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一项多中心队列研究:奥希替尼对比阿法替尼作为 EGFR 突变非小细胞肺癌一线治疗:CJLSG1903 研究。

A multicenter cohort study of osimertinib compared with afatinib as first-line treatment for EGFR-mutated non-small-cell lung cancer from practical dataset: CJLSG1903.

机构信息

Respiratory Center, Matsusaka Municipal Hospital, Matsusaka, Mie, Japan; Department of Biostatistics, Yokohama City University School of Medicine, Yokohama, Kanagawa, Japan.

Department of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.

出版信息

ESMO Open. 2021 Jun;6(3):100115. doi: 10.1016/j.esmoop.2021.100115. Epub 2021 May 10.

Abstract

BACKGROUND

FLAURA, the prospective trial of osimertinib as a first-line therapy compared with first-generation epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs), did not show superior survival benefit for osimertinib in either the subgroup of Asians or the subgroup with the L858R mutation. In addition, the superiority of osimertinib compared with second-generation EGFR-TKI is thus far unclear.

PATIENTS AND METHODS

We reviewed the clinical data of all consecutive patients who were treated with osimertinib or afatinib as first-line therapy between May 2016 and October 2019 from 15 institutions in Japan. We defined the groups based on first-line EGFR-TKI as the afatinib group and the osimertinib group. Outcomes included time to discontinuation of any EGFR-TKI (TD-TKI), overall survival (OS), and time to treatment failure, with propensity score analysis carried out as an exploratory analysis in the survival and subgroup analyses.

RESULTS

A total of 554 patients were enrolled. Data on 326 patients in the osimertinib group, and 224 patients in the afatinib group were analyzed. TD-TKI adjusted by propensity score in the afatinib and osimertinib groups was 18.6 months (95% confidence interval 15.8 to 22.0) and 20.5 months (95% confidence interval 13.8 to not reached), respectively, without significant difference (P = 0.204). OS adjusted by propensity score favored the afatinib group with a significant difference (P = 0.018). Subgroup analysis with propensity score showed that patients with L858R and without brain metastasis had superior survival benefit with afatinib compared with osimertinib (P < 0.001).

CONCLUSIONS

TD-TKI in the afatinib group was not significantly prolonged compared with the osimertinib group in the practical data. In the exploratory analysis of patients with L858R-mutated non-small-cell lung cancer without brain metastasis, afatinib showed more benefit in OS over osimertinib.

摘要

背景

FLAURA 是一项前瞻性试验,比较了奥希替尼作为一线治疗与第一代表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)相比,奥希替尼在亚洲亚组或 L858R 突变亚组中均未显示出生存获益的优势。此外,与第二代 EGFR-TKI 相比,奥希替尼的优势目前尚不清楚。

患者和方法

我们回顾了 2016 年 5 月至 2019 年 10 月期间来自日本 15 家机构的所有连续接受奥希替尼或阿法替尼作为一线治疗的患者的临床数据。我们根据一线 EGFR-TKI 将患者分为阿法替尼组和奥希替尼组。主要结局指标包括任何 EGFR-TKI 停药时间(TD-TKI)、总生存期(OS)和治疗失败时间,采用倾向评分分析对生存和亚组分析进行探索性分析。

结果

共纳入 554 例患者。对奥希替尼组 326 例患者和阿法替尼组 224 例患者的数据进行了分析。阿法替尼组和奥希替尼组的 TD-TKI 经倾向评分校正后分别为 18.6 个月(95%置信区间 15.8-22.0)和 20.5 个月(95%置信区间 13.8-未达到),差异无统计学意义(P=0.204)。OS 经倾向评分校正后阿法替尼组更优,差异有统计学意义(P=0.018)。倾向评分亚组分析显示,无脑转移的 L858R 患者使用阿法替尼的生存获益优于奥希替尼(P<0.001)。

结论

在实际数据中,阿法替尼组的 TD-TKI 并未显著长于奥希替尼组。在无脑转移的 L858R 突变非小细胞肺癌患者的探索性分析中,阿法替尼的 OS 获益优于奥希替尼。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bd4/8134659/1e7a9f9480e4/gr1.jpg

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