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Glasdegib plus intensive/nonintensive chemotherapy in untreated acute myeloid leukemia: BRIGHT AML 1019 Phase III trials.
Cortes, Jorge E; Dombret, Hervé; Merchant, Akil; Tauchi, Tetsuzo; DiRienzo, Christine G; Sleight, Barbara; Zhang, Xiaoxi; Leip, Eric P; Shaik, Naveed; Bell, Timothy; Chan, Geoffrey; Sekeres, Mikkael A.
Afiliação
  • Cortes JE; Georgia Cancer Center, Augusta University, Augusta, GA 30912, USA.
  • Dombret H; Institut de Recherche Saint-Louis, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris Institut Universitaire d`Hematologie Hopital Saint Louis, Paris, France.
  • Merchant A; Department of Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
  • Tauchi T; Department of Hematology, Shin-Yurigaoka General Hospital, Kawasaki, Japan.
  • DiRienzo CG; Pfizer Oncology, Pfizer Inc., New York, NY 10017, USA.
  • Sleight B; Pfizer Oncology, Pfizer Inc., New York, NY 10017, USA.
  • Zhang X; Pfizer Oncology, Pfizer Inc., New York, NY 10017, USA.
  • Leip EP; Pfizer Oncology, Pfizer Inc., New York, NY 10017, USA.
  • Shaik N; Pfizer Oncology, Pfizer Inc., New York, NY 10017, USA.
  • Bell T; Pfizer Oncology, Pfizer Inc., New York, NY 10017, USA.
  • Chan G; Pfizer Oncology, Pfizer Inc., New York, NY 10017, USA.
  • Sekeres MA; Leukemia Program, Cleveland Clinic, Cleveland, OH 44195, USA.
Future Oncol ; 15(31): 3531-3545, 2019 Nov.
Article em En | MEDLINE | ID: mdl-31516032
Glasdegib, an oral Hedgehog pathway inhibitor, has been associated with significantly improved survival when combined with low-dose cytarabine in patients with untreated acute myeloid leukemia (AML) who were unsuitable for intensive chemotherapy, when compared with low-dose cytarabine alone. BRIGHT AML 1019 (NCT03416179) comprises two independently powered Phase III, randomized (1:1), double-blind global trials evaluating oral glasdegib 100 mg once daily or placebo plus one of two standard chemotherapy regimens in adults with untreated AML. The intensive trial combines glasdegib/placebo with cytarabine and daunorubicin (7 + 3), while the nonintensive trial combines glasdegib/placebo with azacitidine. The primary end point of both studies is overall survival. Secondary end points include response, time to and duration of response, event-free survival, safety, patient-reported outcomes and pharmacokinetics. Trial registration number: ClinicalTrials.gov identifier: NCT03416179.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Protocolos de Quimioterapia Combinada Antineoplásica / Protocolos Clínicos Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Protocolos de Quimioterapia Combinada Antineoplásica / Protocolos Clínicos Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article