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Delivering HDAC over 3 or 5 days as consolidation in AML impacts health care resource consumption but not outcome.
Dumas, Pierre-Yves; Bertoli, Sarah; Bérard, Emilie; Leguay, Thibaut; Tavitian, Suzanne; Galtier, Jean; Alric, Camille; Bidet, Audrey; Delabesse, Eric; Rieu, Jean Baptiste; Vial, Jean-Philippe; Vergez, François; Lechevalier, Nicolas; Luquet, Isabelle; Klein, Emilie; Sarry, Audrey; Rey, Héloïse; de Grande, Anne-Charlotte; Despas, Fabien; Pigneux, Arnaud; Récher, Christian.
Afiliação
  • Dumas PY; Centre Hospitalo Universitaire (CHU) Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.
  • Bertoli S; Université de Bordeaux, Bordeaux, France.
  • Bérard E; Institut National de la Santé et de la Recherche Médicale, U1035, Bordeaux, France.
  • Leguay T; Service d'Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.
  • Tavitian S; Université Toulouse III Paul Sabatier, Toulouse, France.
  • Galtier J; Cancer Research Center of Toulouse, Unité Mixte de Recherche (UMR) 1037 INSERM, ERL5294 Centre National de la Recherche Scientifique,Toulouse, France.
  • Alric C; Service d'Epidémiologie, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.
  • Bidet A; UMR 1027, INSERM-Université de Toulouse III, Toulouse, France.
  • Delabesse E; Centre Hospitalo Universitaire (CHU) Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.
  • Rieu JB; Service d'Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.
  • Vial JP; Centre Hospitalo Universitaire (CHU) Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire, Bordeaux, France.
  • Vergez F; Service d'Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.
  • Lechevalier N; CHU Bordeaux, Laboratoire d'Hématologie Biologique, Bordeaux, France.
  • Luquet I; Université Toulouse III Paul Sabatier, Toulouse, France.
  • Klein E; Cancer Research Center of Toulouse, Unité Mixte de Recherche (UMR) 1037 INSERM, ERL5294 Centre National de la Recherche Scientifique,Toulouse, France.
  • Sarry A; Laboratoire d'Hématologie Biologique, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France; and.
  • Rey H; Laboratoire d'Hématologie Biologique, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France; and.
  • de Grande AC; CHU Bordeaux, Laboratoire d'Hématologie Biologique, Bordeaux, France.
  • Despas F; Université Toulouse III Paul Sabatier, Toulouse, France.
  • Pigneux A; Cancer Research Center of Toulouse, Unité Mixte de Recherche (UMR) 1037 INSERM, ERL5294 Centre National de la Recherche Scientifique,Toulouse, France.
  • Récher C; Laboratoire d'Hématologie Biologique, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France; and.
Blood Adv ; 4(16): 3840-3849, 2020 08 25.
Article em En | MEDLINE | ID: mdl-32790847
ABSTRACT
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Protocolos de Quimioterapia Combinada Antineoplásica Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Humans / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Protocolos de Quimioterapia Combinada Antineoplásica Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Humans / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article