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Allogeneic Hematopoietic Stem Cell Transplantation for Adults with Sickle Cell Disease

Overview
Journal J Clin Med
Specialty General Medicine
Date 2019 Oct 5
PMID 31581479
Citations 4
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Abstract

Sickle cell disease (SCD) is an inherited red blood cell disorder that leads to substantial morbidity and early mortality. Acute and chronic SCD-related complications increase with older age, and therapies are urgently needed to treat adults. Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative therapy, but has been used less frequently in adults compared to children. This is, in part, due to (1) greater chronic organ damage, limiting tolerability to myeloablative conditioning regimens, (2) a higher rate of HSCT-related complications in adults versus children with SCD, and (3) limited coverage by public and private health insurance. Newer approaches using nonmyeloablative and reduced-intensity conditioning HSCT regimens have demonstrated better safety and tolerability, with high rates of stable engraftment in SCD adults. This review will focus on the impacts of HSCT, using more contemporary approaches to SCD-related complications in adults.

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References
1.
Gladwin M, Sachdev V, Jison M, Shizukuda Y, Plehn J, Minter K . Pulmonary hypertension as a risk factor for death in patients with sickle cell disease. N Engl J Med. 2004; 350(9):886-95. DOI: 10.1056/NEJMoa035477. View

2.
Desai A, Lei Z, Bahroos N, Maienschein-Cline M, Saraf S, Zhang X . Association of circulating transcriptomic profiles with mortality in sickle cell disease. Blood. 2017; 129(22):3009-3016. PMC: 5454338. DOI: 10.1182/blood-2016-11-752279. View

3.
Fitzhugh C, Hsieh M, Taylor T, Coles W, Roskom K, Wilson D . Cyclophosphamide improves engraftment in patients with SCD and severe organ damage who undergo haploidentical PBSCT. Blood Adv. 2018; 1(11):652-661. PMC: 5727815. DOI: 10.1182/bloodadvances.2016002972. View

4.
Van Besien K, Bartholomew A, Stock W, Peace D, Devine S, Sher D . Fludarabine-based conditioning for allogeneic transplantation in adults with sickle cell disease. Bone Marrow Transplant. 2000; 26(4):445-9. DOI: 10.1038/sj.bmt.1702518. View

5.
Walters M, Patience M, Leisenring W, Eckman J, Buchanan G, Rogers Z . Barriers to bone marrow transplantation for sickle cell anemia. Biol Blood Marrow Transplant. 1996; 2(2):100-4. View