酪氨酸激酶抑制剂在一线治疗表皮生长因子受体突变的晚期NSCLC:来自越南的真实世界数据。

IF 4.1 4区 医学 Q3 ONCOLOGY
Oncology Research Pub Date : 2025-06-26 eCollection Date: 2025-01-01 DOI:10.32604/or.2025.061905
Khanh Toan Nguyen, Thi Huong Pham, VAN Lam Ngo, VAN Tuan Bui, VAN Nhat Nguyen, Thi Phuong Thao Nguyen, Thi Khanh Ha Nguyen, Thi Thuy VAN Nguyen
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引用次数: 0

摘要

目的:本研究旨在评价酪氨酸激酶抑制剂(TKIs)一线治疗表皮生长因子受体(EGFR)突变的晚期非小细胞肺癌(NSCLC)的疗效和不良事件。方法:对2017年1月至2023年8月在越南义安肿瘤医院接受TKIs作为一线治疗的EGFR突变晚期NSCLC患者进行回顾性研究。主要终点包括客观缓解率、无进展生存期和耐受性。次要终点是总生存期。结果:211例患者接受厄洛替尼(74例)、吉非替尼(85例)、阿法替尼(34例)或奥西替尼(18例)一线治疗。总缓解率为76.7%,其中奥西替尼为83.4%,阿法替尼为73.6%,厄洛替尼为77.1%,吉非替尼为76.5%。吉非替尼组的中位无进展生存期为12.2个月(95% CI: 11.1-13.2),厄洛替尼组的中位无进展生存期为13.4个月(95% CI: 10.6-16.2),阿法替尼组的中位无进展生存期为18.4个月(95% CI: 10.1-26.8),奥西替尼组的中位无进展生存期为25.3个月(p = 0.001)。吉非替尼组中位总生存期为21.8个月(95% Cl: 15.0-28.4),厄洛替尼组中位总生存期为30个月(95% Cl: 19.1-40.9) (p = 0.154)。大多数药物相关不良事件为1级或2级。腹泻是阿法替尼组最常见的不良事件,占44.1%;厄洛替尼组皮疹发生率最高,为60.8%;甲沟炎(31.8%)和间质性肺疾病(3.5%)在吉非替尼组中最为常见。结论:TKIs作为EGFR突变晚期NSCLC患者的一线治疗方法,疗效显著,延长生存期,耐受性良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tyrosine kinase inhibitors in first-line treatment of advanced NSCLC with epidermal growth factor receptor mutations: Real-world data from Vietnam.

Tyrosine kinase inhibitors in first-line treatment of advanced NSCLC with epidermal growth factor receptor mutations: Real-world data from Vietnam.

Tyrosine kinase inhibitors in first-line treatment of advanced NSCLC with epidermal growth factor receptor mutations: Real-world data from Vietnam.

Tyrosine kinase inhibitors in first-line treatment of advanced NSCLC with epidermal growth factor receptor mutations: Real-world data from Vietnam.

Aims: The study aimed to evaluate the effectiveness and adverse events of tyrosine kinase inhibitors (TKIs) in the first-line treatment of advanced non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) mutations.

Methods: A retrospective study on advanced NSCLC patients with EGFR mutations treated with TKIs as a first-line therapy at Nghe An Oncology Hospital, Vietnam between January 2017 and August 2023. The primary endpoints included objective response rate, progression-free survival, and tolerability. The secondary endpoint was overall survival.

Results: A total of 211 patients received first-line treatment with Erlotinib (n = 74), Gefitinib (n = 85), Afatinib (n = 34) or Osimertinib (n = 18). The overall response rate was 76.7%, with Osimertinib at 83.4%, Afatinib at 73.6%, Erlotinib at 77.1%, and Gefitinib at 76.5%. The median progression-free survival in the Gefitinib group was 12.2 months (95% CI: 11.1-13.2), 13.4 months (95% CI: 10.6-16.2) in the Erlotinib group, 18.4 months (95% CI: 10.1-26.8) in the Afatinib group and 25.3 months in the Osimertinib group (p = 0.001). The median overall survival was 21.8 months (95% Cl: 15.0-28.4) in the Gefitinib group, 30 months (95% Cl: 19.1-40.9) in the Erlotinib group (p = 0.154). Most drug-related adverse events were grade 1 or 2. Diarrhea was the most frequent adverse event in the Afatinib group at 44.1%; rash was most common in the Erlotinib group at 60.8%; paronychia (31.8%), and interstitial lung disease (3.5%) were most frequent in the Gefitinib group.

Conclusion: The TKIs as first-line therapies for advanced NSCLC patients with EGFR mutated are highly effective, prolong survival, and are well tolerated.

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来源期刊
Oncology Research
Oncology Research 医学-肿瘤学
CiteScore
4.40
自引率
0.00%
发文量
56
审稿时长
3 months
期刊介绍: Oncology Research Featuring Preclinical and Clincal Cancer Therapeutics publishes research of the highest quality that contributes to an understanding of cancer in areas of molecular biology, cell biology, biochemistry, biophysics, genetics, biology, endocrinology, and immunology, as well as studies on the mechanism of action of carcinogens and therapeutic agents, reports dealing with cancer prevention and epidemiology, and clinical trials delineating effective new therapeutic regimens.
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