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低剂量奥希替尼作为表皮生长因子受体突变的晚期非小细胞肺癌患者二线治疗的真实世界疗效

Real-world efficacy of low dose osimertinib as second-line treatment in patients with epidermal growth factor receptor-mutated advanced non-small cell lung cancer.

作者信息

Poh Mau Ern, Balakrishnan Sivasubramaniam, Tan Sin Nee, Zainal Abidin Muhammad Adil, Liam Chong Kin, Tan Jiunn Liang, Pang Yong Kek, Alaga Arvindran, Tho Lye Mun, How Soon Hin

机构信息

Department of Medicine, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.

Kulliyyah of Medicine, International Islamic University Malaysia, Pahang, Malaysia.

出版信息

Transl Lung Cancer Res. 2024 Jul 30;13(7):1649-1659. doi: 10.21037/tlcr-24-243. Epub 2024 Jul 23.

Abstract

BACKGROUND

Response rates of epidermal growth factor receptor ()-mutated advanced non-small cell lung cancer (NSCLC) to lower doses of osimertinib [20 mg once daily (OD) and 40 mg OD] are similar to those of the recommended dose of 80 mg OD, but there is a lack of real-world evidence on the effect of the lower doses of osimertinib on survival outcomes. We conducted this study to assess the efficacy and safety of lower osimertinib doses for patients with -mutated advanced NSCLC whose disease had progressed on earlier generation EGFR tyrosine kinase inhibitors (TKIs) in a real-world clinical practice.

METHODS

This multicenter, retrospective study included patients with -mutated advanced NSCLC treated with low doses of osimertinib after failing first- or second-generation EGFR TKIs due to acquired T790M mutation. Data on demographics, staging, treatment history, best overall response rate (ORR) based on RECIST 1.1, and adverse events (AEs) were collected from the patients' case notes. Descriptive data were described in percentages and medians. Progression-free survival (PFS) and overall survival (OS) were calculated using the Kaplan-Meier method.

RESULTS

Of the 22 patients studied [males =8 and females =14; Eastern Cooperative Oncology Group (ECOG) 1 or 2 =7 and ECOG 3 or 4 =15], 45.5% were on 40 mg OD, 31.8% were on 80 mg every other day (EOD), and 22.7% on 40 mg EOD. First-line EGFR TKIs used included afatinib, erlotinib, and gefitinib. The ORR with lower doses of second-line osimertinib was 77.3%. Overall, the median PFS was 10.0 months [95% confidence interval (CI): 8.6-11.4] and median OS was 13.0 months (95% CI: 9.4-16.6). In patients with ECOG 1 or 2, the median PFS was 18.0 months (95% CI: 5.8-30.2) and the median OS was not reached at the time of analysis. In patients with poor ECOG performance status of 3 and 4, good survival outcomes were also seen with a median PFS of 7.0 months (95% CI: 4.7-9.3) and median OS of 10.0 months (95% CI: 7.5-12.5). All AEs except one case of paronychia were Grade 1. There were no Grade 3 or 4 AEs.

CONCLUSIONS

Treatment with low dose osimertinib demonstrated good efficacy and tolerability in -mutated advanced NSCLC patients who failed first-line treatment with first- or second-generation EGFR TKIs due to T790M mutation.

摘要

背景

表皮生长因子受体(EGFR)突变的晚期非小细胞肺癌(NSCLC)对较低剂量奥希替尼(每日一次20 mg和每日一次40 mg)的反应率与推荐剂量每日一次80 mg相似,但缺乏关于较低剂量奥希替尼对生存结果影响的真实世界证据。我们开展本研究以评估在真实世界临床实践中,较低剂量奥希替尼用于疾病在早期EGFR酪氨酸激酶抑制剂(TKIs)治疗后进展的EGFR突变晚期NSCLC患者的疗效和安全性。

方法

这项多中心回顾性研究纳入了因获得性T790M突变而在第一代或第二代EGFR TKIs治疗失败后接受低剂量奥希替尼治疗的EGFR突变晚期NSCLC患者。从患者病历中收集人口统计学、分期、治疗史、基于RECIST 1.1的最佳总体缓解率(ORR)和不良事件(AE)数据。描述性数据以百分比和中位数表示。采用Kaplan-Meier方法计算无进展生存期(PFS)和总生存期(OS)。

结果

在研究的22例患者中(男性8例,女性14例;东部肿瘤协作组[ECOG] 1或2分7例,ECOG 3或4分15例),45.5%患者接受每日一次40 mg治疗,31.8%患者接受隔日一次80 mg治疗,22.7%患者接受隔日一次40 mg治疗。一线使用的EGFR TKIs包括阿法替尼、厄洛替尼和吉非替尼。二线低剂量奥希替尼的ORR为77.3%。总体而言,中位PFS为10.0个月[95%置信区间(CI):8.6 - 11.4],中位OS为13.0个月(95% CI:9.4 - 16.6)。ECOG 1或2分的患者中,中位PFS为18.0个月(95% CI:5.8 - 30.2),分析时中位OS未达到。ECOG体能状态为3分和4分的患者也有较好的生存结果,中位PFS为7.0个月(95% CI:4.7 - 9.3),中位OS为10.0个月(95% CI:7.5 - 12.5)。除1例甲沟炎外,所有AE均为1级。无3级或4级AE。

结论

对于因T790M突变而一线治疗失败的EGFR突变晚期NSCLC患者,低剂量奥希替尼治疗显示出良好的疗效和耐受性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c861/11304135/949c2da62fe2/tlcr-13-07-1649-f1.jpg

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