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SPIRAL研究的治疗原理与设计:一项针对在既往表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)治疗期间出现进展的老年表皮生长因子受体T790M阳性非小细胞肺癌患者的奥希替尼II期试验。

Treatment rationale and design of the SPIRAL study: A phase II trial of osimertinib in elderly epidermal growth factor receptor T790M-positive nonsmall-cell lung cancer patients who progressed during prior EGFR-TKI treatment.

作者信息

Uchino Junji, Nakao Akira, Tamiya Nobuyo, Kaneko Yoshiko, Yamada Tadaaki, Yoshimura Kenichi, Fujita Masaki, Takayama Koichi

机构信息

Department of Pulmonary Medicine, Kyoto Prefectural University of Medicine, Kyoto Department of Respiratory Medicine, Faculty of Medicine, Fukuoka University, Fukuoka Department of Biostatistics, Innovative Clinical Research Center, Kanazawa University, Kanazawa, Ishikawa, Japan.

出版信息

Medicine (Baltimore). 2018 Jun;97(23):e11081. doi: 10.1097/MD.0000000000011081.

Abstract

BACKGROUND

Advances in epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) treatment led to research on the mechanism of the resistance have revealed that an occurrence of T790M gene mutation generated in exon 20 of the EGFR gene is associated with approximately 50% to 60% of observed resistance. Osimertinib, a 3rd-generation EGFR-TKI, has been shown to be effective against both EGFR tyrosine kinase inhibitor-sensitizing and T790M resistance mutations. In this study, we prospectively investigate the efficacy and safety of osimertinib in elderly patients aged ≥75 years, with ineffective prior EGFR-TKI treatment or with recurrence of EGFR-TKI mutation-positive or T790M mutation-positive nonsmall-cell lung cancer.

PATIENTS AND METHODS

In total, 35 subjects of both sexes aged ≥75 years with T790M mutation will be included. Participants with pulmonary disorders such as idiopathic pulmonary fibrosis, interstitial pneumonia, pneumoconiosis, active radiation pneumonitis, drug-induced pneumonia, and symptomatic brain metastasis will be excluded. Eligible patients will be administrated osimertinib (80 mg/d) until disease progression. The primary outcome is antitumor effect (objective response rate). The secondary outcomes are progression-free survival, overall survival, disease control rate, and safety.

ETHICS AND DISSEMINATION

The protocol was approved by the institutional review boards of Kyoto Prefectural University of Medicine and all the participating hospitals. Written informed consent was obtained from all patients before registration, in accordance with the Declaration of Helsinki. Results of the study will be disseminated via publications in peer-reviewed journals.

TRIAL REGISTRATION

Trial registration number = UMIN000022553.

摘要

背景

表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)治疗的进展促使对其耐药机制的研究,结果显示,表皮生长因子受体(EGFR)基因第20外显子中发生的T790M基因突变与约50%至60%的观察到的耐药情况相关。奥希替尼是一种第三代EGFR-TKI,已被证明对EGFR酪氨酸激酶抑制剂敏感和T790M耐药突变均有效。在本研究中,我们前瞻性地研究了奥希替尼在年龄≥75岁、既往EGFR-TKI治疗无效或EGFR-TKI突变阳性或T790M突变阳性的非小细胞肺癌复发的老年患者中的疗效和安全性。

患者与方法

总共将纳入35名年龄≥75岁且患有T790M突变的男女受试者。患有诸如特发性肺纤维化、间质性肺炎、尘肺病、放射性肺炎、药物性肺炎和有症状的脑转移等肺部疾病的参与者将被排除。符合条件的患者将接受奥希替尼(80mg/天)治疗,直至疾病进展。主要结局是抗肿瘤效果(客观缓解率)。次要结局是无进展生存期、总生存期、疾病控制率和安全性。

伦理与传播

该方案已获得京都府立医科大学及所有参与医院的机构审查委员会的批准。根据《赫尔辛基宣言》,在所有患者登记前均获得了书面知情同意。研究结果将通过在同行评审期刊上发表进行传播。

试验注册

试验注册号=UMIN000022553。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d906/5999479/d1841301b2aa/medi-97-e11081-g001.jpg

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