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Sufficient Immunosuppression with Thymoglobulin Is Essential for a Successful Haplo-Myeloid Bridge in Haploidentical-Cord Blood Transplantation.
- Source :
-
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation [Biol Blood Marrow Transplant] 2015 Oct; Vol. 21 (10), pp. 1839-45. Date of Electronic Publication: 2015 Jun 26. - Publication Year :
- 2015
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Abstract
- In haploidentical (haplo)-cord blood (CB) transplantations, early haplo donor engraftment serves as a myeloid bridge to sustainable CB engraftment and is associated with early neutrophil recovery. The conditioning regimens as published for haplo-cord protocols usually contain serotherapy, such as rabbit antithymocyte globulin (ATG) (Thymoglobulin, Genzyme, Cambridge, MA). However, reducing or omitting serotherapy is an important strategy to improve early immune reconstitution after transplantation. The need for serotherapy in successful haplo-cord transplantation, defined as having a haplo-derived myeloid bridge to CB engraftment, has not been investigated before. Two consecutive cohorts of patients underwent transplantation with haplo-CB. The first group underwent transplantation with haplo-CB for active infection and/or an underlying condition with expected difficult engraftment without a conventional donor available. They received a single unit (s) CB and haplo donor cells (CD34(+) selected, 5 × 10(6) CD34(+)/kg). The second cohort included patients with poor-risk malignancies, not eligible for other treatment protocols. They received a sCB and haplo donor cells (CD19/αβTCR-depleted; 5 × 10(6) CD34(+)/kg). Retrospectively in both cohorts, active ATG (Thymoglobulin) levels were measured and post-hematopoietic cell transplantation area under the curve (AUC) was calculated. The influence of ATG exposure for having a successful haplo-myeloid bridge (early haplo donor engraftment before CB engraftment and no secondary neutropenia) and transplantation-related mortality (TRM) were analyzed as primary endpoints. Twenty patients were included (16 in the first cohort and 4 in the second cohort). In 58% of evaluable patients, there was no successful haplo-derived myeloid bridge to CB engraftment, for which a low post-transplantation ATG exposure appeared to be a predictor (P <.001). TRM in the unsuccessful haplo-bridge group was 70% ± 16% versus 12% ± 12% in the successful haplo-bridge group (P = .012). In conclusion, sufficient in vivo T depletion with ATG is required for a successful haplo-myeloid bridge to CB engraftment.<br /> (Copyright © 2015 American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Adolescent
Adult
Alemtuzumab
Animals
Antibodies, Monoclonal, Humanized therapeutic use
Area Under Curve
Child
Child, Preschool
Dose-Response Relationship, Immunologic
Endpoint Determination
Female
Graft Rejection
Graft Survival
Graft vs Host Disease prevention & control
Humans
Immunosuppressive Agents adverse effects
Immunosuppressive Agents therapeutic use
Infant
Infant, Newborn
Kaplan-Meier Estimate
Lymphocyte Depletion
Male
Middle Aged
Neutrophils immunology
Neutrophils transplantation
Rabbits
Time Factors
Treatment Outcome
Unrelated Donors
Antilymphocyte Serum administration & dosage
Cord Blood Stem Cell Transplantation methods
Haplotypes immunology
Histocompatibility
Immunosuppressive Agents administration & dosage
T-Lymphocytes immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1523-6536
- Volume :
- 21
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
- Publication Type :
- Academic Journal
- Accession number :
- 26119367
- Full Text :
- https://doi.org/10.1016/j.bbmt.2015.06.001