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  3. Prophylactic corticosteroid use prevents engraftment syndrome in patients after autologous stem cell transplantation.
 

Prophylactic corticosteroid use prevents engraftment syndrome in patients after autologous stem cell transplantation.

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BORIS DOI
10.7892/boris.147172
Date of Publication
February 2021
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Institut für Patholog...

Universitätsklinik fü...

Universitätsklinik fü...

Author
Betticher, Christophe
Bacher, Vera Ulrike
Universitätsklinik für Hämatologie und Hämatologisches Zentrallabor
Legros, Myriam
Universitätsklinik für Hämatologie und Hämatologisches Zentrallabor
Zimmerli, Stephan
Universitätsklinik für Infektiologie
Banz Wälti, Yara Sarahorcid-logo
Institut für Pathologie
Mansouri Taleghani, Behrouz
Universitätsklinik für Hämatologie und Hämatologisches Zentrallabor
Pabst, Thomas Niklaus
Universitätsklinik für Medizinische Onkologie
Subject(s)

600 - Technology::610...

500 - Science::570 - ...

Series
Hematological oncology
ISSN or ISBN (if monograph)
1099-1069
Publisher
Wiley
Language
English
Publisher DOI
10.1002/hon.2813
PubMed ID
32979278
Uncontrolled Keywords

autologous stem cell ...

Description
Engraftment syndrome (ES) following autologous stem cell transplantation (ASCT) at the time of neutrophil recovery may comprise fever, rash, pulmonary edema, or diarrhea. Usually, ES is easily manageable using corticosteroids but may prolong hospitalization. In two consecutive cohorts of subsequent patients with myeloma, lymphomas, and testicular/germ cell cancer, we assessed the benefit of corticosteroid use to prevent incidence and severity of ES following ASCT. Whereas Cohort A (82 patients) received no prophylactic corticosteroids, corticosteroids (4 mg dexamethasone oral daily) were started in Cohort B (60 patients) at day +9 until day +13 following ASCT. Steroid prophylaxis significantly reduced the incidence of ES (6/60; 10% vs. 33/82; 40%; p < 0.001). Hospitalization duration was longer in patients with ES than in patients without ES within both cohorts (in Cohort A: p = 0.007; and B: p = 0.011), but did not differ significantly between cohorts A and B. Finally, in Cohort A, there was a trend to an inferior 2-year overall survival rate in patients without ES compared to patients with ES (p = 0.067), but definite conclusions are not yet allowed. Our results suggest that corticosteroid prophylaxis from days +9 to +13 following ASCT significantly reduces the risk of ES and shortens hospitalization duration.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/37433
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hon.2813 (1).pdfAdobe PDF425.45 KBpublisherpublished restricted
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