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1.
The Korean Journal of Internal Medicine ; : 585-594, 2018.
Artigo em Inglês | WPRIM | ID: wpr-714633

RESUMO

BACKGROUND/AIMS: The purpose of the present study was to assess the prevalence of and factors associated with anxiety and depression in Korean patients with advanced gastrointestinal cancer. METHODS: One hundred and twenty consecutive patients with newly diagnosed, advanced gastrointestinal cancer who were scheduled to receive palliative chemotherapy between July 2012 and June 2014 were enrolled in this observational prospective study. Anxiety and depression were assessed using the Hospital Anxiety and Depression Scale (HADS) and Patient Health Questionnaire-9 (PHQ-9). RESULTS: Thirty-seven patients (30.8%) had anxiety or depression with clinical significance according to HADS or PHQ-9. Multivariate analysis identified lower performance status (odds ratio [OR], 4.19; 95% confidence interval [CI], 1.22 to 14.35; p = 0.023), gastric cancer (OR, 5.39; 95% CI, 0.37 to 78.23; p = 0.018), and knowledge of advanced cancer (OR, 15.07; 95% CI, 1.80 to 125.90; p = 0.012) as significantly associated with anxiety or depression. Twenty-one patients with anxiety or depression visited the psycho-oncologic clinic. In these patients, PHQ-9 score (p = 0.008), global health status (p = 0.023), fatigue (p = 0.047), and appetite loss (p = 0.006) improved from baseline to 3 months after study enrollment. CONCLUSIONS: Approximately 30% of Korean patients with advanced gastrointestinal cancer had anxiety or depression. The prevalence of anxiety or depression was higher in patients with poor performance status, gastric cancer, or knowledge of advanced cancer. Psychiatric interventions may be effective in reducing depression and improving quality of life in cancer patients with anxiety or depression.


Assuntos
Humanos , Ansiedade , Apetite , Depressão , Tratamento Farmacológico , Fadiga , Neoplasias Gastrointestinais , Saúde Global , Análise Multivariada , Prevalência , Estudos Prospectivos , Qualidade de Vida , Neoplasias Gástricas
2.
Cancer Research and Treatment ; : 1429-1437, 2016.
Artigo em Inglês | WPRIM | ID: wpr-205893

RESUMO

PURPOSE: Dexamethasone is a mainstay antiemetic regimen for the prevention of chemotherapy-induced nausea and vomiting. The aim of this pilot study was to assess the incidence of and factors associated with steroid-induced diabetes in cancer patients receiving chemotherapy with dexamethasone as an antiemetic. MATERIALS AND METHODS: Non-diabetic patients with newly diagnosed gastrointestinal cancer who received at least three cycles of highly or moderately emetogenic chemotherapy with dexamethasone as an antiemetic were enrolled. Fasting plasma glucose levels, 2-hour postprandial glucose levels, and hemoglobin A1C tests for the diagnosis of diabetes were performed before chemotherapy and at 3 and 6 months after the start of chemotherapy. The homeostasis model assessment of insulin resistance (HOMA-IR) was used as an index for measurement of insulin resistance, defined as a HOMA-IR ≥ 2.5. RESULTS: Between January 2012 and November 2013, 101 patients with no history of diabetes underwent laboratory tests for assessment of eligibility; 77 of these patients were included in the analysis. Forty-five patients (58.4%) were insulin resistant and 17 (22.1%) developed steroid-induced diabetes at 3 or 6 months after the first chemotherapy, which included dexamethasone as an antiemetic. Multivariate analysis showed significant association of the incidence of steroid-induced diabetes with the cumulative dose of dexamethasone (p=0.049). CONCLUSION: We suggest that development of steroid-induced diabetes after antiemetic dexamethasone therapy occurs in approximately 20% of non-diabetic cancer patients; this is particularly significant for patients receiving high doses of dexamethasone.


