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

Authors :
Harmony Leroy
Noémie Gadaud
Emilie Bérard
Emilie Klein
Isabelle Luquet
Jean‐Philippe Vial
Jean‐Baptiste Rieu
Nicolas Lechevalier
Suzanne Tavitian
Thibaut Leguay
Laetitia Largeaud
Audrey Bidet
Eric Delabesse
Audrey Sarry
Anne‐Charlotte deGrande
Christian Récher
Arnaud Pigneux
Sarah Bertoli
Pierre‐Yves Dumas
Source :
Cancer Medicine, Vol 13, Iss 3, Pp n/a-n/a (2024)
Publication Year :
2024
Publisher :
Wiley, 2024.

Abstract

Abstract Background Acute 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. Methods A 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. Results Patient 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. Conclusions These 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.

Details

Language :
English
ISSN :
20457634
Volume :
13
Issue :
3
Database :
Directory of Open Access Journals
Journal :
Cancer Medicine
Publication Type :
Academic Journal
Accession number :
edsdoj.0a123f7bd4524943ae1e40f16745848d
Document Type :
article
Full Text :
https://doi.org/10.1002/cam4.7003