구(mask)를 만든 후 전체 두피에 Bolx-II (Action Products, USA), paraffin wax (Densply, USA), solid thermoplastic 물질(Med-Tec, USA)을 0.5 cm 두께로 동일하게 적용한 Helmet bolus를 각각 제작 하였다. 각 Helmet bolus에 대한 물리적 특성을 평가하기 위해 전산화 단층촬영(computed tomography) (GE, Ultra Light Speed16)을 시행 후 방사선치료계획시스템(radiation therapy planning system) (Philips, Pinnacle)을 이용하여 최적의 치료 계획(radiationtherapy plan)을 세웠으며, 각 조직 보상체(bolus)에 대한 밀도 변화(density variation)화를 분석하였다. 선량 분포(dose distribution)평가(evaluation)를 위해 선량체적히스토그램(Dose-Volume Histogram) (DVH)을 이용해 임상표적체적(Clinical Target Volume) (CTV)에 대한 Dose-homogeneity index (DHI, $D_{90}/D_{10}$), Conformity index (CI, $V_{95}/TV$)를, 정상 뇌 조직(Normal brain tissue)에 있어$V_{20}$, $V_{30}$을 각각 구하여 비교 하였다. 또한 총 제작시간을 측정하여 제작과정에서의 효율성을 평가하였고, 열형광선량계 (Thermoluminescent Dosimeter)를 사용하여 실제 치료 시 각 두피의 표면선량을 확인 하였다. 결 과: Bolx-II, paraffin wax, solid thermoplastic 물질에 대한 밀도측정(density measurement) 결과 $0.952{\pm}0.13g/cm^3$, $0.842{\pm}0.17g/cm^3$, $0.908{\pm}0.24g/cm^3$로 Bolx-II의 밀도변화(density variation)가 가장 작았다. Bolx-II, paraffin wax, solid thermoplastic 물질을 적용한 각 Helmet bolus DHI는 0.89, 0.85, 0.77, CI는 0.86, 0.78, 0.74로 Bolx-II가 가장 우수 하였으며, 정상조직에 있어 뇌(braintissue)의 $V_{20}$은 11.50%, 10.80%, 10.07%, $V_{30}$은 7.62%, 7.40%, 7.31%로 나타났다. 제작 시 총 소요 시간은 30분, 120분, 90분 이였으며, Bolx-II를 적용한 Helmet bolus 제작과정이 가장 간단하였다. 열형광선량계(Thermoluminescent Dosimeter) 측정 결과세 Helmet bolus 모두 ${\pm}7%$ 이내의 선량오차를 보였다. 결 론: Total Scalp의 방사선치료 시 Bolx-II를 사용한 Helmet bolus의 적용은 CTV (Clinical Target Volume)에 대한 Homogeneity와 Conformity를 높여 줄 뿐만 아니라 제작시간 및 제작방법이 간단하여 임상 적용 시 유용하리라 생각된다. Purpose: This study evaluated the usefulness of Helmet bolus device using Bolx-II, paraffin wax, solid thermoplastic material in total scalp irradiation. Materials and Methods: Using Rando phantom, we applied Bolx-II (Action Products, USA), paraffin wax (Densply, USA), solid thermoplastic material (Med-Tec, USA) on the whole scalp to make helmet bolus device. Computed tomography (GE, Ultra Light Speed16) images were acquired at 5 mm thickness. Then, we set up the optimum treatment plan and analyzed the variation in density of each bolus (Philips, Pinnacle). To evaluate the dose distribution, Dose-homogeneity index (DHI, $D_{90}/D_{10}$) and Conformity index (CI, $V_{95}/TV$) of Clinical Target Volume (CTV) using Dose-Volume Histogram (DVH) and $V_{20}$, $V_{30}$ of normal brain tissues. we assessed the efficiency of production process by measuring total time taken to produce. Thermoluminescent dosimeters (TLD) were used to verify the accuracy. Results: Density variation value of Bolx-II, paraffin wax, solid thermoplastic material turned out to be $0.952{\pm}0.13g/cm^3$, $0.842{\pm}0.17g/cm^3$, $0.908{\pm}0.24g/cm^3$, respectively. The DHI and CI of each helmet bolus device which used Bolx-II, paraffin wax, solid thermoplastic material were 0.89, 0.85, 0.77 and 0.86, 0.78, 0.74, respectively. The result of Bolx-II was the best. $V_{20}$ and $V_{30}$ of brain tissues were 11.50%, 10.80%, 10.07% and 7.62%, 7.40%, 7.31%, respectively. It took 30, 120, 90 minutes to produce. The measured TLD results were within ${\pm}7%$ of the planned values. Conclusion: The application of helmet bolus which used Bolx-II during total scalp irradiation not only improves homogeneity and conformity of Clinical Target Volume but also takes short time and the production method is simple. Thus, the helmet bolus which used Bolx-II is considered to be useful for the clinical trials.
