Literature DB >> 30197264

Osimertinib With Ramucirumab in EGFR-mutated, T790M-positive Patients With Progression During EGFR-TKI Therapy: Phase Ib Study.

Hiroaki Akamatsu1, Yasuhiro Koh2, Yuichi Ozawa2, Daichi Fujimoto3, Akito Hata3, Nobuyuki Katakami3, Keisuke Tomii3, Toshio Shimokawa4, Nobuyuki Yamamoto2.   

Abstract

BACKGROUND: Epidermal growth factor receptor (EGFR) T790M mutation is the most frequent mechanism of resistance among patients with progression during EGFR-tyrosine kinase inhibitor (TKI) therapy. A third-generation EGFR-TKI, osimertinib, demonstrated durable efficacy with mild adverse events in a phase III trial and is considered a novel standard regimen. The tolerability of osimertinib monotherapy has allowed for the development of a more efficacious combination regimen. Preclinical and clinical study data have suggested that vascular endothelial growth factor inhibition can enhance EGFR-TKI activity with tolerable toxicity. AIMS: The aim of the present single-arm, phase Ib study is to assess the tolerability of osimertinib combined with ramucirumab in patients with EGFR-mutated, T790M+ lung cancer with progression during EGFR-TKI therapy. The primary endpoint is to assess the safety of osimertinib plus ramucirumab at a fixed dose. The secondary endpoints are the overall response rate, progression-free survival, overall survival, and safety. Six patients will be enrolled in the trial.
Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  EGFR mutation; Osimertinib; Ramucirumab; T790M

Mesh:

Substances:

Year:  2018        PMID: 30197264     DOI: 10.1016/j.cllc.2018.08.001

Source DB:  PubMed          Journal:  Clin Lung Cancer        ISSN: 1525-7304            Impact factor:   4.785


  3 in total

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Authors:  Taiki Hakozaki; Yusuke Okuma; Kana Hashimoto; Yukio Hosomi
Journal:  J Cancer Res Clin Oncol       Date:  2019-07-26       Impact factor: 4.553

2.  Clinical utility of ramucirumab in non-small-cell lung cancer.

Authors:  Dipesh Uprety
Journal:  Biologics       Date:  2019-07-22

3.  Docosahexaenoic Acid Serving As Sensitizing Agents And Gefitinib Resistance Revertants In EGFR Targeting Treatment.

Authors:  Xuansheng Ding; Lei Ge; Chen Qiao; Aiwen Yan; Yuyin Ding; Junye Tao; Qianqian Liu
Journal:  Onco Targets Ther       Date:  2019-12-02       Impact factor: 4.147

  3 in total

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