Role of allogeneic transplantation in chronic myelomonocytic leukemia: an international collaborative analysis

Author:

Robin Marie1ORCID,de Wreede Liesbeth C.2ORCID,Padron Eric3,Bakunina Katerina4,Fenaux Pierre5,Koster Linda6,Nazha Aziz7,Beelen Dietrich W.8,Rampal Raajit K.9,Sockel Katja10,Komrokji Rami S.3ORCID,Gagelmann Nico11ORCID,Eikema Dirk-Jan4,Radujkovic Aleksandar12,Finke Jürgen13ORCID,Potter Victoria14,Killick Sally B.15,Legrand Faezeh16,Solary Eric17ORCID,Broom Angus18,Garcia-Manero Guillermo19,Rizzoli Vittorio20,Hayden Patrick21,Patnaik Mrinal M.22ORCID,Onida Francesco23,Yakoub-Agha Ibrahim24ORCID,Itzykson Raphael42526ORCID

Affiliation:

1. 1Department of Hematology, Transplantation Division, Hôpital Saint-Louis, Paris, France

2. 2Department of Biomedical Data Sciences, Leiden University Medical Center, Leiden, Netherlands;

3. 3Department of Malignant Hematology, H. Lee Moffitt Cancer Center, Tampa, FL;

4. 4European Bone Marrow Transplantation (EBMT) Statistical Unit, Leiden, Netherlands;

5. 5Department of Hematology and Immunology, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris, Paris, France;

6. 6European Bone Marrow Transplantation (EBMT) Data Office Leiden, Leiden, Netherlands;

7. 7Cleveland Clinic, Avon Lake, OH;

8. 8Department of Bone Marrow Transplantation, University Hospital Essen, Essen, Germany;

9. 9Leukemia Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY;

10. 10Division of Hematology, Medical Clinic and Policlinic I, University Hospital Dresden, Technical University (TU) Dresden, Dresden, Germany;

11. 11Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany;

12. 12Department of Internal Medicine V, University Clinic Heidelberg, Heidelberg, Germany;

13. 13Department of Medicine-Hematology, Oncology, Freiburg University Hospital and Medical Faculty, Freiburg, Germany;

14. 14King's College Hospital National Health Service (NHS) Foundation Trust, London, United Kingdom;

15. 15The Royal Bournemouth and Christchurch Hospitals National Health Service (NHS) Foundation Trust, Bournemouth, United Kingdom;

16. 16Programme de Transplantation & Therapie Cellulaire, Centre de Recherche en Cancérologie de Marseille, Institut Paoli Calmettes, Marseille, France;

17. 17INSERM U1287, Université Paris-Saclay, Gustave Roussy Cancer Center, Villejuif, France;

18. 18Western General Hospital, Edinburg, United Kingdom;

19. 19Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX;

20. 20Department of Hematology, U.O. Ematologia Centro Trapianti Midollo Osseo (CTMO) of Hematology, Parma, Italy;

21. 21Department of Hematology, Trinity College Dublin, St. James's Hospital, Dublin, Ireland;

22. 22Division of Hematology, Mayo Clinic, Rochester, MN;

23. 23Bone Marrow Transplantation (BMT) Center - Hematology Unit, Istituto di ricovero e cura a carattere scientifico (IRCCS) Ospedale Maggiore Policlinico Di Milano-University of Milan, Milano, Italy;

24. 24INSERM U1286, Centre Hospitalo-Universitaire (CHU) de Lille, Univ. Lille, Infinite, Lille, France; and

25. 25Génomes, biologie cellulaire et thérapeutique U944, Université Paris Cité, INSERM, Centre National de la Recherche Scientifique (CNRS), Paris, France

26. 26Service Hématologie Adultes, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris, Paris France

Abstract

Abstract To determine the survival benefit of allogeneic hematopoietic cell transplantation (allo-HCT) in chronic myelomonocytic leukemias (CMML), we assembled a retrospective cohort of CMML patients 18-70 years old diagnosed between 2000 and 2014 from an international CMML dataset (n = 730) and the EBMT registry (n = 384). The prognostic impact of allo-HCT was analyzed through univariable and multivariable time-dependent models and with a multistate model, accounting for age, sex, CMML prognostic scoring system (low or intermediate-1 grouped as lower-risk, intermediate-2 or high as higher-risk) at diagnosis, and AML transformation. In univariable analysis, lower-risk CMMLs had a 5-year overall survival (OS) of 20% with allo-HCT vs 42% without allo-HCT (P < .001). In higher-risk patients, 5-year OS was 27% with allo-HCT vs 15% without allo-HCT (P = .13). With multistate models, performing allo-HCT before AML transformation reduced OS in patients with lower-risk CMML, and a survival benefit was predicted for men with higher-risk CMML. In a multivariable analysis of lower-risk patients, performing allo-HCT before transformation to AML significantly increased the risk of death within 2 years of transplantation (hazard ratio [HR], 3.19; P < .001), with no significant change in long-term survival beyond this time point (HR, 0.98; P = .92). In higher-risk patients, allo-HCT significantly increased the risk of death in the first 2 years after transplant (HR 1.46; P = .01) but not beyond (HR, 0.60; P = .09). Performing allo-HCT before AML transformation decreases life expectancy in lower-risk patients but may be considered in higher-risk patients.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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