Publication:
Gemtuzumab Ozogamicin and Stem Cell Mobilization for Autologous Stem Cell Transplantation in Favorable Risk Acute Myeloid Leukemia.

cris.virtualsource.author-orcid0dd4cd15-0e4d-4a28-8df3-d94991823a57
cris.virtualsource.author-orcida02cf60f-3445-4d51-a3c2-15bc7ca6746b
cris.virtualsource.author-orcida0f00c7b-780d-4398-9754-fe2161b10f0e
cris.virtualsource.author-orcidd8f42926-f873-4a1f-839a-49eecd87333a
cris.virtualsource.author-orcid87c04196-fbb6-42b8-97bf-151846fee8ea
cris.virtualsource.author-orcid3ffc609d-4653-413a-a80f-2bf6c2b71f47
cris.virtualsource.author-orcid1b65be99-ede2-4b0e-8e6d-1c720e453513
datacite.rightsopen.access
dc.contributor.authorMartinez Flores, Danaë
dc.contributor.authorAkhoundova Sanoyan, Dilara
dc.contributor.authorSeipel, Katja
dc.contributor.authorLegros, Myriam
dc.contributor.authorKronig, Marie-Noëlle
dc.contributor.authorDaskalakis, Michael
dc.contributor.authorBacher, Vera Ulrike
dc.contributor.authorPabst, Thomas Niklaus
dc.date.accessioned2024-10-26T18:37:04Z
dc.date.available2024-10-26T18:37:04Z
dc.date.issued2024-07-19
dc.description.abstractGemtuzumab ozogamicin (GO), a CD33-targeting antibody drug conjugate, previously showed longer relapse-free survival when combined with induction chemotherapy in patients with favorable-risk acute myeloid leukemia (AML). In this patient population, characterized by lower relapse risk as compared to other ELN risk groups, autologous stem cell transplantation (ASCT) can be used as consolidation strategy. However, there are limited data on the impact of GO on the peripheral blood stem cell (PBSC) mobilization potential. We therefore retrospectively analyzed data from 54 AML patients with favorable-risk AML treated with (n = 17) or without (n = 37) GO during induction treatment. We observed no significant differences in the PBSC mobilization rate between patients treated with vs. without GO. The mobilization success in a first attempt directly following cycle 2 was 65% vs. 70% (p = 0.92); and the mobilization success in a subsequent second attempt after hematologic recovery and repeated stimulation procedure was 24% vs. 19% (p = 0.56). No significant impact on treatment outcome in terms of EFS (p = 0.31) or OS (p = 0.99) was observed. Thus, our results suggest that the addition of GO to induction regimens does not negatively impact PBSC mobilization in favorable-risk AML patients. To our best knowledge, this is the first study comparing the stem cell mobilization potential in favorable-risk AML patients treated with vs. without GO.
dc.description.numberOfPages8
dc.description.sponsorshipUniversitätsklinik für Medizinische Onkologie
dc.description.sponsorshipUniversitätsinstitut für Klinische Chemie (UKC)
dc.description.sponsorshipUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor
dc.identifier.doi10.48350/199327
dc.identifier.pmid39062189
dc.identifier.publisherDOI10.3390/biomedicines12071616
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/179435
dc.language.isoen
dc.publisherMDPI
dc.relation.ispartofBiomedicines
dc.relation.issn2227-9059
dc.relation.organizationDCD5A442C448E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C055E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BA49E17DE0405C82790C4DE2
dc.subjectacute myeloid leukemia (AML) autologous stem cell transplantation (ASCT) gemtuzumab ozogamicin (GO) peripheral blood stem cells (PBSC) stem cell mobilization
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleGemtuzumab Ozogamicin and Stem Cell Mobilization for Autologous Stem Cell Transplantation in Favorable Risk Acute Myeloid Leukemia.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue7
oaire.citation.volume12
oairecerif.author.affiliationUniversitätsklinik für Medizinische Onkologie
oairecerif.author.affiliationUniversitätsklinik für Medizinische Onkologie
oairecerif.author.affiliationUniversitätsinstitut für Klinische Chemie (UKC)
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.contributor.rolecreator
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unibe.date.licenseChanged2024-07-29 09:40:48
unibe.description.ispublishedpub
unibe.eprints.legacyId199327
unibe.refereedtrue
unibe.subtype.articlejournal

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