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American Journal of Hematology | 2001

Response to high-dose intravenous immune globulin as a valuable factor predicting the effect of splenectomy in chronic idiopathic thrombocytopenic purpura patients

Chul Won Choi; Byung Soo Kim; Jae Hong Seo; Sang Won Shin; Yeul Hong Kim; Jun Suk Kim; Sang Kyun Sohn; Jae Seok Kim; Dong Gun Shin; Hun Mo Ryoo; Kyung Hee Lee; Je Jung Lee; Ik Joo Chung; Hyeoung Joon Kim; Jae Yong Kwak; Chang Yeol Yim; Jin Seok Ahn; Jung Ae Lee; Young Suk Park

This study was conducted to verify whether the response to high‐dose intravenous immune globulin (IVIG) was related to the effect of splenectomy in chronic idiopathic thrombocytopenic purpura (ITP) patients. A total of 79 patients over 16 years of age were enrolled in this study. The response to the treatment was classified on the basis of the platelet count as no response (NR, <50 × 109/l), incomplete response (IR, (50–150) × 109/l), and complete response (CR, >150 × 109/l). The response was evaluated after the infusion of high‐dose IVIG, within 2 weeks after splenectomy (immediate response), and during a follow‐up period of more than 6 months after splenectomy (sustained response), respectively. 58 patients (73.4%) showed responses (CR or IR) to high‐dose IVIG. After splenectomy, immediate responses were observed in 73 patients (92%). The response to high‐dose IVIG had no relationship with the immediate response to splenectomy (P = 0.333). A follow‐up evaluation was possible with 58 patients; 6 patients with NR in immediate responses did not show any response during the follow‐up period, and 17 patients relapsed within 6 months after immediate responses, so 35 patients (60.3%) had sustained responses. Responders to IVIG had significantly higher sustained response rates to splenectomy than non‐responders (62% vs. 38%, P = 0.001). These results indicate that the response to high‐dose IVIG could be a valuable factor predicting the sustained response to splenectomy in chronic ITP patients. Am. J. Hematol. 66:197–202, 2001.


Journal of Pain and Symptom Management | 2013

Validation of the Edmonton Symptom Assessment System in Korean Patients With Cancer

Jung Hye Kwon; Seung Hyun Nam; Su-Jin Koh; Young Seon Hong; Kyung Hee Lee; Sang Won Shin; David Hui; Kyun Woo Park; So Young Yoon; Ji Yun Won; Gary Chisholm; Eduardo Bruera

CONTEXTnThe Edmonton Symptom Assessment System (ESAS) is a brief, widely adopted, multidimensional questionnaire to evaluate patient-reported symptoms.nnnOBJECTIVESnTo develop a Korean version of the ESAS (K-ESAS) and to perform a psychometric analysis in Korean patients with advanced cancer.nnnMETHODSnWe tested the K-ESAS in two pilot studies with 15 patients each. We assessed internal consistency, test-retest reliability, and concurrent validity in 163 Korean patients, who completed the K-ESAS along with the Korean versions of the M. D. Anderson Symptom Inventory (K-MDASI) and the Hospital Anxiety and Depression Scale (K-HADS) twice. A total of 38 patients completed the questionnaires again seven days later to assess responsiveness.nnnRESULTSnThe K-ESAS scores had good internal consistency, with a Cronbachs alpha coefficient of 0.88, indicating that no questions had undue influence on the score. Pearson correlation coefficients for K-ESAS symptom scores between baseline and after two to four hours ranged from 0.72 (95% CI 0.64-0.79) to 0.87 (95% CI 0.82-0.90), indicating strong test-retest reliability. For concurrent validity, Pearson correlation coefficients between K-ESAS symptom scores and corresponding K-MDASI symptom scores ranged from 0.70 (95% CI 0.62-0.77) to 0.83 (95% CI 0.77-0.87), indicating good concurrent validity. For the K-HADS, concurrent validity was good for anxiety (r=0.73, 95% CI 0.65-0.79) but moderate for depression (r=0.4, 95% CI 0.26-0.52). For responsiveness, changes in K-ESAS scores after seven days were moderately correlated with changes in K-MDASI scores but weakly correlated with changes in K-HADS scores.nnnCONCLUSIONnThe K-ESAS is a valid and reliable tool for measuring multidimensional symptoms in Korean patients with cancer.


