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박무림 연구실은 의학과 소속으로 혈액종양내과 및 혈액종양학 주제에 기반한 환자 중심 연구를 수행합니다. 혈액종양의 병태생리와 임상 양상을 연계하여 진단적 근거를 정리하고, 질환 경과 및 치료 반응과 관련된 지표를 탐색하는 방향으로 연구를 진행합니다. 또한 환자 데이터를 기반으로 바이오마커와 예후예측 요소를 검토하고, 임상 치료 과정에서 반응 평가 및 추적 관찰 체계를 체계화하는 연구를 수행합니다.

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혈액종양학 기반 진단·병태생리 연구 thumbnail
혈액종양학 기반 진단·병태생리 연구
Hematologic Oncology–Based Diagnosis and Pathophysiology Research
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5개년 연도별 논문 게재 수

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5개년 연도별 피인용 수

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최신 논문
46
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1
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인용수 0
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2022
Busulfan, Melphalan, and Etoposide (BuME) Showed an Equivalent Effect to Busulfan, Cyclophosphamide, and Etoposide (BuCE) As Conditioning Therapy for Autologous Transplantation in Patients with Relapsed or High Risk Non-Hodgkin Lymphoma: A Multicenter Randomized Phase II Study By the Consortium for Improving Survival of Lymphoma (CISL)
Jong-Ho Won, Kyoung Ha Kim, Seug Yun Yoon, Jae Hoon Lee, Mark Lee, Hoon‐Gu Kim, Young Rok, Yong Park, Sung Yong Oh, Ho‐Jin Shin, Won Seog Kim, Sung Kyu Park, JeeHyun Kong, Moo‐Rim Park, Deok‐Hwan Yang, Jae‐Yong Kwak, Hye Jin Kang, Yeung‐Chul Mun
Transplantation and Cellular Therapy
https://doi.org/10.1016/s2666-6367(22)00683-2
Medicine
Busulfan
Etoposide
Melphalan
Cyclophosphamide
Lymphoma
Transplantation
Oncology
Internal medicine
Chemotherapy
2
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인용수 2
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2022
Busulfan, Melphalan, and Etoposide (BuME) Showed an Equivalent Effect to Busulfan, Cyclophosphamide, and Etoposide (BuCE) as Conditioning Therapy for Autologous Stem Cell Transplantation in Patients with Relapsed or High-Risk Non-Hodgkin’s Lymphoma: A Multicenter Randomized Phase II Study bythe Consortium for Improving Survival of Lymphoma (CISL)
Kyoung Ha Kim, Jae Hoon Lee, Mark Lee, Hoon‐Gu Kim, Young Rok, Yong Park, Sung Yong Oh, Ho‐Jin Shin, Won Seog Kim, Seong Kyu Park, Jee Hyun Kong, Moo‐Rim Park, Deok‐Hwan Yang, Jae‐Yong Kwak, Hye Jin Kang, Yeung‐Chul Mun, Jong-Ho Won
IF 4.6 (2022)
Cancer Research and Treatment
PURPOSE: High-dose chemotherapy followed by autologous stem cell transplantation (ASCT) is the standard management for relapsed or high-risk non-Hodgkin's lymphoma (NHL). We reported the busulfan, melphalan, and etoposide (BuME) conditioning regimen was effective in patients with relapsed or high-risk NHL. Moreover, the busulfan, cyclophosphamide, and etoposide (BuCE) conditioning regimen has been used widely in ASCT for NHL. Therefore, based on these encouraging results, this randomized phase II multicenter trial compared the outcomes of BuME and BuCE as conditioning therapies for ASCT in patients with NHL. MATERIALS AND METHODS: Patients were randomly assigned to receive either BuME (n=36) or BuCE (n=39). The BuME regimen was comprised of busulfan (3.2 mg/kg/day, intravenously) administered on days -7, -6, and -5, etoposide (400 mg/m2 intravenously) on days -5 and -4, and melphalan (50 mg/m2/day intravenously) on days -3 and -2. The BuCE regimen was comprised of busulfan (3.2 mg/kg/day intravenously) on days -7, -6, and -5, etoposide (400 mg/m2/day intravenously) on days -5 and -4, and cyclophosphamide (50 mg/kg/day intravenously) on days -3 and -2. The primary endpoint was 2-year progression-free survival (PFS). RESULTS: Seventy-five patients were enrolled. Eleven patients (30.5%) in the BuME group and 13 patients (33.3%) in the BuCE group had disease progression or died. The 2-year PFS rate was 65.4% in the BuME group and 60.6% in the BuCE group (p=0.746). There were no non-relapse mortalities within 100 days after transplantation. CONCLUSION: There were no significant differences in PFS between the two groups. Therefore, busulfan-based conditioning regimens, BuME and BuCE, may be important treatment substitutes for the BCNU-containing regimens.
https://doi.org/10.4143/crt.2022.004
Busulfan
Medicine
Etoposide
Melphalan
Regimen
Autologous stem-cell transplantation
Cyclophosphamide
Transplantation
Internal medicine
Surgery
3
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인용수 7
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2022
Safety and efficacy of nilotinib in adult patients with chronic myeloid leukemia: a post-marketing surveillance study in Korea
Seo‐Yeon Ahn, Sang Kyun Son, Gyu Hyung Lee, Inho Kim, June‐Won Cheong, Won Sik Lee, Byung Soo Kim, Deog‐Yeon Jo, Chul Won Jung, Chu Myoung Seong, Jae Hoon Lee, Young Jin Yuh, Min Kyoung Kim, Hun-Mo Ryoo, Moo‐Rim Park, Su-Hee Cho, Hoon‐Gu Kim, Dae Young Zang, Jinny Park, Hawk Kim, Se-Ryeon Lee, Sung‐Hyun Kim, Myung Hee Chang, Ho Sup Lee, Chul Won Choi, Jihyun Kwon, Sung-Nam Lim, Sukjoong Oh, Inkyung Joo, Dong‐Wook Kim
Blood Research
Background: Nilotinib is a tyrosine kinase inhibitor approved by the Ministry of Food and Drug Safety for frontline and 2nd line treatment of Philadelphia chromosome-positive chronic myeloid leukemia (Ph+ CML). This study aimed to confirm the safety and efficacy of nilotinib in routine clinical practice within South Korea. Methods: An open-label, multicenter, single-arm, 12-week observational post-marketing surveillance (PMS) study was conducted on 669 Korean adult patients with Ph+ CML from December 24, 2010, to December 23, 2016. The patients received nilotinib treatment in routine clinical practice settings. Safety was evaluated by all types of adverse events (AEs) during the study period, and efficacy was evaluated by the complete hematological response (CHR) and cytogenetic response. Results: During the study period, AEs occurred in 61.3% (410 patients, 973 events), adverse drug reactions (ADRs) in 40.5% (271/669 patients, 559 events), serious AEs in 4.5% (30 patients, 37 events), and serious ADRs in 0.7% (5 patients, 8 events). Furthermore, unexpected AEs occurred at a rate of 6.9% (46 patients, 55 events) and unexpected ADRs at 1.2% (8 patients, 8 events). As for the efficacy results, CHR was achieved in 89.5% (442/494 patients), and minor cytogenetic response or major cytogenetic response was achieved in 85.8% (139/162 patients). Conclusion: This PMS study shows consistent results in terms of safety and efficacy compared with previous studies. Nilotinib was well tolerated and efficacious in adult Korean patients with Ph+ CML in routine clinical practice settings.
https://doi.org/10.5045/br.2022.2021137
Nilotinib
Medicine
Adverse effect
Internal medicine
Observational study
Myeloid leukemia
Clinical trial
Tyrosine-kinase inhibitor
Pharmacovigilance
Postmarketing surveillance
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특허 전체보기
상태출원연도과제명출원번호상세정보
소멸2014신규 급성백혈병의 진단용 마커1020140195946
전체 특허

신규 급성백혈병의 진단용 마커

상태
소멸
출원연도
2014
출원번호
1020140195946

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