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回顾性分析 EGFR 突变阳性的晚期非小细胞肺癌患者一线接受奥希替尼治疗的无进展生存期的独立预测因素。

Retrospective analysis of independent predictors of progression-free survival in patients with EGFR mutation-positive advanced non-small cell lung cancer receiving first-line osimertinib.

机构信息

Respiratory Disease Center, Yokohama City University Medical Center, Yokohama, Japan.

Department of Pulmonology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

出版信息

Thorac Cancer. 2022 Oct;13(19):2741-2750. doi: 10.1111/1759-7714.14608. Epub 2022 Aug 18.

Abstract

BACKGROUND

Clinically measurable factors affecting the progression-free survival (PFS) of patients receiving osimertinib as first-line therapy for epidermal growth factor receptor (EGFR) mutation-positive advanced non-small cell lung cancer (NSCLC) have not yet been established.

METHODS

We retrospectively reviewed the medical records of 61 patients treated with osimertinib as primary therapy for EGFR mutation-positive advanced NSCLC at Yokohama City University Medical Center between August 2018 and March 2022. Our objective was to identify the independent predictors of PFS.

RESULTS

The median age of participants was 74 years. Overall, 73.8% had good (0-1) Eastern Cooperative Oncology Group performance status (PS), and 98.4% had histology of adenocarcinoma. The EGFR mutation was exon19 deletion in 52.5% and exon21 L858R in 44.3% of patients. Programmed death-ligand 1 tumor proportion score >50% was observed in 21.3% and liver metastasis in 9.9% of patients. Median PFS was 19.5 months (95% confidence interval [CI]: 10.6-31.6), and overall survival was not reached. The objective response rate was 68.9%, and disease control rate was 93.4%. Multivariate analysis showed that poor PS (2-4) negatively impacted PFS (hazard ratio, 3.79; 95% CI: 1.46-9.87; p = 0.006). Median PFS in the good PS and poor PS groups was 20.4 months (95% CI: 12.4-not evaluable) and 7.2 months (95% CI: 7.2-19.5), respectively. Interstitial lung disease of all grades and grade 3 was observed as an adverse event in 6.6 and 4.9% of patients, respectively.

CONCLUSION

Poor PS was associated with poor prognosis in patients with EGFR mutation-positive advanced NSCLC treated with osimertinib as first-line therapy.

摘要

背景

接受奥希替尼作为表皮生长因子受体(EGFR)突变阳性晚期非小细胞肺癌(NSCLC)一线治疗的患者,其无进展生存期(PFS)的临床可测量因素尚未确定。

方法

我们回顾性分析了 2018 年 8 月至 2022 年 3 月在横滨市立大学医学中心接受奥希替尼作为一线治疗的 61 例 EGFR 突变阳性晚期 NSCLC 患者的病历。我们的目的是确定 PFS 的独立预测因素。

结果

参与者的中位年龄为 74 岁。总体而言,73.8%的患者东部合作肿瘤学组表现状态(PS)良好(0-1),98.4%的患者组织学类型为腺癌。EGFR 突变在 52.5%的患者中为外显子 19 缺失,在 44.3%的患者中为外显子 21 L858R。21.3%的患者程序性死亡配体 1 肿瘤比例评分(TPS)>50%,9.9%的患者有肝转移。中位 PFS 为 19.5 个月(95%置信区间[CI]:10.6-31.6),总生存期未达到。客观缓解率为 68.9%,疾病控制率为 93.4%。多变量分析显示,较差的 PS(2-4)对 PFS 有负面影响(危险比,3.79;95%CI:1.46-9.87;p=0.006)。PS 良好和不良的中位 PFS 分别为 20.4 个月(95%CI:12.4-不可评估)和 7.2 个月(95%CI:7.2-19.5)。所有等级和 3 级的间质性肺病分别在 6.6%和 4.9%的患者中观察到。

结论

在接受奥希替尼作为一线治疗的 EGFR 突变阳性晚期 NSCLC 患者中,较差的 PS 与预后不良相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91b7/9527177/0cc2cad1998c/TCA-13-2741-g001.jpg

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