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We have previously shown that dividing patients with CLL into those with telomeres inside the fusogenic range (TL-IFR) and outside the fusogenic range (TL-OFR) is powerful prognostic tool. Here, we used a high-throughput version of the assay (HT-STELA) to establish whether telomere length could predict for outcome to fludarabine, cyclophosphamide, rituximab (FCR)-based treatment using samples collected from two concurrent phase II studies, ARCTIC and ADMIRE (n = 260). In univariate analysis, patients with TL-IFR had reduced progression-free survival (PFS) (P 

Original publication

DOI

10.1038/s41375-019-0389-9

Type

Journal article

Journal

Leukemia

Publication Date

08/2019

Volume

33

Pages

1953 - 1963

Keywords

Antineoplastic Combined Chemotherapy Protocols, Cyclophosphamide, Disease-Free Survival, Humans, Immunoglobulin Heavy Chains, Immunoglobulin Variable Region, Leukemia, Lymphocytic, Chronic, B-Cell, Mutation, Rituximab, Telomere, Vidarabine