Midostaurin plus Chemotherapy for Acute Myeloid Leukemia with a FLT3 Mutation


Por: Stone, RM, Mandrekar, SJ, Sanford, BL, Laumann, K, Geyer, S, Bloomfield, CD, Thiede, C, Prior, TW, Dohner, K, Marcucci, G, Lo-Coco, F, Klisovic, RB, Wei, A, Sierra, J, Sanz, MA, Brandwein, JM, de Witte, T, Niederwieser, D, Appelbaum, FR, Medeiros, BC, Tallman, MS, Krauter, J, Schlenk, RF, Ganser, A, Serve, H, Ehninger, G, Amadori, S, Larson, RA, Dohner, H

Publicada: 3 ago 2017
Resumen:
BACKGROUND Patients with acute myeloid leukemia (AML) and a FLT3 mutation have poor outcomes. We conducted a phase 3 trial to determine whether the addition of midostaurin - an oral multitargeted kinase inhibitor that is active in patients with a FLT3 mutation - to standard chemotherapy would prolong overall survival in this population. METHODS We screened 3277 patients, 18 to 59 years of age, who had newly diagnosed AML for FLT3 mutations. Patients were randomly assigned to receive standard chemotherapy (induction therapy with daunorubicin and cytarabine and consolidation therapy with high-dose cytarabine) plus either midostaurin or placebo; those who were in remission after consolidation therapy entered a maintenance phase in which they received either midostaurin or placebo. Randomization was stratified according to subtype of FLT3 mutation: point mutation in the tyrosine kinase domain (TKD) or internal tandem duplication (ITD) mutation with either a high ratio (> 0.7) or a low ratio (0.05 to 0.7) of mutant to wild-type alleles (ITD [high] and ITD [low], respectively). Allogeneic transplantation was allowed. The primary end point was overall survival. RESULTS A total of 717 patients underwent randomization; 360 were assigned to the midostaurin group, and 357 to the placebo group. The FLT3 subtype was ITD (high) in 214 patients, ITD (low) in 341 patients, and TKD in 162 patients. The treatment groups were well balanced with respect to age, race, FLT3 subtype, cytogenetic risk, and blood counts but not with respect to sex (51.7% in the midostaurin group vs. 59.4% in the placebo group were women, P = 0.04). Overall survival was significantly longer in the midostaurin group than in the placebo group (hazard ratio for death, 0.78; one-sided P = 0.009), as was event-free survival (hazard ratio for event or death, 0.78; one-sided P = 0.002). In both the primary analysis and an analysis in which data for patients who underwent transplantation were censored, the benefit of midostaurin was consistent across all FLT3 subtypes. The rate of severe adverse events was similar in the two groups. CONCLUSIONS The addition of the multitargeted kinase inhibitor midostaurin to standard chemotherapy significantly prolonged overall and event-free survival among patients with AML and a FLT3 mutation. (Funded by the National Cancer Institute and Novartis; ClinicalTrials.gov number, NCT00651261.)

Filiaciones:
Stone, RM:
 Dana Farber Canc Inst, Dept Med Oncol, 450 Brookline Ave,D-2053, Boston, MA 02115 USA

Mandrekar, SJ:
 Mayo Clin, Div Biomed Stat & Informat, Rochester, MN USA

 Mayo Clin, Alliance Stat & Data Ctr, Rochester, MN USA

Sanford, BL:
 Duke Univ, Alliance Stat & Data Ctr, Durham, NC USA

Laumann, K:
 Mayo Clin, Div Biomed Stat & Informat, Rochester, MN USA

 Mayo Clin, Alliance Stat & Data Ctr, Rochester, MN USA

Geyer, S:
 Mayo Clin, Alliance Stat & Data Ctr, Rochester, MN USA

 Ohio State Univ, Comprehens Canc Ctr, Columbus, OH 43210 USA

Bloomfield, CD:
 Ohio State Univ, Comprehens Canc Ctr, Columbus, OH 43210 USA

Thiede, C:
 Tech Univ Dresden, Univ Klinikum Carl Gustav Carus, Med Klin & Poliklin 1, Dresden, Germany

Prior, TW:
 Ohio State Univ, Comprehens Canc Ctr, Columbus, OH 43210 USA

Dohner, K:
 Univ Hosp Ulm, Dept Internal Med 3, Ulm, Germany

Marcucci, G:
 Ohio State Univ, Comprehens Canc Ctr, Columbus, OH 43210 USA

Lo-Coco, F:
 Univ Tor Vergata, Dept Biomed & Prevent, Rome, Italy

Klisovic, RB:
 Ohio State Univ, Comprehens Canc Ctr, Columbus, OH 43210 USA

Wei, A:
 Alfred Hosp, Dept Clin Haematol, Melbourne, Vic, Australia

 Monash Univ, Melbourne, Vic, Australia

Sierra, J:
 Autonomous Univ Barcelona, Dept Hematol, Hosp Santa Creu & St Pau, Barcelona, Spain

Sanz, MA:
 Univ Valencia, Dept Med, Dept Hematol, Hosp Univ Fe, Valencia, Spain

Brandwein, JM:
 Princess Margaret Hosp, Dept Med Oncol & Hematol, Toronto, ON, Canada

de Witte, T:
 Radboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Studies, Nijmegen, Netherlands

Niederwieser, D:
 Univ Leipzig, Hematol & Oncol, Leipzig, Germany

Appelbaum, FR:
 Fred Hutchinson Canc Res Ctr, Div Clin Res, 1124 Columbia St, Seattle, WA 98104 USA

Medeiros, BC:
 Stanford Univ, Stanford Comprehens Canc Ctr, Div Hematol Oncol, Stanford, CA 94305 USA

Tallman, MS:
 Mem Sloan Kettering Canc Ctr, Dept Med, Leukemia Serv, 1275 York Ave, New York, NY 10021 USA

 Weill Cornell Med Coll, New York, NY USA

Krauter, J:
 Hannover Med Sch, Dept Hematol Hemostasis Oncol & Stem Cell Transpl, Hannover, Germany

Schlenk, RF:
 Univ Hosp Ulm, Dept Internal Med 3, Ulm, Germany

Ganser, A:
 Hannover Med Sch, Dept Hematol Hemostasis Oncol & Stem Cell Transpl, Hannover, Germany

Serve, H:
 Goethe Univ Hosp Frankfurt, Dept Med 2, Hematol Oncol, Frankfurt, Germany

Ehninger, G:
 Tech Univ Dresden, Univ Klinikum Carl Gustav Carus, Med Klin & Poliklin 1, Dresden, Germany

Amadori, S:
 Univ Tor Vergata, Dept Biomed & Prevent, Rome, Italy

Larson, RA:
 Univ Chicago, Dept Med, 5841 S Maryland Ave, Chicago, IL 60637 USA

Dohner, H:
 Univ Hosp Ulm, Dept Internal Med 3, Ulm, Germany
ISSN: 00284793





NEW ENGLAND JOURNAL OF MEDICINE
Editorial
MASSACHUSETTS MEDICAL SOC, WALTHAM WOODS CENTER, 860 WINTER ST,, WALTHAM, MA 02451-1413 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 377 Número: 5
Páginas: 454-464
WOS Id: 000406747100007
ID de PubMed: 28644114
imagen Bronze, Green Accepted

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