Reassessing the Chronic Lymphocytic Leukemia International Prognostic Index in the era of targeted therapies.


Journal

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

Informations de publication

Date de publication:
15 Apr 2024
Historique:
accepted: 02 04 2024
received: 19 09 2023
revised: 01 04 2024
medline: 15 4 2024
pubmed: 15 4 2024
entrez: 15 4 2024
Statut: aheadofprint

Résumé

We evaluated the prognostic value of the Chronic Lymphocytic Leukemia International Prognostic Index (CLL-IPI) using a pooled dataset of CLL-patients treated first-line with targeted drugs (N=991) or chemoimmunotherapy (N=1,256). With a median observation time of 40.5 months, the 3-year progression-free survival (PFS)-rates for targeted drug-treated patients varied by CLL-IPI risk group: 96.5% (low), 87.6% (intermediate), 82.4% (high), and 78.7% (very high). Differences between consecutive CLL-IPI risk groups were observed for intermediate vs. low (HR=3.296, 95%-CI 1.576-6.894, p=0.002), for high vs. intermediate (HR=1.365, 95%-CI 1.003-1.858, p=0.048), but not for very high vs. high. CLL-IPI factors β2-microglobulin, IGHV mutational status, and TP53 status each retained prognostic value for PFS. The 3-year overall survival (OS)-rates by CLL-IPI risk group were 100%, 96%, 93.9%, and 89.4% with no differences between consecutive risk groups. Age, Binet stage, β2-microglobulin, and TP53 status each retained prognostic value for OS. In chemoimmunotherapy patients (median observation time 66.9 months), 3-year PFS-rates for CLL-IPI risk groups were 78.1%, 51.4%, 40.1%, and 16.5%. Corresponding 3-year OS-rates were 97.4%, 93.1%, 81.8%, and 57.3%. In a matched-pair analysis, PFS-differences in targeted therapies (N=812) versus chemoimmunotherapy (N=812) across all risk groups, and OS-differences in all but low-risk patients were demonstrated. The CLL-IPI maintains its prognostic value in predicting PFS outcomes with targeted drugs. With the caveat of a short observation time its impact in predicting survival appears diminished. Targeted therapies showed enhanced outcomes over chemoimmunotherapy, highlighting their effectiveness across various risk groups. Our findings support ongoing assessment of prognostic tools in CLL treatment evolution. CLL2-BIG (NCT02345863), CLL2-BAG (NCT02401503), CLL2-BIO (NCT02689141), CLL2-BCG (NCT02445131), CLL2-GIVe (NCT02758665), CLL13 (NCT02950051), CLL14-trial (NCT02242942), CLL1 (NCT00262782), CLL8 (NCT00281918), and CLL11 (NCT01010061).

Identifiants

pubmed: 38620092
pii: 515747
doi: 10.1182/blood.2023022564
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT00262782', 'NCT01010061', 'NCT00281918']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American Society of Hematology.

Auteurs

Petra Langerbeins (P)

University of Cologne, Germany.

Adam Giza (A)

Department I of Internal Medicine and German CLL Study Group; Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf (CIO ABCD); University of Cologne, Faculty of Medicine and University Hos, Cologne, Germany.

Sandra Robrecht (S)

University Hospital of Cologne, Köln, Germany.

Paula Cramer (P)

Department I of Internal Medicine and German CLL Study Group; Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf (CIO ABCD); University of Cologne, Faculty of Medicine and University Hos, Cologne, Germany.

Julia von Tresckow (J)

Universityhospital Essen, Essen, Germany.

Othman Al-Sawaf (O)

University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.

Anna-Maria Fink (AM)

University Hospital of Cologne, Cologne, Germany.

Moritz Fürstenau (M)

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

Nadine Kutsch (N)

University Hospital of Cologne, Cologne, Germany.

Florian Simon (F)

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

Valentin Goede (V)

St. Marien-Hospital, Cologne, Germany.

Manuela A Hoechstetter (MA)

Interdisciplinary Oncology Center (IOZ) Munich, Hematology and Oncology, Munich, Germany.

Carsten Utoft Niemann (CU)

Rigshospitalet, Copenhagen Ø, Denmark.

Caspar da Cunha-Bang (C)

Rigshospitalet, Copenhagen, Denmark.

Arnon P Kater (AP)

Department of Hematology, Cancer Center Amsterdam, Lymphoma and Myeloma Center Amsterdam, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands, Amsterdam, Netherlands.

Julie Dubois (J)

Cancer Center Amsterdam, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.

Michael Gregor (M)

Luzerner Kantonsspital, Luzern, Switzerland.

Philipp B Staber (PB)

Medical University of Vienna, Austria.

Eugen Tausch (E)

Ulm University, Ulm, Germany.

Christof Schneider (C)

Ulm University, Ulm, Germany.

Stephan Stilgenbauer (S)

Ulm University, Ulm, Germany.

Barbara Eichhorst (B)

University of Cologne, Cologne, Germany.

Kirsten Fischer (K)

University Hospital Cologne, Cologne, Germany.

Michael J Hallek (MJ)

University of Cologne, Cologne, Germany.

Classifications MeSH