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

Author:

Loke Justin12,Labopin Myriam34,Craddock Charles56,Socié Gérard7,Gedde‐Dahl Tobias8,Blaise Didier9,Forcade Edouard10,Salmenniemi Urpu11,Huynh Anne12,Versluis Jurjen13,Yakoub‐Agha Ibrahim14,Labussière‐Wallet Hélène15,Maertens Johan16,Passweg Jakob17,Bulabois Claude Eric18,Gabellier Ludovic19,Mielke Stephan20,Castilla‐Llorente Cristina21,Deconinck Eric2223,Brissot Eolia4,Nagler Arnon24,Ciceri Fabio25,Mohty Mohamad4

Affiliation:

1. University of Birmingham Birmingham UK

2. Dana‐Farber Cancer Institute Boston Massachusetts USA

3. Acute Leukaemia Working Party Paris Study Office European Society for Blood and Marrow Transplantation Paris France

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

5. Birmingham Centre for Cellular Therapy and Transplantation Centre for Clinical Haematology Queen Elizabeth Hospital Birmingham UK

6. University of Warwick Warwick UK

7. Department of Hematology‐BMT Hopital St. Louis Paris France

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

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

10. CHU Bordeaux Hôpital Haut‐leveque Pessac France

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

12. CHU‐Institut Universitaire du Cancer Toulouse Oncopole Toulouse France

13. Erasmus MC Cancer Institute University Medical Center Rotterdam Netherlands

14. CHU de Lille INSERM U995 Lille France

15. Centre Hospitalier Lyon Sud Pavillon Marcel Bérard Lyon France

16. Department of Hematology University Hospital Gasthuisberg Leuven Belgium

17. University Hospital Hematology Basel Switzerland

18. CHU Grenoble Alpes Service d`Hématologie Grenoble France

19. Département d`Hématologie Clinique CHU Lapeyronie Montpellier France

20. Department of Hematology Karolinska University Hospital Stockholm Sweden

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

22. Université de Franche‐Comté EFS INSERM UMR RIGHT Besançon France

23. Hématologie CHU Besançon Besançon France

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

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

Abstract

AbstractIntroductionFor 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.MethodsThis 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.ResultsA 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.ConclusionInitial response to chemotherapy as determined by number of courses to attain CR, retained prognostic relevance even following SCT in CR.

Publisher

Wiley

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