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About:
Infections after T‐replete haploidentical transplantation and high‐dose cyclophosphamide as graft‐versus‐host disease prophylaxis
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wasabi.inria.fr
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research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
Infections after T‐replete haploidentical transplantation and high‐dose cyclophosphamide as graft‐versus‐host disease prophylaxis
Creator
Bramanti, S
Carlo-Stella, C
Casari, E
Castagna, L
Crocchiolo, R
Crocchiolo, Roberto
Lugli, E
Mauro, E
Mavilio, D
Mineri, R
Santoro, A
Sarina, B
Timofeeva, I
Tordato, F
Vai, A
source
PMC
abstract
BACKGROUND: Recently, a platform of T‐cell replete haploidentical hematopoietic stem cell transplantation (haplo‐HSCT) using post‐transplant cyclophosphamide (Cy) has shown high reproducibility and acceptable safety profile. METHOD: This prospective cohort analysis allowed us to collect data on infections among 70 consecutive recipients of haplo‐HSCT affected by various hematologic malignancies. RESULTS: After a median follow‐up of 23 months, cumulative incidence of viral infections was 70% (95% confidence interval [CI] 59–81) at 100 days and 77% (95% CI 67–87) at 1 year; 35 of 65 patients at risk had CMV reactivation (54%) and the rate of polyomavirus‐virus‐associated cystitis was 19% (13/70). Cumulative incidence of bacterial and fungal infections at 1 year were 63% (95% CI 51–75) and 12% (95% CI 4–19), respectively. Of note, only 1 invasive fungal infection occurred beyond 1 year after transplant (day +739). CONCLUSION: In conclusion, despite a high rate of viral infections in the early period, present data suggest a satisfactory infectious profile after T‐cell replete haplo‐HSCT using post‐transplant Cy. These results may help clinicians to improve both prophylactic and therapeutic antimicrobial strategies in this emerging haploidentical setting.
has issue date
2015-03-26
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)
bibo:doi
10.1111/tid.12365
bibo:pmid
25648539
has license
no-cc
sha1sum (hex)
dd021d5e3273bad9458f4deb31f878632a5e624f
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https://doi.org/10.1111/tid.12365
resource representing a document's title
Infections after T‐replete haploidentical transplantation and high‐dose cyclophosphamide as graft‐versus‐host disease prophylaxis
has PubMed Central identifier
PMC7169814
has PubMed identifier
25648539
schema:publication
Transpl Infect Dis
resource representing a document's body
covid:dd021d5e3273bad9458f4deb31f878632a5e624f#body_text
is
schema:about
of
named entity 'graft-versus-host disease'
named entity 'platform'
named entity 'T-cell'
named entity 'All rights reserved'
named entity 'transplantation'
named entity 'hematopoietic stem cell'
named entity 'prophylaxis'
named entity 'hematopoietic stem cell transplantation'
named entity 'reproducibility'
named entity 'graft-versus-host disease'
named entity 'high-dose'
named entity 'pneumonia'
named entity 'pneumonia'
named entity 'hematologic malignancies'
named entity 'candidiasis'
named entity 'primary antibody'
named entity 'CD3'
named entity 'stem cells'
named entity 'CMV'
named entity 'kidney'
named entity 'esophageal cancer'
named entity 'tacrolimus'
named entity 'HSCT'
named entity 'Candida'
named entity 'pathogen'
named entity 'GVHD'
named entity 'cidofovir'
named entity 'relapse'
named entity 'infusion'
named entity 'echinocandin'
named entity 'toxicity'
named entity '10.8'
named entity 'median follow-up'
named entity 'Conditioning regimens'
named entity 'bacterial pneumonia'
named entity 'CD56'
named entity 'progressive multifocal leukoencephalopathy'
named entity 'levofloxacin'
named entity 'CMV'
named entity 'empirical therapy'
named entity 'cyclosporine'
named entity 'Logrank test'
named entity 'CMV'
named entity 'CMV'
named entity 'pneumonia'
named entity 'Italy'
named entity 'memory cells'
named entity 'autologous'
named entity 'T-cell'
named entity 'CMV'
named entity 'GVHD'
named entity 'Neutrophil'
named entity 'pneumonia'
named entity 'ganciclovir'
named entity 'Beckman Coulter'
named entity 'thiotepa'
named entity 'TBI'
named entity 'bacterial infections'
named entity 'prophylaxis'
named entity 'intravenous'
named entity 'HSCT'
named entity 'invasive candidiasis'
named entity 'cyclosporine'
named entity 'pneumonia'
named entity 'risk factor'
named entity 'aminoglycoside'
named entity 'candidemia'
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