Publication:
Feasibility and efficacy of salvage allogeneic stem cell transplantation in AML patients relapsing after autologous stem cell transplantation.

cris.virtualsource.author-orcid7f9e15ad-af15-4392-9c49-2cab178d0677
cris.virtualsource.author-orcida0f00c7b-780d-4398-9754-fe2161b10f0e
cris.virtualsource.author-orcidd8f42926-f873-4a1f-839a-49eecd87333a
cris.virtualsource.author-orcid5f5278c3-d908-45fe-8a4a-885030ed281d
cris.virtualsource.author-orcid3ffc609d-4653-413a-a80f-2bf6c2b71f47
cris.virtualsource.author-orcid1b65be99-ede2-4b0e-8e6d-1c720e453513
datacite.rightsopen.access
dc.contributor.authorShumilov, Evgenii
dc.contributor.authorShakhanova, Inna
dc.contributor.authorFlach, Johanna
dc.contributor.authorSchmidt, Nicole
dc.contributor.authorBürki, Susanne
dc.contributor.authorLegros, Myriam
dc.contributor.authorKronig, Marie-Noëlle
dc.contributor.authorOfran, Yishai
dc.contributor.authorGerull, Sabine
dc.contributor.authorMedinger, Michael
dc.contributor.authorMansouri Taleghani, Behrouz
dc.contributor.authorPassweg, Jakob
dc.contributor.authorHalter, Jörg
dc.contributor.authorBacher, Vera Ulrike
dc.contributor.authorPabst, Thomas Niklaus
dc.date.accessioned2024-10-06T18:50:53Z
dc.date.available2024-10-06T18:50:53Z
dc.date.issued2022-02
dc.description.abstractAutologous hematopoietic cell transplantation (HCT) is suitable for consolidation of favorable-/intermediate-risk AML patients in CR1. However, ~50% of AML patients relapse after autologous HCT, and efficacy of subsequent salvage strategies including allogeneic HCT remains unclear. We studied 123 consecutive patients with newly diagnosed AML undergoing high-dose chemotherapy (HDCT)/autologous HCT in CR1. In relapsing patients afterwards, we analyzed salvage treatments and outcomes focusing particularly on salvage allogeneic HCT. Of 123 patients, 64 (52%) relapsed after autologous HCT. Subsequently, 13 (21%) received palliative therapy, whereas 51 (79%) proceeded to salvage therapy with a curative intent. Of the 47 patients with a curative intent and who did not proceed directly to allogeneic HCT, 23 (49%) achieved CR2 or had ongoing hematologic CR1 despite molecular relapse. Finally, 30 patients (47%) received allogeneic HCT with estimated 3-year leukemia-free and overall survival rates of 33% and 43%. Hematologic remission at allogeneic HCT and lack of acute GvHD had a positive impact on OS and LFS (p < 0.05). Our study suggests that almost 80% of AML patients can undergo salvage therapy following relapse after front-line HDCT/autologous HCT. Allogeneic HCT can provide cure in one third of patients relapsing after front-line HDCT/autologous HCT.
dc.description.numberOfPages8
dc.description.sponsorshipUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor
dc.description.sponsorshipUniversitätsklinik für Medizinische Onkologie
dc.identifier.doi10.48350/161607
dc.identifier.pmid34775480
dc.identifier.publisherDOI10.1038/s41409-021-01521-5
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/57807
dc.language.isoen
dc.publisherSpringer Nature
dc.relation.ispartofBone marrow transplantation
dc.relation.issn1476-5365
dc.relation.organizationDCD5A442C055E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C448E17DE0405C82790C4DE2
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleFeasibility and efficacy of salvage allogeneic stem cell transplantation in AML patients relapsing after autologous stem cell transplantation.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage231
oaire.citation.issue2
oaire.citation.startPage224
oaire.citation.volume57
oairecerif.author.affiliationUniversitätsklinik für Medizinische Onkologie
oairecerif.author.affiliationUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor
oairecerif.author.affiliationUniversitätsklinik für Medizinische Onkologie
oairecerif.author.affiliationUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor
oairecerif.author.affiliationUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor
oairecerif.author.affiliationUniversitätsklinik für Medizinische Onkologie
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unibe.date.licenseChanged2021-11-26 14:09:09
unibe.description.ispublishedpub
unibe.eprints.legacyId161607
unibe.refereedtrue
unibe.subtype.articlejournal

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