• 제목/요약/키워드: Tumor control

검색결과 2,017건 처리시간 0.031초

삼성서울병원 방사선종양학과 종양등록 정보의 타당도 평가 (Evaluation of Tumor Registry Validity in Samsung Medical Center Radiation Oncology Department)

  • 박원;허승재;김대용;신성수;안용찬;임도훈;김선우
    • Radiation Oncology Journal
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    • 제22권1호
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    • pp.33-39
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    • 2004
  • 목적 : 삼성서울병원 방사선종양학과에서는 1994년 개원 초부터 방사선치료를 받은 환자를 대상으로 자체 종양등록시스템을 운영하고 있다. 본 연구에서는 삼성서울병원 방사선종양학과 종양등록시 스템을 소개하고, 종양등록 현황을 분석하고자 하였다. 대상 및 방법 : 삼성서울병원 통합방사선관리 시스템의 한 부분이 종양등록 시스템이다 종양등록 시스템은 환자정보, 진단 정보, 치료정보로 구성되어 있으며, 모든 입력은 한 화면에서 이루어지며, 마우스만 가지고 입력이 가능하다. 2002년 7월까지 종양등록 시스템에 등록된 10,000예의 환자군에서 199명을 무작위 추출하여, 추출된 환자들의 등록된 종양정보와 실제 의무기록을 비교하여 입력이 누락되었거나 다른 정보가 등록되었는지 확인하였다. 결과 : 전체 대상 환자 199예 중 입력 오류가 발생한 경우는 15예(7.5%)에서 17건이었고, 진단정보와 치료정보에서 각각 8건, 9건이었다. 진단정보는 상병, 조직병리, AJCC 병기 및 전신수행능력이 잘못 입력된 경우였고, 치료정보중에는 병용치료 종류, 추적관찰 개시일 및 방사선치료 완결 유무 항목에서 오류가 있었다. 담당 의사별 오류를 분석하여 보았는데, 중복 점검이 시행된 경우에 모류는 3.7%에 불과하였지만 중복 점검이 되지 못한 경우는 15.6%의 오류가 있었다. 결론 : 종양등록 시스템을 이용하여 개별 항목별로는 모두 2% 이내의 오류에 불과하였다. 그러나, 정보의 질을 보다 향상시키기 위해서는 입력자의 성실성 및 종양등록에 대한 전문지식을 높이고, 주기적인 타당도 검사 및 중복점검 체계의 확립이 필요하겠다. 또한, 종합병원정보 시스템과 연계된 항목을 적극 활용할 수 있겠으나, 이를 위해서는 먼저 종합병원정보 시스템 내 종양등록 정보의 수준이 검증되어야 할 것이다.

Sarcopenia in Cancer Patients

  • Chindapasirt, Jarin
    • Asian Pacific Journal of Cancer Prevention
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    • 제16권18호
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    • pp.8075-8077
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    • 2016
  • Sarcopenia, characterized by a decline of skeletal muscle plus low muscle strength and/or physical performance, has emerged to be an important prognostic factor for advanced cancer patients. It is associated with poor performance status, toxicity from chemotherapy, and shorter time of tumor control. There is limited data about sarcopenia in cancer patients and associated factors. Moreover, the knowledge about the changes of muscle mass during chemotherapy and its impact to response and toxicity to chemotherapy is still lacking. This review aimed to provide understanding about sarcopenia and to emphasize its importance to cancer treatment.

Pentoxifylline과 Nicotinamide의 병용에 의한 생체내 방사선 감수성 증강 효과 (Enhancement of in vivo Radiosensitization by Combination with Pentoxifylline and Nicotinamide)