Assuntos
Humanos , Antieméticos , Glicemia , Dexametasona , Diabetes Mellitus , Diagnóstico , Tratamento Farmacológico , Jejum , Neoplasias Gastrointestinais , Glucose , Homeostase , Incidência , Insulina , Resistência à Insulina , Análise Multivariada , Náusea , Projetos Piloto , Vômito
3.
Asian Oncology Nursing ; : 242-250, 2016.
Artigo em Inglês | WPRIM | ID: wpr-67088

RESUMO

PURPOSE: The purpose of the present study was to assess factors associated with quality of life (QOL) and to determine whether anxiety and depression are predictive of QOL in patients with advanced gastrointestinal cancer at initial diagnosis and during the treatment process. METHODS: One hundred and twenty patients with gastrointestinal cancer requiring palliative chemotherapy were enrolled. RESULTS: At baseline, depression, performance status, and anxiety accounted for 55.0% (p<.001) of the variance in global health status score, depression accounted for 22.0% (p<.001) of the variance in functional scales score, and anxiety accounted for 19.0% (p<.001) of the variance in symptom scales score. At 3 months, depression, pain, and performance status accounted for 72.0% (p<.001) of the variance in global health status score, 76.0% (p<.001) of the variance in functional scales score, and 74.0% (p<.001) of the variance in symptom scales score. CONCLUSION: Anxiety and depression were significant predictive factors of QOL in patients with advanced gastrointestinal cancer. Depression and performance status were significant predictive factors of QOL at both baseline and 3 months, and anxiety and pain were significant predictive factors of QOL at baseline and 3 months, respectively.


Assuntos
Humanos , Ansiedade , Depressão , Diagnóstico , Tratamento Farmacológico , Neoplasias Gastrointestinais , Saúde Global , Qualidade de Vida , Pesos e Medidas
4.
Cancer Research and Treatment ; : 150-154, 2013.
Artigo em Inglês | WPRIM | ID: wpr-74598

RESUMO

Pancreatic neuroendocrine tumors (pNETs) are rare neoplasms, which most commonly metastasize to the liver. However, intrathoracic metastases from pNETs are encountered infrequently. This report describes a case of nonfunctioning pNET with multiple cardiac metastases. A 56-year-old male presented with a palpable abdominal mass that showed progressive enlargement. Findings on computed tomography (CT) of the abdomen revealed two relatively well-marginated inhomogeneous low-attenuation masses, one in the head of the pancreas and the other in the tail. Multiple enhancing masses in the left pericardium with myocardial involvement were observed on chest CT and transthoracic echocardiography. Needle biopsies were performed on the mass in the tail of the pancreas and the left ventricular apical pericardium; histologic examination by hematoxylin and eosin morphology and immunohistochemical staining showed pNET in both. This is the first report of pNET with multiple cardiac metastases to previously undescribed metastatic sites.


Assuntos
Humanos , Masculino , Abdome , Biópsia por Agulha , Ecocardiografia , Amarelo de Eosina-(YS) , Cabeça , Neoplasias Cardíacas , Hematoxilina , Fígado , Metástase Neoplásica , Tumores Neuroectodérmicos Primitivos , Tumores Neuroendócrinos , Pâncreas , Pericárdio , Tórax
5.
Cancer Research and Treatment ; : 215-218, 2012.
Artigo em Inglês | WPRIM | ID: wpr-68136

RESUMO

Although metastasis is relatively frequent in cases of renal cell carcinoma (RCC), metastasis in the cervical or supraclavicular lymph node (LN) is relatively rare. Moreover, cases of metastatic RCC with a non-identifiable kidney mass are extremely rare. Here, the authors report a case of metastatic RCC in a supraclavicular LN without a primary kidney lesion. A 69-year-old man presented with a progressively enlarging right supraclavicular mass. Incisional biopsy of the affected supraclavicular LN was performed, and histological examination revealed metastatic RCC. However, no tumor was found in either kidney, despite various examinations. The patient was treated with radiotherapy followed by sunitinib. After three months on sunitinib, a follow-up computed tomography scan revealed that the supraclavicular LN had markedly decreased, and after 20 months, the disease had not progressed. This case suggests that, even when there is no primary kidney lesion, clinicians must consider the possibility of metastatic RCC when evaluating patients with clear cell carcinoma with an unknown primary site.


