Literature DB >> 28419328

Efficacy and safety of osimertinib in a Japanese compassionate use program.

Yutaka Fujiwara1,2, Yasushi Goto1, Shintaro Kanda1, Hidehito Horinouchi1, Noboru Yamamoto1,2, Naomi Sakiyama3, Reiko Ando Makihara3, Yuichiro Ohe1.   

Abstract

BACKGROUND: Osimertinib is a third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) that targets the T790M mutation of EGFR. In 2016, AstraZeneca conducted a compassionate use program for osimertinib in Japan.
METHODS: Eighteen consecutive patients with histologically proven non-small-cell lung cancer (NSCLC) and harboring the T790M EGFR mutation participated in the compassionate use program between 1 April and 25 May 2016, at the National Cancer Center Hospital. We examined the efficacy and safety of osimertinib in a compassionate use program.
RESULTS: All patients had been previously treated with both cytotoxic chemotherapy and EGFR TKIs. Overall response rate was 62.5% (95% confidence interval (CI): 35.9-89.1%). Among the six patients pretreated with a third-generation EGFR TKI, two (33%) responded to osimertinib. On administration with osimertinib, median progression-free and overall survival rates at six months were 66.7% (95% CI: 44.9-88.5) and 88.9% (95% CI: 74.4-100), respectively. Although the toxicity of osimertinib was mild in most patients, three patients had severe adverse events: two developed interstitial lung disease (ILD) and one developed Grade 3 hepatotoxicity. Among these, two (33%) of the six patients who received osimertinib following nivolumab treatment developed severe adverse events, with one each developing Grade 3 hepatotoxicity and Grade 3 ILD. Only one patient visited our hospital seeking to participate in the compassionate program from another hospital.
CONCLUSION: Osimertinib demonstrated efficacy even in patients with heavily pretreated NSCLC harboring the T790M mutation. Some patients pretreated with another third-generation EGFR TKI also responded to osimertinib.
© The Author 2017. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com

Entities:  

Keywords:  acquired resistance; compassionate use program; non-small-cell lung cancer; osimertinib; third-generation EGFR TKI

Mesh:

Substances:

Year:  2017        PMID: 28419328     DOI: 10.1093/jjco/hyx050

Source DB:  PubMed          Journal:  Jpn J Clin Oncol        ISSN: 0368-2811            Impact factor:   3.019


  5 in total

1.  Efficacy and safety of osimertinib in treating EGFR-mutated advanced NSCLC: A meta-analysis.

Authors:  Lilan Yi; Junsheng Fan; Ruolan Qian; Peng Luo; Jian Zhang
Journal:  Int J Cancer       Date:  2019-01-20       Impact factor: 7.396

2.  Efficacy, safety, and resistance profile of osimertinib in T790M mutation-positive non-small cell lung cancer in real-world practice.

Authors:  Dong Kyu Oh; Won Jun Ji; Woo Sung Kim; Chang-Min Choi; Shin-Kyo Yoon; Jin Kyung Rho; Jae Cheol Lee
Journal:  PLoS One       Date:  2019-01-09       Impact factor: 3.240

3.  Characteristics of the Compassionate Use Program in Japan: An Analysis of Expanded Access Clinical Trials from 2016 to 2021.

Authors:  Hideki Maeda; Marika Uchida; Mikiko Kusano; Katsura Tsukamoto; Moeka Yamanoi
Journal:  Clin Pharmacol Ther       Date:  2022-06-07       Impact factor: 6.903

4.  Life-threatening pneumonitis after first-line treatment with osimertinib for primary T790M mutated non-small cell lung cancer.

Authors:  Maik Häntschel; Johannes Niebling; Almut Häring; Max-Felix Häring; Thorben Groß; Marius Horger; Reimer Riessen; Michael Haap; Richard A Lewis; Michael Böckeler; Jürgen Hetzel
Journal:  Thorac Cancer       Date:  2020-05-06       Impact factor: 3.500

5.  The efficacy and safety of osimertinib in treating nonsmall cell lung cancer: A PRISMA-compliant systematic review and meta-analysis.

Authors:  Jing Liu; Xuemei Li; Yinghong Shao; Xiyun Guo; Jinggui He
Journal:  Medicine (Baltimore)       Date:  2020-08-21       Impact factor: 1.817

  5 in total

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