Clinical outcome of therapy-related acute myeloid leukemia patients. Real-life experience in a University Hospital and a Cancer Center in France.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
08 2023
Historique:
revised: 17 06 2023
received: 13 01 2023
accepted: 27 06 2023
medline: 15 9 2023
pubmed: 7 8 2023
entrez: 7 8 2023
Statut: ppublish

Résumé

t-AML occurs after a primary malignancy treatment and retains a poor prognosis. To determine the impact of primary malignancies, therapeutic strategies, and prognostic factors on clinical outcomes of t-AML. A total of 112 adult patients were included in this study. Fifty-Five patients received intensive chemotherapy (IC), 33 non-IC, and 24 best supportive care. At t-AML diagnosis, 42% and 44% of patients presented an unfavorable karyotype and unfavorable 2010 ELN risk profile, respectively. Among treated patients (n = 88), 43 (49%) achieved complete remission: four out of 33 (12%) and 39 out of 55 (71%) in non-IC and IC groups, respectively. With a median follow-up of 5.5 months, the median overall survival (OS) and disease-free survival (DFS) for the whole population were 9 months and 6.3 months, respectively, and for the 88 treated patients 13.5 months and 8.2 months, respectively. Univariate analysis on OS and DFS showed a significant impact of high white blood cells (WBC) and blast counts at diagnosis, unfavorable karyotype and ELN classification. Multivariate analysis showed a negative impact of WBC count at diagnosis and a positive impact of chemotherapy on OS and DFS in the whole population. It also showed a negative impact of previous auto-HCT and high WBC count on OS and DFS and of IC on OS in treated patients which disappeared when we considered only confounding variables (age, previous cancers, marrow blasts, and 2010 ELN classification). In a pair-matched analysis comparing IC treated t-AML with de novo AML, there was no difference of OS and DFS between the two populations. We showed, in this study that t-AML patients with unfavorable features represented almost half of the population. Best outcomes obtained in patients receiving IC must be balanced by known confounding variables and should be improved by using new innovative agents and therapeutic strategies.

Sections du résumé

BACKGROUND
t-AML occurs after a primary malignancy treatment and retains a poor prognosis.
AIMS
To determine the impact of primary malignancies, therapeutic strategies, and prognostic factors on clinical outcomes of t-AML.
RESULTS
A total of 112 adult patients were included in this study. Fifty-Five patients received intensive chemotherapy (IC), 33 non-IC, and 24 best supportive care. At t-AML diagnosis, 42% and 44% of patients presented an unfavorable karyotype and unfavorable 2010 ELN risk profile, respectively. Among treated patients (n = 88), 43 (49%) achieved complete remission: four out of 33 (12%) and 39 out of 55 (71%) in non-IC and IC groups, respectively. With a median follow-up of 5.5 months, the median overall survival (OS) and disease-free survival (DFS) for the whole population were 9 months and 6.3 months, respectively, and for the 88 treated patients 13.5 months and 8.2 months, respectively. Univariate analysis on OS and DFS showed a significant impact of high white blood cells (WBC) and blast counts at diagnosis, unfavorable karyotype and ELN classification. Multivariate analysis showed a negative impact of WBC count at diagnosis and a positive impact of chemotherapy on OS and DFS in the whole population. It also showed a negative impact of previous auto-HCT and high WBC count on OS and DFS and of IC on OS in treated patients which disappeared when we considered only confounding variables (age, previous cancers, marrow blasts, and 2010 ELN classification). In a pair-matched analysis comparing IC treated t-AML with de novo AML, there was no difference of OS and DFS between the two populations.
CONCLUSION
We showed, in this study that t-AML patients with unfavorable features represented almost half of the population. Best outcomes obtained in patients receiving IC must be balanced by known confounding variables and should be improved by using new innovative agents and therapeutic strategies.

Identifiants

pubmed: 37548369
doi: 10.1002/cam4.6322
pmc: PMC10501294
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

16929-16944

Informations de copyright

© 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Amine Belhabri (A)

Department of Hematology, Leon Berard Cancer Center, Lyon, France.

Mael Heiblig (M)

Department of Hematology, University Hospital Lyon Sud, Pierre Benite, France.

Stephane Morisset (S)

Biostatistics Department, Leon Berard Cancer Center, Lyon, France.

Liliana Vila (L)

Department of Hematology, Leon Berard Cancer Center, Lyon, France.

Clémence Santana (C)

Department of Hematology, Leon Berard Cancer Center, Lyon, France.

Emmanuelle Nicolas-Virelizier (E)

Department of Hematology, Leon Berard Cancer Center, Lyon, France.

Sandrine Hayette (S)

Department of biology - GHS, University Hospital Lyon Sud, Pierre Benite, France.

Isabelle Tigaud (I)

Department of biology - GHS, University Hospital Lyon Sud, Pierre Benite, France.

Adriana Plesa (A)

Department of biology - GHS, University Hospital Lyon Sud, Pierre Benite, France.

Hélène Labussiere-Wallet (H)

Department of Hematology, University Hospital Lyon Sud, Pierre Benite, France.

Mohamad Sobh (M)

Research Advisor, Faculty of Medicine, University of Ottawa, Ottawa, Canada.

Anne-Sophie Michallet (AS)

Department of Hematology, Leon Berard Cancer Center, Lyon, France.

Balsat Marie (B)

Department of Hematology, University Hospital Lyon Sud, Pierre Benite, France.

Franck-Emmanuel Nicolini (FE)

Department of Hematology, Leon Berard Cancer Center, Lyon, France.

Yann Guillermin (Y)

Department of Hematology, Leon Berard Cancer Center, Lyon, France.

Fossard Gaëlle (F)

Department of Hematology, University Hospital Lyon Sud, Pierre Benite, France.

Laure Lebras (L)

Department of Hematology, Leon Berard Cancer Center, Lyon, France.

Philippe Rey (P)

Department of Hematology, Leon Berard Cancer Center, Lyon, France.

Lucie Jauffret-Bertholon (L)

Department of Hematology, Leon Berard Cancer Center, Lyon, France.

Marie-Charlotte Laude (MC)

Department of Hematology, Leon Berard Cancer Center, Lyon, France.

Loron Sandrine (L)

Department of Hematology, University Hospital Lyon Sud, Pierre Benite, France.

Mauricette Michallet (M)

Department of Hematology, Leon Berard Cancer Center, Lyon, France.

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