Infectious complications after second allogeneic hematopoietic cell transplant in adult patients with hematological malignancies

We conducted a retrospective review of the infectious complications and outcomes over a 2-year follow-up period of adult patients who received a second allogeneic hematopoietic cell transplant (2nd allo-HCT) during a five-year period at two cancer centers in Michigan. Sixty patients, of whom 44 (73%...

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Veröffentlicht in:Bone marrow transplantation (Basingstoke) 2022-12, Vol.57 (12), p.1820-1826
Hauptverfasser: Maurer, Stephen M., Linder, Kathleen A., Kauffman, Carol A., McDonald, Philip J., Arcobello, Jonathan, Velasco, Jon, Chandrasekar, Pranatharthi H., Revankar, Sanjay G., Miceli, Marisa H.
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Sprache:eng
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Zusammenfassung:We conducted a retrospective review of the infectious complications and outcomes over a 2-year follow-up period of adult patients who received a second allogeneic hematopoietic cell transplant (2nd allo-HCT) during a five-year period at two cancer centers in Michigan. Sixty patients, of whom 44 (73%) had acute leukemia or myelodysplastic syndrome, were studied. The majority ( n  = 37,62%) received a 2nd allo-HCT because of relapsed leukemia. Infection episodes after the 2nd allo-HCT totaled 112. Bacteria were identified in 76 episodes, the majority of which occurred pre-engraftment. The most common infecting organisms were Enterococcus species and Clostridioides difficile . Viral infections, predominantly cytomegalovirus, accounted for 59 infection episodes and occurred mostly in pre-engraftment and early post-engraftment periods. There were 16 proven/probable fungal infections, of which 9 were invasive aspergillosis or candidiasis. Mortality was 45% ( n  = 27) at one year and 65% ( n  = 39) at 2 years after transplant, and 16 deaths (41%) were due to infection. Of those 16 infection deaths, 8 were bacterial, 4 fungal, 2 both bacterial and fungal, and 2 viral. Failure to engraft neutrophils or platelets was significantly associated with decreased survival, p  
ISSN:0268-3369
1476-5365
DOI:10.1038/s41409-022-01827-y