Assuntos
Idoso , Humanos , Biópsia , Carcinoma de Células Renais , Seguimentos , Indóis , Rim , Linfonodos , Metástase Neoplásica , Pirróis
6.
Cancer Research and Treatment ; : 271-274, 2012.
Artigo em Inglês | WPRIM | ID: wpr-90288

RESUMO

Neuroendocrine carcinomas from an unknown primary site are uncommon. The authors report on a case of neuroendocrine carcinoma in a perigastric lymph node (LN) with no primary site. A 52-year-old male patient with early gastric adenocarcinoma underwent treatment by endoscopic submucosal dissection, and, six months later, findings on a computed tomographic scan of the abdomen revealed a LN enlargement measuring 2.0 cm in the perigastric region. The patient underwent subtotal gastrectomy and regional LN dissection under a suggestive preoperative diagnosis of gastric adenocarcinoma with LN metastasis. However, microscopically, no residual tumor was found in the stomach, and the perigastric LN showed poorly differentiated neuroendocrine carcinoma (PDNEC). After an extensive workup, no primary site was identified. The patient also received four cycles of etoposide and cisplatin. Despite its extremely rare incidence, this case suggests that PDNEC of an unknown primary site is limited to a single site, and that resection should be considered in combination with chemotherapy.


Assuntos
Humanos , Masculino , Abdome , Adenocarcinoma , Carcinoma Neuroendócrino , Cisplatino , Etoposídeo , Gastrectomia , Incidência , Linfonodos , Metástase Neoplásica , Neoplasia Residual , Neoplasias Primárias Desconhecidas , Estômago
7.
Journal of Korean Medical Science ; : 304-307, 2011.
Artigo em Inglês | WPRIM | ID: wpr-123273

RESUMO

Interdigitating dendritic cell sarcoma (IDCS) is an extremely rare neoplasm arising from the antigen-presenting cells of the immune system. This disease usually involves the lymph nodes, and rarely, extranodal sites may be affected. The authors report a case of extranodal IDCS presenting in the pleura. A 32-yr-old man presented with progressive chest pain. Imaging studies showed diffuse pleural thickening with pleural effusion. Morphological and immunohistochemical analysis of an incisional biopsy of the pleura were consistent with a diagnosis of IDCS; tumor cells were positive for S100 and CD45, but negative for CD1a, CD21, CD35, B cell and T cell markers. The patient was administered chemotherapy, but died of progressive disease. Although its incidence is extremely rare, this case suggests that extranodal IDCS should be considered in the differential diagnosis of undifferentiated neoplasms and that immunohistochemical staining be performed using appropriate markers.


Assuntos
Adulto , Humanos , Masculino , Sarcoma de Células Dendríticas Interdigitantes/diagnóstico , Evolução Fatal , Pleura/patologia , Neoplasias Pleurais/diagnóstico , Biomarcadores Tumorais
8.
Journal of Korean Medical Science ; : 1754-1758, 2010.
Artigo em Inglês | WPRIM | ID: wpr-15538

RESUMO

This observational study aimed at evaluating recent superwarfarin intoxication of Korean patients. Ten patients were diagnosed as or highly suspicious for superwarfarin intoxication. Case report forms described by attending hematologists of the patients were collected and analyzed. Bleeding symptoms were varied among the patients. Patients uniformly showed prolonged prothrombin time (PT) and activated thromboplastin time (aPTT) with decreased activity of vitamin K dependent coagulation factors. Positive serum brodifacoum test results in 4 of 5 requested patients contributed to confirmatory diagnosis. Psychiatric interview revealed an attempted ingestion in one patient. High dose vitamin K1 therapy promptly corrected prolonged PT and aPTT, but hasty discontinuation caused repeated bleeding diathesis in 6 patients. Route of intoxication was unknown or not definite among 8 of 10 patients. Three patients had a possibility of environmental exposure considering their occupations: there might be intoxication by transdermal absorption or inhalation. Therefore, high dose and prolonged use of vitamin K1 therapy is necessary for effective detoxification. Further detailed investigation on environmental exposure and efforts to improve availability of the blood level test in clinic are requested.


Assuntos
Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , 4-Hidroxicumarinas/intoxicação , Anticoagulantes/intoxicação , Antifibrinolíticos/uso terapêutico , Exposição Ambiental , Hemorragia/induzido quimicamente , Tempo de Tromboplastina Parcial , Tempo de Protrombina , República da Coreia , Resultado do Tratamento , Vitamina K 1/uso terapêutico
9.
Yonsei Medical Journal ; : 52-57, 2010.
Artigo em Inglês | WPRIM | ID: wpr-39510

RESUMO

PURPOSE: This study was designed to investigate whether transduction of lentiviral vectors (LV) carrying human coagulation factor VIII (hFVIII) cDNA into skeletal muscle could increase circulating hFVIII concentrations. MATERIALS AND METHODS: A LV containing bacterial LacZ gene as a control or human FVIII gene was intramuscularly administered into the thigh muscle of 5 weeks old Sparague-Dawley rats. The plasma human FVIII concentration and neutralizing anti-FVIII antibodies were measured for up to 12 weeks in these experimental animals. RESULTS: The plasma human FVIII levels in the rats injected with LV carrying FVIII cDNA peaked at post-injection 1st week (5.19 +/- 0.14 ng/mL vs. 0.21 +/- 0.05 ng/mL in control rats , p < 0.05). Elevated hFVIII concentrations were maintained for 4 weeks (2.52 +/- 0.83 ng/mL vs. 0.17 +/- 0.08 ng/mL in control rats, p < 0.05) after a single intramuscular injection. In the Bethesda assay, neutralizing antibodies for FVIII protein were detected only in FVIII-LV injected rats by the 10th week, but not in control rats. CONCLUSION: This study suggested that a single administration of an advanced generation LV carrying the human FVIII cDNA resulted in elevation of FVIII level in immune competent rats, and that this gene transfer approach to the skeletal muscle could be an effective tool in treatment of hemophilia A.


Assuntos
Animais , Humanos , Masculino , Ratos , Anticorpos/sangue , Fator VIII/genética , Terapia Genética , Vetores Genéticos/genética , Células HeLa , Hemofilia A/terapia , Lentivirus/genética , Músculo Esquelético/metabolismo , Ratos Sprague-Dawley , Transdução Genética , beta-Galactosidase
10.
Korean Journal of Hematology ; : 53-57, 2009.
Artigo em Inglês | WPRIM | ID: wpr-720428

RESUMO

Superwarfarin intoxications that induce profound and prolonged coagulopathy are being increasingly reported, to such an extent that it is becoming a comparatively common intoxication. However, there have been few reported cases of superwarfarin intoxication with an inadvertent cause or an unknown origin. A 58-year-old man with recurrent painless hematuria was found to have an acquired deficiency of vitamin K dependent clotting factors, and a large amount of vitamin K was required to correct the coagulopathy. He had no history of warfarin use or any exposure to rodenticides, but brodifacoum was detected in his serum. It is important for physicians to be aware that significant coagulopathy can occur secondary to superwarfarin intoxication, without any known exposure to substances that might induce this.


Assuntos
Humanos , Pessoa de Meia-Idade , 4-Hidroxicumarinas , Hematúria , Rodenticidas , Vitamina K , Varfarina
11.
Nuclear Medicine and Molecular Imaging ; : 363-365, 2009.
Artigo em Inglês | WPRIM | ID: wpr-33859

RESUMO

Kikuchi's disease is a self-limiting benign disease characterized by cervical lymphadenopathy, but it can be mistaken for malignant disease, and when involved lymph nodes are unusually located, diagnosis can be more difficult. The authors report the case of a 19-year-old man with Kikuchi's disease, who had isolated intraabdominal lymphadenopathy and increased 18-fluoro-deoxyglucose (FDG) uptake in positron emission tomographycomputed tomography (PET-CT). Although its incidence is extremely rare, intra-abdominal Kikuchi's disease with increased FDG uptake in PET-CT image should be considered in the differential diagnosis when constitutional symptoms mimic those of malignant lymphoma.


Assuntos
Humanos , Adulto Jovem , Abdome , Diagnóstico Diferencial , Elétrons , Linfadenite Histiocítica Necrosante , Hidrazinas , Incidência , Linfonodos , Doenças Linfáticas , Linfoma , Tomografia por Emissão de Pósitrons
12.
Korean Journal of Nephrology ; : 355-359, 2009.
Artigo em Inglês | WPRIM | ID: wpr-163516

RESUMO

Hemodialysis (HD) patients continually exposed to heparin are at risk of developing heparin-induced thrombocytopenia (HIT). However, HIT is very rare in chronic HD patients with end-stage renal disease (ESRD). The authors report the case of a chronic HD patient with ESRD who developed HIT complicated by recurrent thrombocytopenia and significant bleeding episodes. A 67-year-old man with diabetic ESRD on chronic HD suddenly developed recurrent acute bleeding episodes and severe thrombocytopenia (platelet count <1.0x10(3)/uL) 2 months prior to presentation. These bleeding episodes and the thrombocytopenia always occurred 1 week after initiating HD with heparin, and improved within 1 week of discontinuing heparin. HIT was confirmed by ELISA for anti-heparin/platelet factor 4 antibody. HD was conducted successfully and thrombocytopenia did not occur after switching argatroban for heparin. This case report suggests that clinicians must consider HIT in the differential diagnosis of thrombocytopenia during maintenance HD.


