Analysis of the factors associated with prognosis in patients with Ph chromosome positive adult acute lymphoblastic leukemia.
- Author:
Shi-he LIU
1
;
Ying-chang MI
;
Xu-ping LIU
;
Yan-ping XUE
;
Hui-jun WANG
;
Shou-geng BIAN
;
Jian-xiang WANG
Author Information
- Publication Type:Journal Article
- MeSH: Adult; Antigens, CD34; metabolism; Chromosome Aberrations; Humans; In Situ Hybridization, Fluorescence; Karyotyping; Precursor Cell Lymphoblastic Leukemia-Lymphoma; genetics; metabolism; pathology; Prognosis; Reverse Transcriptase Polymerase Chain Reaction; Survival Analysis
- From: Chinese Journal of Hematology 2004;25(7):417-420
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate factors associated with survival of patients with Ph chromosome positive adult acute lymphoblastic leukemia (aALL) in a period of 11 years.
METHODSAll the clinical parameters of 31 Ph positive patients were statistically analyzed by SPSS software.
RESULTPh(+) patients account for 15.3% (31/203) of all the aALL patients. Clinically, these patients manifested older in age, higher white blood cell counts with high blast fractions and lower platelet counts (PC). Phenotypically 82.6% of them were common ALL, 39.1% coexpressed myeloid antigens, and 56.5% expressed CD34 antigen. 65.4% of them (17/26) achieved complete remission (CR) and the median remission and survival durations were 4 months and 8 months, respectively. Patients with Ph(+) and additional chromosomal aberrations accounted for 42% of all the Ph(+) patients, including monosomy 7, +Ph, del(9)(p11-12) and add/t(16)(p13), and they had lower PC as compared with those with sole Ph(+) (P = 0.012) and variant Ph translocation (P = 0.01). CD34 positive patients had a shorter remission and survival duration than CD34 negative ones (0 vs 9 months for median remission time, P = 0.024; and 6 vs 12 months for median survival time, P = 0.034). There was no evidence to support the correlation between myeloid antigen expression and survival time in these patients.
CONCLUSIONPh(+) aALL is associated with adverse prognosis and CD34 expression is a poorer prognostic factor in Ph(+) aALL patients. There is no significant clinical difference between Ph(+) aALL with or without additional chromosomal aberrations.