세기조절방사선치료 시 치료 부위에 따른 치료계획 시스템 간 선량평가
김진만,김종식,홍채선,박주영,박수연,주상규,Kim, Jin Man,Kim, Jong Sik,Hong, Chae Seon,Park, Ju Young,Park, Su Yeon,Ju, Sang Gyu 대한방사선치료학회 2013 대한방사선치료학회지 Vol.25 No.2
목 적: 본 연구는 치료계획 시스템인 $Pinnacle^3$ (version 9.2, Philips Medical Systems, USA)과 Eclipse (version 10.0, Varian Medical Systems, USA)을 이용하여 전립선암과 폐암의 세기조절방사선 치료계획시 불균질 부위의 선량 계산 차이를 알고리즘별로 알아보고자 한다. 대상 및 방법: 각 5명의 전립선암 및 폐암 환자를 대상으로, 본원 Protocol에 따른 동일한 조건으로 최적화 계산을 진행하였다. 전립선암 환자의 치료계획은 10 MV, 7Beam을 사용하였으며 2.5 Gy씩 28 fx, 총 70 Gy를 동일 처방하였고, 폐암 환자의 치료계획은 6 MV, 6Beam을 사용하였으며 2 Gy씩 33 fx, 총 66 Gy를 동일 처방하였다. 두 치료계획시스템을 통해 CTV, PTV 및 종양주위의 OAR의 최대선량, 평균선량, 최소선량을 비교하였다. 결 과: 전립선암에서 두 치료계획시스템 모두 CTV와 PTV의 선량변화가 2%이내였으며 종양주변 정상 장기(방광, 대퇴골, 직장)도 선량제약조건을 충족하였다. 폐암에서도 CTV와 PTV는 2%이내의 선량변화를 보였고, 정상 장기(식도, 척수, 양측 폐)도 선량제약 조건을 충족하였다. 하지만, Eclipse 치료계획의 최소선량은 CTV에서 1.9%, PTV에서 3.5% 높았고 양측 폐의 경우 V5 Gy에서 3.0% 높은 차이를 보였다. 결 론: 치료부위에 따른 각각의 치료계획시스템은 본원의 선량제한 조건을 모두 만족하여 임상적 정확성을 확인할 수 있었다. 향후 다양한 부위의 치료계획 연구와 치료계획시스템의 적용은 보다 정확한 치료계획을 위한 방법을 제시할 것이라 사료된다. Purpose: This study executed therapy plans on prostate cancer (homogeneous density area) and lung cancer (non-homogeneous density area) using radiation treatment planning systems such as $Pinnacle^3$ (version 9.2, Philips Medical Systems, USA) and Eclipse (version 10.0, Varian Medical Systems, USA) in order to quantify the difference between dose calculation according to density in IMRT. Materials and Methods: The subjects were prostate cancer patients (n=5) and lung cancer patients (n=5) who had therapies in our hospital. Identical constraints and optimization process according to the Protocol were administered on the subjects. For the therapy plan of prostate cancer patients, 10 MV and 7Beam were used and 2.5 Gy was prescribed in 28 fx to make 70 Gy in total. For lung cancer patients, 6 MV and 6Beam were used and 2 Gy was prescribed in 33 fx to make 66 Gy in total. Through two therapy planning systems, maximum dose, average dose, and minimum dose of OAR (Organ at Risk) of CTV, PTV and around tumor were investigated. Results: In prostate cancer, both therapy planning systems showed within 2% change of dose of CTV and PTV and normal organs (Bladder, Both femur and Rectum out) near the tumor satisfied the dose constraints. In lung cancer, CTV and PTV showed less than 2% changes in dose and normal organs (Esophagus, Spinal cord and Both lungs) satisfied dose restrictions. However, the minimum dose of Eclipse therapy plan was 1.9% higher in CTV and 3.5% higher in PTV, and in case of both lungs there was 3.0% difference at V5 Gy. Conclusion: Each TPS according to the density satisfied dose limits of our hospital proving the clinical accuracy. It is considered more accurate and precise therapy plan can be made if studies on treatment planning for diverse parts and the application of such TPS are made.
