Inferior Outcome of Addition of the Aminopeptidase Inhibitor Tosedostat to Standard Intensive Treatment for Elderly Patients with AML and High Risk MDS.

Détails

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Etat: Public
Version: Final published version
Licence: CC BY 4.0
ID Serval
serval:BIB_E10B8DCDE22C
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Inferior Outcome of Addition of the Aminopeptidase Inhibitor Tosedostat to Standard Intensive Treatment for Elderly Patients with AML and High Risk MDS.
Périodique
Cancers
Auteur⸱e⸱s
Janssen J., Löwenberg B., Manz M., Bargetzi M., Biemond B., Borne PVD, Breems D., Brouwer R., Chalandon Y., Deeren D., Efthymiou A., Gjertsen B.T., Graux C., Gregor M., Heim D., Hess U., Hoogendoorn M., Jaspers A., Jie A., Jongen-Lavrencic M., Klein S., Klift M.V., Kuball J., Lammeren-Venema D.V., Legdeur M.C., Loosdrecht A.V., Maertens J., Kooy MVM, Moors I., Nijziel M., Obbergh F.V., Oosterveld M., Pabst T., Poel M.V., Sinnige H., Spertini O., Terpstra W., Tick L., Velden W.V., Vekemans M.C., Vellenga E., Weerdt O., Westerweel P., Stüssi G., Norden Y.V., Ossenkoppele G.
ISSN
2072-6694 (Print)
ISSN-L
2072-6694
Statut éditorial
Publié
Date de publication
07/02/2021
Peer-reviewed
Oui
Volume
13
Numéro
4
Pages
672
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: epublish
Résumé
Treatment results of AML in elderly patients are unsatisfactory. We hypothesized that addition of tosedostat, an aminopeptidase inhibitor, to intensive chemotherapy may improve outcome in this population. After establishing a safe dose in a run-in phase of the study in 22 patients, 231 eligible patients with AML above 65 years of age (median 70, range 66-81) were randomly assigned in this open label randomized Phase II study to receive standard chemotherapy (3+7) with or without tosedostat at the selected daily dose of 120 mg (n = 116), days 1-21. In the second cycle, patients received cytarabine 1000 mg/m <sup>2</sup> twice daily on days 1-6 with or without tosedostat. CR/CRi rates in the 2 arms were not significantly different (69% (95% C.I. 60-77%) vs 64% (55-73%), respectively). At 24 months, event-free survival (EFS) was 20% for the standard arm versus 12% for the tosedostat arm (Cox-p = 0.01) and overall survival (OS) 33% vs 18% respectively (p = 0.006). Infectious complications accounted for an increased early death rate in the tosedostat arm. Atrial fibrillation was more common in the tosedostat arm as well. The results of the present study show that the addition of tosedostat to standard chemotherapy does negatively affect the therapeutic outcome of elderly AML patients.
Mots-clé
AML, aminopeptidase inhibitor, clinical trial, elderly, high-risk MDS, tosedostat
Pubmed
Web of science
Open Access
Oui
Création de la notice
22/02/2021 14:34
Dernière modification de la notice
12/01/2022 8:14
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