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重新活检可提高阿法替尼与奥希替尼治疗表皮生长因子受体第19外显子缺失的非小细胞肺癌的生存率:台湾的一项多中心研究

Rebiopsy Enhances Survival with Afatinib vs. Osimertinib in EGFR Exon 19 Deletion Non-Small Cell Lung Cancer: A Multicenter Study in Taiwan.

作者信息

Kuo Jerry Shu-Hung, Chang Cheng-Yu, Chang Shih-Chieh, Wei Yu-Feng, Chen Chung-Yu

机构信息

Department of Internal Medicine, National Taiwan University Hospital Yunlin Branch, Yunlin County, Douliu City 640, Taiwan.

Division of Chest Medicine, Department of Internal Medicine, Far Eastern Memorial Hospital, New Taipei City 220, Taiwan.

出版信息

Curr Oncol. 2025 Jan 10;32(1):36. doi: 10.3390/curroncol32010036.

Abstract

BACKGROUND

Afatinib and Osimertinib are first-line treatments for EGFR-mutated advanced non-small cell lung cancer (NSCLC), but their comparative efficacies and the patient groups that benefit the most remain unclear. This multicenter retrospective study evaluated the efficacy of first-line Afatinib and Osimertinib in NSCLC patients with EGFR 19del and no brain metastases at diagnosis.

METHODS

The primary endpoints were time on treatment (ToT) and overall survival (OS). Survival analyses were performed for three groups: Afatinib followed by Osimertinib, Afatinib followed by other therapies, and Osimertinib (alone or followed by other therapies). Rebiopsy practices, including T790M mutation detection, were also analyzed in patients with disease progression on Afatinib.

RESULTS

Among 97 Afatinib-treated and 60 Osimertinib-treated patients, Osimertinib showed a significantly longer ToT (23.3 vs. 16.5 months; = 0.007). Median OS was numerically higher for Afatinib with sequential Osimertinib (40.5 vs. 34.6 months for Osimertinib; = 0.473). Osimertinib demonstrated advantages, with fewer brain metastases upon progression and fewer adverse effects. In the Afatinib group, 64% of patients with disease progression underwent rebiopsy, with 39% testing positive for T790M mutation and subsequently receiving Osimertinib. Rebiopsy was most frequently performed on the lung parenchyma using non-surgical methods.

CONCLUSIONS

In this real-world study, Osimertinib achieved a significantly longer ToT compared to Afatinib in NSCLC patients with EGFR 19del and no brain metastases. The sequential use of Afatinib followed by Osimertinib showed a trend toward improved OS, highlighting the importance of rebiopsy for identifying T790M mutations to guide subsequent therapy.

摘要

背景

阿法替尼和奥希替尼是表皮生长因子受体(EGFR)突变的晚期非小细胞肺癌(NSCLC)的一线治疗药物,但它们的相对疗效以及最能从中获益的患者群体仍不明确。这项多中心回顾性研究评估了一线使用阿法替尼和奥希替尼对诊断时EGFR 19外显子缺失且无脑转移的NSCLC患者的疗效。

方法

主要终点为治疗时间(ToT)和总生存期(OS)。对三组患者进行生存分析:先使用阿法替尼后使用奥希替尼、先使用阿法替尼后使用其他疗法、奥希替尼(单独使用或之后使用其他疗法)。还对阿法替尼治疗期间疾病进展的患者进行了再次活检操作分析,包括T790M突变检测。

结果

在97例接受阿法替尼治疗和60例接受奥希替尼治疗的患者中,奥希替尼的ToT显著更长(23.3个月对16.5个月;P = 0.007)。先使用阿法替尼后使用奥希替尼的患者的中位OS在数值上更高(奥希替尼为34.6个月;P = 0.473)。奥希替尼显示出优势,疾病进展时脑转移较少,不良反应也较少。在阿法替尼组中,64%疾病进展的患者接受了再次活检,其中39%检测到T790M突变阳性,随后接受了奥希替尼治疗。再次活检最常采用非手术方法在肺实质进行。

结论

在这项真实世界研究中,对于EGFR 19外显子缺失且无脑转移的NSCLC患者,奥希替尼的ToT显著长于阿法替尼。先使用阿法替尼后使用奥希替尼显示出OS改善的趋势,突出了再次活检对于识别T790M突变以指导后续治疗的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6757/11763488/f4a07d47aeae/curroncol-32-00036-g001.jpg

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