Korean J Hematol 2001; 36(3):
Published online September 30, 2001
© The Korean Society of Hematology
이제중, 정익주, 양덕환, 조상희, 김형준, 조덕, 양동욱, 남찬은
전남대학교 의과대학 내과학교실,
전남대학교 의과대학 임상병리학교실,
전남대학교 의과대학 의과학연구소
Background :
A number of clinical and biological factors in acute myeloid leukemia (AML) have been used to predict the response to induction treatment or the likelihood of relapse. This study investigated CD34 expression in AML patients to evaluate its clinical and prognostic significance.
Methods : This study included 165 patients with de novo AML who underwent flow cytometry for CD34 at diagnosis between July 1994 and February 2001. To analyze the response to or outcome of therapy, we evaluated 81 patients who received
induction chemotherapy with idarubicin and either cytarabine or N 4 behenoyl-1-D- arabinofuranosylcytosine.
Results:
CD34 was expressed in 38.1±2.7% of mononuclear cells that isolated from AML patients, and 56.4% of the patients with AML were CD34+. There were no significant differences in the clinical and hematological parameters between the
CD34+and CD34- groups. The patients with CD34+ frequently encountered in M2 subtype (49.5%), and cytogenetic abnormality of t(8;21) and karyotypes with poor risk were CD34+ in 66.7% and 92.9% of the cases, respectively. When we compared the CD34+ group with CD34- group, no significant differences were found in CR rate (70.9% vs 76.9%, P=0.61), in median duration of overall survival (16.4±2.4 months vs 25.1±3.9 months, P=0.45), or in disease free survival (P=0.42).
Conclusion :
This study did not show the definitive clinical and prognostic implications of CD34 expression. Further studies with a large number of patients are needed to elucidate the association of CD34 expression with specific subtypes of
AML, such as t(8;21) or t(15;17) karyotypes.
Keywords CD34, Acute myeloid leukemia, Prognosis
Korean J Hematol 2001; 36(3): 197-203
Published online September 30, 2001
Copyright © The Korean Society of Hematology.
이제중, 정익주, 양덕환, 조상희, 김형준, 조덕, 양동욱, 남찬은
전남대학교 의과대학 내과학교실,
전남대학교 의과대학 임상병리학교실,
전남대학교 의과대학 의과학연구소
Je Jung Lee, Ik Joo Chung, Duk Hwan Yang, Sang Hee Cho, Hyeoung Joon Kim, Duck Cho, Dong Wook Ryang, Chan Eun Nam
Department of Internal Medicine, Clinical Pathology, Research Institute of Medical Sciences, Chonnam National University Medical School, kwangju, Korea
Background :
A number of clinical and biological factors in acute myeloid leukemia (AML) have been used to predict the response to induction treatment or the likelihood of relapse. This study investigated CD34 expression in AML patients to evaluate its clinical and prognostic significance.
Methods : This study included 165 patients with de novo AML who underwent flow cytometry for CD34 at diagnosis between July 1994 and February 2001. To analyze the response to or outcome of therapy, we evaluated 81 patients who received
induction chemotherapy with idarubicin and either cytarabine or N 4 behenoyl-1-D- arabinofuranosylcytosine.
Results:
CD34 was expressed in 38.1±2.7% of mononuclear cells that isolated from AML patients, and 56.4% of the patients with AML were CD34+. There were no significant differences in the clinical and hematological parameters between the
CD34+and CD34- groups. The patients with CD34+ frequently encountered in M2 subtype (49.5%), and cytogenetic abnormality of t(8;21) and karyotypes with poor risk were CD34+ in 66.7% and 92.9% of the cases, respectively. When we compared the CD34+ group with CD34- group, no significant differences were found in CR rate (70.9% vs 76.9%, P=0.61), in median duration of overall survival (16.4±2.4 months vs 25.1±3.9 months, P=0.45), or in disease free survival (P=0.42).
Conclusion :
This study did not show the definitive clinical and prognostic implications of CD34 expression. Further studies with a large number of patients are needed to elucidate the association of CD34 expression with specific subtypes of
AML, such as t(8;21) or t(15;17) karyotypes.
Keywords: CD34, Acute myeloid leukemia, Prognosis
Jung Hwan Lee, Hee Young Ju, Ju Kyung Hyun, So Jin Kim, Hee Won Cho, Jae Kyung Lee, Ji Won Lee, Ki Woong Sung, Keon Hee Yoo
Blood Res 2023; 58(4): 181-186Hyery Kim
Blood Res 2020; 55(S1): S5-S13Yumi Park, Jinsook Lim, Seonyoung Kim, Ikchan Song, Kyechul Kwon, Sunhoe Koo, and Jimyung Kim
Blood Res 2018; 53(3): 198-204