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Refined Graft-Versus-Host Disease/Relapse-Free Survival in Transplant From Hla-Identical Related or Unrelated Donors in Acute Myeloid Leukemia Publisher Pubmed



Battipaglia G1, 3 ; Ruggeri A1, 2 ; Labopin M1, 4, 5 ; Volin L6 ; Blaise D7 ; Socie G8 ; Tabrizi R9 ; Cornelissen JJ10 ; Ghavamzadeh A11 ; Huynh A12 ; Wu D13 ; Yakoubagha I14 ; Maertens J15 ; Chevallier P16 Show All Authors
Authors
  1. Battipaglia G1, 3
  2. Ruggeri A1, 2
  3. Labopin M1, 4, 5
  4. Volin L6
  5. Blaise D7
  6. Socie G8
  7. Tabrizi R9
  8. Cornelissen JJ10
  9. Ghavamzadeh A11
  10. Huynh A12
  11. Wu D13
  12. Yakoubagha I14
  13. Maertens J15
  14. Chevallier P16
  15. Mohty M1, 4, 5
  16. Nagler A5, 17

Source: Bone Marrow Transplantation Published:2018


Abstract

Refined graft-versus-host disease (GVHD)/relapse-free survival (GRFS) considers main outcomes of allogeneic stem cell transplant (HSCT), estimating long-term survival without significant morbidity as a surrogate of HSCT success. We compared GRFS in 5059 adults with acute myeloid leukemia (AML), undergoing HSCT in first complete remission from 2000 to 2015 either from a matched sibling (MSD, n = 3731) or unrelated donor (MUD, n = 1328). Median age was 49 (range: 18–76) years. Median follow-up was 32 and 60 months in MSD and MUD, respectively (p < 0.01). Compared to MSD, at 4 years, MUD recipients had lower GRFS, with higher NRM, grade III–IV acute GVHD, and extensive chronic GVHD (HR: 1.42, p < 0.01). We also performed a risk factor analyses, showing unfavorable cytogenetics (HR: 1.42, p < 0.01) and peripheral blood as stem cell source (HR: 1.22, p < 0.01) associated to lower GRFS, while this was higher with in vivo T-cell depletion (TCD, HR: 0.73, p < 0.01) and shorter time from diagnosis to HSCT (HR 0.96, p < 0.01). Different factors, modifiable or not, such as donor type, stem cell source, disease biology, and in vivo TCD, impact on GRFS and this may guide in the future transplant choices to improve morbidity and long-term quality of life. © 2018, Macmillan Publishers Limited, part of Springer Nature.
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