  • 이인태;조문준
    • Radiation Oncology Journal
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    • 제9권1호
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    • pp.7-15
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    • 1991
  • Pentoxifylline (PENTO)는 적혈구의 유동성을 증가시켜 모세혈관의 적혈구 흐름을 증가시킨다. 또한 적혈구내 2,3-DPG를 증가시켜서 산소 친화력을 감소시켜 산소의 해리를 촉진시킨다. Nicotinamide (NA)는 종양내 혈류를 일시적으로 증가시켜서 종양내 급성 저산소 세포의 수를 감소시킨다. PENTO와 NA의 병용이 저산소 세포의 산소화에 의해서 방사선 감수성을 증가시킬 수 있는지를 확인하기 위하여 FSaII생쥐의 섬유육종을 이용하여 실험을 시행하였다. 방사선에 의한 성장 장애가 유의하게 증가하였으며, 증가율은 2.5~2.8이었다. $TCD_{50}$가 대조 종양군에서는 57Gy였으나 PENTO+NA투여 종양군에서는 32Gy로 1.8배의 $TCD_{50}$의 감소를 보였다. 정상피부의 방사선 감수성에는 영향이 없었다. PENTO+NA의 방사선 감수성의 증가를 규명하기 위하여 종양내 혈류의 변화, 종양내 산소농도를 laser Doppler flowmetry와 산소 미소전극 방법으로 측정하였다. PENTO+NA투여후 10분 경과하여 혈류가 유의하게 증가하였으며 종양내 산소 분압도 8 mmHg에서 19 mmHg로 유의하게 증가함을 관찰하였다. 따라서 PEHTO또는 NA단독보다 PENTO+NA병통이 더욱 효과적이라 사료되며 생체내 종양의 방사선 감수성의 증가는 종양내 산소의 증가로 생각되며 더욱 방사선 감수성을 증가시키기 위하여 여러 농도의 PENTO의 단독 또는 NA와의 병용등에 대한 지속적인 연구가 필요하다.

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가토에서 체외 방사선 조사후 재이식한 자가관절의 조직학적 변화 (Histologic Change of Extracorporeal Irradiated Autogenous Joint Transplantation in Rabbit's Knee)

  • 김재도;조명래;유경식;김영창
    • 대한골관절종양학회지
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    • 제5권1호
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    • pp.9-16
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    • 1999
  • A new method of limb sparing by resection, extracorporeal irradiation and reimplantation has several theoretical advantages. This method preserves the mobility of a joint and avoids the problem of loosening or breakage of tumor prosthesis. This study involved using extracorporeal irradiated autogenous joint transplantation for reconstruction after en bloc resection, and observed the periods of functional union and histological changes in irradiated tissue of the knee joint. This study also aimed to clarify whether the degeneration of articular cartilage is induced in rabbits by a single 50Gy dose of irradiation at the knee joint. Twenty New Zealand rabbits about three kilograms were randomized into two groups of 10 rabbits each. In group 1, as control, we resected the knee joint followed by reimplantation without irradiation. Group 2 received extracorporeal irradiation on the resected knee joint followed by reimplantation. Following are the results of these observations. The osteotomy site showed external callus formation in the roentgenographic finding eight weeks after reimplantation. There was marked degenerative changes in the collagen fiber of the irradiated anterior cruciate ligament and meniscus during the fourth week, but new blood-vessel formation was observed in the vicinity. There was degenerative changes in the collagen fiber of articular cartilage treated extracorporeal irradiation at four and eight weeks in the scanning electron micrographic findings. These findings was in contrast to those of subchondral bone which showed decreased cellularity and empty lacuna at four and eight weeks. Autoradiography demonstrated active [$^3H$]uridine incorporation by irradiated chondrocyte at eight weeks after reimplantation. These results indicate that when destruction of the articular cartilage and soft tissue of the knee joint is not severe, extracorporeal irradiation and reimplantation can be used with several advantage in maintaining movement of the joint while avoiding problems of tumor prosthesis and rejection, and therefore extracorporeal irradiated autogenous joint transplantation can be used as a limb-sparing procedure for temporary biological spacer in the childhood bone tumor around the knee.

