Allogeneic Hematopoietic Cell Transplantation for the Treatment of Severe Aplastic Anemia: Evidence-Based Guidelines From the American Society for Transplantation and Cellular Therapy

Allogeneic hematopoietic cell transplantation (HCT) is a potentially curative treatment for severe aplastic anemia (SAA). Existing guidance about HCT in SAA is primarily derived from expert reviews, registry data and societal guidelines; however, transplant-specific guidelines for SAA are lacking. A panel of SAA experts, both pediatric and adult transplant physicians, developed consensus recommendations using Grading of Recommendation, Assessment, Development, and Evaluation (GRADE) methodology employing a GRADE guideline development tool. The panel agrees with previous recommendations for the preferential use of bone marrow as a graft source and the use of rabbit over horse antithymocyte globulin (ATG) for HCT conditioning. Fludarabine containing regimens are preferred for patients at high risk of graft failure and those receiving matched unrelated or haploidentical donor transplant. Given advancements in HCT, the panel does not endorse the historical 40-year age cut-off for considering upfront HCT in adults, acknowledging that fit older patients may also benefit from HCT. The panel also endorses increased utilization of HCT by prioritizing matched unrelated or haploidentical donor HCT over immunosuppressive therapy in children and adults who lack a matched related donor. Finally, the panel suggests either calcineurin inhibitor plus methotrexate or post-transplant cyclophosphamide-based graft-versus-host disease (GVHD) prophylaxis for matched related or matched unrelated donor recipients. These recommendations reflect a significant advancement in transplant strategies for SAA and highlight the importance of ongoing and further research to revisit current evidence in terms of donor choice, conditioning chemotherapy, GVHD prophylaxis and post-transplant immunosuppression.

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Publication Details

Journal
Transplantation and Cellular Therapy
Published
2024-09-20
DOI
https://doi.org/10.1016/j.jtct.2024.09.017
Citations
18
Primary Topic
Hematopoietic Stem Cell Transplantation
Type
article
Field-Weighted Citation Impact
8.18
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article

Allogeneic Hematopoietic Cell Transplantation for the Treatment of Severe Aplastic Anemia: Evidence-Based Guidelines From the American Society for Transplantation and Cellular Therapy

Michael A. Pulsipher, Mehdi Hamadani, Mohamed A. Kharfan‐Dabaja, Paul A. Carpenter et al.
18 citations
Transplantation and Cellular Therapy
Hematopoietic Stem Cell Transplantation
8.18
article

Allogeneic Hematopoietic Cell Transplantation for the Treatment of Severe Aplastic Anemia: Evidence-Based Guidelines From the American Society for Transplantation and Cellular Therapy

Michael A. Pulsipher, Mehdi Hamadani, Mohamed A. Kharfan‐Dabaja, Paul A. Carpenter, Amy Elizabeth Dezern, Sally Arai, Adetola A. Kassim, Blachy J. Dávila Saldaña, Joseph H. Antin, Nelli Bejanyan, Lauri M. Burroughs, Raheel Iftikhar, Zachariah DeFilipp, R. Nakamura, Mahmoud Aljurf
article en
18 citations

Abstract

Allogeneic hematopoietic cell transplantation (HCT) is a potentially curative treatment for severe aplastic anemia (SAA). Existing guidance about HCT in SAA is primarily derived from expert reviews, registry data and societal guidelines; however, transplant-specific guidelines for SAA are lacking. A panel of SAA experts, both pediatric and adult transplant physicians, developed consensus recommendations using Grading of Recommendation, Assessment, Development, and Evaluation (GRADE) methodology employing a GRADE guideline development tool. The panel agrees with previous recommendations for the preferential use of bone marrow as a graft source and the use of rabbit over horse antithymocyte globulin (ATG) for HCT conditioning. Fludarabine containing regimens are preferred for patients at high risk of graft failure and those receiving matched unrelated or haploidentical donor transplant. Given advancements in HCT, the panel does not endorse the historical 40-year age cut-off for considering upfront HCT in adults, acknowledging that fit older patients may also benefit from HCT. The panel also endorses increased utilization of HCT by prioritizing matched unrelated or haploidentical donor HCT over immunosuppressive therapy in children and adults who lack a matched related donor. Finally, the panel suggests either calcineurin inhibitor plus methotrexate or post-transplant cyclophosphamide-based graft-versus-host disease (GVHD) prophylaxis for matched related or matched unrelated donor recipients. These recommendations reflect a significant advancement in transplant strategies for SAA and highlight the importance of ongoing and further research to revisit current evidence in terms of donor choice, conditioning chemotherapy, GVHD prophylaxis and post-transplant immunosuppression.

Transplantation and Cellular TherapyVol. 30(12)
Brigham and Women's Hospital (US), Primary Children's Hospital (US), Children's National (US), Johns Hopkins University (US), Vanderbilt University (US), Medical College of Wisconsin (US), Armed Forces Institute of Pathology (PK), King Faisal Specialist Hospital & Research Centre (SA), Huntsman Cancer Institute (US), Moffitt Cancer Center (US), Massachusetts General Hospital (US), Fred Hutch Cancer Center (US), City of Hope (US), Center for Cancer and Blood Disorders (US), Dana-Farber Cancer Institute (US), Tennessee Oncology (US), Stanford Medicine (US), Mayo Clinic in Florida (US), National University of Medical Sciences (PK), Dana-Farber Brigham Cancer Center (US), Vanderbilt Health (US), Sidney Kimmel Comprehensive Cancer Center (US), Stanford University (US)
Good health and well-being
Openalex Percentile: Top 2%
Hematopoietic Stem Cell Transplantation
8.18
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