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1.
The Korean Journal of Gastroenterology ; : 263-268, 2006.
Article in Korean | WPRIM | ID: wpr-185934

ABSTRACT

BACKGROUND/AIMS: Maximal duration of intravenous (IV) corticosteroid (CS) treatment and efficacy of cyclosporin A (CsA) have not been clarified for patients with severe ulcerative colitis. We aimed to evaluate and compare the effectiveness of CS and CsA combination therapy with prolonged CS therapy alone in patients with severe UC refractory to initial CS therapy. METHODS: We retrospectively reviewed the medical records of 84 episodes of severe UC in 59 patients between April 1999 and May 2005. RESULTS: Among 84 episodes with IV CS therapy, 45 (53.6%) experienced an early response, while 39 (46.4%) did not respond within 2 weeks. The remaining 36 episodes excluding 3 which underwent colectomy were assigned to either combination therapy of IV CS and CsA or prolonged IV CS treatment alone for additional 2 weeks. Twelve of 16 episodes (75.0%) responded to therapy with combinations of IV CsA and CS, and 16 of 20 episodes (80.0%) to prolonged IV CS treatment alone. There was no statistical difference in response and colectomy rate after 4 weeks between CsA-use group and CsA-non-use group (p=1.00). CONCLUSIONS: These results suggest that CS and CsA combination has no additional benefit over prolonged CS therapy alone in terms of short-term response and that CS can be safely prolonged even after the first 14 days of treatment for severe UC.


Subject(s)
Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Antibodies, Monoclonal , Carcinoma, Squamous Cell/metabolism , Cyclin D1/immunology , Cyclin-Dependent Kinase Inhibitor p16/immunology , Esophageal Neoplasms/metabolism , Esophagus/abnormalities , G1 Phase , Immunohistochemistry , Biomarkers, Tumor/metabolism , Tumor Suppressor Protein p53/immunology
2.
Asian Pac J Allergy Immunol ; 2000 Dec; 18(4): 237-43
Article in English | IMSEAR | ID: sea-37030

ABSTRACT

Mutations of the p53 gene have been reported to be of prognostic significance in hepatocellular carcinoma (HCC). However, the clinical associations and prognostic value of anti-p53 antibodies, known to be products of the host immune response to these mutations, have been controversial. Serum anti-p53 antibodies were measured in 121 Thai patients diagnosed with HCC using a specific enzyme-linked immunosorbent assay (ELISA) kit. The clinical/pathological characteristics of the patients were compared with respect to the presence of serum anti-p53 antibodies. Cox regression analysis was performed to assess factor interaction and association with survival. Anti-p53 antibodies were detected in 13.2% (16 of 121) of our patients. There were no differences between groups with regard to age, sex, viral markers (HBsAg or anti-HCV), severity of liver disease and tumor advancement. The median survival rates for patients positive and negative for anti-p53 antibodies were 4.0 and 3.0 months, respectively (p = 0.443, by log-rank test). Multivariate analysis demonstrated that an advanced Okuda stage, lack of therapy and presence of portal vein thrombosis were independent factors related to the prognosis of the patients. Nonetheless, the presence of anti-p53 antibodies did not constitute a predictive variable associated with a poorer prognosis. Serum assay of anti-p53 antibodies, although rapid and easily performed, may not be suitable as an alternative to molecular detection of mutations in assessing tumor advancement and prognosis of patients with HCC.


Subject(s)
Adult , Aged , Aged, 80 and over , Antibodies, Neoplasm/blood , Carcinoma, Hepatocellular/immunology , Female , Humans , Liver Neoplasms/immunology , Male , Middle Aged , Predictive Value of Tests , Prognosis , Proportional Hazards Models , Survival Rate , Thailand/epidemiology , Tumor Suppressor Protein p53/immunology
3.
Journal of Korean Medical Science ; : 59-64, 2000.
Article in English | WPRIM | ID: wpr-43383

ABSTRACT

To determine whether the p53 expression might be a predictor for treatment sponse and overall survival in nodal non-Hodgkin's lymphoma (NHL), we analyzed e expression of p53 in 69 NHL patients. p53 protein expression was analyzed by munohistochemistry with long-term follow up (1-148 months: median 12.2). p53 pression was noted in 23/69 (33.3%) patients. Complete response (CR) rate to stemic chemotherapy was correlated with stage (I/II) (p=0.038), but not with 3 expression (p=0.2856). Poor overall survival was associated with stage =0.0010) or IPI score (p=0.0076), but not with p53 expression (p=0.8601). From ratification analysis by stage, in stage III/IV patients, the p53 positive oup had a trend to be associated with poor overall survival than the p53 gative group. Multivariate analysis revealed that p53 positive group was sociated with less CR rate compared to the p53 negative group (p=0.046), ereas overall survival was correlated with stage (p=0.0320), not with p53 atus. p53 expression was associated with less CR rate in patients with DLBL. rther studies with large numbers of samples and homogenous group of NHL are eded to determine the prognostic value of cell cycle regulator, p53 in NHL.


Subject(s)
Female , Humans , Male , Antibodies, Monoclonal , Cell Cycle Proteins/biosynthesis , Gene Expression , Immunohistochemistry , Immunophenotyping , Lymph Nodes/pathology , Lymph Nodes/metabolism , Lymphoma, Non-Hodgkin/pathology , Lymphoma, Non-Hodgkin/metabolism , Lymphoma, Non-Hodgkin/genetics , Lymphoma, Non-Hodgkin/drug therapy , Middle Aged , Prognosis , Tumor Suppressor Protein p53/immunology , Tumor Suppressor Protein p53/genetics , Tumor Suppressor Protein p53/biosynthesis
4.
Rev. gastroenterol. Perú ; 14(1): 65-8, ene.-abr. 1994. ilus
Article in Spanish | LILACS | ID: lil-132526

ABSTRACT

El gen supresor de tumor P53 se cree que juega un rol importante en la progresión de los tumores malignos a través de la mutación y la expresión aumentada. La inmunohistoquímica de la proteina P53 y el Ki-67 fueron realizados en un carcinoma temprano con epitelio atípico de vesícula biliar. La expresión aumentada de la proteina P53 fue encontrado en el área del adenocarcinoma con una distribución difusa de las células positivas (index:76+/-24 por ciento), y en las áreas de epitelio atípico con focos de células positivas, de distribución difusa (Index:30+/-14 por ciento), mientras el index del Ki-67 fue 6+/- en el área del adenocarcinoma y 6 +/- en el área del epitelio atípico en cada área correspondiente a la medida del P53. Esto sugiere que la expresión aumentada del P53 ocurre en carcinomas tempranos y/o epitelio atípico, al menos en algunos casos y que esto es un evento temprano en el desarrollo del carcinoma de vesícula biliar además de que el epitelio pueda ser parte del carcinoma.


Subject(s)
Humans , Male , Aged , Malignant Carcinoid Syndrome/pathology , Gallbladder/pathology , Carcinoma/physiopathology , Immunohistochemistry , Malignant Carcinoid Syndrome/immunology , Tumor Suppressor Protein p53/analysis , Tumor Suppressor Protein p53/immunology , Tumor Suppressor Protein p53/physiology
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