Development of Video Image-Guided Setup (VIGS) System for Tomotherapy: Preliminary Study
김진성,주상규,홍채선,정재원,손기홍,신정석,신은혁,안성환,한영이,최두호,Kim, Jin Sung,Ju, Sang Gyu,Hong, Chae Seon,Jeong, Jaewon,Son, Kihong,Shin, Jung Suk,Shin, Eunheak,Ahn, Sung Hwan,Han, Youngyih,Choi, Doo Ho Korean Society of Medical Physics 2013 의학물리 Vol.24 No.2
초고압 전산화단층촬영(megavoltage computed tomography, MVCT)이 단층치료(Tomotherapy) 환자의 치료 자세 교정 방법으로 사용되고 있다. MVCT는 부가적인 방사선 피폭뿐만 아니라 전체 치료 시간이 길어지는 단점을 가지고 있다. 이러한 문제점 해결을 위해 비디오 영상기반 환자 치료 자세 교정 시스템(video image-guided setup system, VIGS)을 개발했다. 단층치료 장치내 갠트리에 직각으로 2대의 비디오 카메라를 장착하고 이로부터 얻은 영상을 이용하여 환자의 자세 오차를 측정하는 프로그램을 자체 개발했다. 개발된 시스템은 사용자에 의해 정의된 관심 영역에서의 에지 검출(edge detection) 결과를 기반으로 자동 정합을 통해 자세 오차를 찾도록 고안되었다. 두경부 환자를 묘사하기 위해 휴먼 팬톰을 이용하여 컴퓨터 단층 치료계획 영상을 획득한 후 전산화 치료계획을 수행했다. 실제 치료 상태를 재현하기 위해 고정 용구를 이용하여 팬톰을 고정했으며 전산화치료계획 결과로 부터 팬톰 자세 검증을 위한 기준 MVCT 영상을 획득했다. 팬톰을 치료 위치에 위치시킨 후 MVCT 영상을 얻고 이를 기준 MVCT영상과 비교하여 치료계획시와 동일환 자세가 되도록 위치를 교정했다. 교정된 자세에서 VGIS를 이용하여 기준 비디오 영상을 획득했다. 10회 걸쳐 MVCT 영상을 이용한 자세 교정과 VIGS를 이용한 비디오 영상기반 자세 교정을 각각 수행하여 두 방법간의 교정 값 차이(상관 분석)와 분석 시간을 비교했다. 팬톰 위치 교정 시간은 VIGS 시스템($41.7{\pm}11.2$ seconds)이 MVCT 방법($420{\pm}6$ seconds)에 비해 현저히 적게 조사됐다(p<0.05). 하지만 두 방법간의 위치 오차 분석 결과 통계적으로 유의한 차이는 보이지 않았다(x=0.11 mm, y=0.27 mm, z=0.58 mm, p>0.05). VIGS시스템이 짧은 시간에 정확한 위치 오차 감지 능력을 보여 이의 개발이 단층치료의 절차를 효율적으로 개선하는데 효과적일 것으로 생각된다. At present, megavoltage computed tomography (MVCT) is the only method used to correct the position of tomotherapy patients. MVCT produces extra radiation, in addition to the radiation used for treatment, and repositioning also takes up much of the total treatment time. To address these issues, we suggest the use of a video image-guided setup (VIGS) system for correcting the position of tomotherapy patients. We developed an in-house program to correct the exact position of patients using two orthogonal images obtained from two video cameras installed at $90^{\circ}$ and fastened inside the tomotherapy gantry. The system is programmed to make automatic registration possible with the use of edge detection of the user-defined region of interest (ROI). A head-and-neck patient is then simulated using a humanoid phantom. After taking the computed tomography (CT) image, tomotherapy planning is performed. To mimic a clinical treatment course, we used an immobilization device to position the phantom on the tomotherapy couch and, using MVCT, corrected its position to match the one captured when the treatment was planned. Video images of the corrected position were used as reference images for the VIGS system. First, the position was repeatedly corrected 10 times using MVCT, and based on the saved reference video image, the patient position was then corrected 10 times using the VIGS method. Thereafter, the results of the two correction