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奥希替尼,第三代 EGFR 酪氨酸激酶抑制剂:一项真实世界疗效和安全性的回顾性多中心研究,用于晚期/复发性非小细胞肺癌。

Osimertinib, a third-generation EGFR tyrosine kinase inhibitor: A retrospective multicenter study of its real-world efficacy and safety in advanced/recurrent non-small cell lung carcinoma.

机构信息

Department of Respiratory Medicine, Tochigi Cancer Center, Utsunomiya, Japan.

Pulmonary Division, Department Internal Medicine, Saiseikai Utsunomiya Hospital, Utsunomiya, Japan.

出版信息

Thorac Cancer. 2020 Apr;11(4):935-942. doi: 10.1111/1759-7714.13378. Epub 2020 Mar 4.

Abstract

BACKGROUND

Osimertinib is recommended for T790M mutation-positive advanced non-small cell lung cancer (NSCLC) resistant to first- and second-generation epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs). Recently, some reports exist on the real-world use of osimertinib; however, reports involving third/later-line use are few. Hence, this study was conducted to evaluate the efficacy and safety of osimertinib used in various treatment lines for T790M-positive NSCLC patients.

METHODS

This retrospective, observational, multicenter study included T790M-positive advanced/recurrent NSCLC patients treated with osimertinib from May 2016 to March 2018. The clinical characteristics, efficacy, and adverse events were retrospectively investigated. The Kaplan-Meier method was used to analyze progression-free survival (PFS) and overall survival (OS). PFS-associated clinical characteristics were evaluated using the Cox proportional hazards model.

RESULTS

The objective response rate (ORR) and disease control rate (DCR) were 60.7% and 91.1%, respectively; the median PFS was 11.0 months. There were no significant differences in the median PFS for patients treated with osimertinib as second-line and third-/later-line (14.5 vs. 11.0 months respectively, P = 0.327). Analysis using the Cox proportional hazards model for clinical features affecting PFS also revealed no significant factors. Adverse events of grade ≥ 3 were reported in 15 patients (26.8%); the most common were anemia (n = 3) and cutaneous toxicity (n = 3). Grade 4 neutropenia was observed in one patient; any-grade pneumonitis was observed in six patients (10.7%), including one with grade 3 pneumonitis.

CONCLUSIONS

Osimertinib demonstrated efficacy even when administered as third-/later-line treatment to NSCLC patients. Osimertinib-related pneumonitis was observed more frequently than previously reported.

KEY POINTS

Significant findings of the study Osimertinib shows efficacy even as later-line treatment in T790M mutation-positive NSCLC patients previously treated with EGFR-TKIs. However, the incidence of ≥ grade 3 adverse events, especially pneumonitis, was higher than that previously reported by other studies. What this study adds Osimertinib was approved for previously EGFR-TKI-treated EGFR T790M-positive NSCLC. With the increasing frequency of its use as first-line treatment, this study provides valuable evidence for the efficacy and safety of osimertinib for previously EGFR-TKI-treated NSCLC.

摘要

背景

奥希替尼适用于第一代和第二代表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKI)耐药的 T790M 突变阳性晚期非小细胞肺癌(NSCLC)。最近,有一些关于奥希替尼实际应用的报告;然而,涉及三线或以后线治疗的报告很少。因此,本研究旨在评估奥希替尼在 T790M 阳性 NSCLC 患者的各种治疗线中的疗效和安全性。

方法

本回顾性、观察性、多中心研究纳入了 2016 年 5 月至 2018 年 3 月期间接受奥希替尼治疗的 T790M 阳性晚期/复发性 NSCLC 患者。回顾性调查了临床特征、疗效和不良事件。采用 Kaplan-Meier 法分析无进展生存期(PFS)和总生存期(OS)。使用 Cox 比例风险模型评估与 PFS 相关的临床特征。

结果

客观缓解率(ORR)和疾病控制率(DCR)分别为 60.7%和 91.1%;中位 PFS 为 11.0 个月。奥希替尼二线和三线或以后线治疗的中位 PFS 无显著差异(分别为 14.5 个月和 11.0 个月,P=0.327)。使用 Cox 比例风险模型分析影响 PFS 的临床特征也未发现显著因素。15 例(26.8%)患者出现≥3 级不良事件;最常见的是贫血(n=3)和皮肤毒性(n=3)。1 例患者出现 4 级中性粒细胞减少症,6 例(10.7%)患者出现任何级别肺炎,其中 1 例为 3 级肺炎。

结论

奥希替尼即使作为 NSCLC 患者的三线或以后线治疗,也具有疗效。奥希替尼相关肺炎的发生率高于既往报道。

关键点

研究的重要发现奥希替尼对先前接受 EGFR-TKI 治疗的 EGFR T790M 阳性 NSCLC 患者作为后线治疗具有疗效。然而,≥3 级不良事件的发生率,特别是肺炎,高于其他研究的报道。本研究的重要意义奥希替尼已被批准用于先前接受 EGFR-TKI 治疗的 EGFR T790M 阳性 NSCLC。随着其作为一线治疗的应用频率增加,本研究为奥希替尼用于先前接受 EGFR-TKI 治疗的 NSCLC 的疗效和安全性提供了有价值的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b957/7113046/5a1e04f78829/TCA-11-935-g001.jpg

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