• Radiation Oncology Journal
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• 제14권1호
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• pp.41-52
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• 1996

목적 : 외부 방사선 치료(External Radiation Therapy) 및 Gamma-med (Iridium-192) 고선량 강내 방사선 치료를 받은 자궁 경부암 FIGO stage IIB 환자에서 직장 합병증 발생률 및 이와 관계있는 인자를 후향적으로 분석해 보았다. 대상 및 방법 : 1989년 11월부터 1992년 12월까지 연세암센터 치료방사선과에서 근치적 목적의 외부 및 강내 방사선치료를 받은 FIGO 병기 IIB 자궁경부암 환자 88명을 대상으로 방사선치료후 발생한 직장 합병증 및 이와 연관된 인자들을 분석하여 보았다. 환자들의 연령은 29-83세로 평균치, 중앙치 모두 57세였고 병리조직 분류상 편평상피세포암이 84예 선암이 4예였다. 방사선치료는 외부방사선을 골반 부위에 5-6주 동안 4500-5400cGy 치료하였으며 환자별로 중간 차폐를 시행하였고 고선량 Gamma-med ICR은 A점에 1회당 500cGy씩 1주 2회로 총 3000cGy 조사하였다. 외부 방사선치료시 중앙 차폐까지의 외부 조사량, ICR rectal dose(r) 및 total rectal dose(R), ICRU 38에 따른 ICR rectal dose(Dr)와 total Dr dose(OR), ICR reference volume, TDF, BED(Biologically Effective Dose)를 계산하고 분석해 합병증과의 연관성을 찾아보았다. 대상 환자 88명중 87명($98.9\%$)에서 최저 24개월 이상 추적 관찰이 가능하였으며 중앙치는 40개월(20-66개월)이었다. 결과 : 직장 합병증은 27예에서 발생하였는데($30.7\%$) grade 1이 12예($13.6\%$), 2가 12예($13.6\%$), 3이 3($3.4\%$)예였고 합병증이 발생하는 시기는 망사선치료후 4-43개월(중앙치 16개월, 평균 17.3개월)이었다. 직장 합병증이 발생하지 않은 환자군의 total rectal dose(R)는 $6772.67{\pm}884.02$로 grade 2-3 합병증이 발생한 15명의 R=$7163.0{\pm}838.49$와 유의한 차이를 보였으며 total Dr dose (DR)도 두 군간에 차이를 보였다 또 grade 2-3인 직장 합병증 발생률은 중앙 차폐시 까지의 외부 방사선량과 관계가 있었는데 36Gy이하에서는 $10\%$, 36-40Gy는 $21.4\%$, 40Gy 이상에서는 $29.3\%$의 직장 합병증이 발생하여 중앙 차폐까지 조사된 외부 방사선량이 증가할수록 직장 합병증이 증가함을 알 수 있었다. 직장에 조사된 총직장 조사량(R)에 따라 grade 2-3 합병증 발생률이 증가하였는데 65Gy 이하에서는 $10.5\%$, 65-75Gy는 $17.2\%$, 75Gy이상 조사된 환자군에서는 $28.5\%$로 조사량이 증가할수록 직장 합병증이 증가하는 알상이었으며 ICRU 38 에 따른 total rectal dose (DR)에 대해서도 비슷한 양상이었다. ICR rectal dose(r, Dr)만 따로 분석해 보았는데 방사선량과 직장 합병증간에는 차이가 없었다. 그 외의 인자로 분석한 TDF 와 BED도 grade 2-3의 경우에는 그 값이 증가할수록 증가하는 양상을 보였으나 통계적인 유의성은 없었고 Gamma Dot 에서 계산되는 ICR reference volume도 분석해 보았으나 합병증파의 연관성을 발견할 수 없었다. 결론 : 병기 IIB 자궁경부암 환자에서 외부 방사선치료 및 고선량 강내 방사선치료후 직장 합병증 발생률은 $30.7\%$(grade 2-3: 15예 $17\%$)였다. 직장 합병증 발생에 영향을 미치는 중요한 인자는 직장에 조사된 전골반 방사선량(중앙 차폐까지의 방사선량) 및 고선량 강내 방사선 치료와 합한 총직장 방사선량(r, Dr)으로 나타났으며 이들이 증가할수록 합병증 발생률이 증가하였다.

