Telomere length in chronic lymphocytic leukemia treated with venetoclax-based regimen in GAIA/CLL13 and CLL2-GIVe trials
Telomere length is a prognostic factor in chronic lymphocytic leukemia (CLL), yet its relevance under targeted therapies remains unclear. Here, we analyzed telomere length using qPCR in 917 samples from treatment-naïve CLL patients without TP53 aberrations enrolled in the GAIA/CLL13 trial comparing venetoclax-based combinations with rituximab (RV), obinutuzumab (GV), or obinutuzumab plus ibrutinib (GIV) versus chemoimmunotherapy (CIT). For CLL with TP53 aberrations, samples from 41 treatment-naïve patients receiving GIV in the CLL2-GIVe trial were analyzed. The median telomere lengths in GAIA/CLL13 and CLL2-GIVe were 4.0 kb (1.2-15.2) and 2.8 kb (1.4-14.0), respectively. A prognostic cutoff of 4.17 kb, based on GAIA/CLL13, was used for dichotomization into short and long telomeres. Within GAIA/CLL13, short telomeres significantly correlated with adverse clinical features including advanced Binet stage, high ECOG, high serum ß2-microglobulin and thymidine kinase levels, high lymphocyte count and large lymph nodes (all P<0.01). Among genetic features, short telomeres significantly associated with unmutated IGHV, del(11q), mutations in NOTCH1, SF3B1, XPO1, RPS15, EGR2 and NFKBIE, and karyotypic complexity (all P<0.01). Short telomeres were associated with shorter progression-free survival (PFS) within CIT, RV, GV, GIV in GAIA/CLL13 (all P<0.01) and in CLL2-GIVe (dichotomized by median; P=0.04), and impacted overall survival only in the CIT arm (P=0.024). Multivariable analysis suggested telomere length as an independent prognostic factor for PFS in the overall GAIA/CLL13 cohort. These findings propose telomere length as a prognostic marker for PFS in CLL patients receiving venetoclax-based first-line therapy and could be of relevance for risk stratification in the modern treatment era. NCT02950051
Authors
- Mark‐David Levin (ORCID: https://orcid.org/0000-0003-2139-3547)
- Caspar da Cunha‐Bang (ORCID: https://orcid.org/0000-0002-7800-3098)
- Stephan Stilgenbauer (ORCID: https://orcid.org/0000-0002-6830-9296)
- Tamar Tadmor (ORCID: https://orcid.org/0000-0002-3435-8612)
- Eugen Tausch (ORCID: https://orcid.org/0000-0002-9503-1226)
- Philipp Bernhard Staber (ORCID: https://orcid.org/0000-0001-6729-7708)
- H. Huber
- Billy Michael Chelliah Jebaraj (ORCID: https://orcid.org/0000-0002-6188-1652)
- Anna‐Maria Fink (ORCID: https://orcid.org/0000-0002-7669-7890)
- Carsten Utoft Niemann (ORCID: https://orcid.org/0000-0001-9880-5242)
- Moritz Fürstenau (ORCID: https://orcid.org/0000-0002-6593-0140)
- Kirsten Fischer (ORCID: https://orcid.org/0009-0006-6169-9152)
- Arnon Philip Kater (ORCID: https://orcid.org/0000-0003-3190-1891)
- Sandra Robrecht (ORCID: https://orcid.org/0000-0001-8848-6655)
- Matthias Ritgen (ORCID: https://orcid.org/0000-0002-0957-3804)
- Michael J. Hallek (ORCID: https://orcid.org/0000-0002-7425-4455)
- Patrick D. Thornton (ORCID: https://orcid.org/0000-0002-5126-9590)
- Christof Schneider (ORCID: https://orcid.org/0000-0001-9719-7345)
- Barbara F. Eichhorst (ORCID: https://orcid.org/0000-0001-9990-6918)
- Deyan Yordanov Yosifov (ORCID: https://orcid.org/0000-0002-5473-4398)
- Michael Gregor
- Karl‐Anton Kreuzer
- Can Zhang
Institutions
- Royal College of Surgeons in Ireland (IE)
- University of Cologne (DE)
- Universität Ulm (DE)
- Rigshospitalet (DK)
- Christian-Albrechts-Universität zu Kiel (DE)
- Städtisches Klinikum Karlsruhe (DE)
- Albert Schweitzer Ziekenhuis (NL)
- Cancer Trials Ireland (IE)
- Bnai Zion Medical Center (IL)
- Luzerner Kantonsspital (CH)
- Amsterdam University Medical Centers (NL)
- University Hospital Cologne (DE)
- University Hospital Ulm (DE)
- Deutsche CLL Studiengruppe (DCLLSG) (DE)
- Saarland University (DE)
Publication Details
- Journal
- Blood
- Published
- 2026-10-06
- DOI
- https://doi.org/10.1182/blood.2025032302
- Primary Topic
- Chronic Lymphocytic Leukemia Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00