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A phase 1, first-in-human study of AMG 900, an orally administered pan-Aurora kinase inhibitor, in adult patients with advanced solid tumors.
Carducci, Michael; Shaheen, Montaser; Markman, Ben; Hurvitz, Sara; Mahadevan, Daruka; Kotasek, Dusan; Goodman, Oscar B; Rasmussen, Erik; Chow, Vincent; Juan, Gloria; Friberg, Gregory R; Gamelin, Erick; Vogl, Florian D; Desai, Jayesh.
Afiliação
  • Carducci M; Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, 1M59 Bunting Blaustein Cancer Research Building, 1650 Orleans Street, Baltimore, MD, 21287, USA. Carducci@jhmi.edu.
  • Shaheen M; University of Arizona Cancer Center, Tucson, AZ, USA.
  • Markman B; Monash Health, Melbourne, VIC, Australia.
  • Hurvitz S; University of California Los Angeles, Los Angeles, CA, USA.
  • Mahadevan D; University of Arizona Cancer Center, Tucson, AZ, USA.
  • Kotasek D; Adelaide Cancer Centre, Kurralta Park, Adelaide, SA, Australia.
  • Goodman OB; Comprehensive Cancer Centers of Nevada, Las Vegas, NV, USA.
  • Rasmussen E; Amgen Inc., Thousand Oaks, CA, USA.
  • Chow V; Amgen Inc., Thousand Oaks, CA, USA.
  • Juan G; Amgen Inc., Thousand Oaks, CA, USA.
  • Friberg GR; Amgen Inc., Thousand Oaks, CA, USA.
  • Gamelin E; Amgen Inc., Thousand Oaks, CA, USA.
  • Vogl FD; Amgen Inc., Thousand Oaks, CA, USA.
  • Desai J; Royal Melbourne Hospital, Parkville, VIC, Australia.
Invest New Drugs ; 36(6): 1060-1071, 2018 12.
Article em En | MEDLINE | ID: mdl-29980894
Background Aurora kinase overexpression or amplifications are associated with high proliferation, poor prognosis, and therapeutic resistance in human tumors. AMG 900 is an investigational, oral, selective pan-Aurora kinase inhibitor. Methods This first-in-human trial included dose-escalation and dose-expansion phases ( ClinicalTrials.gov : NCT00858377). Dose escalation evaluated the safety, tolerability, and pharmacokinetics of AMG 900 in advanced solid tumors and determined the maximum tolerated dose (MTD) with/without granulocyte colony-stimulating factor (G-CSF) prophylaxis. Dose expansion evaluated clinical activity in three tumor types: taxane- and platinum-resistant ovarian cancer, taxane-resistant triple-negative breast cancer (TNBC), and castration-resistant and taxane- or cisplatin/etoposide-resistant prostate cancer (CRPC). AMG 900 was administered 4 days on/10 days off at 1-50 mg/day during escalation and at the MTD with G-CSF during expansion. Results AMG 900 showed rapid absorption with fast clearance, supporting once-daily dosing. The MTD was 25 mg/day, increasing to 40 mg/day with G-CSF. Grade ≥ 3 treatment-related adverse events included neutropenia (37%), anemia (23%), leukopenia (14%), and thrombocytopenia (12%). During dose expansion, 3/29 (10.3%, 95% CI: 2.0%-28.0%) evaluable patients with ovarian cancer experienced partial response by central imaging per RECIST 1.1; median duration of response was 24.1 weeks (95% CI: 16.1-34.1). Seven patients (24.1%, 95% CI: 10.3%-43.5%) experienced partial response per Gynecologic Cancer InterGroup criteria; 5/9 patients positive for p53 expression responded to treatment. No objective responses were observed in patients with TNBC or CRPC per RECIST 1.1. Conclusions AMG 900 40 mg/day with G-CSF had manageable toxicity and demonstrated single-agent activity in patients with heavily pretreated, chemotherapy-resistant ovarian cancer.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ftalazinas / Inibidores de Proteínas Quinases / Aurora Quinases / Neoplasias Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ftalazinas / Inibidores de Proteínas Quinases / Aurora Quinases / Neoplasias Idioma: En Ano de publicação: 2018 Tipo de documento: Article