Korean J Hematol 2001; 36(3):
Published online September 30, 2001
© The Korean Society of Hematology
권혁찬, 손승현, 김성현, 김성근, 서봉근, 김재석, 김효진, 한진영
동아대학교 의과대학 내과학교실,
동아대학교 의과대학 임상병리학교실
Background :
Acute myelod leukemia (AML) is a hematologic malignant disease characterized by uncontrolled proliferation of myeloid cells in marrow and arrest in their maturation. It accounts for 70∼80% of chromosomal abnormalities and
t(8;21) has been found in 40% of AML-M2. Because cytogenetic studies can help classifying the disease, providing the clues of disease progression and monitoring remission after chemotherapy, we have performed cytogenetic studies to identify the incidence of t(8;21) and other chromosomal abnormalities and to assure their prognostic significance in patients with AML-M2.
Methods : From August 1998 to July 2000, 38 patients with AML-M2 were treated with ara- C and idarubicin in order to induce complete remission. We evaluated chromosomal abnormalities by high resolution banding technique. We divided patients
into 3 groups. Patients having normal and intermediate risk karyotype belonged to group A, t(8;21) to group B and, unfavorable and undetermined prognostic karyotype to group C.
Results :
The incidence of chromosomal abnormalities was 71% (27/38), and the proportion of A, B, and C group were 40%, 30% and 30%, respectively. The median follow up duration of evaluable patients was 381 (55∼1,295) days. The complete
remission (CR) rate accounted for 79% (30/38). The CR rate in A, B and C group were 88% (14/16), 91% (10/ 11) and 55% (6/11), respectively (P=0.06). The median remission duration had not been reached yet. The median remission duration of group A and B had not been reached yet, but that of group C was 337 days (P=0.60). The overall median survival duration was 567 days, and the median survival duration of group B had not been reached yet, otherwise those that of group A and C were 432 days and 364
days, respectively (P=0.02).
Conclusion :
The incidence of chromosomal abnormalities was observed 71% in patients with AML-M2. The patients with t(8;21) showed higher complete remission rate and tendency to have longer remission duration and survival duration.
Keywords Chromosomal abnormality, Acute myeloid leukemia, t(8;21)
Korean J Hematol 2001; 36(3): 181-188
Published online September 30, 2001
Copyright © The Korean Society of Hematology.
권혁찬, 손승현, 김성현, 김성근, 서봉근, 김재석, 김효진, 한진영
동아대학교 의과대학 내과학교실,
동아대학교 의과대학 임상병리학교실
Hyuk Chan Kwon, Seung Hyun Sohn, Seong Hyun Kim, Seong Geun Kim, Bong Gun Suh, Jae Seok Kim, Hyo Jin Kim, Jin Yeong Han
Department of Internal Medicine, Clinical Pathology, College of Medicine, Dong, A University, Pusan, Korea
Background :
Acute myelod leukemia (AML) is a hematologic malignant disease characterized by uncontrolled proliferation of myeloid cells in marrow and arrest in their maturation. It accounts for 70∼80% of chromosomal abnormalities and
t(8;21) has been found in 40% of AML-M2. Because cytogenetic studies can help classifying the disease, providing the clues of disease progression and monitoring remission after chemotherapy, we have performed cytogenetic studies to identify the incidence of t(8;21) and other chromosomal abnormalities and to assure their prognostic significance in patients with AML-M2.
Methods : From August 1998 to July 2000, 38 patients with AML-M2 were treated with ara- C and idarubicin in order to induce complete remission. We evaluated chromosomal abnormalities by high resolution banding technique. We divided patients
into 3 groups. Patients having normal and intermediate risk karyotype belonged to group A, t(8;21) to group B and, unfavorable and undetermined prognostic karyotype to group C.
Results :
The incidence of chromosomal abnormalities was 71% (27/38), and the proportion of A, B, and C group were 40%, 30% and 30%, respectively. The median follow up duration of evaluable patients was 381 (55∼1,295) days. The complete
remission (CR) rate accounted for 79% (30/38). The CR rate in A, B and C group were 88% (14/16), 91% (10/ 11) and 55% (6/11), respectively (P=0.06). The median remission duration had not been reached yet. The median remission duration of group A and B had not been reached yet, but that of group C was 337 days (P=0.60). The overall median survival duration was 567 days, and the median survival duration of group B had not been reached yet, otherwise those that of group A and C were 432 days and 364
days, respectively (P=0.02).
Conclusion :
The incidence of chromosomal abnormalities was observed 71% in patients with AML-M2. The patients with t(8;21) showed higher complete remission rate and tendency to have longer remission duration and survival duration.
Keywords: Chromosomal abnormality, Acute myeloid leukemia, t(8,21)
Hyuk Chan Kwon
Korean J Hematol 2002; 37(2): 89-96Hee Sue Park
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