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

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Version: Final published version
License: CC BY 4.0
Serval ID
serval:BIB_E10B8DCDE22C
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Inferior Outcome of Addition of the Aminopeptidase Inhibitor Tosedostat to Standard Intensive Treatment for Elderly Patients with AML and High Risk MDS.
Journal
Cancers
Author(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
Publication state
Published
Issued date
07/02/2021
Peer-reviewed
Oui
Volume
13
Number
4
Pages
672
Language
english
Notes
Publication types: Journal Article
Publication Status: epublish
Abstract
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.
Keywords
AML, aminopeptidase inhibitor, clinical trial, elderly, high-risk MDS, tosedostat
Pubmed
Web of science
Open Access
Yes
Create date
22/02/2021 13:34
Last modification date
12/01/2022 7:14
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