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Can haploidentical transplantation meet all patients' needs?
1Division of Hematology, Oncology and Transplantation, University of Minnesota, 420 Delaware Street SE, MMC 480, Minneapolis, MN 55455, USA.
Best Practice & Research. Clinical Haematology
|November 24, 2018
Summary
Hematopoietic stem cell transplantation offers various donor options when a matched sibling is unavailable. Post-transplant cyclophosphamide (PTCy) and specific graft choices improve outcomes by reducing graft-versus-host disease (GVHD).
Area of Science:
- Hematopoietic Stem Cell Transplantation (HSCT)
- Immunology
- Oncology
Background:
- Allotransplantation without an HLA-matched sibling donor involves choices like unrelated donors and umbilical cord blood.
- Haploidentical transplantation has gained popularity, particularly with post-transplant cyclophosphamide (PTCy) for graft-versus-host disease (GVHD) prophylaxis.
Purpose of the Study:
- To review current donor and graft options in allogeneic HSCT.
- To discuss the impact of novel strategies like PTCy and graft source on GVHD.
- To highlight the need for tailored decision-making based on patient-specific factors.
Main Methods:
- Review of current literature and clinical practices in allogeneic HSCT.
- Analysis of outcomes associated with different donor sources (unrelated, cord blood, haploidentical).
- Evaluation of GVHD prophylaxis strategies, including PTCy and graft type (bone marrow vs. peripheral blood stem cells).
Main Results:
- Multiple donor options exist for HSCT when a matched sibling is unavailable.
- PTCy effectively reduces GVHD risk, while bone marrow grafts may lower chronic GVHD compared to peripheral blood stem cells.
- Current evidence does not demonstrate clear superiority of one approach over others; outcomes are influenced by various factors.
Conclusions:
- Advances in HSCT, including PTCy and graft selection, have improved patient outcomes.
- Both PTCy and bone marrow grafts show promise in mitigating GVHD.
- Future research should focus on prospective data to guide individualized HSCT strategies based on patient risk and comorbidity.