• 제목/요약/키워드: Dose-response

검색결과 2,332건 처리시간 0.027초

원발성 간암의 국소 방사선치료 시 선량반응 관계 (Dose Response Relationship in Local Radiotherapy for Hepatocellular Carcinoma)

  • 박희철;성진실;한광협;전재윤;문영명;송재석;서창옥
    • Radiation Oncology Journal
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    • 제19권2호
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    • pp.118-126
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    • 2001
  • 목적 : 본 연구에서는 원발성 간암의 국소 방사선치료 시 조사선량을 높여준 것이 종양의 반응의 향상을 유도하였는지 분석하고자 하였다. 또한, 저선량을 조사하였던 환자들과 고선량을 조사하였던 환자들의 종양의 반응 및 부작용과 이에 영향을 미치는 인자들을 분석함으로써 향후 적절한 조사선량 범위를 결정하는데 유용한 기준을 제시하고자 하였다. 대상 및 방법 : 대상 환자의 선정 기준은 방사선치료의 과거력이 없는 경우, 간외전이가 없는 경우, 간경변증의 정도가 Child's class A 또는 B군인 경우, 종양이 전체 간 용적의 2/3를 넘지 않는 경우, 전신수행도가 ECOG 3기 이상으로 악화되지 않은 경우로 하였다. 1992년 1월부터 2000년 3월까지 원발성 간암에 국소 방사선치료를 시행 받은 환자들 중 158명이 연구 대상에 포함되었다. 조사영역은 종양과 주변 부위 $2\~3\;cm$를 포함하였고 일일 1.8 Gy씩 주 5회 조사되었다. 방사선치료 전과 종료 후 $4\~6$주째의 컴퓨터 단층 촬영 영상 및 자기 공명 영상, 간동맥 혈관 촬영 영상 등을 이용하여 조사영역 내의 종양의 반응을 평가하였다. 주 1회 혈액 검사를 시행하여 말초 혈액 혈구수 및 간기능을 관찰하였다. 치료의 종료 후 체중 증가, 복수, 간종대 등의 소견을 관찰하였고 4주와 8주에 간기능 검사를 시행하였다. 위장관계의 부작용은 상부위장관 내시경을 시행하여 확인하였다. 종양의 관해 정도에 따라 반응군과 비반응군으로 구분한 후 조사선량의 분포를 통계적으로 분석하였다. 또한, 연구대상을 조사선량에 따라 세 군으로 분류하고 종양의 반응과 임상적 특성을 분석하였다. 결과 : 종양의 반응은 106명이 부분 관해를 보여서 반응군의 비율은 $67.1\%$이었다. 완전 관해는 없었다. 종양이 $50\%$ 이하로 감소된 경우가 41명$(25.9\%)$, 종양의 진행을 보인 경우가 11명$(7\%)$이었다. 반응군의 평균 조사선량은 $50.1{\pm}6.6\;Gy$이었고 비반응군의 평균 조사선량은 $44.3{\pm}9.0\;Gy$로 통계적으로 의미 있는 차이를 보였다. 다변량 분석에서도 조사선량이 p-value 0.001로 유일하게 의미 있는 인자로 나타났다. 종양의 반응률은 조사선량이 40 Gy 미만인 군에서 $29.2\%$, 40 Gy에서 50 Gy사이인 군에서 $68.6\%$, 50 Gy를 넘는 환자 군에서 $77.1\%$로 나타났다. 종양의 크기는 40 Gy 미만인 군에서 $9.8{\pm}2.6\;cm$, 40 Gy에서 50 Gy사이인 군에서 $9.8{\pm}2.6\;cm$, 50 Gy를 넘는 환자 군에서 $8.3{\pm}3.2\;cm$로 고선량을 조사한 군에서 작았다. 간문맥 혈전증은 각각 $66.7\%,\;64.7\%,\;37.3\%$에서 양성으로 50 Gy를 넘는 선량이 조사된 군에서 상대적으로 간문맥 혈전증의 양성률이 낮았다. 방사선 간염, 십이지장의 궤양은 조사선량을 증가시킬수록 증가하는 경향을 나타내었다. 경미한 정도의 복수가 발생하거나 전형적인 방사선 간염의 발생, 위장관계의 염증 등이 치료 전 간경변증이 심할수록 현저히 많이 발생하는 경향을 보였다. 결론 : 원발성 간암에서 국소 방사선치료를 시행하는 경우 고선량이 조사될수록 반응군의 비율이 증가하는 선량반응 관계가 성립함을 확인할 수 있었다. 고선량이 조사될수록 대상 환자의 종양의 크기가 작았고 간문맥 혈전증의 비율도 적었는데 이는 병기가 낮은 경우 완치를 목표로 오히려 고선량을 투여하는 경향 때문으로 생각되었다. 조사선량이 50 Gy를 넘는 경우 조사선량의 증가에 따른 반응률의 향상이 현저하지 않은 반면 방사선 간염의 발생은 간경변증의 정도에 크게 영향을 받는다는 점을 고려할 때, 조사선량의 증가는 반드시 치료를 받는 대상 환자의 간기능과 간경변증의 정도 등을 고려하여 조심스럽게 진행되어야 할 것으로 생각된다.

