-Author name in bold denotes the presenting author
-Asterisk * with author name denotes a Non-ASH member
Clinically Relevant Abstract denotes an abstract that is clinically relevant.

PhD Trainee denotes that this is a recommended PHD Trainee Session.

Ticketed Session denotes that this is a ticketed session.

1908 CloB2A2 Reduced-Intensity Conditioning (RIC) Regimen Prior to Allogeneic Stem Cell Transplantation Provides Significant Better Survival Compared to FB2A2 RIC Regimen in Adults with Acute Myeloid Leukemia (AML): A Study on Behalf of the SFGM-TC

Clinical Allogeneic Transplantation: Conditioning Regimens, Engraftment and Acute Transplant Toxicities
Program: Oral and Poster Abstracts
Session: 721. Clinical Allogeneic Transplantation: Conditioning Regimens, Engraftment and Acute Transplant Toxicities: Poster I
Saturday, December 5, 2015, 5:30 PM-7:30 PM
Hall A, Level 2 (Orange County Convention Center)

Patrice Chevallier, MD, PhD1*, Myriam Labopin, MD2*, Regis Peffault de la Tour, MD, PhD3*, Bruno Lioure, MD4*, Jean-Yves Cahn5, Anne Huynh, MD6*, Didier Blaise, MD, PhD7, Pascal Turlure, MD8*, Eric Deconinck9, Natacha Maillard, MD10*, Ibrahim Yakoub-Agha, MD, PhD11, Gaelle Guillerm, MD12*, Nathalie Fegueux, MD13*, Nathalie Contentin, MD14*, Jacques-Olivier Bay, MD, PhD15, Florence Beckerich, MD16*, Jean-Henri Bourhis, MD, PhD17, Marie Y. Detrait, MD18, Stephane Vigouroux19*, Sylvie François, MD20*, Faezeh Legrand, MD21*, Nicole Raus22*, Thierry Guillaume, MD, PhD1* and Mohamad Mohty, MD, PhD23

1Department of Hematology, Nantes University Hospital, Nantes, France
2Department of Hematology and Cell Therapy, Saint Antoine Hospital, Paris, France
3Department of Hematology, Saint Louis Hospital, Paris, France
4Department of Hematology and Oncology, CHU Hautepierre, Strasbourg, France
5Clinique Universitaire d'Hématologie, Grenoble University Hospital, Grenoble, France
6institut universitaire du cancer, Oncopole, TOULOUSE, France
7Programme de Transplantation et Therapie Cellulaire, Institut Paoli Calmettes, Marseille, France
8Hematology Department, CHU Limoges, Limoges, France
9Hematology, INSERM UMR1098 - CHU Jean Minjoz, Besancon, France
10Bone Marrow Transplant Unit Clinical Hematology, Hopital La Miletrie, Poitiers, France
11Hematology, CHU de Lille, Lille, France
12Department of Hematology and Oncology, CH Augustin Morvan, Brest, France
13Department of Hematology, CHU Lapeyronie, Montpellier, France
14Department of Hematology, Centre Henri Becquerel, Rouen, France
15Department of Hematology, Service d'Hematologie Clinique et de Therapie Cellulaire, CHU, Universite d'Auvergne, EA7283, CIC501, Clermont-Ferrand, Clermont-Ferrand, France
16Department of Hematology, CHU Henri Mondor, Creteil, France
17Division of Hematology, Institut Gustave Roussy, Villejuif, France
18Hematology, Hopital Edouard Herriot, HCL, Universite Lyon 1, Lyon, France
19Service d’Hematologie Clinique et Therapie Cellulaire, CHU de Bordeaux, Pessac, France
20CHU Angers, Angers, France
21CHU, Nice, France
22CH Lyon Sud-SFGM-TC, Lyon, France
23Service d’Hématologie et Thérapie Cellulaire, Hôpital Saint-Antoine, Paris, France

Purpose: The FB2A2 (fludarabine, intermediate doses of busulfan and ATG) reduced-intensity conditioning (RIC) regimen is considered as a standard RIC regimen in many centers worldwide. Recently, we have reported the prospective good results of a clofarabine-busulfan containing RIC regimen (CloB2A2) in adults with high-risk acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) in complete remission (CR) at time of transplant (Chevallier et al, Haematologica, 2014). Thus, this regimen may prove to be superior to the FB2A2 regimen in patients with AML/MDS.

