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  • 1
    In: The Korean Journal of Hematology, The Korean Society of Hematology, Vol. 44, No. 4 ( 2009), p. 304-
    Type of Medium: Online Resource
    ISSN: 1738-7949
    Language: English
    Publisher: The Korean Society of Hematology
    Publication Date: 2009
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  • 2
    In: The Korean Journal of Hematology, The Korean Society of Hematology, Vol. 41, No. 4 ( 2006), p. 302-
    Type of Medium: Online Resource
    ISSN: 1738-7949
    Language: Korean
    Publisher: The Korean Society of Hematology
    Publication Date: 2006
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  • 3
    In: Blood, American Society of Hematology, Vol. 108, No. 11 ( 2006-11-16), p. 1982-1982
    Abstract: Effectiveness and safety of combining gemtuzumab ozogamicin (GO) with attenuated dose of standard induction chemotherapy (CTx) were prospectively assessed in 16 elderly patients with previously untreated AML. The drug was administered at a dose of 6mg/m2 as a single 2-h IV infusion on day 1. Following GO, abbreviated schedule of standard induction CTx consisted of idarubicin (IDA, 12mg/m2/d) and N4-behenoyl-1-β-arabinofuranosyl cytosine (BH-AC, 300mg/m2/d, 2-h infusion) was administered from day 2 for 3 and 5 days, respectively (Group A). Eligible criteria were as following; age ≥55 years, previously untreated AML, ECOG performance status (PS) of 0 to 2, and adequate organ function. Patients with diagnosis of FAB subtype M3, significant comorbidities, or uncontrolled infection were excluded. All patients were required to express CD33 at least 〉 20% by flow cytometry. The clinical effect of combining GO and CTx in terms of CR rate, induction mortality and myelotoxicity was compared with historical cohort of patients who had been treated previously with the same regimen of induction CTx but without GO at our center. Patients in historical cohort were subdivided into standard (IDA+BH-AC, 3+7, Group B) and abbreviated (IDA+BH-AC, 2~3+5, Group C) CTx group, respectively. All patients received the 1st consolidation CTx consisted of fludarabine, cytarabine, mitoxantrone, and G-CSF (FLANG). The 2nd consolidation CTx was comprised of IDA and BH-AC (3+5). Patients after completion of consolidation CTx cycle received reduced intensity stem cell transplantation (SCT) or autologous SCT according to the HLA-matched donor status. 34 and 28 patients were included in Group B and C, respectively. There were no significant differences in pretreatment patient characteristics among 3 groups except patients’ age . Patients’ age was significantly higher in Group A. The rate of response to induction chemotherapy was significantly higher in GO combination group (87.5% vs 58.8% vs 50% in Group A, B and C, respectively) (P = 0.044) (Figure 1). In Group A, thirteen patients (81.3%) achieved CR, and 1 patient (6.3%) achieved CR with incomplete platelet recovery (CRp). Early death during induction occurred in 6.3%, 11.8%, and 14.3% of patients of Group A, B, and C, respectively (P = 0.724) (Figure 1). Estimated probability of overall survival was 51.3% with a median follow up duration of 7.1 months in Group A. We observed a significantly higher CR rate in patients who received GO combined with conventional chemotherapy but without increasing the risk of early death. We conclude that although the small numbers of cases included and follow up duration was relatively short in this study, frontline gemtuzumab ozogamicin in combination with conventional CTx was effective and safe approach in elderly patients with AML. Larger studies are now required in order to define the possible role of this regimen in the treatment of elderly AML patients. Figure Figure
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
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    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2006
    detail.hit.zdb_id: 1468538-3
    detail.hit.zdb_id: 80069-7
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  • 4
    In: Blood, American Society of Hematology, Vol. 108, No. 11 ( 2006-11-16), p. 5334-5334
