Role of Hematopoietic Stem Cell Transplantation in Acute Promyelocytic Leukemia

The indication of hematopoietic stem cell transplantation (HSCT) in acute promyelocytic leukemia (APL) has evolved historically from a widespread use in front-line therapy during the pre-ATRA era to a virtual rejection of this indication for patients treated with modern treatments. HSCT in first com...

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Main Authors: Jaime Sanz, Pau Montesinos, Miguel A. Sanz
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-03-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2021.614215/full
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author Jaime Sanz
Jaime Sanz
Pau Montesinos
Pau Montesinos
Miguel A. Sanz
Miguel A. Sanz
author_facet Jaime Sanz
Jaime Sanz
Pau Montesinos
Pau Montesinos
Miguel A. Sanz
Miguel A. Sanz
author_sort Jaime Sanz
collection DOAJ
description The indication of hematopoietic stem cell transplantation (HSCT) in acute promyelocytic leukemia (APL) has evolved historically from a widespread use in front-line therapy during the pre-ATRA era to a virtual rejection of this indication for patients treated with modern treatments. HSCT in first complete remission could only be considered for an extremely small fraction of patients with persistent MRD at the end of consolidation or for those who relapse. In the pre-ATO era, relapsed patients were usually treated with readministration of ATRA and chemotherapy as salvage therapy, generally containing high-dose cytarabine and an anthracycline, followed by further post-remission chemotherapy and/or HSCT. ATO-based regimens are presently regarded as the first option for relapsed APL. The selection of the most appropriate post-remission treatment option for patients in second CR (CR2), as well as the modality of HSCT when indicated, depends on several variables, such as pre-transplant molecular status, duration of first remission, age, and donor availability. Although with a moderate level of evidence, based on recent retrospective studies, autologous HSCT would be at present the preferred option for consolidation for patients in molecular CR2. Allogeneic HSCT could be considered in patients with a very early relapse or those beyond CR2. Nevertheless, the superiority of HSCT as consolidation over other alternatives without transplantation has recently been questioned in some studies, which justify a prospective controlled study to resolve this still controversial issue.
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spelling doaj.art-5b9b92d280384e4186e86f379285fce22022-12-21T20:33:26ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2021-03-011110.3389/fonc.2021.614215614215Role of Hematopoietic Stem Cell Transplantation in Acute Promyelocytic LeukemiaJaime Sanz0Jaime Sanz1Pau Montesinos2Pau Montesinos3Miguel A. Sanz4Miguel A. Sanz5Department of Hematology, Hospital Universitari i Politècnic La Fe, Valencia, SpainCentro de Investigación Biomédica en Red de Cáncer, Instituto Carlos III, Madrid, SpainDepartment of Hematology, Hospital Universitari i Politècnic La Fe, Valencia, SpainCentro de Investigación Biomédica en Red de Cáncer, Instituto Carlos III, Madrid, SpainDepartment of Hematology, Hospital Universitari i Politècnic La Fe, Valencia, SpainCentro de Investigación Biomédica en Red de Cáncer, Instituto Carlos III, Madrid, SpainThe indication of hematopoietic stem cell transplantation (HSCT) in acute promyelocytic leukemia (APL) has evolved historically from a widespread use in front-line therapy during the pre-ATRA era to a virtual rejection of this indication for patients treated with modern treatments. HSCT in first complete remission could only be considered for an extremely small fraction of patients with persistent MRD at the end of consolidation or for those who relapse. In the pre-ATO era, relapsed patients were usually treated with readministration of ATRA and chemotherapy as salvage therapy, generally containing high-dose cytarabine and an anthracycline, followed by further post-remission chemotherapy and/or HSCT. ATO-based regimens are presently regarded as the first option for relapsed APL. The selection of the most appropriate post-remission treatment option for patients in second CR (CR2), as well as the modality of HSCT when indicated, depends on several variables, such as pre-transplant molecular status, duration of first remission, age, and donor availability. Although with a moderate level of evidence, based on recent retrospective studies, autologous HSCT would be at present the preferred option for consolidation for patients in molecular CR2. Allogeneic HSCT could be considered in patients with a very early relapse or those beyond CR2. Nevertheless, the superiority of HSCT as consolidation over other alternatives without transplantation has recently been questioned in some studies, which justify a prospective controlled study to resolve this still controversial issue.https://www.frontiersin.org/articles/10.3389/fonc.2021.614215/fullacute promyelocytic leukaemiahematopoietic (stem) cell transplantation (HCT)all-trans retinoic acid (ATRA)arsenic trioxiderelapse
spellingShingle Jaime Sanz
Jaime Sanz
Pau Montesinos
Pau Montesinos
Miguel A. Sanz
Miguel A. Sanz
Role of Hematopoietic Stem Cell Transplantation in Acute Promyelocytic Leukemia
Frontiers in Oncology
acute promyelocytic leukaemia
hematopoietic (stem) cell transplantation (HCT)
all-trans retinoic acid (ATRA)
arsenic trioxide
relapse
title Role of Hematopoietic Stem Cell Transplantation in Acute Promyelocytic Leukemia
title_full Role of Hematopoietic Stem Cell Transplantation in Acute Promyelocytic Leukemia
title_fullStr Role of Hematopoietic Stem Cell Transplantation in Acute Promyelocytic Leukemia
title_full_unstemmed Role of Hematopoietic Stem Cell Transplantation in Acute Promyelocytic Leukemia
title_short Role of Hematopoietic Stem Cell Transplantation in Acute Promyelocytic Leukemia
title_sort role of hematopoietic stem cell transplantation in acute promyelocytic leukemia
topic acute promyelocytic leukaemia
hematopoietic (stem) cell transplantation (HCT)
all-trans retinoic acid (ATRA)
arsenic trioxide
relapse
url https://www.frontiersin.org/articles/10.3389/fonc.2021.614215/full
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