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Poor graft function after T cell-depleted allogeneic hematopoietic stem cell transplant
Ronit Reich-Slotky1, Naima Al-Mulla2, Rania Hafez3
1Hackensack University Medical Center, Hackensack, NJ, USA.
Leukemia & Lymphoma
|July 15, 2020
Summary
Persistent graft failure (PGF) affects over half of transplant patients, leading to higher non-relapse mortality. Key factors include ABO incompatibility, acute GVHD, and CMV viremia, impacting blood counts and transfusion needs.
Area of Science:
- Hematology
- Transplantation Immunology
- Oncology
Background:
- Persistent graft failure (PGF) is a critical complication after hematopoietic stem cell transplantation (HCT).
- Understanding PGF contributors is crucial for improving outcomes in HCT recipients with donor chimerism.
Purpose of the Study:
- To investigate the factors associated with PGF in HCT recipients.
- To determine the impact of PGF on overall survival (OS) and progression-free survival (PFS).
Main Methods:
- Analysis of 104 HCT recipients surviving ≥100 days without relapse or major complications.
- Defined PGF by surrogate parameters: low hemoglobin, red blood cell (RBC) transfusion dependence, low platelet count, or low absolute neutrophil count (ANC).
- All patients received T cell depletion (alemtuzumab or ATG).
Main Results:
- 52% of patients met PGF criteria.
- Significant associations found between major ABO incompatibility and low platelets (OR=4.7), acute GVHD and low hemoglobin (OR=3.7), and CMV viremia and low ANC (OR=3.0).
- Non-relapse mortality (NRM) was significantly higher in the PGF group (45.5%) compared to the adequate graft function group (16.7%).
Conclusions:
- PGF is common and associated with specific clinical factors in T cell-depleted HCT.
- PGF significantly increases NRM, highlighting the need for early identification and management.
- Further research is warranted to mitigate PGF and improve long-term HCT outcomes.
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