Assuntos
Idoso , Humanos , Diagnóstico Diferencial , Ensaio de Imunoadsorção Enzimática , Hemorragia , Heparina , Falência Renal Crônica , Ácidos Pipecólicos , Diálise Renal , Trombocitopenia
13.
Korean Journal of Medicine ; : 236-240, 2009.
Artigo em Coreano | WPRIM | ID: wpr-7187

RESUMO

Granulocytic sarcoma (GS) is a rare extramedullary tumor composed of immature myeloid precursor cells. GS is associated with acute or chronic myeloid leukemia; it has rarely been reported in non-leukemic patients. We report two cases of GS with unusual presentations; neither had bone marrow involvement. The first case was a GS presenting with multiple intra-abdominal masses in a 43-year-old man. Computed tomography (CT) of the abdomen showed masses in the small bowel and right adrenal gland. The second case was a patient with a GS presenting with symptoms of spinal cord compression in a 32-year-old man. Magnetic resonance imaging (MRI) showed an extradural mass in the spinal canal at the T3-T5 levels. Blood smear and bone marrow studies were normal. These cases show that GS should be included in the differential diagnosis of intra-abdominal masses and extradural spinal cord tumors, even in the absence of leukemia.


Assuntos
Adulto , Humanos , Abdome , Glândulas Suprarrenais , Medula Óssea , Diagnóstico Diferencial , Leucemia , Imageamento por Ressonância Magnética , Sarcoma Mieloide , Canal Medular , Compressão da Medula Espinal , Neoplasias da Medula Espinal
14.
Korean Journal of Blood Transfusion ; : 1-8, 2008.
Artigo em Coreano | WPRIM | ID: wpr-57133

RESUMO

BACKGROUND: Hemophilia B is an inheritable X-linked bleeding disorder that occurs as a consequence of genetic alterations within the factor IX (IX) gene. In the present study, pseudotyped HIV-I-derived lentiviral vectors expressing human IX (lentivirus-IX) were assessed for the ability to produce an active human IX in the animals transduced with lentivirus-IX. METHODS: The IX concentrations and activated partial thromboplastin times (aPTT) were measured from the supernatants of HeLa cells that were transduced with lentivirus-IX. In an animal study, we injected 1microgram of lentivirus-IX into the hind limbs of Sparague-Dawley (SD) rats. The IX concentrations were measured from the plasma of the vehicle injected rats and the plasma of the lentivirus-IX injected rats for 8 weeks. RESULTS: The in vitro expression of human IX was detected in a dose-dependent manner following the transduction of lentivirus-IX into the HeLa cells (control: 10+/-3 vs. 100 ng of lentivirus-IX: 1486+/-50 ng/mL, P<0.05). The aPTT also showed the tendency of dose-dependent decrease (control: 83.9+/-0.5 vs. 50 ng of lentivirus-IX: 80.1+/- 0.8 sec), but this was not statistically significant. In the animal experiment, the plasma IX concentration from the lentivirus-IX transduced rats (n=3) was significantly increased compared to the vehicle-injected rats (n=4) (5.9+/-3.9 vs. 46.4+/-20.6 ng/mL) at post-injection 1 week. CONCLUSION: This study demonstrated that in vivo delivery of lentiviral vectors expressing human IX to the muscle cells has the potential to be a therapeutic modality for hemophilia B.