• 대한방사선치료학회:학술대회논문집
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• 대한방사선치료학회 2005년도 춘계학술대회 초록집
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• pp.23-26
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• 2005

재발한 vulva tumor의 근접 치료에 있어서 정상조직의 장애와 tumor volume내의 dose uniformity는 치료성적에 매우 중요한 요인이다. 이를 개선하기 위하여 modified MUPIT applicator를 제작하여 modified MUPIT applicator의 적용에 대한 유용성을 평가하고자 한다. modified MUPIT applicator는 template, cylinder, interstitial needle로 구성되었으며, tumor volume을 정하기 위하여 CT를 시행하였다. CT image를 이용하여 interstitial needle의 삽입 위치를 확인하고 수술실에서 template 를 치료 부위에 고정을 시키고 cylinder를 vaginal cavity에 삽입한 후 interstitial needle을 tumor volume 내에 삽입 하였다. tumor volume내에서 interstitial needle의 정확한 위치를 확인하기 위하여 CT를 시행하였으며 orthogonal film을 이용하여 computer planning을 실시하였다. daily tumor dose는 600 cGy, BID로 3000 cGy를 조사하였으며 치료 시 rectal dose를 평가하기 위하여 TLD를 이용하여 anal verge를 기준으로 5개 지점에서 rectal dose를 측정하였다. rectal dose는 34.1 cGy, 57.1 cGy, 103.8 cGy, 162.7 cGy, 165.7 cGy로 측정되었으며 EBRT(whole pelvis RT), ICR과 overlap되는 지점은 34.1 cGy, 57.1 cGy로 매우 우수하게 평가되었다. 결론적으로 자체 제작한 modified MUPIT applicator 사용하여 interstitial brachytherapy를 시행함으로써 EBRT로 cover하기 어려운 환자의 tumor volume내에서 irregularity를 효율적으로 극복할 수 있었고 우수한 rectal dose 분포를 통하여 rectal complication의 발생 확률을 현저히 감소시킬 수 있었다.

• Radiation Oncology Journal
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• 제21권4호
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• pp.276-282
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• 2003

목적: 자궁경부암의 고선량률 근접치료는 근치적 치료에서 중요한 역할을 차지하나 만성합병증 특히 직장합병증의 위험도 증가하게 된다. 이에 저자들은 직장합병증과 직장 방사선선량을 비교하여 합병증과 관련된 인자를 알아보고자 하였다. 대상 및 방법: 1995년 7월부터 2001년 12월까지 자궁경부암으로 진단받고 근치적 방사선치료로 외부방사선치료와 고선량률 강내치료를 모두 받은 환자 222명을 대상으로 하였다. 외부방사선치료의 총방사선량 중앙값은 50.4 Gy(30.6$\~$56.4 Gy)이고 고선량률 강내치료는 이리듐(Ir)-192를 이용하여 point A에 3$\~$5.5 Gy (중앙값 4 Gy), 조사횟수는 5$\~$8회(중앙값 6회)로 주 2회 조사하여 총 15$\~$32.5 Gy (중앙값 24 Gy)를 조사하였다. 환자의 중앙 추적기간은 39개월(6$\~$90개월)이었다 결과: 만성 직장합병증은 21명(9.5$\%$)에서 관찰되었다. 이들은 모두 직장출혈을 보였으며 다른 합병증은 나타나지 않았다. 직장합병증이 발생하기까지의 시간은 방사선치료 종료 후 3$\~$44개월(중앙값 13개월)이었다. 이전의 결과와 마찬가지로 직장합병증을 보인 군의 계산직장선량은 합병증을 보이지 않았던 군과 비슷하고 그 차이가 통계적으로 유의하지 않았다. 그러나 직장합병증을 보인 군의 측정직장선량의 평균값과 BED는 합병증을 보이지 않았던 군에 비해 높았으며 통계적으로 유의한 차이를 보였다. 측정 직장선량이 16 Gy를 넘거나 측정 직장선량과 A point 선량과의 비가 70$\%$를 넘는 경우 또는 측정 직장선량의 BED가 120 Gy$_{3}$을 넘는 경우는 직장 합병증의 가능성이 유의하게 증가하였다. 결론: 자궁경부암에서 고선량률 강내치료시 TLD를 이용한 생체 내 선량측정을 하고 이를 조정함으로써 만성 직장합병증을 예측하고 그 가능성을 줄일 수 있을 것으로 생각된다.

