安洛替尼加奥西替尼治疗奥西替尼耐药非鳞状非小细胞肺癌的渐进进展:一项回顾性研究

IF 2.3 3区 医学 Q3 ONCOLOGY
Yu Hua, Minghui Liu, Boshi Li, Hongbing Zhang, Zihe Zhang, Yanan Wang, Jinghao Liu, Xin Li, Yongwen Li, Sen Wei, Hongyu Liu, Jun Chen
{"title":"安洛替尼加奥西替尼治疗奥西替尼耐药非鳞状非小细胞肺癌的渐进进展:一项回顾性研究","authors":"Yu Hua, Minghui Liu, Boshi Li, Hongbing Zhang, Zihe Zhang, Yanan Wang, Jinghao Liu, Xin Li, Yongwen Li, Sen Wei, Hongyu Liu, Jun Chen","doi":"10.1111/1759-7714.70071","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Previous studies have shown that anlotinib plus third-generation epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) overcome acquired resistance to EGFR-TKIs in patients with advanced EGFR-mutant nonsmall cell lung cancer (NSCLC). This study aimed to retrospectively evaluate whether anlotinib plus osimertinib overcame acquired resistance in patients with nsq-NSCLC who gradually progressed after first-line EGFR-TKI treatment.</p><p><strong>Methods: </strong>This study included patients with nsq-NSCLC who developed gradual progression after first-line osimertinib treatment, underwent an anlotinib plus osimertinib regimen in Tianjin Medical University General Hospital, and had available data from October 8, 2020 to October 14, 2023. Outcomes included the efficacy, assessed by progression-free survival (PFS), of anlotinib plus osimertinib treatment (PFS1) and prior osimertinib treatment (PFS2), to disease progression, objective response rate (ORR), disease control rate (DCR), and safety as assessed by the incidence of treatment-related toxicities.</p><p><strong>Results: </strong>A total of 28 patients with nsq-NSCLC were included, with a median follow-up of 12 months (range, 7.8-16.2). Treatment with anlotinib plus osimertinib led to a median PFS1 of 10.0 months (95% confidence interval [CI], 8.4-11.6). With a median follow-up from prior osimertinib therapy of 31.5 months (range, 20.8-42.2), the median PFS2 was 22.0 months (95% CI, 17.5-26.5). The ORR to combination therapy was 3.6% (95% CI, 0.2-20.2) and the DCR was 85.7% (95% CI, 67.3-96.0). All patients experienced treatment-related toxicities, with 10.7% showing grade 3, and none were grade ≥ 4.</p><p><strong>Conclusions: </strong>Anlotinib plus osimertinib exhibited encouraginsg anti-tumor activity and had a manageable safety profile in patients with nsq-NSCLC showing gradual progression on osimertinib.</p>","PeriodicalId":23338,"journal":{"name":"Thoracic Cancer","volume":"16 10","pages":"e70071"},"PeriodicalIF":2.3000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12093106/pdf/","citationCount":"0","resultStr":"{\"title\":\"Anlotinib Plus Osimertinib in Osimertinib-Resistant Nonsquamous Nonsmall Cell Lung Cancer With Gradual Progression: A Retrospective Study.\",\"authors\":\"Yu Hua, Minghui Liu, Boshi Li, Hongbing Zhang, Zihe Zhang, Yanan Wang, Jinghao Liu, Xin Li, Yongwen Li, Sen Wei, Hongyu Liu, Jun Chen\",\"doi\":\"10.1111/1759-7714.70071\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Previous studies have shown that anlotinib plus third-generation epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) overcome acquired resistance to EGFR-TKIs in patients with advanced EGFR-mutant nonsmall cell lung cancer (NSCLC). This study aimed to retrospectively evaluate whether anlotinib plus osimertinib overcame acquired resistance in patients with nsq-NSCLC who gradually progressed after first-line EGFR-TKI treatment.</p><p><strong>Methods: </strong>This study included patients with nsq-NSCLC who developed gradual progression after first-line osimertinib treatment, underwent an anlotinib plus osimertinib regimen in Tianjin Medical University General Hospital, and had available data from October 8, 2020 to October 14, 2023. Outcomes included the efficacy, assessed by progression-free survival (PFS), of anlotinib plus osimertinib treatment (PFS1) and prior osimertinib treatment (PFS2), to disease progression, objective response rate (ORR), disease control rate (DCR), and safety as assessed by the incidence of treatment-related toxicities.</p><p><strong>Results: </strong>A total of 28 patients with nsq-NSCLC were included, with a median follow-up of 12 months (range, 7.8-16.2). Treatment with anlotinib plus osimertinib led to a median PFS1 of 10.0 months (95% confidence interval [CI], 8.4-11.6). With a median follow-up from prior osimertinib therapy of 31.5 months (range, 20.8-42.2), the median PFS2 was 22.0 months (95% CI, 17.5-26.5). The ORR to combination therapy was 3.6% (95% CI, 0.2-20.2) and the DCR was 85.7% (95% CI, 67.3-96.0). All patients experienced treatment-related toxicities, with 10.7% showing grade 3, and none were grade ≥ 4.</p><p><strong>Conclusions: </strong>Anlotinib plus osimertinib exhibited encouraginsg anti-tumor activity and had a manageable safety profile in patients with nsq-NSCLC showing gradual progression on osimertinib.</p>\",\"PeriodicalId\":23338,\"journal\":{\"name\":\"Thoracic Cancer\",\"volume\":\"16 10\",\"pages\":\"e70071\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12093106/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Thoracic Cancer\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1111/1759-7714.70071\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Thoracic Cancer","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/1759-7714.70071","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:先前的研究表明,anlotinib联合第三代表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)可以克服晚期egfr突变的非小细胞肺癌(NSCLC)患者对EGFR-TKIs的获得性耐药。本研究旨在回顾性评估在一线EGFR-TKI治疗后逐渐进展的nsq-NSCLC患者,anlotinib + osimertinib是否克服了获得性耐药。方法:本研究纳入了天津医科大学总医院的nsq-NSCLC患者,这些患者在接受一线奥西替尼治疗后逐渐进展,接受了安洛替尼加奥西替尼方案,数据时间为2020年10月8日至2023年10月14日。结果包括通过无进展生存期(PFS)评估的安洛替尼加奥西替尼治疗(PFS1)和既往奥西替尼治疗(PFS2)对疾病进展的疗效、客观缓解率(ORR)、疾病控制率(DCR)以及通过治疗相关毒性发生率评估的安全性。结果:共纳入28例nsq-NSCLC患者,中位随访时间为12个月(范围7.8-16.2)。anlotinib + osimertinib治疗导致中位PFS1为10.0个月(95%可信区间[CI], 8.4-11.6)。既往奥西替尼治疗的中位随访时间为31.5个月(范围,20.8-42.2),中位PFS2为22.0个月(95% CI, 17.5-26.5)。联合治疗的ORR为3.6% (95% CI, 0.2-20.2), DCR为85.7% (95% CI, 67.3-96.0)。所有患者均出现治疗相关毒性,10.7%为3级,无≥4级。结论:Anlotinib + osimertinib显示出令人鼓舞的抗肿瘤活性,并且在nsq-NSCLC患者中具有可控的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anlotinib Plus Osimertinib in Osimertinib-Resistant Nonsquamous Nonsmall Cell Lung Cancer With Gradual Progression: A Retrospective Study.