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홍삼의 에탄올 추출물의 감마선 조사를 통한 항암효과 증대 (The Ethanol Extract of Red Ginseng Enhances Anti-Tumor Effects Using Co60 Gamma Irradiation)

  • 허정무;김동호
    • Journal of Applied Biological Chemistry
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    • 제54권1호
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    • pp.15-20
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    • 2011
  • 홍삼은 우리나라에서 오랜 역사동안 여러 질병을 치료하는데 사용되었다. 본 연구에서는 홍삼 에탄올 추출물에 감마선을 1~5kGy 범위에서 조사를 하는 새로운 기법을 개발하고자 한다. 감마선 조사된 홍삼 추출물(IHRG)의 진세노사이드의 조성변화를 관찰하기 위해서 HPLC 분석을 이용하였다. 그 결과, 홍삼 에탄올 추출물에 감마선 1 kGy와 5 kGy를 조사한 처리군에서 진세노사이드의 조성에 변화는 관찰되지 않았다. MTT 분석법을 이용하여 사람의 전립선암세포주인 PC-3세포에서의 IHRG의 세포독성을 살펴 본 결과, 감마선을 처리하지 않은 홍삼추출액(HRG) 보다 더 높은 세포독성을 보였다. $LD_{50}$ 농도가 IHRG-1(1 kGy)에서는 $30{\mu}g/mL$, IHRG-5 (5 kGy)에서는 $15{\mu}g/mL$로 나타났다. 이러한 세포독성이 Annexin V/PI 분석 및 핵의 염색법인 DAPI 염색을 통하여 IHRG를 처리한 군들에서 전형적인 apoptosis를 관찰할 수 있었다. 또한, 산화적 스트레스(ROS)의 유발이 IHRG 처리군에서 나타났다. BALB/c 마우스에 암세포를 이식시킨 모델에서 IHRG에 의한 암세포 증식억제 효과를 살펴 본 결과, 암세포 증식 억제율이 HRG에서 21.1%인 반면에, IHRG-1에서 56.9%, IHRG-5에서 76.1%로 나타났다. 이들 결과들 통해, HRG에 어떤 생리활성 물질이나 성분들이 감마선 조사에 의해 항암효과를 증대시킨 것으로 사료된다.

Risk factors for locoregional recurrence in patients with pathologic T3N0 rectal cancer with negative resection margin treated by surgery alone

  • Baek, Jong Yun;Yu, Jeong Il;Park, Hee Chul;Choi, Doo Ho;Yoo, Gyu Sang;Cho, Won Kyung;Lee, Woo-Yong;Yun, Seong Hyeon;Cho, Yong Beom;Park, Yoon Ah;Kim, Hee Cheol
    • Radiation Oncology Journal
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    • 제37권2호
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    • pp.110-116
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    • 2019
  • Purpose: This study aimed to identify prognostic factors for locoregional recurrence (LRR) in pT3N0 rectal cancer patients who were treated with surgery alone and had negative resection margin including circumferential resection margin (CRM) for optimal indication of adjuvant radiotherapy. Materials and Methods: We reviewed patients with pT3N0 rectal cancer who were treated via upfront surgery and had no other adjuvant treatment from January 2003 to December 2012. In total, 122 patients who had negative resection margin including negative CRM were included in the analysis. Results: The median follow-up period after surgery was 60 months (range, 3 to 161 months). During this time, 6 patients (4.9%) experienced LRR at the anastomotic site (4 patients), and regional lymphatic area (2 patients). The estimated 5-year rates of overall survival, recurrence-free survival, and LRR-free survival were 96.7%, 84.6%, and 94.0%, respectively. Multivariate analysis showed that level of tumor ≤5 cm was a significant prognostic factor for LRR-free survival (LRRFS) (p = 0.04; hazard ratio = 7.08; 95% confidence interval, 1.06-47.30). Patients with level of tumor ≤5 cm had an estimated 5-year LRRFS of 66.8%, which was much higher than 2.3% in patients with level of tumor >5 cm. There was no significant factor for recurrence-free survival or overall survival. Conclusion: In T3N0 rectal cancer, adjuvant chemoradiotherapy should be recommended in patients with level of tumor ≤5 cm for better local control. However, in patients with pT3N0 disease, negative resection margin, and level of tumor >5 cm, adjuvant chemoradiotherapy should be carefully suggested.