• Asian Pacific Journal of Cancer Prevention
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• 제15권15호
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• pp.6115-6120
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• 2014

Background: To compare the KKU-model rectal tube (KKU-tube) and the conventional rectal tube (CRT) for checking rectal doses during high-dose-rate intracavitary brachytherapy (HDR-ICBT) of cervical cancer. Materials and Methods: Between February 2010 and January 2011, thirty -two patients with cervical cancer were enrolled and treated with external beam radiotherapy (EBRT) and intracavitary brachytherapy (ICBT). The KKU-tube and CRT were applied intrarectally in the same patients at alternate sessions as references for calculation of rectal doses during ICBT. The gold standard references of rectum anatomical markers which are most proximal to radiation sources were anterior rectal walls (ARW) adjacent to the uterine cervix demonstrated by barium sulfate suspension enema. The calculated rectal doses derived from actual anterior rectal walls, CRT and the anterior surfaces of the KKU-tubes were compared by using the paired t-test. The pain caused by insertion of each type of rectal tube was assessed by the visual analogue scale (VAS). Results: The mean dose of CRT was lower than the mean dose of ARW ($Dmean_0-Dmean_1$) by $80.55{\pm}47.33cGy$ (p-value <0.05). The mean dose of the KKU-tube was lower than the mean dose of ARW ($Dmean_0-Dmean_2$) by $30.82{\pm}24.20cGy$ (p-value <0.05). The mean dose difference [($Dmean_0-Dmean_1$)-($Dmean_0-Dmean_2$)] was $49.72{\pm}51.60cGy$, which was statistically significant between 42.32 cGy -57.13 cGy with the t-value of 13.24 (p-value <0.05). The maximum rectal dose by using CRT was higher than the KKU-tube as much as 75.26 cGy and statistically significant with the t-score of 7.55 (p-value <0.05). The mean doses at the anterior rectal wall while using the CRTs and the KKU-tubes were not significantly different (p-value=0.09). The mean pain score during insertion of the CRT was significantly higher than the KKU-tube by a t-score of 6.15 (p-value <0.05) Conclusions: The KKU-model rectal tube was found to be an easily producible, applicable and reliable instrument as a reference for evaluating the rectal dose during ICBT of cervical cancer without negative effects on the patients.

• 대한한의학방제학회지
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• 제12권2호
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• pp.95-108
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• 2004

Objective: We made the genital organs inflammatory mice model by vaginal injection of Lipopolysaccharide(LPS), and we intended to make study about anti-inflammatory effects of Gangyeong-Tang, among oral and rectal medication and Herbal-Acupuncture treatment. Method: The female ICR(20-30g) mice were used, the temperature was controlled within $22{\pm}0.5^{\circ}C$ and water and food was not limited. The environment was manipulated to simulate 12 hours of day and 12 hours of night. After LPS injection into vagina, we confirmed on-set of inflammation. 2 days before LPS injection, we started to medicate Gangyeong-Tang in Oral and Rectal and Aqua-acupucture treatment. After 3days from LPS injection, we mesured the White Blood Cell(WBC), Interrleukin-6(IL-6), Tumor Necrosis Factor-${\alpha}$(TNF-${\alpha}$) in blood which was collected from the Retro-orbital Plexus. Results: 1. We made the genital organs inflammatory mice model by vaginal injection of LPS successfully. 2. The number of WBC was decreased significantly as we medicated Gangyeong- Tang in Oral 1g/kg dose, 3g/kg dose and Rectal 1g/kg dose, rectal 3g/kg dose. 3. The concentration of IL-6 was decreased significantly as we medicated Gangyeong-Tang in all group of the Oral, Rectal, Herbal-Acupuncture treatment. 4. The concentration of TNF-${\alpha}$ was decreased significantly as we medicated Gangyeong-Tang in Oral 3g/kg dose and Rectal 1g/kg dose, Rectal 3g/kg dose group. Herbal-Acupuncture treatment group datas showed reductive tendency. Conclusion: As a result of this experiment, we made the genital organs inflammatory mice model by vaginal injection of LPS successfully and demonstrated anti-inflammatory effect of Gangyeong-Tang.