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Genetic radiation risks: a neglected topic in the low dose debate

  • Schmitz-Feuerhake, Inge;Busby, Christopher;Pflugbeil, Sebastian
    • Environmental Analysis Health and Toxicology
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    • 제31권
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    • pp.1.1-1.13
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    • 2016
  • Objectives To investigate the accuracy and scientific validity of the current very low risk factor for hereditary diseases in humans following exposures to ionizing radiation adopted by the United Nations Scientific Committee on the Effects of Atomic Radiation and the International Commission on Radiological Protection. The value is based on experiments on mice due to reportedly absent effects in the Japanese atomic bomb (A-bomb) survivors. Methods To review the published evidence for heritable effects after ionising radiation exposures particularly, but not restricted to, populations exposed to contamination from the Chernobyl accident and from atmospheric nuclear test fallout. To make a compilation of findings about early deaths, congenital malformations, Down's syndrome, cancer and other genetic effects observed in humans after the exposure of the parents. To also examine more closely the evidence from the Japanese A-bomb epidemiology and discuss its scientific validity. Results Nearly all types of hereditary defects were found at doses as low as one to 10 mSv. We discuss the clash between the current risk model and these observations on the basis of biological mechanism and assumptions about linear relationships between dose and effect in neonatal and foetal epidemiology. The evidence supports a dose response relationship which is non-linear and is either biphasic or supralinear (hogs-back) and largely either saturates or falls above 10 mSv. Conclusions We conclude that the current risk model for heritable effects of radiation is unsafe. The dose response relationship is non-linear with the greatest effects at the lowest doses. Using Chernobyl data we derive an excess relative risk for all malformations of 1.0 per 10 mSv cumulative dose. The safety of the Japanese A-bomb epidemiology is argued to be both scientifically and philosophically questionable owing to errors in the choice of control groups, omission of internal exposure effects and assumptions about linear dose response.

동집단 자료의 주의력 결핍 과잉행동 장애를 종점으로 한 납의 벤치마크 용량 하한 도출 (Derivation of benchmark dose lower limit of lead for ADHD based on a longitudinal cohort data set)

  • 김병수;김대희;하미나;권호장
    • Journal of the Korean Data and Information Science Society
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    • 제25권5호
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    • pp.987-998
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    • 2014
  • 본 연구에서는 우리나라 환경부에서 최근에 구축한 아동 동집단 경시적 자료인 아동 건강과 환경 연구 (CHEER) 자료에 기초하여 주의력 결핍 과잉행동 장애 (ADHD)와 혈중 납 농도의 상관을 선형혼합모형을 사용하여 규명하고, CHEER 자료의 경시적 특성으로 나타나는 ADHD 점수의 "평균으로의 회귀" 현상을 보고하고자 한다. 또한 ADHD를 종점으로 한 혈중 납 농도의 용량-반응 곡선을 도출하며, 이렇게 도출된 용량-반응 곡선에 기초하여 몇 가지 상황 하에서 독성기준치인 벤치마크 용량 하한 (BMDL)을 유도한다.