International Journal of Hematology | 2001

Long-Term Engraftment Stability of Peripheral Blood Stem Cells Cryopreserved Using the Dump-Freezing Method in a −80°C Mechanical Freezer with 10% Dimethyl Sulfoxide

Chul Won Choi; Byung Soo Kim; Jae Hong Seo; Sang Won Shin; Yeul Hong Kim; Jun Suk Kim

In this study, we summarize our long-term follow-up data of 24 patients who underwent autologous peripheral blood stem cell transplantation (PBSCT) using the dump-freezing method in a −80°C freezer. Collected peripheral blood mononuclear cells were mixed with a cryoprotectant solution consisting of autologous plasma and 20% dimethyl sulfoxide, then placed in a −80°C freezer. The recovery rate of mononuclear cells (MNCs), colony-forming unit—granulocyte/macrophage (CFU-GM) colonies, and CD34+ cells were calculated. Engraftment time (with neutrophil count > 0.5 × 109/L, platelet count > 50 ×109/L) and normal hemopoiesis (neutrophil count > 2 ×109/L, platelet count > 100 ×109/L) were evaluated. Median duration of cryopreservation was 76 days. The mean recovery rates of MNCs, CFU-GM colonies, and CD34+ cells were 93.4%, 78.4%, and 95.3%, respectively. The median engraftment times of neutrophils and platelets were 8 and 27 days, respectively. The median normal hemopoiesis times of neutrophil and platelet were 31 and 45 days, respectively. Nine patients are alive and in complete remission (CR). Seven patients in first CR sustained normal hemopoiesis with a median duration of 35 months. Two patients, who achieved second CR after salvage chemotherapy due to a leukemia relapse after PBSCT, maintained engraftment status for 24 and 28 months, and 1 reached normal hemopoiesis. These results demonstrate that PBSCT using the dump-freezing method in a −80°C freezer leads to acceptable long-term engraftment stability.


Annals of Hematology | 2005

The cutoff value of serum ferritin for the diagnosis of iron deficiency in community-residing older persons

Chul Won Choi; Woo Ri Cho; Kyong Hwa Park; In Keun Choi; Jae Hong Seo; Byung Soo Kim; Sang Won Shin; Yeul Hong Kim; Jun Suk Kim; Juneyoung Lee

The serum ferritin assay is the best single blood test for the diagnosis of iron deficiency. Previous studies with elderly anemic patients have suggested that ferritin level less than 45xa0μg/L is indicative of iron deficiency. The subjects of these studies were hospitalized patients with anemia, however. We thus conducted a prospective study to determine the normal minimum level of serum ferritin of community-dwelling older adults by assessing the ratio of serum transferrin receptor to the log ferritin level (sTfR-F index). We conducted the anemia survey between October and November 2002. A total of 1,254 apparently healthy older adults, aged between 60 and 95 years, from three urban community dwellings participated in the survey. Among these individuals, 156 subjects who were anemic or whose serum ferritin level was less than 100xa0μg/L were selected. The soluble transferrin receptor assay was performed and the sTfR-F index was calculated. The receiver operating characteristic curve analysis was performed. Based on the data, serum ferritin level of 22xa0μg/L was selected as the cutoff value for the diagnosis of iron deficiency in community-dwelling older adults. Applying the serum ferritin cutoff of 22xa0μg/L and the sTfR-F index cutoff of 1.5, the sensitivity of the assay was 89.5% (34 of 38) and the specificity was 89.0% (105 of 118). In conclusion, for the diagnosis of iron deficiency of community-residing older adults, we suggest the serum ferritin cutoff value of 22xa0μg/L obtained by use of the sTfR-F index. The value is lower than the previous value established for hospitalized and anemic older adults.


