Jin-Hwang Liu
Taipei Veterans General Hospital
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Publication
Featured researches published by Jin-Hwang Liu.
British Journal of Haematology | 2002
Liang-Tsai Hsiao; Hung-Ming Chung; Jen-Tsun Lin; Tzeon-Jye Chiou; Jin-Hwang Liu; Frank S. Fan; Wei-Shu Wang; Chueh-Chuan Yen; Po-Min Chen
Summary. Between seven and 21% of patients treated with the specific tyrosine kinase inhibitor STI571 have been reported to develop mild‐to‐moderate severity of adverse cutaneous reactions. We report a patient in the blast crisis phase of chronic myeloid leukaemia who developed a life‐threatening cutaneous reaction, Stevens–Johnson syndrome, following 1 week of STI571 therapy. This report may serve to remind the clinician about the possible severe cutaneous side‐effects of STI571 before instituting more extensive clinical application of this agent in the future.
Cancer | 2008
Chun-Yu Liu; Po-Min Chen; Tzeon-Jye Chiou; Jin-Hwang Liu; Jen-Kou Lin; Tzu-Chen Lin; Wei-Shone Chen; Jeng-Kae Jiang; Huann-Sheng Wang; Wei-Shu Wang
It is known that the uridine‐diphosphoglucuronosyl transferase 1A1 (UGT1A1)*28 polymorphism reduces UGT1A1 enzyme activity, which may lead to severe toxicities in patients who receive irinotecan. This study was conducted to assess the influence of this polymorphism on the efficacy and toxicity of irinotecan treatment in Chinese patients with metastatic colorectal carcinoma (CRC).
Transplantation | 1990
Po-Min Chen; Sheng Fan; Chia-Jui Liu; Hsieh Rk; Jin-Hwang Liu; Ming-Wei Chuang; Ren-Shyan Liu; Cheng-Hwai Tzeng
The hepatitis B virus (HBV) infection and its resulting hepatic abnormalities are very high in prevalence among the Taiwan population. They also seem to compose a major problem to patients subjected to bone marrow transplantation (BMT) due to intensive chemoradiotherapy. In this study, the sera of 42 patients were investigated before and after BMT to detect the presence of HBV markers and to test their liver function (LF). Being followed-up for 3–12 months after BMT, 12 out of 27 were found to have altered HBV markers according to the classification of the following: seroconversion of HBsAg, clearance of HBsAb, appearance of HBeAg, clearance of HBeAb, and acute hepatitis. Thirty-seven out of 42 patients (88.1%) were found in routine LF test to develop one or more abnormality; however, 90% of them turned normal within one year after BMT. Only one patient died of complications associated with fulminant hepatitis. In conclusion, the previous hepatic damage from HBV infection appears unlikely to increase the risk of posttransplant morbidity and mortality.
Annals of Hematology | 2008
Ming-Huang Chen; Liang-Tsai Hsiao; Tzeon-Jye Chiou; Jin-Hwang Liu; Jyh-Pyng Gau; Hao-Wei Teng; Wei-Shu Wang; Ta-Chung Chao; Chueh-Chuan Yen; Po-Min Chen
Several reports recently found that patients with B cell non-Hodgkin’s lymphoma (NHL) had a higher carrier rate of hepatitis B surface antigen (HBsAg). The current study aimed to examine the hepatitis B virus (HBV) infection status of NHL patients in Taiwan, an HBV-endemic area. Serum HBV and serum hepatitis C virus were measured in 471 NHL patients and 1,013 non-lymphoma cancer patients enrolled between February 2000 and March 2007. Furthermore, nested polymerase chain reaction of HBV-DNA was used to examine the sera from selected patients in these two populations and healthy volunteers for the presence of occult HBV infection. The infection rates (as indicated by the rates of HBsAg and occult HBV) were compared between different groups. There was a higher incidence of HBV infection in B cell NHL patients (23.5%), especially patients with diffuse large B lymphoma, than solid tumor patients (15.6%, P = 0.001). Among HbsAg-negative patients, those with B cell NHL had a higher prevalence of occult HBV infection (6%) than those with non-lymphoma solid tumors and healthy volunteers, 0% and 0.9%, respectively (P = 0.005). B cell NHL patients, even HBsAg-negative B cell NHL patients, but not T cell NHL patients, have a higher incidence of HBV infection than patients with solid tumors. Our findings support the etiologic role of HBV infection in B cell NHL.
Journal of Gastroenterology and Hepatology | 2005
Jen-Tsun Lin; Wei-Shu Wang; Chueh-Chuan Yen; Jin-Hwang Liu; Mu-Hua Yang; Ta-Chon Chao; Po-Min Chen; Tzeon-Jye Chiou
Aims: Colorectal carcinoma in patients under 40 years of age usually has a poor prognosis. Controversies still exist regarding the features and the prognosis of colorectal cancer in young patients.
Cancer | 2001
Chueh-Chuan Yen; Yann-Jang Chen; Jung-Ta Chen; Jiun-Yi Hsia; Po-Min Chen; Jin-Hwang Liu; Frank S. Fan; Tzeon-Jye Chiou; Wei-Shu Wang; Chi-Hung Lin
Esophageal carcinoma is a major cause of cancer‐related deaths among males in Taiwan. However, to date, the genetic alterations that accompany this lethal disease are not understood.
