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. 2021 Oct;56(10):2489-2496.
doi: 10.1038/s41409-021-01367-x. Epub 2021 Jun 14.

Cryopreservation of unrelated donor hematopoietic stem cells: the right answer for transplantations during the COVID-19 pandemic?

Affiliations

Cryopreservation of unrelated donor hematopoietic stem cells: the right answer for transplantations during the COVID-19 pandemic?

Jesus Fernandez-Sojo et al. Bone Marrow Transplant. 2021 Oct.

Erratum in

Abstract

Cryopreservation was recommended to ensure continuity of unrelated donor (UD) hematopoietic stem cell transplantation (HSCT) during COVID-19 pandemic. However, its impact on clinical outcomes and feasibility was not well known. We compared 32 patients who underwent UD HSCT using cryopreserved peripheral blood stem cells (PBSC) during the COVID-19 pandemic with 32 patients who underwent UD HSCT using fresh PBSC in the previous period. Median neutrophil engraftment was 17.5 and 17.0 days with cryopreserved and fresh grafts, respectively. Non-significant delays were found in platelet recovery days (25.5 versus 19.0; P = 0.192) and full donor chimerism days (35.0 and 31.5; P = 0.872) using cryopreserved PBSC. The rate of acute graft-versus-host disease at 100 days was 41% (95% CI [21-55%]) in cryopreserved group versus 31% (95% CI [13-46%]) in fresh group (P = 0.380). One-hundred days progression-relapse free survival and overall survival did not differ significantly. During COVID-19 pandemic, six frozen UD donations were not transfused and logistical and clinical issues regarding cryopreservation procedure, packaging, and transporting appeared. In summary, UD HSCT with cryopreserved PBSC was safe during this challenging time. More efforts are needed to ensure that all frozen grafts are transplanted and cryopreservation requirements are harmonized.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1. Cumulative incidence of hematological recovery and full donor chimerism according to UD HSC (cryopreserved versus fresh).
The cumulative incidences of A neutrophil recovery, B platelet recovery, and C full donor chimerism are shown for the groups of patients who underwent UD HSCT with either cryopreserved (solid line) or fresh PBSC (dashed line).
Fig. 2
Fig. 2. Cumulative incidence of acute GVHD and preemptive CMV treatment disease, PFS, and OS according to UD HSC (cryopreserved versus fresh).
The cumulative incidences of A acute graft-versus-host disease (GVHD), B preemptive therapy on CMV disease, C progression-relapse-free survival, and D overall survival are shown for the groups of patients who underwent UD HSCT with either cryopreserved (solid line) or fresh grafts (dashed line).

References

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