Delivering HDAC over 3 or 5 days as consolidation in AML impacts health care resource consumption but not outcome.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
25 08 2020
Historique:
received: 01 06 2020
accepted: 14 07 2020
entrez: 14 8 2020
pubmed: 14 8 2020
medline: 15 5 2021
Statut: ppublish

Résumé

Postremission treatment is crucial to prevent relapse in acute myeloid leukemia (AML). High-dose cytarabine delivered every 12 hours on days 1, 3, and 5 (HDAC-135) is the standard of care for younger adult patients with AML. Although this standard has been unsuccessfully challenged by other treatment regimens, including multiagent chemotherapy, the timing of HDAC administration has attracted little attention. Here, we retrospectively compared the safety, efficacy, and health care resource consumption associated with HDAC-135 and another standard, condensed HDAC-123 regimen, as consolidation treatment in younger AML patients in first complete response. This study included 221 patients (median age, 46.6 years; range, 18-60 years). HDAC-123 and HDAC-135 were used in 92 and 129 patients, respectively. Both regimens were associated with similar rates of relapse-free survival, cumulative incidence of relapse, nonrelapse mortality, and overall survival, including in core binding factor AML subgroup in which levels of minimal residual disease reduction were similar in both schedules. Hematological recovery times regarding neutrophils and platelets were significantly shorter in patients receiving HDAC-123, with an average difference of 3 to 4 days for each consolidation cycle. The total duration of hospitalization for the whole postremission program was shorter with HDAC-123 (32 days; interquartile ratio [IQR], 22.0,36.5) compared with HDAC-135 (41 days; IQR, 30.5, 50.0) (P < .0001). In conclusion, the condensed HDAC-123 regimen induced faster hematological recovery and therefore significantly reduced the length of hospital stay without affecting treatment response or outcome in younger AML patients.

Identifiants

pubmed: 32790847
pii: S2473-9529(20)31143-5
doi: 10.1182/bloodadvances.2020002511
pmc: PMC7448603
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3840-3849

Informations de copyright

© 2020 by The American Society of Hematology.

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Auteurs

Pierre-Yves Dumas (PY)

Centre Hospitalo Universitaire (CHU) Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.
Université de Bordeaux, Bordeaux, France.
Institut National de la Santé et de la Recherche Médicale, U1035, Bordeaux, France.

Sarah Bertoli (S)

Service d'Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.
Université Toulouse III Paul Sabatier, Toulouse, France.
Cancer Research Center of Toulouse, Unité Mixte de Recherche (UMR) 1037 INSERM, ERL5294 Centre National de la Recherche Scientifique,Toulouse, France.

Emilie Bérard (E)

Service d'Epidémiologie, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.
UMR 1027, INSERM-Université de Toulouse III, Toulouse, France.

Thibaut Leguay (T)

Centre Hospitalo Universitaire (CHU) Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.

Suzanne Tavitian (S)

Service d'Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.

Jean Galtier (J)

Centre Hospitalo Universitaire (CHU) Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.

Camille Alric (C)

Service d'Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.

Audrey Bidet (A)

CHU Bordeaux, Laboratoire d'Hématologie Biologique, Bordeaux, France.

Eric Delabesse (E)

Université Toulouse III Paul Sabatier, Toulouse, France.
Cancer Research Center of Toulouse, Unité Mixte de Recherche (UMR) 1037 INSERM, ERL5294 Centre National de la Recherche Scientifique,Toulouse, France.
Laboratoire d'Hématologie Biologique, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France; and.

Jean Baptiste Rieu (JB)

Laboratoire d'Hématologie Biologique, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France; and.

Jean-Philippe Vial (JP)

CHU Bordeaux, Laboratoire d'Hématologie Biologique, Bordeaux, France.

François Vergez (F)

Université Toulouse III Paul Sabatier, Toulouse, France.
Cancer Research Center of Toulouse, Unité Mixte de Recherche (UMR) 1037 INSERM, ERL5294 Centre National de la Recherche Scientifique,Toulouse, France.
Laboratoire d'Hématologie Biologique, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France; and.

Nicolas Lechevalier (N)

CHU Bordeaux, Laboratoire d'Hématologie Biologique, Bordeaux, France.

Isabelle Luquet (I)

Laboratoire d'Hématologie Biologique, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France; and.

Emilie Klein (E)

CHU Bordeaux, Laboratoire d'Hématologie Biologique, Bordeaux, France.

Audrey Sarry (A)

Service d'Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.

Héloïse Rey (H)

Service d'Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.

Anne-Charlotte de Grande (AC)

Centre Hospitalo Universitaire (CHU) Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.

Fabien Despas (F)

Département de Pharmacologie Médicale et Clinique, Centre de Pharmacovigilance, Pharmacoépidémiologie et Information sur les Médicaments, INSERM, UMR-1027, Pharmacoépidémiologie, évaluation de l'utilisation des médicaments et de la sécurité des médicaments, Centre d'Investigation Clinique 1426, CHU de Toulouse, Toulouse, France.

Arnaud Pigneux (A)

Centre Hospitalo Universitaire (CHU) Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.
Université de Bordeaux, Bordeaux, France.
Institut National de la Santé et de la Recherche Médicale, U1035, Bordeaux, France.

Christian Récher (C)

Service d'Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.
Université Toulouse III Paul Sabatier, Toulouse, France.
Cancer Research Center of Toulouse, Unité Mixte de Recherche (UMR) 1037 INSERM, ERL5294 Centre National de la Recherche Scientifique,Toulouse, France.

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