    Abstract: Time to relapse of acute leukemia after allogeneic hematopoietic stem cell transplantation (allo-HSCT) is variable. The relapse kinetics may be influenced by graft-versus-leukemic (GVL) reaction mediated by donor immune cells and inflammatory cytokines. We wondered if the inflammatory cytokines released during the occurrence of the early post-transplantation inflammatory events may affect GVL effect thus influencing the relapse kinetics. We retrospectively analyzed the correlation between early post-transplantation inflammatory events and relapse kinetics in 55 patients with acute leukemia who relapsed following allo-HSCT. Patients were divided into two groups, early and late-relapsed group according to the time to relapse from transplantation. Multivariate logistic regression analysis revealed that the incidences of conditioning associated diarrhea (CAD) ≥ 500ml/day and febrile episode (FE) were significantly lower in the early-relapsed group than in the late-relapsed group (P=0.046 and 0.014, respectively). Serum levels of C-reactive protein, a surrogate marker of inflammation, on day 21 after transplantation (CRP21) were significantly lower in the early-relapsed group than in the late-relapsed group (P=0.009). FE, CAD ≥ 500ml/day and CRP21 were independent predictable factors for relapse kinetics based on multivariate Cox regression analysis (P=0.037, 0.002 and 0.025; hazard ratio=0.360, 0.221 and 0.971, respectively). Our analysis indicated the inflammatory events in early post-transplantation period could delay the relapse of acute leukemia early after allo-HSCT presumably because GVL effect was enhanced with the cytokines released by the events. Figure 1 Cumulative Incidences of relapse according to the presence of febrite episode (A) and conditioning regimens associated diarrhea ≥ 500mg/day (B) based on multivariate Cox regression analysis. The patients who had either febrite episode (FE) or server conditioning regimens associated diarrhea (CAD) ≥ 500mg/day in early posttransplantation period at longer relapse free survival compared with the patients who did not (P=0.035 and 0.002). Figure 1. Cumulative Incidences of relapse according to the presence of febrite episode (A) and conditioning regimens associated diarrhea ≥ 500mg/day (B) based on multivariate Cox regression analysis. The patients who had either febrite episode (FE) or server conditioning regimens associated diarrhea (CAD) ≥ 500mg/day in early posttransplantation period at longer relapse free survival compared with the patients who did not (P=0.035 and 0.002).
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
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    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2006
    detail.hit.zdb_id: 1468538-3
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  • 5
    In: Blood, American Society of Hematology, Vol. 108, No. 11 ( 2006-11-16), p. 2992-2992
    Abstract: Purpose: The role of allogeneic stem cell transplantation (SCT) for adult acute lymphoblastic leukemia (ALL) remains unclear because interpretation of transplantation outcome is complicated by the criteria used to select patients for transplantation and by the relatively small number of patients studied. Moreover, whether SCT from an unrelated donor could be a treatment option of equal value in a case lacking a compatible related donor remains controversial. The aim of the present study was to determine the graft-versus-leukemia (GVL) effect and risk factors affecting outcome of 218 adults with ALL who received allogeneic SCT during the last 10 years (1995 to 2004). Patients and Methods: The study population was 218 consecutive adults receiving an allogeneic SCT from matched sibling (n=162) or unrelated (n=56; 40 matched, 16 mismatched) donors at the Catholic Hematopoietic Stem Cell Transplantation Center in Korea. Their median age was 30 years (range, 15–61 years). One hundred eighty-three (83.9%) patients had high-risk criteria, and of these, 69 (31.7%) had t(9;22)/BCR-ABL and 7 (3.2%) had t(4;11)/MLL-AF4. One hundred sixty-five patients (75.7%) were transplanted in first complete remission (CR1); 23 (10.5%) in CR2; and 30 (13.8%) were resistant to chemotherapy before transplantation. Most patients (n=206, 94.5%) received a preparative treatment of total body irradiation (TBI)-containing regimen (TBI/cyclophosphamide for CR1, TBI/cytarabine/melphalan for 〉 CR1). Graft-versus-host disease (GVHD) prophylaxis was attempted by administering calcineurin inhibitor (cyclosporine for sibling, tacrolimus for unrelated) plus methotrexate. Results: With a median follow-up of 52 months (range, 15+ to 130+ months) after SCT, the 5-year probability of disease-free survival (DFS) was 51.3%±3.5% for all patients; 62.4%±4.3% for patients in CR1; and 11.3%±4.4% for patients in 〉 CR1 at transplantation. There was no difference in DFS for sibling and unrelated transplant patients in CR1 (65.2%±4.3% v 62.3%±8.0%). Multivariate Cox regression analysis showed that the most powerful predictive factor affecting relapse and DFS was disease status at transplantation (CR1 v 〉 CR1, p 〈 0.001). The presence of chronic GVHD was also found to be significantly associated with favorable outcome (p 〈 0.001). Conclusion: Our data in combination with recent studies suggest that matched related or unrelated allogeneic SCT should be performed in CR1 in adults with ALL. Further studies to develop treatment strategies to reduce leukemic cell burden and to enhance GVL effect are needed. The indications for allogeneic SCT also should be continuously evaluated.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
