Granulocyte Colony-Stimulating Factor Is Safe and Well Tolerated following Allogeneic Transplantation in Patients with Sickle Cell Disease.


Journal

Transplantation and cellular therapy
ISSN: 2666-6367
Titre abrégé: Transplant Cell Ther
Pays: United States
ID NLM: 101774629

Informations de publication

Date de publication:
03 2022
Historique:
received: 04 11 2021
revised: 19 12 2021
accepted: 20 12 2021
pubmed: 28 12 2021
medline: 21 4 2022
entrez: 27 12 2021
Statut: ppublish

Résumé

Granulocyte colony-stimulating factor (G-CSF) used after hematopoietic stem cell transplantation (HSCT) can enhance neutrophil recovery in patients rendered neutropenic by the preparative regimen. G-CSF is contraindicated in patients with sickle cell disease (SCD), because life-threatening complications can ensue in the presence of sickle vasculopathy. The safety profile of G-CSF after HSCT for SCD has not been described, however. We report clinical outcomes in the first 100 days post-HSCT in 62 patients supported with G-CSF until neutrophil recovery on a clinical trial of reduced- intensity conditioning HSCT for SCD. The patients received G-CSF for a median of 9 days (range, 5 to 33 days) post-transplantation from the best available stem cell source. Preparation for transplantation included a target hemoglobin S level of ≤45%. Neutrophil engraftment (absolute neutrophil count >0.5 × 10

Identifiants

pubmed: 34958973
pii: S2666-6367(21)01449-4
doi: 10.1016/j.jtct.2021.12.016
pii:
doi:

Substances chimiques

Granulocyte Colony-Stimulating Factor 143011-72-7

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

174.e1-174.e5

Informations de copyright

Copyright © 2021 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Niketa C Shah (NC)

Department of Pediatric Hematology Oncology and Bone Marrow transplant, Yale University, New Haven, Connecticut. Electronic address: Niketa.shah@yale.edu.

Sweta Bhoopatiraju (S)

St. Louis University, St. Louis, Missouri.

Allistair Abraham (A)

Center for Cancer and Blood Disorders, Children's National Hospital, Washington, DC.

Eric Anderson (E)

Division of Hematology Oncology, Rady Children's Hospital, San Diego, California.

Martin Andreansky (M)

Blood and Marrow transplant Program, Baylor College of Medicine, San Antonio, Texas.

Monica Bhatia (M)

Department of Pediatrics, Pediatric Stem Cell Transplant, Irving Medical Center, University of Columbia, New York, New York.

Sonali Chaudhury (S)

Division of Pediatric Hematology Oncology and Stem Cell Transplantation, Lurie Children's Hospital, Northwestern University, Chicago, Illinois.

Geoff D E Cuvelier (GDE)

Manitoba Blood and Marrow Transplant Program, Cancer Care Manitoba, Winnipeg, Manitoba, Canada.

Kamar Godder (K)

Cancer and Blood Disorders Center, Nicklaus Children's Hospital, Miami, Florida.

Michael Grimley (M)

Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital, Cincinnati, Ohio.

Gregory Hale (G)

Cancer and Blood Disorder Institute, All Children's, St. Petersburg, Florida.

Naynesh Kamani (N)

Center for Cancer and Blood Disorders, Children's National Hospital, Washington, DC.

David Jacobsohn (D)

Center for Cancer and Blood Disorders, Children's National Hospital, Washington, DC.

Alexander Ngwube (A)

Center for Cancer and Blood Disorder, Phoenix Children's Hospital, Phoenix, Arizona.

Andrew L Gilman (AL)

ICON, Raleigh, North Carolina.

Jodi Skiles (J)

Department of Pediatric Cancer and Blood Disorders, Riley Children's Hospital, Indianapolis, Indiana.

Lolie C Yu (LC)

Center for Cancer and Blood Disorders, Children's Hospital/LSUHSC, New Orleans, Louisiana.

Shalini Shenoy (S)

Division of Pediatric Hematology Oncology, Washington University, St. Louis, Missouri.

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