Clinical and molecular characteristics and treatment patterns of adolescent and young adult patients with chronic lymphocytic leukaemia.


Journal

British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544

Informations de publication

Date de publication:
07 2021
Historique:
revised: 25 03 2021
received: 19 01 2021
accepted: 29 03 2021
pubmed: 12 5 2021
medline: 17 12 2021
entrez: 11 5 2021
Statut: ppublish

Résumé

Chronic lymphocytic leukaemia (CLL) rarely presents in adolescent and young adult (AYA) patients (patients aged 15-39 years). Disease characteristics and outcomes of AYA patients with CLL are not well understood, particularly in the era of novel oral targeted therapies. We analysed outcomes of 227 AYA patients with CLL diagnosed in the last two decades and evaluated at our institution. Median time to first treatment (TTFT) was 2·2 years, and five- and 10-year overall survival (OS) were 90% and 78%, respectively. Pre-treatment elevated beta 2-microglobulin, advanced Rai stage, del(11q) or del(17p) by FISH, unmutated IGHV and CD38 positivity were associated with both shorter TTFT and OS. Within the subgroup of patients who received oral targeted therapy at any time, del(11q) or del(17p) and complex karyotype were associated with shorter OS. First-line treatment choice was significantly associated with time to second treatment (P < 0·001). Patients harbouring del(11q) or del(17p) experienced shorter time to Richter transformation and were more likely to undergo an allogeneic stem cell transplant. There was a significant association between age and both OS and time to Richter transformation. Our study is the first analysis of AYA patients with CLL with a large number of patients treated with oral targeted therapies.

Identifiants

pubmed: 33973230
doi: 10.1111/bjh.17498
pmc: PMC9284944
mid: NIHMS1703741
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

61-68

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States

Informations de copyright

© 2021 British Society for Haematology and John Wiley & Sons Ltd.

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Auteurs

Hua-Jay J Cherng (HJ)

Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Nadya Jammal (N)

Department of Clinical Pharmacy, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Shilpa Paul (S)

Department of Clinical Pharmacy, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Xuemei Wang (X)

Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Koji Sasaki (K)

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Philip Thompson (P)

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Jan Burger (J)

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Alessandra Ferrajoli (A)

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Zeev Estrov (Z)

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Susan O'Brien (S)

Chao Family Comprehensive Cancer Center, University of Irvine, Orange County, CA, USA.

Michael Keating (M)

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

William G Wierda (WG)

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Nitin Jain (N)

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

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Classifications MeSH