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    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2006
    detail.hit.zdb_id: 1468538-3
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  • 6
    In: Blood, American Society of Hematology, Vol. 112, No. 11 ( 2008-11-16), p. 5005-5005
    Abstract: Extranodal NK/T-cell lymphoma, nasal type is common in Asians rather than in Western populations. This special subtype responds poorly to intensive chemotherapy regimens or has a significant relapse rate in spite of low IPI and loco-regional staging. The presence of the EBV genome within tumor cells raised the possibility of developing therapeutic strategies directed at viral targets. The primary objectives of this prospective, single center, nonrandomized phase II trial are the evaluation of efficacy by determination of progression-free survival after concurrent administration of peginterferon alfa-2a (PEGASYS®, provided by Roche Korea) and chemoradiotherapy in patients with extranodal NK/T cell lymphoma. In addition, we evaluated the efficacy of peginterferon alfa-2a maintenance therapy for 3 years. All seven patients with newly diagnosed CD56+ EBV+ extranodal NK/T-cell lymphoma were enrolled onto a prospective clinical trial. Step 1; PEGASYS® 180 mcg was administered once weekly on D1, D8 of ProMACE-CytaBOM. 1, 2 cycles. Step 2; PEGASYS® 180 mcg will be administered once weekly on D1, D8, D15, D22 of involved-filed irradiation 3600 cGy (180 cGy × 20, for 4 weeks). Step 3; PEGASYS® 180 mcg will be administered once weekly on D1, D8 of ProMACE-CytaBOM. 3, 4 cycles. Step 4; PEGASYS® 180 mcg will be administered every two weeks after hematologic recovery of high-dose therapy and autologous PBSCT for 3 years. In case of advanced stage and non-nasal lesion, Step 2 was omitted and ProMACE-CytaBOM was extended to 6 cycles. EBV DNA copy based on real-time PCR was monitored. Of all 7 patients, 6 patients achieved complete response and 1 patient was dead due to pneumonia during chemotherapy. With a median follow-up of 26 months (3–36 months), the 3-year PFS were 67%. Of 6 assessable patients, five patients extended to peginterferon alfa-2a maintenance therapy and four patients showed PFS. Among two relapsed patients, one patient refused a peginterferon alfa-2a maintenance therapy and eventually relapsed 3 months later. Titer of EBV DNA copy in whole blood was significantly decreased compared with the titer on initial diagnosis. The main toxicities of peginterferon alfa-2a were mild flu-like symptoms. This pilot study suggests that larger prospective randomized studies are needed to define the role of peginterferon alfa-2a concurrent administration during induction therapy and maintenance therapy in EBV-associated extranodal NK/T-cell lymphoma.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
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    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2008
    detail.hit.zdb_id: 1468538-3
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  • 7
    In: Blood, American Society of Hematology, Vol. 112, No. 11 ( 2008-11-16), p. 4593-4593
    Abstract: Background & Objectives: Recently, T cells in BM have attracted renewed interest because they are now known to have different surface phenotypes, subsets, and activation states from those in the periphery. Memory T cells undergo extensive migration from the blood to the BM and vice versa. The BM plays an important role in preferential homing and extensive proliferation of memory T cells, and contributes considerably to the longlived memory T cell pool. BM T cells are more activated than their splenic counterparts and have a higher rate of local proliferation. Although BM-T (NK1.1– CD4+ or CD8+) cells did not induce lethal GVH disease, even at high cell numbers, BM-T cells mediated vigorous graft-versus-tumor activity and facilitated engraftment of hematopoietic progenitor cells. These studies suggested that BM-T cells could be a useful cellular source for adoptive immunotherapy following ABMT, instead of peripheral T cells. Non-myeloablative bone marrow transplantation (NMT) and allogeneic mixed chimerism can provide an environment adequate for diminishing susceptibility to DLI-mediated GVHD and an immunological platform for DLI in both mouse and human models. In patients treated with DLI, a successful GVL effect is often associated