Tolerability and Efficacy of Treatment With Azacytidine as Prophylactic or Preemptive Therapy for Myeloid Neoplasms After Allogeneic Stem Cell Transplantation.


Journal

Clinical lymphoma, myeloma & leukemia
ISSN: 2152-2669
Titre abrégé: Clin Lymphoma Myeloma Leuk
Pays: United States
ID NLM: 101525386

Informations de publication

Date de publication:
06 2020
Historique:
received: 23 07 2019
revised: 11 10 2019
accepted: 15 10 2019
pubmed: 3 4 2020
medline: 1 6 2021
entrez: 3 4 2020
Statut: ppublish

Résumé

Azacytidine (AZA) has been used as a promising treatment for relapse after allogeneic transplantation. A clear benefit has been demonstrated when treating patients with a reduced disease burden, thus a prophylactic and preemptive approach to these patients has emerged. We retrospectively analyzed patients with myeloid malignancies treated with azacytidine in the posttransplantation setting between September 2013 and April 2018 in a single tertiary care hospital. Of 32 patients analyzed, 21 were treated for prophylactic use and 11 preemptively, with a median follow-up of 20 months. Prophylactic treatment consisted of AZA at 32 mg/m In the prophylactic group, all patients are alive at 1 year with an event-free survival (EFS) of 95%, as only 1 patient relapsed. In the preemptive group, 1-year EFS was 54% and 1-year overall survival was 82%. Low-dose AZA in posttransplantation patients with myeloid neoplasms is a well-tolerated therapy with the potential to prevent relapse and maintain stable remissions. Randomized prospective trials are needed to determine patient selection and dosage, timing, and duration of treatment.

Sections du résumé

INTRODUCTION/BACKGROUND
Azacytidine (AZA) has been used as a promising treatment for relapse after allogeneic transplantation. A clear benefit has been demonstrated when treating patients with a reduced disease burden, thus a prophylactic and preemptive approach to these patients has emerged.
MATERIALS AND METHODS
We retrospectively analyzed patients with myeloid malignancies treated with azacytidine in the posttransplantation setting between September 2013 and April 2018 in a single tertiary care hospital. Of 32 patients analyzed, 21 were treated for prophylactic use and 11 preemptively, with a median follow-up of 20 months. Prophylactic treatment consisted of AZA at 32 mg/m
RESULTS
In the prophylactic group, all patients are alive at 1 year with an event-free survival (EFS) of 95%, as only 1 patient relapsed. In the preemptive group, 1-year EFS was 54% and 1-year overall survival was 82%.
CONCLUSION
Low-dose AZA in posttransplantation patients with myeloid neoplasms is a well-tolerated therapy with the potential to prevent relapse and maintain stable remissions. Randomized prospective trials are needed to determine patient selection and dosage, timing, and duration of treatment.

Identifiants

pubmed: 32234295
pii: S2152-2650(19)32059-2
doi: 10.1016/j.clml.2019.10.011
pii:
doi:

Substances chimiques

Azacitidine M801H13NRU

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

377-382

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Carolina Marini (C)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Eolia Brissot (E)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France; Sorbonne University, INSERM UMRs 948, Centre de Recherche Saint-Antoine (CRSA), Paris, France.

Abdulhamid Bazarbachi (A)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Rémy Duléry (R)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France; Sorbonne University, INSERM UMRs 948, Centre de Recherche Saint-Antoine (CRSA), Paris, France.

Simona Sestili (S)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Giorgia Battipaglia (G)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France; Sorbonne University, INSERM UMRs 948, Centre de Recherche Saint-Antoine (CRSA), Paris, France.

Clémence Médiavilla (C)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France; Sorbonne University, INSERM UMRs 948, Centre de Recherche Saint-Antoine (CRSA), Paris, France.

Annalisa Paviglianiti (A)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Ramdane Belhocine (R)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Francoise Isnard (F)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Simona Lapusan (S)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Rosa Adaeva (R)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Anne Bannet (A)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Zoé van de Wiegert (Z)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Anne Vekhoff (A)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Tounes Ledraa (T)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Ollivier Legrand (O)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France; Sorbonne University, INSERM UMRs 948, Centre de Recherche Saint-Antoine (CRSA), Paris, France.

Myriam Labopin (M)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Agnes Bonnin (A)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Annalisa Ruggeri (A)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France.

Florent Malard (F)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France; Sorbonne University, INSERM UMRs 948, Centre de Recherche Saint-Antoine (CRSA), Paris, France.

Mohamad Mohty (M)

Department of Clinical Hematology, Saint-Antoine Hospital, AP-HP, Paris, France; Sorbonne University, INSERM UMRs 948, Centre de Recherche Saint-Antoine (CRSA), Paris, France. Electronic address: mohamad.mohty@inserm.fr.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH