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1047 Alternative Donor Transplantation for Severe Aplastic Anemia: A Comparative Study of the Saawp EBMTClinically Relevant Abstract

Program: Oral and Poster Abstracts
Type: Oral
Session: 732. Allogeneic Transplantation: Disease Response and Comparative Treatment Studies: Donor and Conditioning Regimen Selection
Hematology Disease Topics & Pathways:
Research, adult, Bone Marrow Failure Syndromes, Clinical Research, Aplastic Anemia, Diseases, Therapies, registries, young adult , Study Population, Human
Monday, December 11, 2023: 5:00 PM

Juan Montoro1*, Dirk-Jan Eikema Sr.2*, Joe Tuffnell Sr.3*, Victoria Potter4*, Krzysztof Kalwak Sr.5*, Stijn Halkes Sr.6*, Aleksandr Kulagin Sr.7*, Matthew P. Collin Sr., MD, PhD8, Robert Wynn Sr.9*, Stephen Robinson Jr.10*, Emma Nicholson Sr.11*, Henrik Sengeloev12*, Jennifer Clay Sr., MD, PhD13*, Khaled Halahleh Sr., MD14*, Elena Skorobogatova Sr.15*, Jakob Passweg Sr.16*, Stephan Mielke, MD17, Samppa Ryhanen Sr., MD, PhD18, Ben Carpenter, MD, PhD19*, Tobias Gedde-Dahl, MD20*, Eleni Tholouli, MD21*, Renato Fanin, MD22*, Philippe Lewalle Sr., MD23*, Austin Kulasekararaj, MD, MBBS, FRCPath, MRCP24, Antonio M Risitano, MD, PhD25 and Regis Peffault De Latour26*

1Hematology Department, Hospital La Fe, Valencia, Spain
2EBMT Statistical Unit, Leiden, Netherlands
3EBMT Statisitcal Unit, Leiden, Netherlands
4Department of Haematological Medicine, King's College Hospital NHS, London, United Kingdom
5Fundacja "Na Ratunek Dzieciom z Choroba Nowotworowa", Wroclaw, Poland
6Leiden University Hospital, Leiden, Netherlands
7b. First State Pavlov Medical University of St. Petersburg, Raisa Gorbacheva Memorial Research Institute for Paediatric Oncology, Hematology, and Transplantation, St-Petersburg, Russia, St. Petersburg, RUS
8Northern Centre for Bone Marrow Transplantation, Newcastle University, Newcastle Upon Tyne, GBR
9Royal Manchester Children's Hospital, MANCHESTER, United Kingdom
10University Hospitals Bristol, Bristol, GBR
11Royal Marsden Hospital, LONDON, United Kingdom
12Rigshospitalet, Copenhagen, Denmark
13Yorkshire Blood & Marrow Transplant Program, Leeds, United Kingdom
14King Hussein Cancer Centre Adult BMT Program, AMMAN, Jordan
15The Russian Federationn Children's Research Hospital, MOSCOW, Russian Federation
16University Hospital | Basel, Basel, Switzerland
17Department of Cellular Therapy and Allogeneic Stem Cell Transplantation, Karolinska Institute & University Hospital, Stockholm, Stockholms Laen, Sweden
18Hospital For Children and Adolescent, Helsinki University Central Hospital, Helsinki, FIN
19University College London Hospitals NHS Foundation Trust, London, United Kingdom
20Oslo University Hospital, Rikshospitalet, Clinic for Cancer Medicine, Hematology Department, Section for Stem Cell Transplantation, Oslo, Norway
21Manchester Royal Infirmary, Clinical Haematology Department, Manchester, United Kingdom
22Hematology, Azienda Sanitaria Universitaria Integrata di Udine, Udine, Italy
23Hôpital Universitaire de Bruxelles (HUB), Institut Jules Bordet, Hematology Department, Brussels, BEL
24Department of Haematological Medicine, King's College Hospital, London, United Kingdom
25University of Naples, Avellino, Italy
26Hôpital Saint-Louis,, Paris, France

Alternative donor transplantation for severe aplastic anemia: a comparative study of the SAAWP EBMT

INTRODUCTION

Allogeneic stem cell transplantation (allo-SCT) from an HLA-matched sibling donor (MSD) is considered the standard of care for younger patients with severe aplastic anemia (SAA). For patients lacking a suitable MSD, matched unrelated donors (MUD) have increasingly been used for SAA patients who do not respond to immunosuppressive therapy. However, a significant number of SAA patients who require allo-SCT are unable to access a fully HLA-matched unrelated donor or experience delays in finding one. In such cases, other alternative options, such as mismatched unrelated donors (MMUD), and haploidentical family donors (Haplo), have been explored.

Limited research exists on MUD, MMUD, and Haplo allo-SCT efficacy and safety in SAA. Drawing definitive conclusions for the optimal alternative donor transplant approach remains challenging.

This study compares the outcomes of allo-SCT from MUD, MMUD, and Haplo donors in patients with SAA from the SAAWP EBMT.

PATIENTS AND METHODS

Inclusion criteria

All patients diagnosed with SAA who underwent their first allo-SCT between January 2012 and December 2021 from either a MUD, MMUD or Haplo, were included. Only transplants from Haplo donors who received post-transplant cyclophosphamide (PTCy) as prophylaxis for graft-versus-host disease (GVHD) were considered.

Statistical Analysis

The study utilized statistical methods such as Kaplan-Meier estimation, Log-Rank test, competing risks analysis, and Cox proportional hazards regression. The analyses included OS, EFS, GRFS, NRM, aGVHD, cGVHD, and graft failure. The statistical software R and relevant packages were used.

RESULTS

Patient and Transplantation Characteristics

Table 1 summarizes patient and transplant characteristics for the 1652 participants.

Engraftment

Neutrophil recovery at 28 days was 85% (95% CI; 83–87) for MUD, 84% (95% CI; 80–88) for MMUD, and 75% (95% CI; 69–81) for Haplo (p = 0.033). Platelet engraftment at 100 days was 88% (95% CI; 86–91) for MUD, 82% (95% CI; 78–87) for MMUD and 72% (95% CI; 65–78) for Haplo (p < 0.001).

Graft failure

The 1-year cumulative incidence of primary graft failure (PGF) for the MUD, MMUD, and Haplo cohorts was 4% (95% CI; 3–6%), 5% (95% CI; 3–8%) and 16% (95% CI; 11–21%), respectively (p < 0.001). In multivariable analysis, compared with MUD, Haplo (HR, 3.72; 95% CI, 1.97-7.03; p<0.001) was associated with a higher PGF. Other predictors for a higher PGF are shown in Table 2.

GVHD

The cumulative incidence of aGVHD grades II–IV at 100 days for the MUD, MMUD, and Haplo cohorts was 13% (95% CI; 11–15), 22% (95% CI; 17–26), and 18% (95% CI; 13–24), respectively (p < 0.001). In multivariable analysis, MMUD was associated with an increased risk of aGVHD grades II–IV, when compared with MUD (HR 1.97; 95% CI, 1.4–2.77; p < 0.001). Other predictors associated with a higher risk of aGVHD grades II–IV are shown in Table 2.

The 3-year cumulative incidence of cGVHD for the MUD, MMUD, and Haplo cohorts was 18% (95% CI; 15–20), 19% (95% CI; 14–24), and 18% (95% CI; 11–24), respectively (p = 0.9).

NRM

The 3-year cumulative incidence of NRM was 12% (95% CI; 10–14) for MUD, 17% (95% CI; 13–22) for MMUD, and 22% (95% CI; 15–28) for Haplo (p < 0.001).

Survival

The 3-year EFS for the MUD, MMUD, and Haplo cohorts was 73% (95% CI; 71–76), 64% (95% CI; 59–70), and 53% (95% CI; 46–61), respectively (p < 0.001), whereas OS was 81% (95% CI; 79–84), 74% (95% CI; 69–79), and 63% (95% CI; 54–71), respectively (p < 0.001). In multivariable analysis, compared to MUD, MMUD (HR, 1.54; 95% CI, 1.12-2.11; p = 0.007) and Haplo (HR, 1.97; 95% CI, 1.35-2.86; p<0.001) were associated with worse survival. Other predictors for a worse OS are shown in Table 2.

The 3-year GRFS for the MUD, MMUD, and Haplo cohorts was 71% (95% CI; 68–74), 66% (95% CI; 60–72), and 53% (95% CI; 44–61), respectively (p < 0.001). In multivariable analysis, compared with MUD, MMUD (HR, 1.42; 95% CI, 1.1-1.82; p = 0.006) and Haplo (HR, 1.71; 95% CI, 1.27-2.31; p<0.001) were associated with worse GRFS. Other factors associated with a worse GRFS are shown in Table 2.

CONCLUSION

In conclusion, our study supports MUD transplantation as the preferred option for SAA patients without a MSD. While MMUD and Haplo transplants are feasible, MMUD appears more favorable than Haplo, even in the era of PTCy.

Disclosures: Mielke: SWECARNET: Other: Founder/Leadership (via my institution) ; ScientifyResearch: Other: Founder (spouse) ; Immunicum/Mendes, Miltenyi: Other: Participation on a Data Safety Monitoring Board or Advisory Board; Celgene/BMS, Novartis, Janssen, Gilead/KITE, JSMO, Pfizer: Speakers Bureau. Carpenter: Vertex Pharmaceuticals: Membership on an entity's Board of Directors or advisory committees; Novartis: Membership on an entity's Board of Directors or advisory committees; BlueBird Bio: Membership on an entity's Board of Directors or advisory committees. Kulasekararaj: F. Hoffmann-La Roche Ltd: Consultancy, Membership on an entity's Board of Directors or advisory committees; Amgen: Honoraria, Membership on an entity's Board of Directors or advisory committees; Samsung: Consultancy; Novartis: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; Achillion: Consultancy; Alexion, AstraZeneca Rare Disease: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; Celgene/BMS: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; Akari Therapeutics: Consultancy; BioCryst: Consultancy. Risitano: Novartis: Consultancy, Honoraria; F. Hoffmann-La Roche Ltd: Consultancy, Honoraria, Research Funding; Alexion, AstraZeneca Rare Disease: Consultancy, Honoraria, Research Funding. Peffault De Latour: Jazz Pharmaceuticals: Honoraria.

*signifies non-member of ASH