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一项奥希替尼一线治疗老年 EGFR 突变阳性晚期 NSCLC 的 II 期临床试验:SPIRAL-0 研究。

A Phase II Trial on Osimertinib as a First-Line Treatment for EGFR Mutation-Positive Advanced NSCLC in Elderly Patients: The SPIRAL-0 Study.

机构信息

Department of Respiratory Medicine, Uji-Tokushukai Medical Center, Uji, Japan.

Department of Respiratory Medicine, Japanese Red Cross Kyoto Daini Hospital, Kyoto, Japan.

出版信息

Oncologist. 2022 Nov 3;27(11):903-e834. doi: 10.1093/oncolo/oyac193.

Abstract

BACKGROUND

Osimertinib is one of the standard first-line treatments for advanced non-small cell lung cancer in patients with epidermal growth factor receptor (EGFR) mutations, because it achieves significantly longer progression-free survival (PFS) than conventional first-line treatments (hazard ratio: 0.46). However, the efficacy and safety of osimertinib as a first-line treatment for patients aged ≥75 years remain unclear.

METHODS

This phase II study was performed to prospectively investigate the efficacy and safety of osimertinib for elderly patients with EGFR mutation-positive advanced non-small cell lung cancer. The primary endpoint was 1-year PFS rate; secondary endpoints were overall response rate (ORR), PFS, overall survival (OS), and safety.

RESULTS

Thirty-eight patients were included in the analysis. The 1-year PFS rate was 59.4% (95% confidence interval [CI], 46.1%-72.7%), which did not meet the primary endpoint (the threshold 1-year PFS rate of 50% predicted using data from the NEJ003 study). The most common grade 3/4 adverse events were rash/dermatitis acneiform/ALT increased/hypokalemia (2 patients, 5%). Seven patients developed pneumonitis (17.5%). There were no other cases of treatment discontinuation due to adverse events other than pneumonitis.

CONCLUSION

Although this study did not meet the primary endpoint, osimertinib was tolerable for elderly patients with EGFR mutation-positive advanced non-small cell lung cancer. (Japan Registry of Clinical Trials [JRCT] ID number: jRCTs071180007).

摘要

背景

奥希替尼是表皮生长因子受体(EGFR)突变的晚期非小细胞肺癌患者的标准一线治疗药物之一,因为它比传统的一线治疗方法(风险比:0.46)显著延长了无进展生存期(PFS)。然而,奥希替尼作为 75 岁及以上患者的一线治疗药物的疗效和安全性仍不清楚。

方法

这项 II 期研究旨在前瞻性地研究奥希替尼治疗 EGFR 突变阳性的晚期非小细胞肺癌老年患者的疗效和安全性。主要终点是 1 年 PFS 率;次要终点是总缓解率(ORR)、PFS、总生存期(OS)和安全性。

结果

38 例患者纳入分析。1 年 PFS 率为 59.4%(95%置信区间 [CI],46.1%-72.7%),未达到主要终点(使用 NEJ003 研究数据预测的 1 年 PFS 率 50%的阈值)。最常见的 3/4 级不良事件是皮疹/痤疮样皮炎/ALT 升高/低血钾(2 例,5%)。7 例发生肺炎(17.5%)。除肺炎外,无其他因不良事件而停止治疗的病例。

结论

尽管本研究未达到主要终点,但奥希替尼对 EGFR 突变阳性的晚期非小细胞肺癌老年患者是可耐受的。(日本临床试验注册中心 [JRCT] 编号:jRCTs071180007)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b17/9632307/02361e7a5c29/oyac193f0001.jpg

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