다분할조사에 의한 마우스공장소낭선 세포의 선량반응곡선 (Dose- Response Curves of Mouse Jejunal Crypt Cells by Multifractionated Irradiation)

  • 홍성언;안치열
    • Radiation Oncology Journal
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    • 제4권2호
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    • pp.89-97
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    • 1986
  • Co-60 치료기로 마우스 전신에 다분할조사(단일 2, 3, 4, 5, 8, 10, 12, 16회 분할 조사)후 공장소 낭선세포측정법으로 소낭선세포의 재생능력에 대한 선량반응 곡선을 작성하고, 단일선량생존곡선을 분석하여 다음과 같은 결론을 얻었다. 1) 분할조사회수가 증가함에 따라 생존곡선은 고선량으로 이동하고 경사도는 점차 낮아졌다. 2) 단일선량생존곡선에서 Dq=460 cGy로 비교적 broad shoulder를 가지며 initial slope$(^1Do)$는 475 cGy이 었다. 3) $180\~450cGy$까지 분할 조사한 경우 분할조사간격당 평균회복선량은 분할조사선량의 약 $50\%$이었다. 4) 등가효과를 나타내는 분할조사선량과 이에 해당하는 총선량의 역수를 산출하여 선형회귀분석한 $\alpha/\beta$ 값은 8.3Gy로 조기반응조직의 범위(6-l4Gy)에 속하였다. 5) LQ model은 방사선치료에 사용되고 있는 모든 선량에 적용이 가능하고, $\alpha,\;\beta$ 두 요소만 필요하므로, 실질적으로 편리하게 적응할 수 없다. 다분할조사에 대한 stem cell의 반응을 이해함으로써, 실제방사선치료시 위장관에 대한 급성손상을 극소화시키는 변형된 치료방법을 도입하고 다른 조직에도 응용할 수 있는 방사선생물학적 자료가 될 것으로 사료된다.

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Novel Dosimeter for Low-Dose Radiation Using Escherichia coli PQ37

  • Park, Seo-Hyoung;Kim, Tae-Hwan;Cho, Chul-Koo;Lee, Yeon-Hee
    • Journal of Microbiology and Biotechnology
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    • 제11권3호
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    • pp.524-528
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    • 2001
  • The measurement of radiation response using simple and informative techniques would be of great value in studying the genetic risk following occupational, therapeutic, or accidental exposure to radiation. When patients receive radiation therapy, many suffer from side effects. Since each patient receives a different dose due to different physical conditions, it is important to measure the exact dose of radiation received by each patient to lessen the side effects. Even though several biological dosimetric systems have already been developed, there is no ideal system that can satisfy all the criteria for an idean dosimetric system, especially for low-dose radiation as used in radiation therapy. In this study, an SOS Chromotest of E. coli PQ37 was evaluated as a novel dosimeter for low-dose gamma-rays. E. coli PQ37 was originally developed to screen chemical mutagens using the SOS Chromotest-a colorimtric assay, based on the induction of ${\beta}$-galactosidase ue to DNA damage. The survival fraction of E. coli PQ37 decreased dose-dependently with an increasing dose of cobalt-60 gamma-rays. Also, a good linear correlation was found between the biological damage revealed by the ${\beta}$-galactosidase expression and the doses of gamma-rays. The expression of ${\beta}$-galactosidase activity that responded to low-dose radiation under 1 Gy was $Y=0.404+(0.089{\pm}0.3)D+(-0.018{\pm}0.16)D^2$ (Y, absorbance at 420 nm; D, Dose of irradiation) as calculated using Graph Pad In Plot and Excel. When a rabbit was fed with capsules containing an agar block embdded with E. coli PQ37 showed a linear response to the radiation doses. Accordingly, the results confirm that E. coli PQ37 can be used as a sensitive biological dosimeter fro cobalt-60 gamma-rays. To the best of our knowledge, this is the first time that a bacterium has been used as a biological dosimeter, especially for low-dose radiation.

