We have isolated the 3Π BCR breakpoint junction of a complex BCR-ABL1 rearrangement found in leukemic cells with a cytogenetically normal karyotype, and the corresponding germline fragment that spanned the 3Π BCR recombination site. Fluorescence in situ hybridization localized the 3Π BCR recombinati
Characteristics and outcome of patients with Philadelphia chromosome negative, bcr/abl negative chronic myelogenous leukemia
β Scribed by Francesco Onida; Greg Ball; Hagop M. Kantarjian; Terry L. Smith; Armand Glassman; Maher Albitar; Barbara Scappini; Mary Beth Rios; Michael J. Keating; Miloslav Beran
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 150 KB
- Volume
- 95
- Category
- Article
- ISSN
- 0008-543X
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β¦ Synopsis
Abstract
BACKGROUND
Up to 5% of patients with chronic myelogenous leukemia (CML) do not have the Philadelphia (Ph) translocation t(9;22)(q34;q11) or a bcr/abl molecular rearrangement. Although the diagnostic criteria of this entity are still under debate, there is general agreement that patients with Ph negative, bcr/abl negative CML have a severe clinical course that is not affected significantly by current treatment options.
METHODS
A population of 76 patients with bcr/abl negative CML who had received minimal or no previous therapy was characterized carefully with the intent of investigating clinical and hematologic variables and their association with survival by univariate, correlation, and multivariate analyses. A group of 73 patients with Ph negative CML who were not tested for the bcr/abl rearrangement (bcr/abl unknown) was analyzed separately and used for extension of the analysis.
RESULTS
In the bcr/abl negative patient population, the median overall survival was 24 months. At the time of the analysis, 38 patients (50%) had died, and blastic transformation preceded death in 31%. Chromosomal abnormalities were found in 30% of the 76 patients, with trisomy 8 the most common abnormality. Complex chromosomal abnormalities were rare, and monosomy 7 was not observed. Survival was not affected significantly by treatment. Multivariate analysis identified older age (> 65 years), anemia (hemoglobin < 10 g/dL), and severe leukocytosis (white blood cells > 50 Γ 10^9^/L) as variables with independent prognostic significance for poor survival. A prognostic scoring system stratified patients into a lowβrisk group (53%) and a highβrisk group (47%), with median survivals of 38 months and 9 months, respectively.
CONCLUSIONS
Bcr/abl negative CML is a distinct clinical entity associated with very poor prognosis. Two risk categories are identifiable using a simple scoring system based on age, hemoglobin level, and leukocyte number. Cancer 2002;95:1673β84. Β© 2002 American Cancer Society.
DOI 10.1002/cncr.10832
π SIMILAR VOLUMES
## Abstract ## BACKGROUND Anecdotal cases of chromosomal abnormalities in Philadelphia chromosome (Ph)βnegative metaphases have been reported in patients with chronic myelogenous leukemia (CML) in the chronic phase during treatment with interferon and, more recently, with imatinib. This phenomenon