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

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

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BORIS DOI
10.48350/199327
Date of Publication
July 19, 2024
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Universitätsinstitut ...

Universitätsklinik fü...

Author
Martinez Flores, Danaë
Akhoundova Sanoyan, Dilara
Universitätsklinik für Medizinische Onkologie
Seipel, Katja
Universitätsklinik für Medizinische Onkologie
Legros, Myriam
Universitätsinstitut für Klinische Chemie (UKC)
Kronig, Marie-Noëlle
Universitätsklinik für Medizinische Onkologie
Daskalakis, Michael
Universitätsklinik für Hämatologie und Hämatologisches Zentrallabor
Bacher, Vera Ulrike
Universitätsklinik für Hämatologie und Hämatologisches Zentrallabor
Pabst, Thomas Niklaus
Universitätsklinik für Medizinische Onkologie
Subject(s)

600 - Technology::610...

Series
Biomedicines
ISSN or ISBN (if monograph)
2227-9059
Publisher
MDPI
Language
English
Publisher DOI
10.3390/biomedicines12071616
PubMed ID
39062189
Uncontrolled Keywords

acute myeloid leukemi...

Description
Gemtuzumab 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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/179435
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biomedicines-12-01616-v2.pdftextAdobe PDF346.76 KBpublishedOpen
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