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Prognostic impact of prevalent chronic lymphocytic leukemia stereotyped subsets: analysis within prospective clinical trials of the German CLL Study Group

Authors :
Kirsten Fischer
Barbara Eichhorst
Richard Rosenquist
Hartmut Döhner
Kostas Stamatopoulos
Paolo Ghia
Eugen Tausch
Michael Hallek
Sonia Jaramillo
Valentin Goede
Manuela Hoechstetter
Sandra Robrecht
Andreas Agathangelidis
Johannes Bloehdorn
Christof Schneider
Stephan Stilgenbauer
Jasmin Bahlo
Jaramillo, S.
Agathangelidis, A.
Schneider, C.
Bahlo, J.
Robrecht, S.
Tausch, E.
Bloehdorn, J.
Hoechstetter, M.
Fischer, K.
Eichhorst, B.
Goede, V.
Hallek, M.
Dohner, H.
Rosenquist, R.
Ghia, P.
Stamatopoulos, K.
Stilgenbauer, S.
Source :
Haematologica
Publication Year :
2020
Publisher :
Fondazione Ferrata Storti, 2020.

Abstract

Almost one-third of all patients with chronic lymphocytic leukemia (CLL) express stereotyped B-cell receptor immunoglobulins (BcR IG) and can be assigned to distinct subsets, each with a particular BcR IG. The largest stereotyped subsets are #1, #2, #4 and #8, associated with specific clinico-biological characteristics and outcomes in retrospective studies. We assessed the associations and prognostic value of these BcR IG in prospective multicenter clinical trials reflective of two different clinical situations: (i) early-stage patients ('watch and wait' arm of the CLL1 trial) (n=592); (ii) patients in need of treatment, enrolled in three phase III trials (CLL8, CLL10, CLL11), treated with different chemo-immunotherapies (n=1,861). Subset #1 was associated with del(11q), higher CLL International Prognostic Index (CLL-IPI) scores and similar clinical course to CLL with unmutated immunoglobulin heavy variable (IGHV) genes (U-CLL) in both early and advanced stage groups. IGHV-mutated (M-CLL) subset #2 cases had shorter time-to-first-treatment (TTFT) versus other M-CLL cases in the early-stage cohort (hazard ratio [HR]: 4.2, confidence interval [CI]: 2-8.6, P

Details

Language :
English
ISSN :
15928721 and 03906078
Volume :
105
Issue :
11
Database :
OpenAIRE
Journal :
Haematologica
Accession number :
edsair.doi.dedup.....16bb71f778dcdc08bd458eeaabf69310