Timing of Alemtuzumab With Respect to Day of Bone Marrow Infusion and its Effects Upon Engraftment and Graft-Versus-Host Disease in Patients With Sickle Cell Disease: A Single-Institutional Study. Issue 8 (November 2020)
- Record Type:
- Journal Article
- Title:
- Timing of Alemtuzumab With Respect to Day of Bone Marrow Infusion and its Effects Upon Engraftment and Graft-Versus-Host Disease in Patients With Sickle Cell Disease: A Single-Institutional Study. Issue 8 (November 2020)
- Main Title:
- Timing of Alemtuzumab With Respect to Day of Bone Marrow Infusion and its Effects Upon Engraftment and Graft-Versus-Host Disease in Patients With Sickle Cell Disease
- Authors:
- Sahdev, Indira
Brochstein, Joel
Werther, Nan
Stiles, Jessica - Abstract:
- Abstract : The possible impact of "late" alemtuzumab (administered on days −10 to −8) versus "early" alemtuzumab (−19 to −17) with respect to engraftment and acute/chronic graft-versus-host disease (GvHD) in a group of 25 pediatric patients with sickle cell disease undergoing bone marrow transplantation following conditioning with alemtuzumab, fludarabine, and melphalan is reported. The first 9 patients received "late" alemtuzumab followed by bone marrow transplantation from HLA-matched sibling donors. The next 16 patients undergoing matched sibling transplants received "early" alemtuzumab. In the "late" group, 1 patient (11%) developed acute GvHD. Six patients (67%) achieved sustained engraftment. Three patients (33%) experienced graft rejection, leading to termination of enrollment of patients on this regimen. In the "early" alemtuzumab group, acute and chronic GvHD developed in 43% and 25% patients, respectively. None of the patients experienced graft rejection in this group of patients. Three patients developed stable mixed chimerism and 13 patients demonstrated 100% donor chimerism at 1 year post-transplant and beyond. These results suggest a benefit with respect to engraftment of administering "early" versus "late" alemtuzumab in this reduced-intensity conditioning regimen, however, with the possible cost of an increase in acute, and possibly chronic GvHD.
- Is Part Of:
- Journal of pediatric hematology/oncology. Volume 42:Issue 8(2020)
- Journal:
- Journal of pediatric hematology/oncology
- Issue:
- Volume 42:Issue 8(2020)
- Issue Display:
- Volume 42, Issue 8 (2020)
- Year:
- 2020
- Volume:
- 42
- Issue:
- 8
- Issue Sort Value:
- 2020-0042-0008-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-11
- Subjects:
- sickle cell disease -- alemtuzumab -- reduced-intensity conditioning -- hematopoietic stem cell transplantation -- graft failure -- graft-versus-host disease
Pediatric hematology -- Periodicals
Tumors in children -- Periodicals
618.9215 - Journal URLs:
- http://journals.lww.com/jpho-online/pages/default.aspx ↗
http://gateway.tx.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=00043426-000000000-00000 ↗
http://www.jpho-online.com/ ↗
http://journals.lww.com/jpho-online/pages/default.aspx ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/MPH.0000000000001930 ↗
- Languages:
- English
- ISSNs:
- 1077-4114
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5030.183000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 22441.xml