Cancer Chemotherapy and Pharmacology | 2006

Phase II study with a combination of epirubicin, cisplatin, UFT, and leucovorin in advanced hepatocellular carcinoma

Seok Jin Kim; Hee Yun Seo; Jong Gwon Choi; Hye Ryoung Sul; Hwa Jung Sung; Kyong Hwa Park; In Keun Choi; Sang Cheul Oh; So Young Yoon; Jae Hong Seo; Chul Won Choi; Byung Soo Kim; Sang Won Shin; Yeul Hong Kim; Jun Suk Kim

Purpose: Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide. Because HCC usually presents as an advanced disease and occurs in the background of liver cirrhosis, most patients are not suitable for treatment with curative intent, thus effective systemic chemotherapy is required. However, the outcome of systemic chemotherapy has been disappointing in advanced HCC. This study was conducted to test the efficacy and toxicity of the combined regimen of epirubicin, cisplatin, and UFT moderated by leucovorin in advanced or recurrent HCC. Patients and methods: All 53 patients received epirubicin (50xa0mg/m2 i.v.) on day 1 and cisplatin (60xa0mg/m2 i.v.) after epirubicin administration. Oral UFT 400–600xa0mg/day, determined by body surface area, and leucovorin 75xa0mg/day were administered for 21 consecutive days, followed by a 7-day drug free interval. Results: Nine had a partial response, representing 16.9% of response rate (95% confidence interval rate; 7.0–26.8%) with median response duration of 17.1xa0weeks (95% CI; 5.0–29.3xa0weeks, range; 7.1–51.7xa0weeks). Fifteen patients had stable disease and the disease progressed in 26 patients. The median overall survival for the patients was 24.6xa0weeks (95% CI; 17.3–31.9xa0weeks, range; 3.0–131.3xa0weeks). The main toxicities were hematologic toxicities including neutropenia, which reached grade 3/4 in 17 patients (38.5%), and grade 3 or 4 thrombocytopenia in five patients (9.4%). Conclusion: The combination of epirubicin, cisplatin, and UFT moderated by leucovorin showed modest anti-tumor activity with relatively tolerable toxicities. However, a randomized phase III trial based on this regimen is warranted to clarify its survival benefit in patients with advanced HCC.


Yonsei Medical Journal | 2005

Hematopoietic Differentiation of Embryoid Bodies Derived from the Human Embryonic Stem Cell Line SNUhES3 in Co-culture with Human Bone Marrow Stromal Cells

Seok Jin Kim; Byung Soo Kim; Suck Won Ryu; Ji Hyun Yoo; Jee Hyun Oh; Chang Hee Song; Sun Haeng Kim; Dong Seop Choi; Jae Hong Seo; Chul Won Choi; Sang Won Shin; Yeul Hong Kim; Jun Suk Kim

Human embryonic stem (ES) cells can be induced to differentiate into hematopoietic precursor cells via two methods: the formation of embryoid bodies (EBs) and co-culture with mouse bone marrow (BM) stromal cells. In this study, the above two methods have been combined by co-culture of human ES-cell-derived EBs with human BM stromal cells. The efficacy of this method was compared with that using EB formation alone. The undifferentiated human ES cell line SNUhES3 was allowed to form EBs for two days, then EBs were induced to differentiate in the presence of a different serum concentration (EB and EB/high FBS group), or co-cultured with human BM stromal cells (EB/BM co-culture group). Flow cytometry and hematopoietic colony-forming assays were used to assess hematopoietic differentiation in the three groups. While no significant increase of CD34+/CD45- or CD34+/CD38- cells was noted in the three groups on days 3 and 5, the percentage of CD34+/CD45- cells and CD34+/CD38- cells was significantly higher in the EB/BM co-culture group than in the EB and EB/high FBS groups on day 10. The number of colony-forming cells (CFCs) was increased in the EB/BM co-culture group on days 7 and 10, implying a possible role for human BM stromal cells in supporting hematopoietic differentiation from human ES cell-derived EBs. These results demonstrate that co-culture of human ES-cell-derived EBs with human BM stromal cells might lead to more efficient hematopoietic differentiation from human ES cells cultured alone. Further study is warranted to evaluate the underlying mechanism.


Asia-pacific Journal of Clinical Oncology | 2010

Mitomycin‐C, 5‐fluorouracil, and leucovorin as a salvage therapy in patients with metastatic colorectal adenocarcinoma

Eun Joo Kang; Yoon Ji Choi; Jung Seon Kim; Seung Tae Kim; Kyong Hwa Park; In Keun Choi; Sang Chul Oh; Jae Hong Seo; Sang Won Shin; Jun Suk Kim; Yeul Hong Kim

Aim:u2003 There is no further treatment option for metastatic colon patients who are refractory to standard chemotherapy and to whom novel biological agents are not available. We evaluated the outcomes of mitomycin‐C, 5‐fluorouracil (5‐FU) and leucovorin in patients with metastatic colon cancer previously treated with oxaliplatin/5‐FU/leucovorin and irinotecan/5‐FU/leucovorin.


