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Efficacy of imatinib mesylate (STI571) in chronic neutrophilic leukemia with t(15;19): Case report

Authors
 In Keun Choi  ;  Byung-Soo Kim  ;  Jun Suk Kim  ;  Yeul Hong Kim  ;  Young-Kee Kim  ;  Yunjung Cho  ;  Soo-Young Yoon  ;  Sang Won Shin  ;  Chul Won Choi  ;  Jae Hong Seo  ;  Sang Cheul Oh  ;  So Young Yoon  ;  Kyong Hwa Park  ;  Hwa Jung Sung  ;  Jong Gwon Choi  ;  Hyeryoung Sul  ;  Hee Yun Seo  ;  Sookwon Ryu  ;  Kyung-A Lee 
Citation
 AMERICAN JOURNAL OF HEMATOLOGY, Vol.77(4) : 366-369, 2004 
Journal Title
AMERICAN JOURNAL OF HEMATOLOGY
ISSN
 0361-8609 
Issue Date
2004
MeSH
Antineoplastic Agents/administration & dosage ; Antineoplastic Agents/therapeutic use* ; Benzamides ; Biopsy, Needle ; Bone Marrow/pathology ; Humans ; Imatinib Mesylate ; Leukemia, Neutrophilic, Chronic/blood ; Leukemia, Neutrophilic, Chronic/drug therapy* ; Leukemia, Neutrophilic, Chronic/genetics ; Leukemia, Neutrophilic, Chronic/pathology ; Leukocyte Count ; Male ; Middle Aged ; Neutrophils/pathology ; Piperazines/administration & dosage ; Piperazines/therapeutic use* ; Pyrimidines/administration & dosage ; Pyrimidines/therapeutic use* ; Receptor, Platelet-Derived Growth Factor beta/genetics* ; Remission Induction ; Translocation, Genetic ; Treatment Outcome
Keywords
chronic neutrophilic leukemia ; imatinib mesylate ; t(15 ; 19)
Abstract
Chronic neutrophilic leukemia (CNL) is a rare hematologic disorder, for which there is no standard therapy. Recently, STI (imatinib mesylate) has been shown to be effective in treating patients with chronic myeloproliferative disorder (CMPD) displaying the translocation of the PDGFβR gene. Here, we present a case of a patient with CNL carrying t(15;19)(q13;p13.3) who achieved a cytogenetic remission following treatment with imatinib, 400 mg daily. After failure of alpha interferon and hydroxyurea therapy, a durable and complete clinical and cytogenic remission was induced by imatinib. To our knowledge, this is the first case with CNL who showed complete response with cytogenic remission after treatment of imatinib. The mechanism of response to this molecule is unknown in our case (other oncogenes than c-kit, tyrosine kinase, or PDGFR may be involved). The patient remains in complete remission with an excellent performance status after 7 months of therapy. We demonstrate here that imatinib can induce a clinical and cytogenetic response in a case of CNL associated with a novel translocation other than a 5q33 rearrangement. Further studies including the molecular cloning of the t(15;19)(q13;p13.3) will be important in understanding the pathophysiology of CNL with a heterogeneous clinical course and the exploitation of the basic mechanisms of imatinib treatment. Am. J. Hematol. 77:366–369, 2004.
Full Text
http://onlinelibrary.wiley.com/doi/10.1002/ajh.20197/abstract
DOI
10.1002/ajh.20197
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers
Yonsei Authors
Lee, Kyung A(이경아) ORCID logo https://orcid.org/0000-0001-5320-6705
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/111295
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