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真实世界中奥希替尼预处理经验在表皮生长因子受体 T790M 突变阳性局部晚期或转移性非小细胞肺癌患者中的应用。

Real-world osimertinib pretreatment experience in patients with epidermal growth factor receptor T790M mutation-positive locally advanced or metastatic non-small cell lung cancer.

机构信息

Department of Internal Medicine, Division of Pulmonary Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan.

School of Medicine and Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan.

出版信息

PLoS One. 2024 May 16;19(5):e0303046. doi: 10.1371/journal.pone.0303046. eCollection 2024.

Abstract

Osimertinib has demonstrated efficacy in patients with epidermal growth factor receptor (EGFR) T790M-positive non-small cell lung cancer (NSCLC) in clinical trials. However, real-world data on its effectiveness remain scarce. Taiwanese patients with T790M-positive locally advanced or metastatic NSCLC and progressive disease following treatment with at least one EGFR tyrosine kinase inhibitor (TKI) were enrolled from the osimertinib early access program. Of the 419 patients (mean age, 63 years; female, 67%), 53% were heavily pretreated (≥ third-line [3L]), making osimertinib a fourth-line (4L) intervention. The median progression-free survival (PFS) was 10.5 months (95% confidence interval [CI]: 8.95-11.41); the 18-month PFS rate was 26.5%. The median overall survival (OS) was 19.0 months (95% CI: 16.30-20.95); the 24-month OS rate was 40.9%. The objective response rate was 32.46%, and the disease control rate was 86.38%. The median time to treatment discontinuation of osimertinib monotherapy was 11.9 months (95% CI: 10.49-13.11). Subgroup analyses of median PFS and OS in the chemotherapy combination group vs. the osimertinib monotherapy group yielded no difference. Central nervous system (CNS) metastasis, number of prior lines of therapy, and types of initial EGFR-TKIs did not significantly impact outcomes. The median PFS values were 9.0 (95% CI: 5.18-11.34) and 10.9 (95% CI: 9.18-11.90) months with and without CNS metastasis, respectively, and 10.8 (95% CI: 8.59-12.69), 13.6 (95% CI: 10.89-16.3), and 9.2 (95% CI: 7.8-10.62) months for second-line (2L), 3L, and ≥4L therapy, respectively. In patients who received osimertinib as 2L therapy, the median PFS values in response to prior afatinib, erlotinib and gefitinib treatment were 11.2 (95% CI: 4.85-4.79), 10.5 (95% CI: 8.59-20.26) and 8.7 (95% CI: 7.21-16.79) months, respectively. Overall, real-world data from Taiwan support the clinical benefits of osimertinib in EGFR T790M -positive NSCLC.

摘要

奥希替尼在临床试验中已被证明对表皮生长因子受体(EGFR)T790M 阳性非小细胞肺癌(NSCLC)患者有效。然而,关于其疗效的真实世界数据仍然很少。台湾的 T790M 阳性局部晚期或转移性 NSCLC 患者,在至少一种 EGFR 酪氨酸激酶抑制剂(TKI)治疗后出现进展,符合奥希替尼早期准入计划的条件。在 419 名患者(平均年龄 63 岁;女性占 67%)中,53%的患者接受了大量预处理(≥三线[3L]),这使得奥希替尼成为四线(4L)干预药物。中位无进展生存期(PFS)为 10.5 个月(95%置信区间[CI]:8.95-11.41);18 个月的 PFS 率为 26.5%。中位总生存期(OS)为 19.0 个月(95%CI:16.30-20.95);24 个月的 OS 率为 40.9%。客观缓解率为 32.46%,疾病控制率为 86.38%。奥希替尼单药治疗的中位停药时间为 11.9 个月(95%CI:10.49-13.11)。化疗联合组与奥希替尼单药组的中位 PFS 和 OS 亚组分析无差异。中枢神经系统(CNS)转移、治疗线数和初始 EGFR-TKIs 的类型均未显著影响结局。有和无脑转移的中位 PFS 值分别为 9.0(95%CI:5.18-11.34)和 10.9(95%CI:9.18-11.90),二线(2L)、三线(3L)和≥四线(4L)治疗的中位 PFS 值分别为 10.8(95%CI:8.59-12.69)、13.6(95%CI:10.89-16.3)和 9.2(95%CI:7.8-10.62)。在接受奥希替尼二线治疗的患者中,既往阿法替尼、厄洛替尼和吉非替尼治疗的中位 PFS 值分别为 11.2(95%CI:4.85-4.79)、10.5(95%CI:8.59-20.26)和 8.7(95%CI:7.21-16.79)个月。总体而言,来自台湾的真实世界数据支持奥希替尼在 EGFR T790M 阳性 NSCLC 中的临床获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cbb/11098304/f8407be180e1/pone.0303046.g001.jpg

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