Improved Post remission survival of non- favorable risk Acute Myelogenous Leukemia (AML) patients following initial remission induction therapy with FLAG+/-Idarubicin versus 3 + 7 (Anthracycline + Cytarabine).


Journal

Leukemia research
ISSN: 1873-5835
Titre abrégé: Leuk Res
Pays: England
ID NLM: 7706787

Informations de publication

Date de publication:
06 2020
Historique:
received: 09 01 2020
revised: 03 02 2020
accepted: 10 02 2020
pubmed: 5 3 2020
medline: 6 10 2020
entrez: 5 3 2020
Statut: ppublish

Résumé

The fludarabine, high dose cytarabine and G-CSF with or without idarubicin combination regimen, referred to as FLAG+/-Ida, is commonly used as a salvage regimen for relapsed/refractory AML but its use as initial induction therapy has been more limited. The impact of choice of induction regimen on post remission survival remains unclear. We retrospectively analyzed 304 consecutive AML patients, with non-favorable NCCN risk who received initial treatment at our center with either 7 + 3 (n = 86) or FLAG+/-Ida (n = 218). Patients in the FLAG+/-Ida group were more likely to achieve remission after one course of induction (74 % vs 62 %, p < 0.001) and had a faster time to achieve CR (30 days vs 37.5, p < 0.001) compared to 7 + 3. The time from diagnosis to transplant was shorter among CR patients after FLAG+/-Ida compared to 7 + 3 (115 vs. 151 days, p < 0.003). The 3-year post-remission OS and DFS was significantly better for patients receiving FLAG-Ida at 54 % and 49 % compared to 39 % and 32 % for 7 + 3 respectively (P = 0.01). Factors associated with post-remission survival included age at CR1, NCCN risk, induction regimen (FLAG+/-Ida vs 3 + 7 h 0.62, p = 0.01) and receipt of HCT. Our data, with the limitations inherent to a retrospective analysis, shows that achieving CR after FLAG+/-Ida has better post remission survival than 7 + 3.

Identifiants

pubmed: 32127177
pii: S0145-2126(20)30023-0
doi: 10.1016/j.leukres.2020.106318
pii:
doi:

Substances chimiques

Cytarabine 04079A1RDZ
Granulocyte Colony-Stimulating Factor 143011-72-7
Vidarabine FA2DM6879K
Idarubicin ZRP63D75JW

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106318

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors have no financial conflict of interest related to this manuscript

Auteurs

Melhem M Solh (MM)

Blood and Marrow Transplant Program at Northside Hospital, Atlanta, GA, United States. Electronic address: msolh@bmtga.com.

Scott R Solomon (SR)

Blood and Marrow Transplant Program at Northside Hospital, Atlanta, GA, United States.

Lawrence E Morris (LE)

Blood and Marrow Transplant Program at Northside Hospital, Atlanta, GA, United States.

Xu Zhang (X)

Center for Clinical and Translational Sciences, University of Texas Health Science Center at Houston, United States.

H Kent Holland (HK)

Blood and Marrow Transplant Program at Northside Hospital, Atlanta, GA, United States.

Asad Bashey (A)

Blood and Marrow Transplant Program at Northside Hospital, Atlanta, GA, United States; Center for Clinical and Translational Sciences, University of Texas Health Science Center at Houston, United States.

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Classifications MeSH