Acta Haematologica | 2005

Prevalence of iron deficiency anemia in community-dwelling older persons as measured by the transferrin receptor-ferritin index

Chul Won Choi; Kyong Hwa Park; In Keun Choi; Seok Jin Kim; Jae Hong Seo; Byung Soo Kim; Sang Won Shin; Yeul Hong Kim; Jun Suk Kim

community-dwelling older adults using the sTfR-F index. We conducted the anemia survey in three urban districts (Guro, Yangcheon and Gwanak) located in the southwestern part of Seoul in 2002. In this survey, a total of 1,254 subjects over the age of 60 years were selected from a cross-sectional study, the results of which have been published previously [2] . In brief, all the subjects lived in their own homes and were fully ambulatory with unlimited activities of daily living. Informed consent was obtained from all subjects, and then a complete medical history was taken and laboratory testing including a complete blood cell count with a reticulocyte count and iron profi les was performed. Anemia was defi ned according to the World Health Organization criteria, i.e. a hemoglobin level of ! 13 g/dl in men and ! 12 g/dl in women. In case of anemia, we performed the sTfR assay using a commercial kit based on a polyclonal antibody in a sandwich enzyme immunoassay (R&D Systems, Minneapolis, Minn., USA). According to the manufacturer, the central 95th percentile of the reference distribution of the sTfR concentration is 8.7–28.1 nmol/l. We then calculated the sTfR-F index (ratio of sTfR and log ferritin level). All the sTfR assays were performed in duplicate. IDA was considered present if the subject had anemia and the sTfR-F index was 1 1.5. Anemia is the most common hematologic problem encountered in older adults, and its prevalence increases with age [1, 2] . The common causes of anemia among older persons are anemia of chronic disease, iron defi ciency caused by gastrointestinal bleeding, cobalamin defi ciency, folate defi ciency and the myelodysplasia. Among these causes, the diagnosis of iron defi ciency anemia (IDA) is important because proper iron therapy can improve the symptoms, and treatment may help indicate an occult gastrointestinal pathology such as malignancy [3, 4] . There are few reports regarding the prevalence of IDA in older persons, and epidemiologic studies on East Asian populations are scarce. Moreover, the results of such studies have been variable according to the diagnostic criteria used. Previously published reports have used serum ferritin levels to diagnose IDA, but the cutoff levels were different in the various studies. The interpretation of the serum ferritin level in older adults is sometimes complicated because its level increases with age and with concomitant chronic illnesses [5, 6] . Therefore, we measured the soluble transferrin receptor (sTfR), which is not infl uenced by ageing or chronic diseases [7, 8] , and we calculated the ratio of sTfR to the log ferritin level (sTfR-F index) to make the test more specifi c. An index value of


Japanese Journal of Clinical Oncology | 2004

Serum Vascular Endothelial Growth Factor per Platelet Count in Hepatocellular Carcinoma: Correlations with Clinical Parameters and Survival

Seok Jin Kim; In Keun Choi; Kyong Hwa Park; So Young Yoon; Sang Cheul Oh; Jae Hong Seo; Chul Won Choi; Byung Soo Kim; Sang Won Shin; Yeul Hong Kim; Jun Suk Kim


American Journal of Hematology | 2004

Prevalence and characteristics of anemia in the elderly: Cross‐sectional study of three urban Korean population samples

Chul Won Choi; Juneyoung Lee; Kyong Hwa Park; So Young Yoon; In Keun Choi; Sang Cheul Oh; Jae Hong Seo; Byung Soo Kim; Sang Won Shin; Yeul Hong Kim; Jun Suk Kim

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Jae Hong Seo

Korea University Medical Center

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Jun Suk Kim

Korea University Medical Center

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Yeul Hong Kim

Korea University Medical Center

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Chul Won Choi

Korea University Medical Center

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In Keun Choi

Korea University Medical Center

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Kyong Hwa Park

Korea University Medical Center

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Sang Cheul Oh

Korea University Medical Center

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So Young Yoon

Korea University Medical Center

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