Treatment, risk factors, and outcome of adults with relapsed AML after reduced intensity conditioning for allogeneic stem cell transplantation

Author:

Schmid Christoph1,Labopin Myriam2,Nagler Arnon3,Niederwieser Dietger4,Castagna Luca5,Tabrizi Reza6,Stadler Michael7,Kuball Jürgen8,Cornelissen Jan9,Vorlicek Jiri10,Socié Gerard11,Falda Michele12,Vindeløv Lars13,Ljungman Per14,Jackson Graham15,Kröger Nicolaus16,Rank Andreas1,Polge Emmanuelle2,Rocha Vanderson11,Mohty Mohamad17,

Affiliation:

1. Klinikum Augsburg, University of Munich, Munich, Germany;

2. EBMT Study Office, Faculté de Medicines St Antoine, Paris, France;

3. Chaim Sheba Medical Center, Tel-Hashomer, Israel;

4. University Hospital, Leipzig, Germany;

5. Institute Paoli Calmettes, Marseilles, France;

6. Centre Hospitalier Universitaire, Bordeaux, France;

7. Michael Stadler Medizinische Hochschule, Hannover, Germany;

8. University Medical Center, Utrecht, The Netherlands;

9. Erasmus MC–Daniel den Hoed Cancer Centre, Rotterdam, The Netherlands;

10. University Hospital, Brno, Czech Republik;

11. Hôpital St Louis, Paris, France;

12. Azienda Ospedaliera S. Giovanni, Torino, Italy;

13. Rigshospitalet, Copenhagen, Denmark;

14. Huddinge University Hospital, Huddinge, Sweden;

15. Royal Victoria Infirmary, New Castle, United Kingdom;

16. University Hospital Eppendorf, Hamburg, Germany; and

17. Hôtel Dieu, University of Nantes, Nantes, France

Abstract

Abstract Because information on management and outcome of AML relapse after allogeneic hematopoietic stem cell transplantation (HSCT) with reduced intensity conditioning (RIC) is scarce, a retrospective registry study was performed by the Acute Leukemia Working Party of EBMT. Among 2815 RIC transplants performed for AML in complete remission (CR) between 1999 and 2008, cumulative incidence of relapse was 32% ± 1%. Relapsed patients (263) were included into a detailed analysis of risk factors for overall survival (OS) and building of a prognostic score. CR was reinduced in 32%; remission duration after transplantation was the only prognostic factor for response (P = .003). Estimated 2-year OS from relapse was 14%, thereby resembling results of AML relapse after standard conditioning. Among variables available at the time of relapse, remission after HSCT > 5 months (hazard ratio [HR] = 0.50, 95% confidence interval [CI], 0.37-0.67, P < .001), bone marrow blasts less than 27% (HR = 0.53, 95% CI, 0.40-0.72, P < .001), and absence of acute GVHD after HSCT (HR = 0.67, 95% CI, 0.49-0.93, P = .017) were associated with better OS. Based on these factors, 3 prognostic groups could be discriminated, showing OS of 32% ± 7%, 19% ± 4%, and 4% ± 2% at 2 years (P < .0001). Long-term survival was achieved almost exclusively after successful induction of CR by cytoreductive therapy, followed either by donor lymphocyte infusion or second HSCT for consolidation.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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