Assuntos
Animais , Humanos , Ratos , Experimentação Animal , Fatores de Coagulação Sanguínea , Extremidades , Fator IX , Terapia Genética , Células HeLa , Hemofilia A , Hemofilia B , Hemorragia , Lentivirus , Células Musculares , Plasma , Tromboplastina
15.
Korean Journal of Hematology ; : 197-205, 2007.
Artigo em Coreano | WPRIM | ID: wpr-720794

RESUMO

BACKGROUND: The aim of this study was to investigate the prevalence, clinical and laboratory findings of hereditary hemolytic anemia (HHA) in Korea from 1997 to 2006 and to develop the appropriate diagnostic approach for HHA. METHODS: By the use of questionnaires, information on the clinical and laboratory findings ofHHA diagnosed from 1997 to 2006 in Korea was collected and analyzed retrospectively. A total of 431 cases were enrolled in this study from 46 departments of 35 hospitals. RESULTS: The overall frequency of HHA did not change through the 10-year period for pediatrics but did show an increasing tendency for internal medicine. The overall male to female sex ratio did not show sex predominance (1.17:1), but a significant male predominance with a ratio of 1.49:1 was seen for pediatrics while a significant female predominance with a ratio of 1:1.97 was seen forinternal medicine. Of the total cases, 74.2% (282/431) were diagnosed before the age of 15 years. The etiologies of HHA were classified as red cell membrane defects, hemoglobinopathies, red cell enzyme deficiencies and unknown causes. There were 382 cases (88.6%) of red cell membrane defects with 376 cases (87.2%) of hereditary spherocytosis and 6 cases (1.4%) of hereditary elliptocytosis, 20 cases (4.6%) of hemoglobinopathies with 18 cases (4.2%) of beta-thalassemia, a case (0.2%) of alpha-thalassemia and a case (0.2%) of Hemoglobin Madrid, 7 cases (1.6%) of red cell enzyme deficiencies with 5 cases (1.2%) of glucose-6- phosphate dehydrogenase (G-6-PD) deficiency, a case (0.2%) of pyruvate kinase (PK) deficiency and a case (0.2%) of enolase deficiency, and 22 cases (5.1%) of unknown causes. The most common chief complaint in pediatric patients was pallor and that in adult patients was jaundice. In the red cell membrane defect group of patients, the level of hemoglobin was significantly higher than in adult patients. The mean corpuscular volume, mean corpuscular hemoglobin, corrected reticulocyte count, total and indirect bilirubin level and lactate dehydrogenase levels in the hemoglobinopathy group of patients were significantly lower than the values in the red cell membrane defect group of patients. The mean concentration of G-6-PD was 0.8+/-0.7U/1012RBC in the G-6-PD deficient patients, PK was 1.7U/1010 RBC in the PK deficient patient, and the level of enolase was 0.04U/g of Hb in the enolase deficient patient. CONCLUSION: The most prevalent cause of HHA in Korea during 1997 to 2006 was hereditary spherocytosis, but HHA by other causes such as hemoglobinopathy and red cell enzyme deficiency gradually increased with the development of molecular diagnostic methods and increasing general interest. However, the etiologies of HHA need to be pursued further in 5.1% of the patients. An systematic standard diagnostic approach is needed in a nationwide prospective study for correct diagnoses and appropriate management of HHA.


Assuntos
Adulto , Feminino , Humanos , Masculino , Talassemia alfa , Anemia Hemolítica Congênita , Talassemia beta , Bilirrubina , Membrana Celular , Diagnóstico , Eliptocitose Hereditária , Índices de Eritrócitos , Hemoglobinopatias , Medicina Interna , Icterícia , Coreia (Geográfico) , L-Lactato Desidrogenase , Oxirredutases , Palidez , Patologia Molecular , Pediatria , Fosfopiruvato Hidratase , Prevalência , Piruvato Quinase , Contagem de Reticulócitos , Estudos Retrospectivos , Razão de Masculinidade , Inquéritos e Questionários
16.
Korean Journal of Medicine ; : 567-572, 2006.
Artigo em Coreano | WPRIM | ID: wpr-117423

RESUMO

Metastatic cancer from breast cancer is not uncommon and it often involves multiple organs. Gastric metastasis from breast cancer is much rarer than lung, bone and lymph node metastasis. Most of the symptoms are nonspecific, so it is not easy to differentiate primary gastric cancer from gastric metastasis from the breast. In particular, gastric and breast cancers are the two most common cancers among Korean women, so efforts should be made to distinguish primary gastric cancer from gastric metastasis because treatment and prognosis are very different between two. A few cases have been reported in Korea concerning gastric metastasis from breast cancer. We report here a case of gastric metastasis from infiltrating duct carcinoma of the breast.


