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PMID: 12149225 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

V(H) mutation status, CD38 expression level, genomic aberrations, and survival in chronic lymphocytic leukemia.

Blood ·Vol. 100 ·No. 4 ·2002-08-15 ·Pages 1410-6

Kröber A, Seiler T, Benner A, Bullinger L, Brückle E, Lichter P, Döhner H, Stilgenbauer S

Abstract

In chronic lymphocytic leukemia (CLL), biologic risk factors such as immunoglobulin variable heavy chain gene (V(H)) mutation status, CD38 expression level, and genomic aberrations have recently been identified, but the relative prognostic impact of the individual parameters is unknown. In the current study, we analyzed V(H) mutation status by polymerase chain reaction and sequencing (n = 300), genomic aberrations by fluorescence in situ hybridization (+3q, 6q-, +8q, 11q-, +12q, 13q-, t(14q), 17p-) (n = 300), and CD38 expression by triple-color FACS (CD5, CD19, CD38) (n = 157) in a unicentric CLL cohort. The prognostic influence of V(H) mutation rate and CD38 expression level was tested by maximally selected log-rank statistics. A corrected P value (P(cor)) for a cutoff level allowing the best separation of 2 subgroups with different survival probabilities was identified at 97% V(H) homology (95% confidence interval [CI], 96%-98% homology, P(cor) <.001) and at 7% CD38 expression (95% CI, 20%-71% expression, P(cor) =.02). In univariate analyses, unmutated V(H) genes and high CD38 expression levels predicted for shorter survival times. The overall incidence of genomic aberrations was similar in the V(H) unmutated and V(H) mutated subgroups. High-risk genomic aberrations such as 17p- and 11q- occurred almost exclusively in the V(H) unmutated subgroup, whereas favorable aberrations such as 13q- and 13q- as single abnormalities were overrepresented in the V(H) mutated subgroup. In multivariate analysis, unmutated V(H), 17p deletion, 11q deletion, age, WBC, and LDH were identified as independent prognostic factors, indicating a complementary role of V(H) mutation status and genomic aberrations to predict outcome in CLL.

MeSH Terms
ADP-ribosyl Cyclase ADP-ribosyl Cyclase 1 Antigens, CD Antigens, Differentiation/analysis Chromosome Aberrations Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 12 Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 17 Flow Cytometry Gene Deletion Humans Immunoglobulin Heavy Chains/genetics Immunoglobulin Variable Region/genetics In Situ Hybridization, Fluorescence L-Lactate Dehydrogenase/blood Leukemia, Lymphocytic, Chronic, B-Cell/genetics,immunology Leukocyte Count Membrane Glycoproteins Mutation NAD+ Nucleosidase/analysis Polymerase Chain Reaction Prognosis Sequence Analysis, DNA Survival Rate Trisomy
Chemicals
Antigens, CD Antigens, Differentiation Immunoglobulin Heavy Chains Immunoglobulin Variable Region Membrane Glycoproteins L-Lactate Dehydrogenase ADP-ribosyl Cyclase CD38 protein, human NAD+ Nucleosidase ADP-ribosyl Cyclase 1
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Kröber Alexander
Abteilung Innere Medizin III, University of Ulm, Germany.
Seiler Till
Benner Axel
Bullinger Lars
Brückle Elsbeth
Lichter Peter
Döhner Hartmut
Stilgenbauer Stephan
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
2002-08-15
Pages
1410-6
Language
English
Region
United States
NLM ID
7603509
Subset
IM
Corrections
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