• Radiation Oncology Journal
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• 제1권1호
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• pp.103-109
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• 1983

47 out of 56 cases of intact uterine cervix cancer treated by radiation at the Hanyang University Hospital were followed 18 months or more after treatment. (7 patients died before 18 months, 2 cases lost to follow-up). Age distribution reveal 5 cases in 30's, 18 cases in 40's, 17 cases in 50's, 7 cases in 60's. Histologically, all cases were squamous cell type except one case of adenocarcinoma. 1. 45 cases were treated by combined external Co-60 irradiation and intracavitary irradiation by Cs-137 small sources. 1 case was treated by external irradiation only, and 1 case by intracavitary only. 2. Rectal injuries were observed in 13 cased (27.6%), 4 cases in Grade 1, 8 cased in Grade 2 and 1 cases in Grade 3 which needed surgical management. 3. Average intervals of rectal injury following treatment was 9.2 months varying from 5 to 15 months. 4. Relation between rectal injury and point A dose reveal 6 cases between 7000-7999 rad and 6 cases between 8000-8999 rad and 1 case above 9000 rad. Even though there is no direct relation between point A dose and rectal injury, it is expected that rectal injury increases as point A dose increase. 5. In the normal condition, rectal injury can't be attributed to one major cause. Radiation dose, small source distribution, general condition of patients, local anatomy of the individual patient, history of PID and previous surgery, all play complex roles.

• Radiation Oncology Journal
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• 제32권2호
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• pp.57-62
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• 2014

Purpose: To evaluate association between equivalent dose in 2 Gy (EQD2) to rectal point dose and gastrointestinal toxicity from whole pelvic radiotherapy (WPRT) and intracavitary brachytherapy (ICBT) in cervical cancer patients who were evaluated by rectosigmoidoscopy in Faculty of Medicine, Chiang Mai University. Materials and Methods: Retrospective study was designed for the patients with locally advanced cervical cancer, treated by radical radiotherapy from 2004 to 2009 and were evaluated by rectosigmoidoscopy. The cumulative doses of WPRT and ICBT to the maximally rectal point were calculated to the EQD2 and evaluated the association of toxicities. Results: Thirty-nine patients were evaluated for late rectal toxicity. The mean cumulative dose in term of EQD2 to rectum was 64.2 Gy. Grade 1 toxicities were the most common findings. According to endoscopic exam, the most common toxicities were congested mucosa (36 patients) and telangiectasia (32 patients). In evaluation between rectal dose in EQD2 and toxicities, no association of cumulative rectal dose to rectal toxicity, except the association of cumulative rectal dose in EQD2 >65 Gy to late effects of normal tissue (LENT-SOMA) scale ${\geq}$ grade 2 (p = 0.022; odds ratio, 5.312; 95% confidence interval, 1.269-22.244). Conclusion: The cumulative rectal dose in EQD2 >65 Gy have association with ${\geq}$ grade 2 LENT-SOMA scale.