methods were compared. The results demonstrated that patient positioning using a video-imaging method ($41.7{\pm}11.2$ seconds) significantly reduces the overall time of the MVCT method ($420{\pm}6$ seconds) (p<0.05). However, there was no meaningful difference in accuracy between the two methods (x=0.11 mm, y=0.27 mm, z=0.58 mm, p>0.05). Because VIGS provides a more accurate result and reduces the required time, compared with the MVCT method, it is expected to manage the overall tomotherapy treatment process more efficiently.
사차원전산화단층촬영과 호흡연동 직각 Kilovolt 준비 영상을 이용한 간 종양의 움직임 분석
주상규(Sang Gyu Ju),홍채선(Chae Seon Hong),박희철(Hee Chul Park),안종호(Jong Ho Ahn),신은혁(Eunhyuk Shin),신정석(Jung Suk Shin),김진성(Jin Sung Kim),한영이(Youngyih Han),임도훈(Do Hoon Lim),최두호(Doo Ho Choi) 대한방사선종양학회 2010 Radiation Oncology Journal Vol.28 No.3
목 적: 4-dimensional computed tomography (4DCT) 영상과 on board imaging (OBI) 및 real time position management (RPM) 장치로 매 회 치료 시마다 얻은 호흡연동 직각 kilovolt (KV) 준비 영상(gated orthogonal kilovolt setup image)을 이용해 간암 환자를 치료하는 동안 발생하는 종양 위치의 불확실성을 평가하고자 했다. 대상 및 방법: 3차원입체조형치료가 예정된 20명의 간암 환자를 대상으로 RPM과 전산화단층촬영모의치료기를 이용해 치료계획용 4DCT를 시행했다. 표적 근처에 위치한 간동맥화학색전술 후 집적된 리피오돌(lipiodol) 혹은 횡격막을 종양의 위치 변이를 측정하는 표지자로 선택했다. 표지자의 위치 차이를 이용해 온라인 분할간 및 분할중 내부 장기 변이와 움직임 진폭을 측정했다. 측정된 자료의 정량적 평가를 위해 통계 분석을 실시했다. 결 과: 20명 환자로부터 측정된 표지자의 분할간변이의 중앙값은 X (transaxial), Y (superior-inferior), Z (anteriorposterior)축에서 각각 0.00 cm (범위, -0.50∼0.90 cm), 0.00 cm (범위, -2.4∼1.60 cm), 0.00 cm (범위, -1.10∼0.50 cm) 였다. 4명의 환자에서 X, Y, Z축 중 하나 이상에서 0.5 cm를 초과하는 변이가 관찰되었다. 4DCT와 호흡연동 직각 준비 영상으로부터 얻은 표적의 움직임 진폭의 차이는 X, Y, Z 축에서 각각 중앙값이 -0.05 cm (범위,-0.83∼0.60 cm), -0.15 cm (범위, -2.58∼1.18 cm), -0.02 cm (범위, -1.37∼0.59 cm) 였다. 두 영상간 표적의 움직임 진폭 차이가 1 cm를 초과하는 환자가 Y축 방향으로 3명 관찰되었으며, 0.5 cm 초과 1 cm 미만의 차이를 보이는 환자도 Y축과 Z축 방향을 합쳐 5명 관찰되었다. 분할중 표지자 위치 변이의 중앙값은 X, Y, Z축에서 각각 0.00 cm (범위, -0.30∼0.40 cm), -0.03 cm (범위, -1.14∼0.50 cm), 0.05 cm (범위, -0.30∼0.50 cm)였으며 2명의 환자에서 1 cm를 초과하는 변이가 Y축 방향으로 관찰되었다. 결 론: 4DCT와 호흡연동 직각 KV 준비 영상으로 얻은 표지자의 분할간, 분할중 및 움직임 진폭에서 큰 변이가 관찰되었다. Purpose: In order to evaluate the positional uncertainty of internal organs during radiation therapy for treatment of liver cancer, we measured differences in inter- and intra-fractional variation of the tumor position and tidal amplitude using 4-dimentional computed radiograph (DCT) images and gated orthogonal setup kilovolt (KV) images taken on every treatment using the on board imaging (OBI) and real time position management (RPM) system. Materials and Methods: Twenty consecutive patients who underwent 3-dimensional (3D) conformal radiation therapy for treatment of liver cancer participated in this study. All patients received a 4DCT simulation with an RT16 scanner and an RPM system. Lipiodol, which was updated near the target volume after transarterial