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2023 World Conference on Lung Cancer (Posters)
P2.09. Efficacy of Anlotinib in T790M-positive NSC ...
P2.09. Efficacy of Anlotinib in T790M-positive NSCLC Patients with Osimertinib Resistance: A Retrospective and Exploratory Study - PDF(Abstract)
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Pdf Summary
A retrospective and exploratory study was conducted to evaluate the efficacy of Anlotinib in patients with non-small cell lung cancer (NSCLC) who developed resistance to Osimertinib, a targeted therapy for EGFR mutations. The study collected data from 268 NSCLC patients with the EGFR T790M mutation who had become resistant to Osimertinib and compared the efficacy of antiangiogenic-based therapy (using Anlotinib) with immunotherapy and chemotherapy.<br /><br />The results showed that patients receiving antiangiogenic-based therapy had a significantly longer progression-free survival (PFS) compared to those receiving immunotherapy or chemotherapy. The objective response rate (ORR) and disease control rate (DCR) were also higher in the antiangiogenic-based therapy group.<br /><br />Subgroup analysis revealed that Anlotinib-based therapy may have more benefits in terms of PFS and overall survival (OS) compared to Bevacizumab-based therapy. In in vitro experiments, Anlotinib alone or in combination with Osimertinib demonstrated potent cytotoxicity to T790M-mutant NSCLC cells with acquired Osimertinib resistance.<br /><br />These findings suggest that antiangiogenic-based therapy, particularly using Anlotinib, could be an effective treatment option for EGFR-mutant NSCLC patients who have developed resistance to Osimertinib. The study highlights the potential of targeting angiogenesis in the treatment of Osimertinib-resistant NSCLC. These results have implications for the management of patients with metastatic NSCLC and provide valuable insights for future treatment strategies.
Asset Subtitle
Ya Chen
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Speaker
Ya Chen
Topic
Metastatic NSCLC: Targeted Therapy - EGFR/HER2
Keywords
Anlotinib
NSCLC
Osimertinib resistance
antiangiogenic-based therapy
immunotherapy
chemotherapy
progression-free survival
EGFR mutations
cytotoxicity
angiogenesis
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