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Reduced-dose whole-brain radiotherapy with tumor bed boost after upfront high-dose methotrexate for primary central nervous system lymphoma

  • Lee, Tae Hoon;Lee, Joo Ho;Chang, Ji Hyun;Ye, Sung-Joon;Kim, Tae Min;Park, Chul-Kee;Kim, Il Han;Kim, Byoung Hyuck;Wee, Chan Woo
    • Radiation Oncology Journal
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    • 제38권1호
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    • pp.35-43
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    • 2020
  • Purpose: This retrospective study compares higher-dose whole-brain radiotherapy (hdWBRT) with reduced-dose WBRT (rdWBRT) in terms of clinical efficacy and toxicity profile in patients treated for primary central nervous system lymphoma (PCNSL). Materials and Methods: Radiotherapy followed by high-dose methotrexate (HD-MTX)-based chemotherapy was administered to immunocompetent patients with histologically confirmed PCNSL between 2000 and 2016. Response to chemotherapy was taken into account when prescribing the radiation dose to the whole brain and primary tumor bed. The whole brain dose was ≤23.4 Gy for rdWBRT (n = 20) and >23.4 Gy for hdWBRT (n = 68). Patients manifesting cognitive disturbance, memory impairment and dysarthria were considered to have neurotoxicity. A median follow-up was 3.62 years. Results: The 3-year overall survival (OS) and progression-free survival (PFS) were 70.0% and 48.9% with rdWBRT, and 63.2% and 43.2% with hdWBRT. The 3-year OS and PFS among patients with partial response (n = 45) after chemotherapy were 77.8% and 53.3% with rdWBRT, and 58.3% and 45.8% with hdWBRT (p > 0.05). Among patients with complete response achieved during follow-up, the 3-year freedom from neurotoxicity (FFNT) rate was 94.1% with rdWBRT and 62.4% with hdWBRT. Among patients aged ≥60 years, the 3-year FFNT rate was 87.5% with rdWBRT and 39.1% with hdWBRT (p = 0.49). Neurotoxicity was not observed after rdWBRT in patients aged below 60 years. Conclusion: rdWBRT with tumor bed boost combined with upfront HD-MTX is less neurotoxic and results in effective survival as higher-dose radiotherapy even in partial response after chemotherapy.

폐암의 방사선치료 결과 (Result of Radiation Therapy for the Lung Cancer)

  • 김주영;최명선;서원혁
    • Radiation Oncology Journal
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    • 제7권2호
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    • pp.213-225
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    • 1989
  • An analysis has been made of two hundred seven patients who were treated at the department of Radiation Oncology of Korea University Hospital for lung cancer from January 1981 through December 1986. There were 137 patients of nonsmall cell carcinoma (137/207, 66%), 26 patients of small cell carcinoma (26/207, 12.5%) and 44 patients of unproven histology. By aims of treatment, there were 104 patients (104/207, 50%) treated for cure, 89 patients (89/207, 42.9%) for palliation and 14 patients treated postoperatively. In 22 out of 207 patients, chemotherapy was done with radiotherapy, 12 of which were patients with small cell carcinoma. Stage II patients were 49 (49/207, 23.6%), stage III patients were 157 (157/207, 75.8%) and one patient had an occult cancer The tumor was initial Iy measured by CAT scan and chest X-rays in the 165 (165/207, 79.7%) patients, among which 117 patients had tumor diameter more than 5cm and 48 patients less than 5cm. Radiation therapy was given with Cobalt 60 teletherapy unit and the treatment volume encompassed primary tumor and the mediastinum. For curative aim, daily tumor dose of 180 cGy was given up to the range of 5,400~6,120cGy/30~34F/6~7 week period and for palliative aim, daily tumor dose of 300 cGy was given up to the range of 3,600~4,500 cGy/12~15F/2~3 week period. Postoperatively, mediastinum was treated for total dose of 5,040 cGy/28F/5.5 week period. 123 patients (123/207, 59%) were followed up after completion of radiotherapy for 14 months to 7 years. Local tumor response to the irradiation was measured by chest X-ray taken at one month follow up and was evaluated for response rate, if they were regressed more than 50% or less than 50% of the initial tumor size. The treatment results were as follows; 1. The median survival time was 8.5 months and survival rates for 1 year, 2 year and 5 year was 25%, 3.5% and 1% of nonsmall cell lung ca of 74 evaluable patients. 2. More than 50% of local tumor response rate was obtained in about half of overall cases; 90.5% for small cell ca, 50% for squamous cell ca, 25% for adenoca and 57% for large cell ca. 3. Response rate more than 50% was seen in the 50% of the patient group with tumor diameter more than 5cm and in the 55% of those with tumor diameter less than 5cm. 4. By total raidation dose given, patient group which was given 5,400~6,120 cGy equivalent dose or higher showed tumor response rate more than 50% in 53% of the patients, whereas the group with dose less than 5,400cGy equivalent, in 25% of the patients. 5. Survival rate for 6 month, 1 year and 2 year was compared between the group of local tumor response rate more than 50% vs. group with response rate less than 50%; 74% vs. 43%, 33% vs, 23%, 10% vs. 1%, respectively. 6. Local failure was seen in 21%(44/207) of the patients, which occured mostly within 15 months after completion of radiation therapy. Distant metastases were seen in 49.7%(103/207) of the patients, of which 43 cases were found before initiation of radiotherapy. The most common metastatic sites were bone and brain. In this sutdy, 1 year,2 year and S year survival rates were somewhat poor compared to the other studies. It mainly seems to be due to the poor general status of the patients and the far-advanced stage of the disease. In nonsmall cell cancer patients who had limited local disease and had small primary tumor size, we observed better local response. In addition, dose higher than 6,000 cGy group showed better tumor control than lower dose group. Survival rate was better for the local control group. For imporvement of local control of the lung cancer and hence, the survival of the patients with lung cancer, proper radical radiotherapy with high dose for localized disease is needed. New modality of treatment such as high LET beam in radiation therapy or drugs for the advanced disease as well as early diagnosis is also needed.

