Anti-Thymocyte-Globulin as part of the preparative regimen prevents graft failure and severe Graft versus Host disease (GvHD) in allogeneic stem celltransplantation from unrelated donors

Citation
N. Kroger et al., Anti-Thymocyte-Globulin as part of the preparative regimen prevents graft failure and severe Graft versus Host disease (GvHD) in allogeneic stem celltransplantation from unrelated donors, ANN HEMATOL, 80(4), 2001, pp. 209-215
Citations number
25
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
ANNALS OF HEMATOLOGY
ISSN journal
09395555 → ACNP
Volume
80
Issue
4
Year of publication
2001
Pages
209 - 215
Database
ISI
SICI code
0939-5555(200104)80:4<209:AAPOTP>2.0.ZU;2-4
Abstract
To reduce the incidence of GvHD and the rate of graft failure in unrelated stem cell transplantation, we incorporate anti-thymocyte globulin in the pr eparative regimen in 98 patients with hematological or inherited storage di sease. The median age was 32 years (range: 1-56) and 84 patients underwent transplantation from HLA-A,-B and DR identical donor, while in 14 patients the donor were mismatched either in HLA- A, -B or -DR locus. Only one patient with chronic myelocytic leukemia (CML) and blast crisis ha d a primary graft failure (1%). Grade II-IV acute GVHD occurred in 37 patie nts (37%), grade III/IV GVHD developed in 15 patients (15%). Chronic GvHD w as observed in 29%, and only 12 patients had extensive GVHD (17%). After a median follow-up of 34 months (range, 9-90), the estimated overall survival at 3 years for all patients is 58% (CI 95%: 48%-68%), and the estimated di sease-free survival at 3 years is 49% (CI 95%: 38%-60%). For patients with CML transplanted in first chronic phase or accelerated phase (n=40), the es timated overall survival at 3 pears is 70% (CI 95%: 56%-84%), and the estim ated disease-free survival at 3 years is 58% (CI 95%: 17%-85%). ATG in unre lated stem cell transplantation reduces the risk of severe acute and chroni c GVHD and of graft failure without an obvious increase of severe infection . Further follow-up is mandatory to determine the incidence of late relapse .