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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
Publisher :
American Society of Hematology

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

Database :
OpenAIRE
Accession number :
edsair.doi...........f57abf9094f416349bbd7f9ecc75fc32