Literature DB >> 21120480

A two-part phase II study of cediranib in patients with advanced solid tumours: the effect of food on single-dose pharmacokinetics and an evaluation of safety, efficacy and imaging pharmacodynamics.

Claire L Mitchell1, J P B O'Connor, C Roberts, Y Watson, A Jackson, S Cheung, J Evans, J Spicer, A Harris, C Kelly, S Rudman, M Middleton, A Fielding, J Tessier, H Young, G J M Parker, G C Jayson.   

Abstract

BACKGROUND: Cediranib (RECENTIN™) is an oral, highly potent VEGF inhibitor. This study evaluated the effect of food on the pharmacokinetics of cediranib and compared the administration of continual cediranib via two dosing strategies using this as a platform to investigate pharmacodynamic imaging biomarkers.
METHODS: Sixty patients were randomised to receive two single doses of cediranib in either fed/fasted or fasted/fed state (Part A). In continual dosage phase (Part B), patients were randomised to a fixed-dose or dose-escalation arm. Exploratory pharmacodynamic assessments were performed using DCE-MRI and CT enhancing fraction (EnF).
RESULTS: In part A, plasma AUC and C (max) of cediranib were lower in the presence of food by a mean of 24 and 33%, respectively (94% CI: AUC, 12-34% and C (max), 20-43%), indicating food reduces cediranib plasma exposure. In part B, cediranib 30 mg/day appeared to be the most sustainable for chronic dosing. Continuous cediranib therapy was associated with sustained antivascular effects up to 16 weeks, with significant reductions in DCE-MRI parameters and CT EnF.
CONCLUSIONS: It is recommended that cediranib be administered at least 1 h before or 2 h after food. Evidence of antitumour activity was observed, with significant sustained effects upon imaging vascular parameters.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 21120480     DOI: 10.1007/s00280-010-1534-3

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  8 in total

Review 1.  Dynamic contrast-enhanced MRI in clinical trials of antivascular therapies.

Authors:  James P B O'Connor; Alan Jackson; Geoff J M Parker; Caleb Roberts; Gordon C Jayson
Journal:  Nat Rev Clin Oncol       Date:  2012-02-14       Impact factor: 66.675

2.  Population pharmacokinetic and exposure simulation analysis for cediranib (AZD2171) in pooled Phase I/II studies in patients with cancer.

Authors:  Jianguo Li; Nidal Al-Huniti; Anja Henningsson; Weifeng Tang; Eric Masson
Journal:  Br J Clin Pharmacol       Date:  2017-03-27       Impact factor: 4.335

3.  Population exposure-safety analysis of cediranib for Phase I and II studies in patients with cancer.

Authors:  Nidal Al-Huniti; Klas Petersson; Weifeng Tang; Eric Masson; Jianguo Li
Journal:  Br J Clin Pharmacol       Date:  2018-01-31       Impact factor: 4.335

4.  A phase II trial of single-agent bevacizumab in patients with recurrent anaplastic glioma.

Authors:  Teri N Kreisl; Weiting Zhang; Yazmin Odia; Joanna H Shih; John A Butman; Dima Hammoud; Fabio M Iwamoto; Joohee Sul; Howard A Fine
Journal:  Neuro Oncol       Date:  2011-08-24       Impact factor: 12.300

Review 5.  Clinical Pharmacokinetics and Pharmacodynamics of Cediranib.

Authors:  Weifeng Tang; Alex McCormick; Jianguo Li; Eric Masson
Journal:  Clin Pharmacokinet       Date:  2017-07       Impact factor: 6.447

6.  A phase II study of cediranib, an oral VEGF inhibitor, in previously untreated patients with metastatic or recurrent malignant melanoma.

Authors:  Elaine McWhirter; Ian Quirt; Thomas Gajewski; Gregory Pond; Lisa Wang; June Hui; Amit Oza
Journal:  Invest New Drugs       Date:  2016-02-03       Impact factor: 3.850

7.  DCE-MRI assessment of the effect of Epstein-Barr virus-encoded latent membrane protein-1 targeted DNAzyme on tumor vasculature in patients with nasopharyngeal carcinomas.

Authors:  Wei-Hua Liao; Li-Fang Yang; Xiao-Yu Liu; Gao-Feng Zhou; Wu-Zhong Jiang; Bob-Lei Hou; Lun-Quan Sun; Ya Cao; Xiao-Yi Wang
Journal:  BMC Cancer       Date:  2014-11-18       Impact factor: 4.430

8.  Vascular effects, efficacy and safety of nintedanib in patients with advanced, refractory colorectal cancer: a prospective phase I subanalysis.

Authors:  Klaus Mross; Martin Büchert; Annette Frost; Michael Medinger; Peter Stopfer; Matus Studeny; Rolf Kaiser
Journal:  BMC Cancer       Date:  2014-07-11       Impact factor: 4.430

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.