• 한국의학물리학회지:의학물리
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• 제3권1호
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• pp.45-52
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• 1992

수술중방사선치료는 개복후 가능한 광범위하게 병소를 절제한 후 방사선에 예민한 장기는 조사면적 밖으로 밀어내고 국소재발이 높은 부위에만 전자선을 사용하여 한번만에 다량의 방사선을 조사하므로서 정상조직의 손상을 최소화하면서 국소재발을 최대로 저하시키는 방법이다. 수술중방사선치료를 실시하는 병원마다 사용하는 cone의 모양, 시행방법, 조사선량등이 모두 달라 수술중방사선치료시 사용된 cone의 선량분포도 및 치료면적의 범위, 누설선량등은 치료효과의 중요한 지표가 된다. 대장직장암의 수술중 방사선치료를 위하여 본 교실에서 제작한 IORT cone의 선량분포 특성을 비교 검토하였다.

• Radiation Oncology Journal
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• 제31권2호
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• pp.81-87
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• 2013

Purpose: To describe chronic rectal mucosal damage after pelvic radiotherapy (RT) for cervical cancer and correlate these findings with clinical symptoms and radiation dose. Materials and Methods: Thirty-two patients who underwent pelvic RT were diagnosed with radiation-induced proctitis based on endoscopy findings. The median follow-up period was 35 months after external beam radiotherapy (EBRT) and intracavitary radiotherapy (ICR). The Vienna Rectoscopy Score (VRS) was used to describe the endoscopic findings and compared to the European Organization for Research and Treatment of Cancer (EORTC)/Radiation Therapy Oncology Group (RTOG) morbidity score and the dosimetric parameters of RT (the ratio of rectal dose calculated at the rectal point [RP] to the prescribed dose, biologically effective dose [BED] at the RP in the ICR and EBRT plans, ${\alpha}/{\beta}$ = 3). Results: Rectal symptoms were noted in 28 patients (rectal bleeding in 21 patients, bowel habit changes in 6, mucosal stools in 1), and 4 patients had no symptoms. Endoscopic findings included telangiectasia in 18 patients, congested mucosa in 20, ulceration in 5, and stricture in 1. The RP ratio, $BED_{ICR}$, $BED_{ICR+EBRT}$ was significantly associated with the VRS (RP ratio, median 76.5%; $BED_{ICR}$, median 37.1 $Gy_3$; $BED_{ICR+EBRT}$, median 102.5 $Gy_3$; p < 0.001). The VRS was significantly associated with the EORTC/RTOG score (p = 0.038). Conclusion: The most prevalent endoscopic findings of RT-induced proctitis were telangiectasia and congested mucosa. The VRS was significantly associated with the EORTC/RTOG score and RP radiation dose.

• Journal of Pharmaceutical Investigation
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• 제24권3호
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• pp.115-129
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• 1994

In the present study, quantitative and qualitative histology was used to assess the effects of ibuprofen suppositories with various treatments on the rectal mucosa of rats. Two suppositories were prepared with Witepsol W35 and compared with two commercial ibuprofen suppositories Reference I (Showa Pharm.ind., Tokyo, Japan), Reference II (P.Pharm., Seoul, Korea). Single and multiple dose(dosing interval 4 hr, n=4) studies were conducted. All suppositories significantly increased epithelial cell loss, but the extent of rectal irritation was variable. These studies showed that the incorporation of ibuprofen into the suppository bases increases the morphological change in rectal tissue both for the single and multiple administrations of suppositories, but which was significantly recovered within 24 hr although the interanimal variability in scores was very substantial. Multiple administration of ibuprofen suppositories caused significant damage to rectal mucosa, but it must be considered that these were under the severe condition, that is, interval of administration (4 hr) was three times shorter than normal interval of administration and dose was fifteen times larger than usual human dose. Aluminum oxide $(Al_2O_3)$, a dispersing agent, slightly increased the irritation of rectal mucosa in rats at 5 hr and 24 hr after multiple administration, but it was possible to ignore the difference of irritation in the data at 5hr and 24hr after single administration. Finally, it was concluded that Witepsol W35 and ibuprofen had a slight rectal mucosa-irritating effect on the usual human dose, and ibuprofen suppositories prepared with Witepsol W35 or Witepsol W35, $Al_2O_3$ showed almost similar extent of rectal irritation with commercial ibuprofen products.