High karyotypic complexity is an independent prognostic factor in patients with CLL treated with venetoclax combinations.


Journal

Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509

Informations de publication

Date de publication:
03 08 2023
Historique:
accepted: 05 04 2023
received: 17 01 2023
medline: 4 8 2023
pubmed: 12 5 2023
entrez: 12 5 2023
Statut: ppublish

Résumé

Complex karyotypes have been associated with inferior outcomes in chronic lymphocytic leukemia (CLL) treated with chemoimmunotherapy (CIT), whereas their prognostic impact in the context of venetoclax-based treatments is still debated. In this prospective analysis on karyotype complexity in CLL, we evaluated the impact of complex (≥3 chromosomal aberrations [CAs], CKTs) and highly complex karyotypes (≥5 CAs; hCKTs) as well as specific aberrations in previously untreated patients without TP53 aberrations undergoing either CIT or time-limited venetoclax-based therapies in the phase 3 GAIA/CLL13 trial. Karyotype analyses were available for 895 of 926 patients (96.7%), of whom 153 (17%) had a CKT and 43 (5%) hCKT. In the CIT arm, CKT was associated with shorter progression-free survival (PFS) (hazard ratio [HR] 2.58; 95% confidence interval [95% CI], 1.54-4.32; P < .001) and overall survival (HR, 3.25; 95% CI, 1.03-10.26; P = .044). In the pooled venetoclax arms, a multivariable analysis identified hCKTs (HR, 1.96; 95% CI, 1.03-3.72; P = .041), but not CKTs, as independent adverse prognosticators for PFS. The presence of translocations (unbalanced and/or balanced) was also independently associated with shorter PFSs in the venetoclax arms. CIT led to the acquisition of additional CAs (mean CAs, 2.0-3.4; from baseline to CLL progression), whereas karyotype complexity remained stable after venetoclax-based treatments (2.0, both time points). This analysis establishes highly complex karyotypes and translocations as adverse prognostic factors in the context of venetoclax-based combination treatments. The findings of this study support the incorporation of karyotyping into the standard diagnostic workup of CLL, because it identifies patients at high risk of poor treatment outcomes and thereby improves prognostication. This trial was registered at www.clinicaltrials.gov as #NCT02950051.

Identifiants

pubmed: 37172204
pii: 495806
doi: 10.1182/blood.2023019634
doi:

Substances chimiques

Bridged Bicyclo Compounds, Heterocyclic 0
venetoclax N54AIC43PW

Banques de données

ClinicalTrials.gov
['NCT02950051']

Types de publication

Clinical Trial, Phase III Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

446-459

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023 by The American Society of Hematology.

Auteurs

Moritz Fürstenau (M)

Department I of Internal Medicine, Faculty of Medicine and University Hospital Cologne, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, German CLL Study Group, University of Cologne, Cologne, Germany.

Yvonne J Thus (YJ)

Department of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.

Sandra Robrecht (S)

Department I of Internal Medicine, Faculty of Medicine and University Hospital Cologne, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, German CLL Study Group, University of Cologne, Cologne, Germany.

Clemens H M Mellink (CHM)

Genome Diagnostics Laboratory, Section Cytogenetics, Department of Human Genetics, Cancer Center Amsterdam, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.

Anne-Marie van der Kevie-Kersemaekers (AM)

Genome Diagnostics Laboratory, Section Cytogenetics, Department of Human Genetics, Cancer Center Amsterdam, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.

Julie Dubois (J)

Department of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.

Julia von Tresckow (J)

Clinic for Hematology and Stem Cell Transplantation, West German Cancer Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

Michaela Patz (M)

Department I of Internal Medicine, Faculty of Medicine and University Hospital Cologne, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, German CLL Study Group, University of Cologne, Cologne, Germany.

Michael Gregor (M)

Division of Hematology, Cantonal Hospital of Lucerne, Lucerne, Switzerland.
Swiss Group for Clinical Cancer Research, Berne, Switzerland.

Patrick Thornton (P)

Department of Haematology, Beaumont Hospital, RCSI University of Medicine and Health Sciences, Cancer Trials Ireland, Dublin, Ireland.

Philipp B Staber (PB)

Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Tamar Tadmor (T)

Hematology, Bnai-Zion Medical Center, Haifa, Israel.

Mark-David Levin (MD)

Department of Internal Medicine, Albert Schweitzer Hospital, Dordrecht, The Netherlands.