Biotechnology Progress | 2002
Suh-Chin Wu; Gloria Yia‐Ling Huang; Jin-Hwang Liu
In gene therapy, retrovirus and adenovirus vectors are extensively used as gene‐delivery vehicles and further large‐scale processing of these viral vectors will be increasingly important. This study examined stationary and microcarrier cell culture systems with respect to the production of a retrovirus vector (encoding a monounit hammerhead ribozyme gene with an intron) and an adenovirus vector (encoding a reporter lacZ gene). Cytodex 1 and Cytodex 3 solid microcarriers were found to be able to provide good cell growth and high‐titer vector production in suspension cultures. Porous microcarriers such as Cytopore 2 gave slightly lower but still efficient growth but produced significantly lower titers of retrovirus and adenovirus vector from the producer cells. The specific retrovirus production was not proportionally related to the specific growth rate of the producer cells. High MOI infection was essential for high‐titer production of adenovirus vector in 293 cells. Hydrodynamic shear forces on microcarrier‐grown cells increased the production yield for retrovirus vector but decreased for adenovirus vector. The cellular productivity was much more efficient for adenovirus vector produced in 293 cells as compared to the retrovirus vector produced in PA317‐RCM1 cells. These findings can provide further insight into the feasibility of applying microcarrier cell culture technology to produce gene‐therapy virus vectors.
Scandinavian Journal of Infectious Diseases | 2003
Jen-Tsun Lin; Wei-Shu Wang; Chueh-Chuan Yen; Jin-Hwang Liu; Tzeon-Jye Chiou; Mu-Hua Yang; Ta-Chon Chao; Po-Min Chen
We describe a case of Chryseobacterium indologenes bacteremia in a leukemia patient with chronic graft-versus-host disease (GVHD) 6 months after allogeneic bone marrow transplantation. Blood cultures from a vein and via Hickman catheter grew C. indologenes. The patient was successfully treated with piperacillin/tazobactam and the infection did not recur. Our case indicates that C. indologenes infection can occur in patients with GVHD after allogeneic BMT and might be treated with a single agent, piperacillin/tazobactam without the removal of intravascular catheter.1
World Journal of Surgery | 2004
Wei-Shone Chen; Ming-yi Chung; Jin-Hwang Liu; Jacqueline Ming Liu; Jen-Kou Lin
Despite widespread use of laparoscopic surgery for colorectal operations, its application for curative resection of colorectal cancer is still controversial. One of the major concerns is the impact of the laparoscopic procedure on dissemination of tumor cells. The main purpose of this study was to investigate the impact of laparoscopic surgery on circulating tumor cells in colorectal cancer patients. Quantitation of circulating free tumor cells (FTCs) was performed preoperatively, during the operation, and 14 days later by means of real-time quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) targeting guanylyl cyclase C (GCC) mRNA in 42 colorectal cancer patients undergoing laparoscopic resections. Despite an increasing trend of FTC detection in patients with advancing stage, there is no significant difference in the preoperative FTC level by disease stage. No elevation in FTC level was found during the laparoscopic procedure in most patients compared with their preoperative FTC value. Patients with a persistently high FTC load [per nucleated blood cells (NBCs)] (> 102 FTCs/106 NBCs) 2 weeks postoperatively portends a poor prognosis regarding disease recurrence and tumor-related mortality when compared to those with an undetectable or low FTC load (≤ 102 FTCs/106 NBCs). We concluded that the laparoscopic procedure itself had no significantly deleterious effect on circulating FTCs and that the detection of FTCs by real-time qRT-PCR might be of clinical importance during the postoperative follow-up for colorectal cancer patients.
Transplantation | 1999
Po-Min Chen; Tzeon-Jye Chiou; Frank S. Fan; Jacqueline M. Liu; Hsieh Rk; Chueh-Chuan Yen; Wei-Shu Wang; Jin-Hwang Liu
BACKGROUND Bone marrow transplantation (BMT) is effective treatment for many hematologic disease, but performed in a population with a high endemic hepatitis B virus carrier rate, the incidence of liver function impairment and fulminant hepatitis (FH) is expected to be raised. METHODS Forty-three hepatitis B virus carriers received high-dose chemotherapy and BMT, 32 patients received an allogeneic graft, and 11 patients autologous marrow. Acute graft-versus-host disease prophylaxis consisted of methotrexate on day 1, 3, 6, and 11 and cyclosporine for 6 months. RESULTS After a median follow-up period of 68 months (range: 1-11.5 years), 26 (81.3%) allogeneic BMT patients developed impaired liver function (LF), 5 progressed to FH on day 93, 169, 170, 180, and 468, respectively, and died after an average of 13.8 days (range: 1-45 days). Whereas only 4 (36.4%) autologous BMT patients developed impaired LF, and none FH. Impaired LF (P=0.026, chi-square), and FH (odds ratio=12.86, P=0.009 for coefficient) were significantly related to an allogeneic marrow graft, and the timing of liver function impairment coincided with cyclosporine withdrawal. Hepatitis B surface antigen (HbsAg) disappeared from the serum in 4/14 (28.6%) patients receiving a marrow graft from an HbsAg+ donor. HbsAg was not detected in the serum after BMT in 2/11 (18.2%) autologous BMT patients. CONCLUSIONS Hepatitis B virus carriers receiving a marrow graft from an HbsAg+ donor have a significantly increased risk of FH.