Effects of FasL Expression in Oral Squamous Cell Cancer

  • Fang, Li;Sun, Lin;Hu, Fang-Fang;Chen, Qiao-Er
    • Asian Pacific Journal of Cancer Prevention
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    • 제14권1호
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    • pp.281-285
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    • 2013
  • Purpose: To probe the role of FasL in cell apoptosis in oral squamous cell carcinomas (OSCCs). Methods: The expression of Fas/FasL was assessed in 10 cases of normal oral epithelium, 38 cases of OSCC and tumor infiltrating lymphocytes (TIL), and 11 cases of metastatic lymph nodes by immunohistochemistry. Apoptosis of tumor cells and TIL was detected by terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling assay (TUNEL). FasL-induction of T cell apoptosis was tested by co-culture assay in vitro with SCC-9 and Jurkat T cells. Results: The 10 cases of normal oral epithelium all demonstrated extensive expression of Fas, the positive rate being largely down-regulated in OSCC (21/38) (P<0.05) compared to the normal (10/10). At the same time, the positive rate of FasL significantly increased in OSCC (P<0.05) especially those with lymph node metastasis (P<0.05). The positive rates of Fas in well and middle differentiated OSCC were higher than those in poor differentiated OSCC (P<0.05). The AI of tumor cells in Fas-positive OSCC was remarkably higher than that in Fas-negative OSCC (P<0.01), with a positive correlation between Fas expression and cell differentiation as well as apoptosis (r=0.68, P<0.01). The AI of tumor cells in FasL positive OSCC was remarkably lower than that in control while the AI of TIL was higher than in FasL negative OSCC (P<0.05). The AI of tumor cells reversely correlated with that of TIL (r = -0. 72, P<0.05). It was found that SCC-9 cells expressing functional FasL could induce apoptosis of Jurkat cells as demonstrated by co-culture assays. As a conclusion, it is evident that OSCC cells expressing FasL can induce apoptosis in Fas-expressing T cells. Conclusions: In progression of OSCC, expression of the Fas/FasL changes significantly. The results suggest that FasL is a mediator of immune privilege in OSCC and may serve as an marker for predicting malignant change in oral tissues.

Down Regulation of miR-34a and miR-143 May Indirectly Inhibit p53 in Oral Squamous Cell Carcinoma: a Pilot Study

  • Manikandan, Mayakannan;Rao, Arunagiri Kuha Deva Magendhra;Arunkumar, Ganesan;Rajkumar, Kottayasamy Seenivasagam;Rajaraman, Ramamurthy;Munirajan, Arasambattu Kannan
    • Asian Pacific Journal of Cancer Prevention
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    • 제16권17호
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    • pp.7619-7625
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    • 2015
  • Background: Aberrant microRNA expression has been associated with the pathogenesis of a variety of human malignancies including oral squamous cell carcinoma (SCC). In this study, we examined primary oral SCCs for the expression of 6 candidate miRNAs, of which five (miR-34a, miR-143, miR-373, miR-380-5p, and miR-504) regulate the tumor suppressor TP53 and one (miR-99a) is involved in AKT/mTOR signaling. Materials and Methods: Tumor tissues (punch biopsies) were collected from 52 oral cancer patients and as a control, 8 independent adjacent normal tissue samples were also obtained. After RNA isolation, we assessed the mature miRNA levels of the 6 selected candidates against RNU44 and RNU48 as endogenous controls, using specific TaqMan miRNA assays. Results: miR-34a, miR-99a, miR-143 and miR-380-5p were significantly down-regulated in tumors compared to controls. Moreover, high levels of miR-34a were associated with alcohol consumption while those of miR-99a and miR-143 were associated with advanced tumor size. No significant difference was observed in the levels of miR-504 between the tumors and controls whereas miR-373 was below the detection level in all but two tumor samples. Conclusions: Low levels of miR-380-5p and miR-504 that directly target the 3'UTR of TP53 suggest that p53 may not be repressed by these two miRNAs in OSCC. On the other hand, low levels of miR-34a or miR-143 may relieve MDM4 and SIRT1 or MDM2 respectively, which will sequester p53 indicating an indirect mode of p53 suppression in oral tumors.