Caspar da Cunha-Bang (C)

Department of Hematology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Christof Schneider (C)

Division of CLL, Department of Internal Medicine III, University of Ulm, Ulm, Germany.

Christian Bjoern Poulsen (CB)

Department of Hematology, Zealand University Hospital, Roskilde, Roskilde, Denmark.

Thomas Illmer (T)

BAG Freiberg-Richter, Jacobasch, Wolf, Illmer, Dresden, Germany.

Björn Schöttker (B)

Hämatologisch-onkologische Schwerpunktpraxis Würzburg, Würzburg, Germany.

Ann Janssens (A)

Department of Hematology, Universitaire Ziekenhuizen Leuven, Leuven, Belgium.

Ilse Christiansen (I)

Department of Hematology, Aalborg University Hospital, Aalborg, Denmark.

Thomas Nösslinger (T)

Department of Internal Medicine III, Hanusch Hospital, Vienna, Austria.

Michael Baumann (M)

Swiss Group for Clinical Cancer Research, Berne, Switzerland.
Department of Oncology, Kantonsspital St. Gallen, St. Gallen, Switzerland.

Holger Hebart (H)

Department of Oncology, Stauferklinikum, Mutlangen, Germany.

Tobias Gaska (T)

Hematology and Oncology, Brüderkrankenhaus, Paderborn, Germany.

Josien C Regelink (JC)

Department of Haematology, Meander Medisch Centrum, Amersfoort, The Netherlands.

Ellen C Dompeling (EC)

Department of Hematology, Isala Ziekenhuis, Zwolle, The Netherlands.

Vesa Lindström (V)

Department of Hematology, Comprehensive Cancer Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.

Gunnar Juliusson (G)

Department of Hematology, Skåne University Hospital, Lund, Sweden.

Anouk Widmer (A)

Swiss Group for Clinical Cancer Research, Berne, Switzerland.
Department of Medical Oncology and Haematology, Universitätsspital Zürich, Zürich, Switzerland.

Jeroen Goede (J)

Swiss Group for Clinical Cancer Research, Berne, Switzerland.
Clinic for Medical Oncology and Hematology, Cantonal Hospital of Winterthur, Winterthur, Switzerland.

Neta Goldschmidt (N)

Department of Hematology, Hadassah Medical Center, Jerusalem, Israel.

Florian Simon (F)

Department I of Internal Medicine, Faculty of Medicine and University Hospital Cologne, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, German CLL Study Group, University of Cologne, Cologne, Germany.

Nisha De Silva (N)

Department I of Internal Medicine, Faculty of Medicine and University Hospital Cologne, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, German CLL Study Group, University of Cologne, Cologne, Germany.

Anna-Maria Fink (AM)

Department I of Internal Medicine, Faculty of Medicine and University Hospital Cologne, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, German CLL Study Group, University of Cologne, Cologne, Germany.

Kirsten Fischer (K)

Department I of Internal Medicine, Faculty of Medicine and University Hospital Cologne, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, German CLL Study Group, University of Cologne, Cologne, Germany.

Clemens-Martin Wendtner (CM)

Department of Hematology, Oncology, Immunology, Palliative Care, Infectious Diseases and Tropical Medicine, German CLL Study Group, Munich Clinic Schwabing, Munich, Germany.

Matthias Ritgen (M)

Department II of Internal Medicine, University of Schleswig-Holstein, Kiel, Germany.

Monika Brüggemann (M)

Department II of Internal Medicine, University of Schleswig-Holstein, Kiel, Germany.

Eugen Tausch (E)

Division of CLL, Department of Internal Medicine III, University of Ulm, Ulm, Germany.

Marcel Spaargaren (M)

Department of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.

Eric Eldering (E)

Department of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.

Stephan Stilgenbauer (S)

Division of CLL, Department of Internal Medicine III, University of Ulm, Ulm, Germany.

Carsten U Niemann (CU)

Department of Hematology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Michael Hallek (M)

Department I of Internal Medicine, Faculty of Medicine and University Hospital Cologne, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, German CLL Study Group, University of Cologne, Cologne, Germany.

Barbara Eichhorst (B)

Department I of Internal Medicine, Faculty of Medicine and University Hospital Cologne, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, German CLL Study Group, University of Cologne, Cologne, Germany.

Karl-Anton Kreuzer (KA)

Department I of Internal Medicine, Faculty of Medicine and University Hospital Cologne, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, German CLL Study Group, University of Cologne, Cologne, Germany.

Arnon P Kater (AP)

Department of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.

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