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患者特征是否会影响 EGFR 酪氨酸激酶抑制剂的治疗效果?一项真实世界研究中,一线 EGFR-TKIs 治疗的东亚晚期非小细胞肺癌患者的生存结局的网络荟萃分析

Do patient characteristics affect EGFR tyrosine kinase inhibitor treatment outcomes? A network meta-analysis of real-world survival outcomes of East Asian patients with advanced non-small cell lung cancer treated with first-line EGFR-TKIs.

机构信息

Divisions of Pulmonary & Critical Care Medicine, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Kaohsiung, Taiwan.

Ph.D. Program in Environmental and Occupational Medicine, College of Medicine, and Research Center for Precision Environmental Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.

出版信息

Thorac Cancer. 2023 Nov;14(32):3208-3216. doi: 10.1111/1759-7714.15111. Epub 2023 Sep 22.

DOI:10.1111/1759-7714.15111
PMID:37737541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10643796/
Abstract

BACKGROUND

Despite the well-established efficacies of tyrosine kinase inhibitors (TKIs) in epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC), there is limited real-world evidence comparing their effectiveness according to patients' clinical characteristics. This network meta-analysis (NMA) compared survival outcomes among first-line EGFR-TKIs in different subgroups of East Asian patients with advanced NSCLC.

METHODS

This NMA included real-world observational studies reporting outcomes with TKIs in patients aged >65 years, with baseline brain metastasis, with different Eastern Cooperative Oncology Group (ECOG) statuses, or with different common EGFR mutation types.

RESULTS

In patients with the EGFR L858R mutation, afatinib resulted in significantly longer progression-free survival (PFS) than erlotinib (hazard ratio [HR]: 0.59, 95% confidence interval [CI]: 0.46-0.75) and gefitinib (HR: 0.41, 95% CI: 0.32-0.53). Similarly, in patients with the EGFR Del19 mutation, afatinib and erlotinib resulted in significantly longer PFS than gefitinib (HR: 0.48 with 95% CI: 0.33-0.71 and HR: 0.54 with 95% CI: 0.36-0.80, respectively). Moreover, afatinib resulted in significantly longer PFS than gefitinib in patients with brain metastasis (HR: 0.53, 95% CI: 0.33-0.87) or ECOG status 0-1 (HR: 0.37, 95% CI: 0.23-0.59).

CONCLUSION

This NMA suggests that afatinib results in similar PFS to erlotinib and superior PFS than gefitinib in patients with Del19 mutant NSCLC, aged ≥65 years, with ECOG scores of 0-1, and with baseline brain metastasis.

摘要

背景

尽管表皮生长因子受体 (EGFR) 突变型非小细胞肺癌 (NSCLC) 的酪氨酸激酶抑制剂 (TKI) 的疗效已得到充分证实,但根据患者的临床特征比较其疗效的真实世界证据有限。本网络荟萃分析 (NMA) 比较了不同亚组东亚晚期 NSCLC 患者一线 EGFR-TKI 的生存结局。

方法

本 NMA 纳入了报告 TKI 治疗年龄 >65 岁、基线有脑转移、不同东部合作肿瘤学组 (ECOG) 状态或不同常见 EGFR 突变类型患者结局的真实世界观察性研究。

结果

在 EGFR L858R 突变患者中,阿法替尼的无进展生存期 (PFS) 明显长于厄洛替尼 (风险比 [HR]:0.59,95%置信区间 [CI]:0.46-0.75) 和吉非替尼 (HR:0.41,95% CI:0.32-0.53)。同样,在 EGFR Del19 突变患者中,阿法替尼和厄洛替尼的 PFS 明显长于吉非替尼 (HR:0.48,95% CI:0.33-0.71 和 HR:0.54,95% CI:0.36-0.80)。此外,阿法替尼在有脑转移 (HR:0.53,95% CI:0.33-0.87) 或 ECOG 评分 0-1 (HR:0.37,95% CI:0.23-0.59) 的患者中,PFS 明显长于吉非替尼。

结论

本 NMA 表明,阿法替尼在 Del19 突变型 NSCLC 患者、年龄≥65 岁、ECOG 评分为 0-1 和基线有脑转移患者中,与厄洛替尼的 PFS 相似,而优于吉非替尼。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f95/10643796/8783e038fc3f/TCA-14-3208-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f95/10643796/eecd3ced3c47/TCA-14-3208-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f95/10643796/9ec8d106b5c6/TCA-14-3208-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f95/10643796/c37c98e3fa41/TCA-14-3208-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f95/10643796/8783e038fc3f/TCA-14-3208-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f95/10643796/eecd3ced3c47/TCA-14-3208-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f95/10643796/9ec8d106b5c6/TCA-14-3208-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f95/10643796/c37c98e3fa41/TCA-14-3208-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f95/10643796/8783e038fc3f/TCA-14-3208-g005.jpg

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