chemoembolization or diaphragm was chosen as a surrogate for the evaluation of the position difference of internal organs. Two reference orthogonal (anterior and lateral) digital reconstructed radiograph (DRR) images were generated using CT image sets of 0% and 50% into the respiratory phases. The maximum tidal amplitude of the surrogate was measured from 3D conformal treatment planning. After setting the patient up with laser markings on the skin, orthogonal gated setup images at 50% into the respiratory phase were acquired at each treatment session with OBI and registered on reference DRR images by setting each beam center. Online inter-fractional variation was determined with the surrogate. After adjusting the patient setup error, orthogonal setup images at 0% and 50% into the respiratory phases were obtained and tidal amplitude of the surrogate was measured. Measured tidal amplitude was compared with data from 4DCT. For evaluation of intra-fractional variation, an orthogonal gated setup image at 50% into the respiratory phase was promptly acquired after treatment and compared with the same image taken just before treatment. In addition, a statistical analysis for the quantitative evaluation was performed. Results: Medians of inter-fractional variation for twenty patients were 0.00 cm (range, −0.50 to 0.90 cm), 0.00 cm (range, −2.40 to 1.60 cm), and 0.00 cm (range, −1.10 to 0.50 cm) in the X (transaxial), Y (superiorinferior), and Z (anterior-posterior) directions, respectively. Significant inter-fractional variations over 0.5 cm were observed in four patients. Min addition, the median tidal amplitude differences between 4DCTs and the gated orthogonal setup images were −0.05 cm (range, −0.83 to 0.60 cm), −0.15 cm (range, −2.58 to 1.18 cm), and −0.02 cm (range, −1.37 to 0.59 cm) in the X, Y, and Z directions, respectively. Large differences of over 1 cm were detected in 3 patients in the Y direction, while differences of more than 0.5 but less than 1 cm were observed in 5 patients in Y and Z directions. Median intra-fractional variation was 0.00 cm (range, −0.30 to 0.40 cm), −0.03 cm (range, −1.14 to 0.50 cm), 0.05 cm (range, −0.30 to 0.50 cm) in the X, Y, and Z directions, respectively. Significant intra-fractional variation of over 1 cm was observed in 2 patients in Y direction. Conclusion: Gated setup images provided a clear image quality for the detection of organ motion without a motion artifact. Significant intra- and inter-fractional variation and tidal amplitude differences between 4DCT and gated setup images were detected in some patients during the radiation treatment period, and therefore, should be considered when setting up the target margin. Monitoring of positional uncertainty and its adaptive feedback system can enhance the accuracy of treatments.