Assuntos
Feminino , Humanos , Neoplasias da Mama , Mama , Coreia (Geográfico) , Pulmão , Linfonodos , Metástase Neoplásica , Prognóstico , Neoplasias Gástricas , Estômago
17.
Journal of Korean Medical Science ; : 932-937, 2005.
Artigo em Inglês | WPRIM | ID: wpr-16330

RESUMO

The potential therapeutic benefit of introducing IFN-gamma and GM-CSF genes in combination with the HSVtk suicide gene into subcutaneously implanted CT26 tumor cells was compared with that from each treatment alone. Cells, unmodified or retrovirally transduced with HSVtk or IFN-gamma/GM-CSF genes, were inoculated subcutaneously into syngeneic BALB/c mice in various combinations. HSVtk gene, with intraperitoneal ganciclovir treatment, reduced tumor volume by 81% at locally inoculated tumor sites (p<0.01) and by 25% at distantly inoculated tumor sites (p=0.052). IFN-gamma/GM-CSF genes showed a 56% tumor volume reduction at local tumor sites (p<0.01) and 15% volume reduction at remote tumor sites, although this was not statistically significant. The combination of HSVtk (with GCV) and IFN-gamma/GM-CSF genes showed an 81% volume reduction at local tumor sites (p<0.01) and a 43% volume reduction at remote tumor sites (p<0.01). Thus, the combination of HSVtk and IFN-gamma/GM-CSF gene therapy produced greater therapeutic efficacy than either treatment alone.


Assuntos
Animais , Masculino , Camundongos , Linhagem Celular , Linhagem Celular Tumoral , Terapia Genética/métodos , Genes Transgênicos Suicidas , Fator Estimulador de Colônias de Granulócitos e Macrófagos/biossíntese , Antígenos H-2/metabolismo , Interferon gama/biossíntese , Camundongos Endogâmicos BALB C , Neoplasias Experimentais/terapia , Simplexvirus/enzimologia , Timidina Quinase/genética , Transdução Genética
18.
Cancer Research and Treatment ; : 330-334, 2003.
Artigo em Inglês | WPRIM | ID: wpr-226926

RESUMO

PURPOSE: The outcomes of a surgical approach for patients with an esophageal carcinoma remain unsatisfactory despite its high complication rates. We conducted a phase II trial, using combined FP (5-fluorouracil and cisplatin) chemotherapy and concurrent radiotherapy, as a definitive therapy for patients with esophageal cancer. MATERIALS AND METHODS: Patients with histologically proven esophageal cancer were enrolled onto this study. The treatment consisted of four courses of chemotherapy and six and a half weeks of radiotherapy. The patients received chemotherapy in weeks 1, 5, 12 and 16 (5-fluorouracil 1, 000 mg/m2 on days 1 to 4 and cisplatin 75 mg/m2 on day 1). Radiotherapy was administered at a dose of 59.4 Gy, in five 1.8 Gy fractions a week. RESULTS: A total of 22 eligible patients entered the study. Of the 19 evaluable patients, a complete response occurred in 7 (37%), and a partial response in 8 (42%). After a median follow-up of 35 months, the overall survival rate was 32% at three years and the median survival was 11 months. Fourteen (64%) received planned dose of radio-therapy and 13 (59%) received more than three courses of chemotherapy. However, there was no difference in three-year survival rates between the patients that received less than three courses of chemotherapy and those that received three or more courses (31% vs. 32%). The major treatment related toxicity was mucositis, which developed in every patient, with grades III or IV in thirteen (59%) patients. During the treatment, the patients lost, on average, 3.8% of their body weight. The mean hospital stay was 23 days, with a total duration of treatment of 74 days. CONCLUSIONS: Concurrent FP chemoradiotherapy was effective as a definitive therapy for patients with esophageal cancer. The major toxicity was mucositis. Although the treatment was relatively feasible, a randomized trial of reduced courses of chemotherapy is warranted.