Background: Previous studies have shown that anlotinib plus third-generation epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) overcome acquired resistance to EGFR-TKIs in patients with advanced EGFR-mutant nonsmall cell lung cancer (NSCLC). This study aimed to retrospectively evaluate whether anlotinib plus osimertinib overcame acquired resistance in patients with nsq-NSCLC who gradually progressed after first-line EGFR-TKI treatment.

Methods: This study included patients with nsq-NSCLC who developed gradual progression after first-line osimertinib treatment, underwent an anlotinib plus osimertinib regimen in Tianjin Medical University General Hospital, and had available data from October 8, 2020 to October 14, 2023. Outcomes included the efficacy, assessed by progression-free survival (PFS), of anlotinib plus osimertinib treatment (PFS1) and prior osimertinib treatment (PFS2), to disease progression, objective response rate (ORR), disease control rate (DCR), and safety as assessed by the incidence of treatment-related toxicities.

Results: A total of 28 patients with nsq-NSCLC were included, with a median follow-up of 12 months (range, 7.8-16.2). Treatment with anlotinib plus osimertinib led to a median PFS1 of 10.0 months (95% confidence interval [CI], 8.4-11.6). With a median follow-up from prior osimertinib therapy of 31.5 months (range, 20.8-42.2), the median PFS2 was 22.0 months (95% CI, 17.5-26.5). The ORR to combination therapy was 3.6% (95% CI, 0.2-20.2) and the DCR was 85.7% (95% CI, 67.3-96.0). All patients experienced treatment-related toxicities, with 10.7% showing grade 3, and none were grade ≥ 4.

Conclusions: Anlotinib plus osimertinib exhibited encouraginsg anti-tumor activity and had a manageable safety profile in patients with nsq-NSCLC showing gradual progression on osimertinib.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Thoracic Cancer
Thoracic Cancer ONCOLOGY-RESPIRATORY SYSTEM
CiteScore
5.20
自引率
3.40%
发文量
439
审稿时长
2 months
期刊介绍: Thoracic Cancer aims to facilitate international collaboration and exchange of comprehensive and cutting-edge information on basic, translational, and applied clinical research in lung cancer, esophageal cancer, mediastinal cancer, breast cancer and other thoracic malignancies. Prevention, treatment and research relevant to Asia-Pacific is a focus area, but submissions from all regions are welcomed. The editors encourage contributions relevant to prevention, general thoracic surgery, medical oncology, radiology, radiation medicine, pathology, basic cancer research, as well as epidemiological and translational studies in thoracic cancer. Thoracic Cancer is the official publication of the Chinese Society of Lung Cancer, International Chinese Society of Thoracic Surgery and is endorsed by the Korean Association for the Study of Lung Cancer and the Hong Kong Cancer Therapy Society. The Journal publishes a range of article types including: Editorials, Invited Reviews, Mini Reviews, Original Articles, Clinical Guidelines, Technological Notes, Imaging in thoracic cancer, Meeting Reports, Case Reports, Letters to the Editor, Commentaries, and Brief Reports.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信