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Titel:

Midostaurin plus intensive chemotherapy for younger and older patients with AML and FLT3 internal tandem duplications.

Dokumenttyp:
Article; Clinical Trial, Phase II; Journal Article; Research Support, Non-U.S. Gov't
Autor(en):
Döhner, Hartmut; Weber, Daniela; Krzykalla, Julia; Fiedler, Walter; Wulf, Gerald; Salih, Helmut; Lübbert, Michael; Kühn, Michael W M; Schroeder, Thomas; Salwender, Hans; Götze, Katharina; Westermann, Jörg; Fransecky, Lars; Mayer, Karin; Hertenstein, Bernd; Ringhoffer, Mark; Tischler, Hans-Joachim; Machherndl-Spandl, Sigrid; Schrade, Anika; Paschka, Peter; Gaidzik, Verena I; Theis, Frauke; Thol, Felicitas; Heuser, Michael; Schlenk, Richard F; Bullinger, Lars; Saadati, Maral; Benner, Axel; Larson,...     »
Abstract:
We conducted a single-arm, phase 2 trial (German-Austrian Acute Myeloid Leukemia Study Group [AMLSG] 16-10) to evaluate midostaurin with intensive chemotherapy followed by allogeneic hematopoietic-cell transplantation (HCT) and a 1-year midosta urin maintenance therapy in adult patients with acute myeloid leukemia (AML) and fms-related tyrosine kinase 3 (FLT3) internal tandem duplication (ITD). Patients 18 to 70 years of age with newly diagnosed FLT3-ITD-positive AML were eligible. Primary and key secondary endpoints were event-free survival (EFS) and overall survival (OS). Results were compared with a historical cohort of 415 patients treated on 5 prior AMLSG trials; statistical analysis was performed using a double-robust adjustment with propensity score weighting and covariate adjustment. Results were also compared with patients (18-59 years) treated on the placebo arm of the Cancer and Leukemia Group B (CALGB) 10603/RATIFY trial. The trial accrued 440 patients (18-60 years, n = 312; 61-70 years, n = 128). In multivariate analysis, EFS was significantly in favor of patients treated within the AMLSG 16-10 trial compared with the AMLSG control (hazard ratio [HR], 0.55; P < .001); both in younger (HR, 0.59; P < .001) and older patients (HR, 0.42; P < .001). Multivariate analysis also showed a significant beneficial effect on OS compared with the AMLSG control (HR, 0.57; P < .001) as well as to the CALGB 10603/RATIFY trial (HR, 0.71; P = .005). The treatment effect of midostaurin remained significant in sensitivity analysis including allogeneic HCT as a time-dependent covariate. Addition of midostaurin to chemotherapy was safe in younger and older patients. In comparison with historical controls, the addition of midostaurin to intensive therapy led to a significant improvement in outcome in younger and older patients with AML and FLT3-ITD. This trial is registered at clinicaltrialsregistry.eu as Eudra-CT number 2011-003168-63 and at clinicaltrials.gov as NCT01477606.
Zeitschriftentitel:
Blood Adv
Jahr:
2022
Band / Volume:
6
Heft / Issue:
18
Seitenangaben Beitrag:
5345-5355
Volltext / DOI:
doi:10.1182/bloodadvances.2022007223
PubMed:
http://view.ncbi.nlm.nih.gov/pubmed/35486475
Print-ISSN:
2473-9529
TUM Einrichtung:
290; Klinik und Poliklinik für Innere Medizin III, Hämatologie und Onkologie
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