Volume 56, Issue 1 pp. 164-169
TRANSPLANTATION AND CELLULAR ENGINEERING

Pretransplant platelet transfusion refractoriness is not associated with platelet nonengraftment in T-replete hematopoietic progenitor cell transplantation for hematologic malignancies

Ashleigh Scott

Corresponding Author

Ashleigh Scott

Department of Haematology and Bone Marrow Transplantation, Royal Brisbane and Women's Hospital, Herston

Pathology Queensland, Herston

Australian Red Cross Blood Service, Kelvin Grove

Address reprint requests to: Ashleigh Scott, Department of Cancer Care Services (Haematology/Bone Marrow Transplantation), Royal Brisbane and Women's Hospital, Butterfield Street, Herston, Queensland 4006, Australia; e-mail: [email protected].Search for more papers by this author
Shoma Baidya

Shoma Baidya

Australian Red Cross Blood Service, Kelvin Grove

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Jason Butler

Jason Butler

Department of Haematology and Bone Marrow Transplantation, Royal Brisbane and Women's Hospital, Herston

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Kirk Morris

Kirk Morris

Department of Haematology and Bone Marrow Transplantation, Royal Brisbane and Women's Hospital, Herston

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Alycia Thornton

Alycia Thornton

Pathology Queensland, Herston

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Glen A. Kennedy

Glen A. Kennedy

Department of Haematology and Bone Marrow Transplantation, Royal Brisbane and Women's Hospital, Herston

The University of Queensland, St Lucia, Queensland, Australia

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First published: 11 August 2015
Citations: 6

Abstract

BACKGROUND

Cellular engraftment after allogeneic hematopoietic progenitor cell transplantation (HPCT) can be affected by pre-HPCT antibodies against donor human leukocyte antigen (HLA; donor-specific antibodies [DSAs]), which are commonly acquired by either pregnancy or transfusion. Issues regarding high assay sensitivity and variable interpretation limit routine screening for DSAs. Platelet (PLT) transfusion refractoriness (PTR) is relatively common in patients with hematologic malignancies, and anti-HLA alloantibodies can be identified in up to 20% of cases. For patients with PTR undergoing subsequent allogeneic HPCT, however, the effect if any on subsequent PLT nonengraftment is unknown.

STUDY DESIGN AND METHODS

We conducted a retrospective study of 480 adults who underwent T-replete HPCT for hematologic malignancy and compared the posttransplantation clinical outcomes between patients who were PTR before HPCT and those who were not.

RESULTS

Multivariate analysis demonstrated that PTR was not directly associated with PLT nonengraftment or graft failure, but did predict for early intensive care unit admission, which was the only variable associated with these outcomes (p < 0.0001).

CONCLUSION

Our findings suggest that PTR before HPCT identifies patients at higher risk of early clinical rather than immunologic complications.

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