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Gene Expression Biodosimetry: Quantitative Assessment of Radiation Dose with Total Body Exposure of Rats

  • Saberi, Alihossein;Khodamoradi, Ehsan;Birgani, Mohammad Javad Tahmasebi;Makvandi, Manoochehr
    • Asian Pacific Journal of Cancer Prevention
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    • 제16권18호
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    • pp.8553-8557
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    • 2016
  • Background: Accurate dose assessment and correct identification of irradiated from non-irradiated people are goals of biological dosimetry in radiation accidents. Objectives: Changes in the FDXR and the RAD51 gene expression (GE) levels were here analyzed in response to total body exposure (TBE) to a 6 MV x-ray beam in rats. We determined the accuracy for absolute quantification of GE to predict the dose at 24 hours. Materials and Methods: For this in vivo experimental study, using simple randomized sampling, peripheral blood samples were collected from a total of 20 Wistar rats at 24 hours following exposure of total body to 6 MV X-ray beam energy with doses (0.2, 0.5, 2 and 4 Gy) for TBE in Linac Varian 2100C/D (Varian, USA) in Golestan Hospital, in Ahvaz, Iran. Also, 9 rats was irradiated with a 6MV X-ray beam at doses of 1, 2, 3 Gy in 6MV energy as a validation group. A sham group was also included. After RNA extraction and DNA synthesis, GE changes were measured by the QRT-PCR technique and an absolute quantification strategy by taqman methodology in peripheral blood from rats. ROC analysis was used to distinguish irradiated from non-irradiated samples (qualitative dose assessment) at a dose of 2 Gy. Results: The best fits for mean of responses were polynomial equations with a R2 of 0.98 and 0.90 (for FDXR and RAD51 dose response curves, respectively). Dose response of the FDXR gene produced a better mean dose estimation of irradiated "validation" samples compared to the RAD51 gene at doses of 1, 2 and 3 Gy. FDXR gene expression separated the irradiated rats from controls with a sensitivity, specificity and accuracy of 87.5%, 83.5% and 81.3%, respectively, 24 hours after dose of 2 Gy. These values were significantly (p<0.05) higher than the 75%, 75% and 75%, respectively, obtained using gene expression of RAD51 analysis at a dose of 2 Gy. Conclusions: Collectively, these data suggest that absolute quantification by gel purified quantitative RT-PCR can be used to measure the mRNA copies for GE biodosimetry studies at comparable accuracy to similar methods. In the case of TBE with 6MV energy, FDXR gene expression analysis is more precise than that with RAD51 for quantitative and qualitative dose assessment.

