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Addition of lenalidomide to intensive treatment in younger and middle-aged adults with newly diagnosed AML: the HOVON-SAKK-132 trial

Authors :
Löwenberg, Bob
Pabst, Thomas
Maertens, Johan
Gradowska, Patrycja
Biemond, Bart J.
Spertini, Olivier
Vellenga, Edo
Griskevicius, Laimonas
Tick, Lidwine W.
Jongen-Lavrencic, Mojca
van Marwijk Kooy, Marinus
Vekemans, Marie-Christiane
van der Velden, Walter J. F. M.
Beverloo, Berna
Michaux, Lucienne
Graux, Carlos
Deeren, Dries
de Weerdt, Okke
van Esser, Joost W. J.
Bargetzi, Mario
Klein, Saskia K.
Gadisseur, Alain
Westerweel, Peter E.
Veelken, Hendrik
Gregor, Michael
Silzle, Tobias
van Lammeren-Venema, Daniëlle
Moors, Ine
Breems, Dimitri A.
Hoogendoorn, Mels
Legdeur, Marie-Cecile J. C.
Fischer, Thomas
Kuball, Juergen
Cornelissen, Jan
Porkka, Kimmo
Juliusson, Gunnar
Meyer, Peter
Höglund, Martin
Gjertsen, Bjorn T.
Janssen, Jeroen J. W. M.
Huls, Gerwin
Passweg, Jakob
Cloos, Jacqueline
Valk, Peter J. M.
van Elssen, Catharina H. M. J.
Manz, Markus G.
Floisand, Yngvar
Ossenkoppele, Gert J.
Source :
Blood Advances; February 2021, Vol. 5 Issue: 4 p1110-1121, 12p
Publication Year :
2021

Abstract

Lenalidomide, an antineoplastic and immunomodulatory drug, has therapeutic activity in acute myeloid leukemia (AML), but definitive studies about its therapeutic utility have been lacking. In a phase 3 study, we compared 2 induction regimens in newly diagnosed patients age 18 to 65 years with AML: idarubicine-cytarabine (cycle 1) and daunorubicin and intermediate-dose cytarabine (cycle 2) without or with lenalidomide (15 mg orally on days 1-21). One final consolidation cycle of chemotherapy or autologous stem cell transplantation (auto-SCT) or allogeneic SCT (allo-SCT) was provided according to a prognostic risk and minimal residual disease (MRD)–adapted approach. Event-free survival (EFS; primary end point) and other clinical end points were assessed. A second random assignment in patients in complete response or in complete response with incomplete hematologic recovery after cycle 3 or auto-SCT involved 6 cycles of maintenance with lenalidomide (10 mg on days 1-21) or observation. In all, 392 patients were randomly assigned to the control group, and 388 patients were randomly assigned to lenalidomide induction. At a median follow-up of 41 months, the study revealed no differences in outcome between the treatments (EFS, 44% ± 2% standard error and overall survival, 54% ± 2% at 4 years for both arms) although in an exploratory post hoc analysis, a lenalidomide benefit was suggested in SRSF2-mutant AML. In relation to the previous Dutch-Belgian Hemato-Oncology Cooperative Group and Swiss Group for Clinical Cancer Research (HOVON-SAKK) studies that used a similar 3-cycle regimen but did not pursue an MRD-guided approach, these survival estimates compare markedly more favorably. MRD status after cycle 2 lost prognostic value in intermediate-risk AML in the risk-adjusted treatment context. Maintenance with lenalidomide showed no apparent effect on relapse probability in 88 patients randomly assigned for this part of the study.

Details

Language :
English
ISSN :
24739529 and 24739537
Volume :
5
Issue :
4
Database :
Supplemental Index
Journal :
Blood Advances
Publication Type :
Periodical
Accession number :
ejs55384554
Full Text :
https://doi.org/10.1182/bloodadvances.2020003855