A phase Ib GOELAMS study of the mTOR inhibitor RAD001 in association with chemotherapy for AML patients in first relapse

被引:45
|
作者
Park, S. [1 ,2 ]
Chapuis, N. [2 ,3 ]
St Marcoux, F. [4 ]
Recher, C. [5 ]
Prebet, T. [6 ]
Chevallier, P. [7 ]
Cahn, J-Y [8 ]
Leguay, T. [9 ]
Bories, P. [10 ]
Witz, F. [11 ]
Lamy, T. [12 ]
Mayeux, P. [2 ]
Lacombe, C. [2 ,3 ]
Demur, C. [5 ]
Tamburini, J. [1 ,2 ]
Merlat, A. [13 ]
Delepine, R. [14 ]
Vey, N. [6 ]
Dreyfus, F. [1 ,2 ]
Bene, M. C. [11 ]
Ifrah, N. [15 ]
Bouscary, D. [2 ]
机构
[1] Hop Cochin, AP HP, Inst Cochin, Serv Hematol,INSERM U1016, F-75014 Paris, France
[2] Inst Cochin, INSERM U1016, CNRS UMR8104, Dept Immunohematol, Paris, France
[3] Hop Cochin, AP HP, Serv Hematol Biol, F-75014 Paris, France
[4] CHU Limoges, Hop Dupuytren, Serv Pharmacol Toxicol & Pharmacovigilance, Limoges, France
[5] Univ Toulouse, Hop Purpan, Toulouse, France
[6] Hop Paoli Calmettes, Marseille, France
[7] CHU Nantes, Serv Hematol, F-44035 Nantes 01, France
[8] CHU Grenoble, CNRS UJF, UMR5525, F-38043 Grenoble, France
[9] CHU Bordeaux, Pessac, France
[10] CHU Strasbourg, F-67000 Strasbourg, France
[11] CHU Nancy, Serv Hematol, Nancy, France
[12] CHU Rennes, Serv Hematol, Rennes, France
[13] BU Oncol Novartis Pharma SAS, Novartis, France
[14] CHU Bretonneau, F-37044 Tours, France
[15] CHU Angers, Serv Hematol, Angers, France
关键词
AML; relapse; RAD001; mTORC1; ACUTE MYELOID-LEUKEMIA; REMISSION-INDUCTION THERAPY; ACUTE MYELOGENOUS LEUKEMIA; MAMMALIAN TARGET; ANTILEUKEMIC ACTIVITY; RAPAMYCIN; EVEROLIMUS; SURVIVAL; COMBINATION; CYTARABINE;
D O I
10.1038/leu.2013.17
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The mTORC1 signaling pathway is constitutively activated in almost all acute myelogenous leukemia (AML) patients. We conducted a phase Ib trial combining RAD001 (everolimus), an allosteric inhibitor of mTORC1, and conventional chemotherapy, in AML patients under 65 years of age at first relapse (clinical trial NCT 01074086). Increasing doses of RAD001 from 10-70mg were administrated orally on days 1 and 7 (d1 and d7) of a 3+7 daunorubicin + cytarabine conventional induction chemotherapy regimen. Twenty-eight patients were enrolled in this trial. The treatment was well tolerated with <10% toxicity, mainly involving the gastrointestinal tract and lungs. In this phase Ib trial, the RAD001 maximum tolerated dose was not reached at 70 mg. Sixty-eight percent of patients achieved CR, of which 14 received a double induction. Eight subsequently were intensified with allogeneic-stem cell transplant. Strong plasma inhibition of P-p70S6K was observed after RAD001 administration, still detectable at d7 (d7) at the 70mg dosage. CR rates in patients with RAD001 areas under or above the curve median were 53% versus 85%. A 70mg dose of RAD001 at d1 and d7 of an induction chemotherapy regimen for AML has acceptable toxicity and may improve treatment.
引用
收藏
页码:1479 / 1486
页数:8
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