개심술시 Activated Clotting Time 을 이용한 Heparin 투여 조절에 관한 임상적 고찰 (Control of heparinization by activated clotting time during extracorporeal circulation)

  • 서충헌
    • Journal of Chest Surgery
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    • 제16권3호
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    • pp.281-288
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    • 1983
  • Heparinization is an essential step in extracorporeal circulation for open heart surgery. But wide individual variation to heparin effect sometimes makes it difficult to anticoagulate safely or neutralize appropriately. Because the conventional set protocol of heparinization did not consider this individual variation, a new method of control of heparinization was proposed by Dr. Brian Bull in 1974. We compared the group in which a conventional set protocol was used [Control group] with the other in which a new protocol modified from that of Bull was used [ACT group], on the aspects of the dosages of heparin and protamine administered and postoperative bleeding. Our conventional protocol [Control group] consisted of: 1. Initial heparin was given at dose of 350U/Kg into the right atrium prior to bypass. 2. Additional heparin was given every hour during E.C.C., as much as a half of the Initial dose. 3. 600U of heparin was mixed into every 100ml. of priming solution. 4. The protamine dose was calculated by totalling the units of heparin given to the patient and giving 1 .8mg. of protamine per 100 units of heparin. ACT protocol [ACT group] consisted of: 1. Initial heparinization was same as that of conventional protocol. 2. ACT`s were checked before [A point] and 10 minutes after initial heparinization [B point]. With these 2 points, a dose response curve was drawn. 3. Heparin for the priming solution was same as in control group. 4. Every 30 minutes during E.C.C., ACT`s were checked with Hemochron [International Technidyne Corp.]. ACT between 450 and 600 seconds was regarded as safety zone. If ACT checked at a time was below 450 seconds, heparin dose was calculated on the dose-response curve to lengthen ACT to 480 seconds and was given into the oxygenator. 5. About 10 minutes before the term of E.C.C., ACT was checked to estimate the blood heparin level at the time. Then, protamine dose was calculated at dose of 1.Stag per 100 units of heparin. The calculated dose of protamine was mixed into 50 to lO0ml of 5% Dextrose Water and dripped intravenously during the period of 15 minutes. Compared these two groups mentioned above, results were obtained as follows: 1. Mean value of normal ACT checked with Hemochron on 30 preoperative patients was 124 seconds [range 95-145 sec.]. 2. Doses of heparin and protamine given to the patient were decreased in ACT group as much as 32.2% and 62.2% respectively. 3. Postoperative bleeding and transfusion were also decreased in ACT group in 60.5% and 67.1% respectively. 4. Our modified dose-response curve did not cause any problems in the control of heparinization. 5. Initial heparinization [Heparin 350U/Kg] was sufficient for the most patients until 60 minutes under extracorporeal circulation. 6. We used 1.5mg of protamine to neutralize 100 units of heparin. But smaller dose of protamine may be sufficient for appropriate neutralization.

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흰쥐를 이용한 에페드린의 약물남용가능성 평가 (Evaluation on the Abuse Liability of Ephedrine Using Rats)

  • 류승렬;김혜진;홍진태;이종권;이선희;이병무;김부영
    • 약학회지
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    • 제43권5호
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    • pp.682-688
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    • 1999
  • Abuse liability of ephedrine was investigated by measurement of locomotor activity and self-administration in Sprague-Dawley rats. Locomotor activity was determined in rats treated with 3, 10 and 30 mg/kg ephedrine for 14 days. Self-administration by ephedrine (0.23, 1 and 2.3 mg/kg) was examined in food-trained rats. We also examined effect of dopamine receptor antagonist (spiperone, $30{\;}\mu\textrm{g}/kg$) on the ephedrine-induced response of self-administration. Body weight was not statistically difference between control and ephedrine treatment group, but locomotor activity was dose-dependently increased. Self-administration for ephedrine was decreased in the early response (day 1 and 2) but the response was increased by higher dose of ephedrine. Self-administration was decreased by dopamine receptor antagonist (spiperone). These data showed that ephedrine increased locomotor activity and induced response of self-administration, and the effects of ephedrine were partially related to the dopaminergic system, which suggest the ephedrine may have abuse liability.

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