Patients and Methods:

The aim of this study was to compare outcomes between adult AML/MDS patients who have received, between 2009 and 2015, in 26 French centers, either a FB2A2 RIC regimen (n=170, male 61%, median age: 58 years, AML 86%, CR1 79%) or the CloB2A2 RIC regimen (n=39, including the 16 cases treated within the prospective trial mentioned above, male 62%, median age: 61 years, AML 62%, CR1 64%). The FB2A2  and CloB2A2 regimens consisted of either 30 mg/m²/day Fludarabine for 5 days or 30mg/m²/day Clofarabine for 4 or 5 days, each combined with 3.2 mg/kg/day Busulfan for 2 days and 2.5 mg/kg/day Anti-thymocyte globulin (ATG, Thymoglobuline) for 2 days.  As GVHD prophylaxis, cyclosporine (CsA) alone was used in case of related donor in both groups, and for the 16 CloB2A2 patients treated within the prospective trial, while CsA+ MMF were used in case of unrelated donors. The two groups were not statistically different in term of gender, median age and performans status at transplant, median white blood count at diagnosis, median time between diagnosis and transplant, type of donors or cytogenetics for AML patients. Conversely, there were more AML patients (86% vs 62%, p=0.0004) and more patients in CR1 (79% vs 64%, p=0.04) in the FB2A2 group. Also, CloB2A2 patients were transplanted more recently (median year of transplant: 2014 vs 2011, p<0.0001).

Results: All patients engrafted, except one in the FB2A2 group. Median time of neutrophils recovery was similar between both groups (FB2A2: 17 days vs CloB2A2: 18 days, p=0.10). With a median follow-up of 28 and 14 months in the FB2A2 and the CloB2A2 groups, respectively, 2-year overall survival (OS) were 59% (51.4-66.7) for the former vs 77% (62.8-91.1) for the latter, p=0.07, 2-year leukemia-free survival (LFS) were 52.7% (44.9-60.4) vs 64% (48.1-79.9), p=0.23, 2-year relapse incidence were 31.1% (24.2-38.4) vs 27.5% (14-42.9), p=0.58, 2-year non relapse mortality were 16.2% (5.8-31.3) vs 8.5% (2.1-20.7), p=0.26 and 2-year chronic GVHD were 13.8% (8.3-20.5) vs 23.9% (8.1-44.2), p=0.12. Incidences of grade 2-4 or grade 3-4 acute GVHD were similar between both groups: FB2A2 22% vs CloB2A2 23%, p=0.86, and 8% vs 3%, p=0.31. In multivariate analysis, FB2A2 RIC regimen was significantly associated with lower OS and LFS (HR: 2.45; 95%CI: 1.08-5.55, p=0.03; and HR: 2.32; 95%CI: 1.12-4.79, p=0.02) contrary to CR1 status which was associated with significant higher survivals (HR: 0.48; 95%CI: 0.28-0.83, p=0.008 and HR: 0.42; 95%CI: 0.25-0.70, p=0.001). MDS (HR: 1.88; 95%CI: 1.03-3.43, p=0.03) and higher WBC at diagnosis (>median) (HR: 1.76; 95%CI: 1.10-2.82, p=0.01) were also significantly associated with lower LFS. However, when considering AML and MDS patients separately, benefit of CLOB2A2 RIC regimen appears to be restricted to AML patients (2-year OS FB2A2: 58.1% vs CloB2A2: 80.2%; HR: 2.45; 95%CI: 1.08-5.55, p=0.03; and 2-year LFS FB2A2: 53.6%, vs CloB2A2: 76.9%; HR: 2.32; 95%CI: 1.12-4.79, p=0.02).

Conclusion: This retrospective comparison suggests that the CloB2A2 RIC regimen can likely provide a higher survival compared to the use of a FB2A2 RIC regimen for AML patients. A prospective phase 3 randomized study is warranted.

Disclosures: Deconinck: JANSSEN: Other: Travel for international congress ; NOVARTIS: Other: Travel for international congress ; ALEXION: Other: Travel for international congress ; ROCHE: Research Funding ; PFIZER: Research Funding ; CHUGAI: Other: Travel for international congress ; LFB loboratory: Consultancy . Mohty: Janssen: Honoraria ; Celgene: Honoraria .

*signifies non-member of ASH