Assuntos
Humanos , Peso Corporal , Quimiorradioterapia , Cisplatino , Tratamento Farmacológico , Neoplasias Esofágicas , Seguimentos , Tempo de Internação , Mucosite , Radioterapia , Taxa de Sobrevida
19.
Korean Journal of Hematology ; : 176-182, 2003.
Artigo em Coreano | WPRIM | ID: wpr-720473

RESUMO

BACKGROUND: Erythropoietin (EPO) is a 30.4kDa glycoprotein that serves as the primary regulator of red cell production in mammals. Recombinant erythropoietin has been used in the treatment of anemia associated with numerous chronic diseases. Ex vivo therapy of recombinant EPO, however, requires large dose and frequent administration, which gives financial impact to the patients. In vivo delivery of EPO using gene therapy method can solve this problem. METHODS: Recombinant lentiviral vectors containing the rat EPO gene were made by co-transfection of 293T cell with pRRL-cPPT-CMV-EPO-PRE-SIN, pMDL, pVSVG, and pREV plasmids. These viruses were concentrated and intramusculary injected into the groin muscles of Fisher 344 rats. Sequential complete blood counts were measured periodically thereafter. RESULTS: Virus doses of 6x107 infectious units and 6x106 infectious units produced significantly increased hemoglobin and hematocrit values, being 24.9+/-0.19g/dL, 66.9+/-0.62% (P < 0.01, N=5) and 18.4+/-0.55g/dL, 54.6+/-1.71%(P < 0.01, N=5), respectively at 40 weeks after injection, over values of control animals receiving normal saline (15.2+/-0.42g/dL, 44.6+/-0.49%, N=5). CONCLUSION: Lentiviral vectors are able to transduce skeletal muscle and are capable of achieving sustained expression and systemic delivery of EPO following intramuscular administration. Gene therapy using lentiviral vectors may provide a practical strategy for in vivo delivery of therapeutic proteins.


Assuntos
Animais , Humanos , Ratos , Anemia , Contagem de Células Sanguíneas , Doença Crônica , Eritropoetina , Terapia Genética , Glicoproteínas , Virilha , Hematócrito , Mamíferos , Músculo Esquelético , Músculos , Plasmídeos
20.
Cancer Research and Treatment ; : 296-301, 2002.
Artigo em Coreano | WPRIM | ID: wpr-82341

RESUMO

The combination of chemotherapy and radiotherapy is emerging as the new standard modality for the treatment of locally advanced head and neck cancer, due to the inherent functional and cosmetic sequelae associated with its surgical management. Combination chemotherapy with 5-fluorouracil and cisplatin (FP) is one of the most active regimens for the head and neck cancer. Furthermore, both agents are known to act as radiosensitizer. This study was conducted to determine the efficacy, feasibility, and the toxicities of concurrent FP chemotherapy with radiotherapy. MATERIALS AND METHODS: Patients with histologically proven locally advanced head and neck cancer (T3-4 or node positive) were enrolled in the study. Patients received 5-fluorouracil, 1,000 mg/m2/day, continuously for 4 days, and cisplatin, 75 mg/m2, on day 1. This regimen was given every four weeks. The radiotherapy (45 Gy) was started on day 1 of the first cycle, and administered in 25 fractions. Following a three-week interval, the radiotherapy was resumed on day 1 of the third cycle of chemotherapy, and administered in 15 fractions (27 Gy). RESULTS: Of the 31 eligible patients included, 28 were able to be evaluated for the tumor response. The response rate for the 28 patients was 93% (16 complete responses, 10 partial responses). Disease free survival for the 16 complete responders was 37 months (median, 1 ~41 months), with a median follow-up time of 31 months. The 1-, 2-, and 3-year survival rates were 82%, 69%, and 63%, respectively. Regarding the feasibility of this treatments, only nineteen patients (61%) received the complete courses of scheduled treatments. The median duration of admission for all patients was 39 days. Grade 3 or 4 stomatitis were observed in 25 patients (83%) and appeared as the dose limiting toxicity of this regimen CONCLUSION: Although FP chemotherapy with concurrent radiotherapy is toxic, it is an effective and relatively feasible treatment for locally advanced head and neck cancer. The majority of patients experienced severe stomatitis, which appeared as the dose limiting toxicity of this regimen.


Assuntos
Humanos , Quimiorradioterapia , Cisplatino , Intervalo Livre de Doença , Tratamento Farmacológico , Quimioterapia Combinada , Fluoruracila , Seguimentos , Neoplasias de Cabeça e Pescoço , Cabeça , Radioterapia , Estomatite , Taxa de Sobrevida
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