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

cris.virtual.author-orcid0000-0003-4474-3132
cris.virtualsource.author-orcid3ffc609d-4653-413a-a80f-2bf6c2b71f47
cris.virtualsource.author-orcida0f00c7b-780d-4398-9754-fe2161b10f0e
cris.virtualsource.author-orcid50113cbc-046c-4bec-9e6b-bd6f9b06d6eb
cris.virtualsource.author-orcidc441561b-2f62-41ef-8e09-fb335467e1b9
cris.virtualsource.author-orcid5f5278c3-d908-45fe-8a4a-885030ed281d
cris.virtualsource.author-orcid1b65be99-ede2-4b0e-8e6d-1c720e453513
datacite.rightsrestricted
dc.contributor.authorBetticher, Christophe
dc.contributor.authorBacher, Vera Ulrike
dc.contributor.authorLegros, Myriam
dc.contributor.authorZimmerli, Stephan
dc.contributor.authorBanz Wälti, Yara Sarah
dc.contributor.authorMansouri Taleghani, Behrouz
dc.contributor.authorPabst, Thomas Niklaus
dc.date.accessioned2024-09-02T16:18:03Z
dc.date.available2024-09-02T16:18:03Z
dc.date.issued2021-02
dc.description.abstractEngraftment 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.
dc.description.numberOfPages8
dc.description.sponsorshipUniversitätsklinik für Infektiologie
dc.description.sponsorshipInstitut für Pathologie
dc.description.sponsorshipUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor
dc.description.sponsorshipUniversitätsklinik für Medizinische Onkologie
dc.identifier.doi10.7892/boris.147172
dc.identifier.pmid32979278
dc.identifier.publisherDOI10.1002/hon.2813
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/37433
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofHematological oncology
dc.relation.issn1099-1069
dc.relation.organizationDCD5A442C055E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BF89E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C448E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BB13E17DE0405C82790C4DE2
dc.subjectautologous stem cell transplantation corticosteroid prophylaxis engraftment syndrome lymphoma myeloma
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.subject.ddc500 - Science::570 - Life sciences; biology
dc.titleProphylactic corticosteroid use prevents engraftment syndrome in patients after autologous stem cell transplantation.
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage104
oaire.citation.issue1
oaire.citation.startPage97
oaire.citation.volume39
oairecerif.author.affiliationUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor
oairecerif.author.affiliationUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor
oairecerif.author.affiliationUniversitätsklinik für Infektiologie
oairecerif.author.affiliationInstitut für Pathologie
oairecerif.author.affiliationUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor
oairecerif.author.affiliationUniversitätsklinik für Medizinische Onkologie
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unibe.date.licenseChanged2020-11-02 15:11:44
unibe.description.ispublishedpub
unibe.eprints.legacyId147172
unibe.refereedtrue
unibe.subtype.articlejournal

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