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}
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.
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.