Osimertinib for patients with poor performance status and EGFR T790M mutation-positive advanced non-small cell lung cancer: a phase II clinical trial

被引:0
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作者
Kazuhisa Nakashima
Yuichi Ozawa
Haruko Daga
Hisao Imai
Motohiro Tamiya
Takaaki Tokito
Takahisa Kawamura
Hiroaki Akamatsu
Yuko Tsuboguchi
Toshiaki Takahashi
Nobuyuki Yamamoto
Keita Mori
Haruyasu Murakami
机构
[1] Division of Thoracic Oncology,Department of Internal Medicine, Division of Medical Oncology & Respiratory Medicine
[2] Shizuoka Cancer Center,Internal Medicine III
[3] Shimane University Faculty of Medicine,Department of Medical Oncology
[4] Wakayama Medical University,Division of Respiratory Medicine
[5] Osaka City General Hospital,Department of Thoracic Oncology
[6] Gunma Prefectural Cancer Center,Department of Medicine, Division of Respirology, Neurology, and Rheumatology
[7] Osaka International Cancer Institute,Clinical Research Center
[8] Kurume University School of Medicine,undefined
[9] Shizuoka Cancer Center,undefined
来源
Investigational New Drugs | 2020年 / 38卷
关键词
T790M mutation-positive; Non-small-cell lung cancer; Osimertinib; Poor performance status;
D O I
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学科分类号
摘要
Osimertinib is a molecularly targeted agent used to treat non-small cell lung cancer (NSCLC) patients with an epidermal growth factor receptor (EGFR) T790M mutation. However, its efficacy and safety profile when patients have poor performance status (PS) is unknown. Therefore, we conducted an open-label, multi-center, single-arm phase II study to evaluate its efficacy and safety in EGFR T790M mutation-positive NSCLC patients with Eastern Cooperative Oncology Group PS scores of between 2 and 4. Patients received 80 mg of osimertinib once daily. Our primary endpoint was progression-free survival. Eighteen patients were enrolled between June 2017 and November 2018. The median age was 77 years (range: 55–85 years). Ten, six, and two patients had PS scores of 2, 3, and 4, respectively. All patients had adenocarcinoma with common EGFR mutations and had been treated with first- or second-generation EGFR- tyrosine kinase inhibitors previously. The overall median progression-free survival was 7.0 months (90% confidence interval: 5.5–8.9 months). The overall response rate and median overall survival were 53% and 12.7 months, respectively. Moreover, improved PS scores were observed in 72% of the patients. Although the incidence of grade 3 adverse events was low, with no grade 4 or 5 events observed, three patients required treatment cessation due to the development of interstitial lung disease. Osimertinib therapy could be beneficial for EGFR T790M mutation-positive advanced NSCLC patients with poor PS. This trial was registered with the Japan Registry of Clinical Trials on March 12, 2019 (trial no. jRCT1041180081).
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页码:1854 / 1861
页数:7
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