Dismal outcome of refractory or relapsing patients with myelodysplasia‐related acute myeloid leukemia partially alleviated by intensive chemotherapy

Author:

Leroy Harmony1,Gadaud Noémie2,Bérard Emilie3,Klein Emilie4ORCID,Luquet Isabelle5,Vial Jean‐Philippe4,Rieu Jean‐Baptiste5,Lechevalier Nicolas4ORCID,Tavitian Suzanne2,Leguay Thibaut1,Largeaud Laetitia5,Bidet Audrey4,Delabesse Eric5,Sarry Audrey2,de Grande Anne‐Charlotte1,Récher Christian2ORCID,Pigneux Arnaud16,Bertoli Sarah2ORCID,Dumas Pierre‐Yves16ORCID

Affiliation:

1. CHU Bordeaux, Service d'Hématologie Clinique et de Thérapie Cellulaire Bordeaux France

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

3. Centre Hospitalier Universitaire de Toulouse, Service d'Epidémiologie, CERPOP, Inserm, Université Toulouse III Paul Sabatier Toulouse France

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

5. Laboratoire d'Hématologie Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse‐Oncopole Toulouse France

6. Université de Bordeaux, Bordeaux, Institut National de la Santé et de la Recherche Médicale Bordeaux France

Abstract

AbstractBackgroundAcute myeloid leukemia (AML) with myelodysplasia‐related characteristics is a heterogeneous subset of AML that has been challenged throughout the history of myeloid malignancies classifications, considered to have similar outcomes as intermediate‐ or adverse‐risk AML depending on the subgroup. However, little is known about the fate of these patients in refractory or relapsed situation (R/R) after first line therapy.MethodsA large series of R/R AML patients, recorded in the French DATAML registry, have received either intensive chemotherapy (ICT), azacitidine (AZA) as single agent, or best supportive care (BSC). A cohort of 183 patients (median age 63‐year‐old) with what was called at the time AML‐MRC has been explored, and data are reported here.ResultsPatient status was refractory for 93, while 90 had relapsed. Respectively, 88, 34, and 61 were included in the three treatment arms. The median OS of the whole cohort was 4.2 months (95%CI: 3.1–5.6) with a mean 1‐year overall survival of 24% ± 3.2%. There was no significant survival difference between refractory and relapsed patients. The BSC group had overall a significantly worse outcome (p = 0.0001), and this remained true in both refractory (p = 0.01) and relapsed (p = 0.002) patients. Similar survivals were observed in both groups comparing ICT and AZA.ConclusionsThese data, reporting about an ill‐explored population, indicate the poor prognosis of this condition where both ICT and AZA can be proposed. The latter, which was demonstrated here to be a feasible option, should be added to new targeted therapies.

Publisher

Wiley

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