Prognostic impact of number of induction courses to attain complete remission in patients with acute myeloid leukemia transplanted with either a matched sibling or human leucocyte antigen 10/10 or 9/10 unrelated donor: An Acute Leukemia Working Party European Society for Blood and Marrow Transplantation study.

AML MRD induction chemotherapy stem cell transplant

Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
06 Apr 2024
Historique:
revised: 14 02 2024
received: 21 12 2023
accepted: 16 02 2024
medline: 7 4 2024
pubmed: 7 4 2024
entrez: 6 4 2024
Statut: aheadofprint

Résumé

For the majority of patients with acute myeloid leukemia (AML) an allogeneic stem cell transplant (SCT) in first complete remission (CR) is preferred. However, whether the number of courses required to achieve CR has a prognostic impact is unclear. It is unknown which factors remain important in patients requiring more than one course of induction to attain remission. This Acute Leukaemia Working Party study from the European Society for Blood and Marrow Transplantation identified adults who received an allograft in first CR from either a fully matched sibling or 10/10 or 9/10 human leucocyte antigen (HLA)-matched unrelated donor (HLA-A, HLA-B, HLA-C, HLA-DR, or HLA-DQ). Univariate and multivariate analyses were undertaken to identify the prognostic impact of one or two courses of induction to attain CR. A total of 4995 patients were included with 3839 (77%) patients attaining a CR following one course of induction chemotherapy (IND1), and 1116 patients requiring two courses (IND2) to attain CR. IND2 as compared to IND1 was a poor prognostic factor in a univariate analysis and remained so in a multivariate Cox model, resulting in an increased hazard ratio of relapse (1.38; 95% confidence interval [CI], 1.16-1.64; p = .0003) and of death (1.27; 95% CI, 1.09-1.47; p = .002). Adverse prognostic factors in a multivariate analysis of the outcomes of patients requiring IND2 included age, FLT3-ITD, adverse cytogenetics, and performance status. Pretransplant measurable residual disease retained a prognostic impact regardless of IND1 or IND2. Initial response to chemotherapy as determined by number of courses to attain CR, retained prognostic relevance even following SCT in CR.

Identifiants

pubmed: 38581695
doi: 10.1002/cncr.35308
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 The Authors. Cancer published by Wiley Periodicals LLC on behalf of American Cancer Society.

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Auteurs

Justin Loke (J)

University of Birmingham, Birmingham, UK.
Dana-Farber Cancer Institute, Boston, Massachusetts, USA.

Myriam Labopin (M)

Acute Leukaemia Working Party, Paris Study Office, European Society for Blood and Marrow Transplantation, Paris, France.
Hematology Department, AP-HP, Sorbonne Universités, INSERM, Centre de Recherche Saint-Antoine (CRSA), Saint Antoine Hospital, Paris, France.

Charles Craddock (C)

Birmingham Centre for Cellular Therapy and Transplantation, Centre for Clinical Haematology, Queen Elizabeth Hospital, Birmingham, UK.
University of Warwick, Warwick, UK.

Gérard Socié (G)

Department of Hematology-BMT, Hopital St. Louis, Paris, France.

Tobias Gedde-Dahl (T)

Hematology Department, Oslo University Hospital, Rikshospitalet Clinic for Cancer Medicine, Oslo, Norway.

Didier Blaise (D)

Programme de Transplantation & Therapie Cellulaire Centre de Recherche en Cancérologie de Marseille, Marseille, France.

Edouard Forcade (E)

CHU Bordeaux Hôpital Haut-leveque, Pessac, France.

Urpu Salmenniemi (U)

HUCH Comprehensive Cancer Center, Stem Cell Transplantation Unit, Helsinki, Finland.

Anne Huynh (A)

CHU-Institut Universitaire du Cancer Toulouse, Oncopole, Toulouse, France.

Jurjen Versluis (J)

Erasmus MC Cancer Institute University Medical Center, Rotterdam, Netherlands.

Ibrahim Yakoub-Agha (I)

CHU de Lille, INSERM U995, Lille, France.

Hélène Labussière-Wallet (H)

Centre Hospitalier Lyon Sud, Pavillon Marcel Bérard, Lyon, France.

Johan Maertens (J)

Department of Hematology, University Hospital Gasthuisberg, Leuven, Belgium.

Jakob Passweg (J)

University Hospital, Hematology, Basel, Switzerland.

Claude Eric Bulabois (CE)

CHU Grenoble Alpes, Service d`Hématologie, Grenoble, France.

Ludovic Gabellier (L)

Département d`Hématologie Clinique, CHU Lapeyronie, Montpellier, France.

Stephan Mielke (S)

Department of Hematology, Karolinska University Hospital, Stockholm, Sweden.

Cristina Castilla-Llorente (C)

Department of Hematology, Gustave Roussy Cancer Campus BMT Service, Villejuif, France.

Eric Deconinck (E)

Université de Franche-Comté, EFS, INSERM, UMR RIGHT, Besançon, France.
Hématologie, CHU Besançon, Besançon, France.

Eolia Brissot (E)

Hematology Department, AP-HP, Sorbonne Universités, INSERM, Centre de Recherche Saint-Antoine (CRSA), Saint Antoine Hospital, Paris, France.

Arnon Nagler (A)

Hematology Division, Chaim Sheba Medical Center, Tel Hashomer, Ramat Gan, Israel.

Fabio Ciceri (F)

Hematology and Bone Marrow Transplantation Unit, Università Vita Salute San Raffaele, Milan, Italy.

Mohamad Mohty (M)

Hematology Department, AP-HP, Sorbonne Universités, INSERM, Centre de Recherche Saint-Antoine (CRSA), Saint Antoine Hospital, Paris, France.

Classifications MeSH