with conversion to complete donor chimerism, supporting the concept of a graft-versus-host (GVH) response as part of the GVL effect. Thus, a quiet chimeric conversion following DLI is desirable to reach an optimal DLI-mediated GVL effect, without the occurrence of GVHD. Although in a mouse model, the administration of non-tolerant donor spleen cells to established mixed chimeras has been shown to convert mixed hematopoietic chimerism to full donor chimerism, without the concomitant development of GVHD, DLI in humans frequently results in serious GVHD and life-threatening complications. However, the use of BM-T cells, as compared with spleen T cells (SP-T), as the DLI source has not been investigated in allogeneic mixed chimerism prepared with NMT. In this study, we evaluated the beneficial alloreactivity of DLI using cryopreserved BM-T cells, a by-product obtained during the T cell depletion (TCD) procedure in BM grafting, to effectively induce chimeric conversion without the occurrence of GVHD in MHC-mismatched NMT. Methods: Cells were prepared using established procedures. During the T cell depletion (TCD) procedure in BM grafting, BM-T cells were obtained as a by-product and then cryopreserved for subsequent DLI using BM-T cells 21 days after the bone marrow transplant. Results: The administration of 5–10 × 105 BM-T (Thy1.2+) cells in mixed chimeras resulted in complete chimeric conversion, with self-limited graft-versus-host disease (GVHD) and no pathological changes. However, the administration of 5–10 × 105 SP-T (Thy1.2+) cells resulted in persistent mixed chimerism, with pathological GVHD signs in the liver and intestine. Conclusion: Our results suggest that DLI using BM-T cells, even in small numbers, could be more potent for inducing chimeric conversion in mixed chimerism than DLI using SP-T cells. Further study is needed to determine whether cryopreserved BM-T cells are an effective cell source for DLI to consolidate donor-dominant chimerism in clinical practice, without concerns about GVHD.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
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    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2008
    detail.hit.zdb_id: 1468538-3
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  • 8
    In: The Korean Journal of Internal Medicine, Korean Association of Internal Medicine, Vol. 24, No. 3 ( 2009), p. 252-
    Type of Medium: Online Resource
    ISSN: 1226-3303
    Language: English
    Publisher: Korean Association of Internal Medicine
    Publication Date: 2009
    detail.hit.zdb_id: 2500508-X
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  • 9
    In: Blood, American Society of Hematology, Vol. 106, No. 11 ( 2005-11-16), p. 1277-1277
    Abstract: Objective: To investigate the immunoregulatory effects of allogeneic mixed chimerism induced by T-cell depleted, nonmyeloablative bone marrow transplantation (TCD-NMT) on chronic inflammatory arthritis and autoimmunity developed in interleukin-1 receptor antagonist-deficient (IL-1Ra−/ −) mice. Methods: IL-1Ra−/ − mice (H-2kd) were treated with anti-asialoGM1 Ab, TBI 500 cGy, and TCD-NMT from C57BL/6 mice (H-2kb). Engraftment and chimerism were evaluated on peripheral blood (PB), lymph node, and spleen by multi-color flow cytometry. The severity of arthritis was evaluated by clinical score and histopathology. IgG1 and IgG2a subtype of anti-type II collagen (CII) were measured in PB samples. After T cells were stimulated with CII, ovalbumin, and phytohemagglutinin, T-cell proliferation response and cytokines production (INF-g, TNF-a, IL-10, and IL-17) in culture supernatant were assayed. Results: All the transplanted IL-1Ra mice showed marked improvement of arthritis within 3 weeks after transplantation as well as successful induction of mixed chimerism. Mice in mixed chimerism showed higher level of anti-CII IgG1 and lower level of anti-CII IgG2a and weaker T cell proliferative response than in control groups, such as no-treatment and conditioning only without BM rescue. In mixed chimera, INF-g, TNF-a and IL-17 production from CII-stimulated T cells was significantly suppressed and IL-10 production was significantly increased as compared to the control groups. Conclusion: These observations indicate that the introduction of allogeneic mixed chimerism has a strong immunoregulatroy potential to correct established chronic inflammatory arthritis and autoimmunity originating from dysregulated proinflammatory cytokine network.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
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    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2005
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