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Case Report: Allogeneic Stem Cell Transplantation Following Induction With CPX-351 in Patients With Acute Myeloid Leukemia Is Feasible

Acute myeloid leukemia with myelodysplasia-related changes (AML-MRC) and treatment-related acute myeloid leukemia (tAML) after chemotherapy or radiation therapy for other neoplasms are associated with poor outcomes. CPX-351, a dual-drug liposomal encapsulation of daunorubicin and cytarabine, has bee...

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Autores principales: Vucinic, Vladan, Jentzsch, Madlen, Schwind, Sebastian, Bach, Enrica, Leiblein, Sabine, Remane, Yvonne, Rieprecht, Susanne, Otto, Sandra, Kubasch, Anne-Sophie, Behre, Gerhard, Cross, Michael, Platzbecker, Uwe, Franke, Georg-Nikolaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7526474/
https://www.ncbi.nlm.nih.gov/pubmed/33042819
http://dx.doi.org/10.3389/fonc.2020.01746
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author Vucinic, Vladan
Jentzsch, Madlen
Schwind, Sebastian
Bach, Enrica
Leiblein, Sabine
Remane, Yvonne
Rieprecht, Susanne
Otto, Sandra
Kubasch, Anne-Sophie
Behre, Gerhard
Cross, Michael
Platzbecker, Uwe
Franke, Georg-Nikolaus
author_facet Vucinic, Vladan
Jentzsch, Madlen
Schwind, Sebastian
Bach, Enrica
Leiblein, Sabine
Remane, Yvonne
Rieprecht, Susanne
Otto, Sandra
Kubasch, Anne-Sophie
Behre, Gerhard
Cross, Michael
Platzbecker, Uwe
Franke, Georg-Nikolaus
author_sort Vucinic, Vladan
collection PubMed
description Acute myeloid leukemia with myelodysplasia-related changes (AML-MRC) and treatment-related acute myeloid leukemia (tAML) after chemotherapy or radiation therapy for other neoplasms are associated with poor outcomes. CPX-351, a dual-drug liposomal encapsulation of daunorubicin and cytarabine, has been shown to improve outcomes in AML-MRC and tAML compared with standard 7+3 regimens. Here we report the cases of four consecutive patients with AML-MRC or tAML who received CPX-351 as outpatient induction therapy immediately followed by allogeneic hematopoietic stem cell transplantation (allo-HSCT). Two patients received allo-HSCT in remission (one in complete remission and one in partial remission) and two patients received allo-HSCT in aplasia (one at 11 days and one at 52 days after the start of induction therapy with CPX-351). With a median follow-up of 188 days after allo-HSCT, all but one patient are alive and two are in remission. Further studies will help define and expand the role of CPX-351 in the treatment of AML-MRC and tAML, especially in patients expected to undergo allo-HSCT.
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spelling pubmed-75264742020-10-09 Case Report: Allogeneic Stem Cell Transplantation Following Induction With CPX-351 in Patients With Acute Myeloid Leukemia Is Feasible Vucinic, Vladan Jentzsch, Madlen Schwind, Sebastian Bach, Enrica Leiblein, Sabine Remane, Yvonne Rieprecht, Susanne Otto, Sandra Kubasch, Anne-Sophie Behre, Gerhard Cross, Michael Platzbecker, Uwe Franke, Georg-Nikolaus Front Oncol Oncology Acute myeloid leukemia with myelodysplasia-related changes (AML-MRC) and treatment-related acute myeloid leukemia (tAML) after chemotherapy or radiation therapy for other neoplasms are associated with poor outcomes. CPX-351, a dual-drug liposomal encapsulation of daunorubicin and cytarabine, has been shown to improve outcomes in AML-MRC and tAML compared with standard 7+3 regimens. Here we report the cases of four consecutive patients with AML-MRC or tAML who received CPX-351 as outpatient induction therapy immediately followed by allogeneic hematopoietic stem cell transplantation (allo-HSCT). Two patients received allo-HSCT in remission (one in complete remission and one in partial remission) and two patients received allo-HSCT in aplasia (one at 11 days and one at 52 days after the start of induction therapy with CPX-351). With a median follow-up of 188 days after allo-HSCT, all but one patient are alive and two are in remission. Further studies will help define and expand the role of CPX-351 in the treatment of AML-MRC and tAML, especially in patients expected to undergo allo-HSCT. Frontiers Media S.A. 2020-09-16 /pmc/articles/PMC7526474/ /pubmed/33042819 http://dx.doi.org/10.3389/fonc.2020.01746 Text en Copyright © 2020 Vucinic, Jentzsch, Schwind, Bach, Leiblein, Remane, Rieprecht, Otto, Kubasch, Behre, Cross, Platzbecker and Franke. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Vucinic, Vladan
Jentzsch, Madlen
Schwind, Sebastian
Bach, Enrica
Leiblein, Sabine
Remane, Yvonne
Rieprecht, Susanne
Otto, Sandra
Kubasch, Anne-Sophie
Behre, Gerhard
Cross, Michael
Platzbecker, Uwe
Franke, Georg-Nikolaus
Case Report: Allogeneic Stem Cell Transplantation Following Induction With CPX-351 in Patients With Acute Myeloid Leukemia Is Feasible
title Case Report: Allogeneic Stem Cell Transplantation Following Induction With CPX-351 in Patients With Acute Myeloid Leukemia Is Feasible
title_full Case Report: Allogeneic Stem Cell Transplantation Following Induction With CPX-351 in Patients With Acute Myeloid Leukemia Is Feasible
title_fullStr Case Report: Allogeneic Stem Cell Transplantation Following Induction With CPX-351 in Patients With Acute Myeloid Leukemia Is Feasible
title_full_unstemmed Case Report: Allogeneic Stem Cell Transplantation Following Induction With CPX-351 in Patients With Acute Myeloid Leukemia Is Feasible
title_short Case Report: Allogeneic Stem Cell Transplantation Following Induction With CPX-351 in Patients With Acute Myeloid Leukemia Is Feasible
title_sort case report: allogeneic stem cell transplantation following induction with cpx-351 in patients with acute myeloid leukemia is feasible
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7526474/
https://www.ncbi.nlm.nih.gov/pubmed/33042819
http://dx.doi.org/10.3389/fonc.2020.01746
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