Protective Effect of Selenium on Experimental Colon Carcinogenesis in Mice Fed a Low Iron Diet

  • Park, Hyun-Ji;Kim, Jun-Hyeong;Kang, Bong-Su;Nam, Sang-Yoon;Kim, Jong-Soo;Jeong, Jae-Hwang;Kim, Eun-Young;Lee, Beom-Jun;Yun, Young-Won
    • 한국식품위생안전성학회지
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    • 제26권4호
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    • pp.388-397
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    • 2011
  • Selenium (Se) is known to prevent from several cancers, while iron (Fe) is known to be associated with high risk of cancers. The role of Se on colon carcinogenesis was investigated in an animal model induced by azoxymethane (AOM) and dextran sodium sulfate (DSS) in low Fe mice. Six-week old ICR mice fed on a low Fe diet (4.5 ppm Fe; generally 10 times lower than normal Fe) with three different Se (0.02, 0.1 or 0.5 ppm) levels for 24 weeks. The animals received weekly three ($0{\sim}2^{nd}$ weeks) i.p. injections of AOM (10 mg/kg RW), followed by 2% DSS with drinking water for 1 week to induce the colon cancer. There were five experimental groups including vehicle, positive control (normal Fe level, AOM/DSS), Low Fe (LFe) + AOM/DSS+Low Se (LSe), LFe + AOM/DSS + medium Se (MSe) and LFe + AOM/DSS + high Se (HSe) groups. HSe group showed a 66.7% colonic tumor incidence, MSe group showed a 69.2% tumor incidence, and LSe group showed a 80.0% tumor incidence. The tumor incidence was negatively associated with Se levels of diets. Tumor multiplicity in Hse group was significantly low compared to the other groups (p < 0.05). With increasing Se levels of diets, the primary anti-proliferating cell nuclear antigen (PCNA)-positive cells were decreased and apoptotic bodies were increased in a dose-dependent manner. Se-dependent glutathione peroxidase activity and its protein level were dependent on the levels of Se of diets. Malondialdehyde level in liver was lowest in Hse group among experimental groups. These findings indicate that dietary Se is chemopreventive for colon cancer by increasing antioxidant activity and decreasing cell proliferation in Fe-deficient mice.

The Antitumor Effects of Selenium Compound $Na_5SeV_5O_{18}{\cdot}3H_2O$ in K562 Cell

  • Yang, Jun-Ying;Wang, Zi-Ren
    • Archives of Pharmacal Research
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    • 제29권10호
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    • pp.859-865
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    • 2006
  • With an approach to study the anti-tumor effects and mechanism of selenium compound, we investigated the anti-tumor activity and mechanism of $Na_5SeV_5O_{18}{\cdot}3H_2O$ (NaSeVO) in K562 cells. The results showed that $0.625{\sim}20\;mg/L$ NaSeVO could significantly inhibit the proliferation of K562 cells in vitro in a time- and concentration-dependent manner as determined by microculture tetrazolium (MTT) assay, the IC50 values were 14.41 (4.45-46.60) and 3.45 (2.29-5.22) mg/L after 48 hand 72 h treatment with NaSeVO respectively. In vivo experiments demonstrated that i.p. administration of 5, 10 mg/kg NaSeVO exhibited an significant inhibitory effect on the growth of transplantation tumor sarcoma 180 (S180) and hepatoma 22 (H22) in mice, with inhibition rate 26.8% and 58.4% on S180 and 31.3% and 47.4% on H22, respectively. Cell cycle studies indicated that the proportion of G0/G1 phase was increased at 2.5 mg/L while decreased at 10 mg/L after treatment for 24, 48 h. Whereas S phase was decreased at 2.5-5 mg/L and markedly increased at 10 mg/L after treatment for 48 h. After treatment for 24 h, 10 mg/L NaSeVO also markedly increased S and G2/M phases. Take together, the result clearly showed that NaSeVO markedly increased S and G2/M phases at 10 mg/L. The study of immunocytochemistry showed that the expression bcl-2 is significantly inhibited by 10 mg/L NaSeVO, and bax increased. Morphology observation also revealed typical apoptotic features. NaSeVO also significantly caused the accumulation of $Ca^{2+}$ and $Mg^{2+}$, reactive oxygen species (ROS) and the reduction of pH value and mitochondrial membrane potential in K562 cells as compared with control by confocal laser scanning microscope. These results suggest that NaSeVO has anti-tumor effects and its mechanism is attributed partially to apoptosis induced by the elevation of intracellular $Ca^{2+}$, $Mg^{2+}$ and ROS concentration, and a reduction of pH value and mitochondria membrane potential (MMP).