At three years, patients with acute lymphoblastic leukaemia are still at risk for relapse. Results of the international MRC UKALLXII/ECOG E2993 trial.


Journal

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

Informations de publication

Date de publication:
10 2020
Historique:
received: 18 12 2019
revised: 02 03 2020
accepted: 05 03 2020
pubmed: 29 3 2020
medline: 17 3 2021
entrez: 29 3 2020
Statut: ppublish

Résumé

Late relapse [>3 years from complete remission (CR)] in acute lymphoblastic leukaemia (ALL), is unusual. Data from the MRC UKALLXII/ECOG E2993 trial are presented to evaluate the incidence and characteristics of late relapse in adult ALL. Of 1,909 patients, 1,752 (92%) achieved CR and among these 757 (43·2%) relapsed; 691 (91·3%) within three years and 66 (8·7%) beyond. Among these 66 patients, median time to relapse was 47 (37-144) months. Relapse beyond three years occurred in 3·8% of all who achieved CR. The cumulative risk of relapse was 40%, 43% and 45% at three, five and ten years respectively. Out of the 1 752 patients who achieved CR, 11·7% underwent autologous and 40·6% allogeneic transplant, while in CR1. Of the autologous patients, 43·2% relapsed early and 3·4% relapsed late. However, among the allogeneic patients, 13·2% relapsed early and only 1·3% late. The five-year overall survival from relapse was 5·8% and 20% in the early and late relapse patients respectively. In conclusion, late relapse in adults with ALL is not uncommon, and is associated with better outcome after relapse compared to early relapse.

Identifiants

pubmed: 32220069
doi: 10.1111/bjh.16616
pmc: PMC7687130
mid: NIHMS1593966
doi:

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

37-43

Subventions

Organisme : NCI NIH HHS
ID : UG1 CA233290
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233234
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189859
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA232760
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180820
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180794
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180853
Pays : United States

Informations de copyright

© 2020 British Society for Haematology and John Wiley & Sons Ltd.

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Auteurs

Chezi Ganzel (C)

Shaare Zedek Medical Center, Jerusalem, Israel.
Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Xin V Wang (XV)

Dana Farber Cancer Institute - ECOG-ACRIN Biostatistics Center, Boston, MA, USA.

Jacob M Rowe (JM)

Shaare Zedek Medical Center, Jerusalem, Israel.
Rambam Medical Center, Haifa, Israel.

Susan M Richards (SM)

Clinical Trial Service Unit, Oxford, UK.

Georgina Buck (G)

Clinical Trial Service Unit, Oxford, UK.

David I Marks (DI)

University Hospitals Bristol National Health Service Foundation Trust, Bristol, UK.

Mark R Litzow (MR)

Mayo Clinic, Rochester, MN, USA.

Elisabeth M Paietta (EM)

Montefiore Medical Center, Bronx, NY, USA.

Letizia Foroni (L)

Hammersmith Hospital, London, UK.

Selina M Luger (SM)

University of Pennsylvania, Philadelphia, PA, USA.

Cheryl L Willman (CL)

The University of New Mexico, Albuquerque, NM, USA.

Charles G Mullighan (CG)

St Jude Children's Research Hospital, Memphis, TN, USA.

Kathryn G Roberts (KG)

St Jude Children's Research Hospital, Memphis, TN, USA.

Peter H Wiernik (PH)

Our Lady of Mercy Medical Center, Bronx, NY, USA.

Dan Douer (D)

Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Hillard M Lazarus (HM)

Case Western Reserve University, Cleveland, OH, USA.

Martin S Tallman (MS)

Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Anthony H Goldstone (AH)

University College London, London, UK.

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