AI Article Synopsis

  • The study evaluated the effectiveness of osimertinib compared to the traditional PC regimen (pemetrexed + cisplatin) in patients with advanced non-small cell lung cancer.
  • Results showed that osimertinib had a significantly higher response and disease control rate, along with lower adverse events than the conventional treatment.
  • Additionally, osimertinib reduced levels of serum carcinoembryonic antigen (CEA) and vascular endothelial growth factor (VEGF), and it improved both 1-year and 2-year survival rates in patients.

Article Abstract

Objective: To assess the clinical efficacy of osimertinib in patients with advanced non-small cell lung cancer and its effect on serum carcinoembryonic antigen (CEA) and vascular endothelial growth factor (VEGF) expression.

Methods: Between July 2018 and January 2020, 80 patients with advanced non-small cell lung cancer were assessed for eligibility and recruited. The patients were assigned at a ratio of 1 : 1 to receive either the PC regimen (pemetrexed + cisplatin) (conventional group) or osimertinib (experimental group). The primary endpoint was the clinical efficacy, and the secondary endpoints were the adverse events, expression of serum CEA and VEGF, and 2-year survival.

Results: Osimertinib was associated with a significantly higher response rate and disease control rate versus pemetrexed plus cisplatin ( < 0.05). Osimertinib resulted in a significantly lower incidence of adverse events versus the PC regimen ( < 0.05). Patients given osimertinib had significantly lower levels of CEA and VEGF versus those given pemetrexed plus cisplatin ( < 0.05). Osimertinib was associated with a significantly higher 1-year and 2-year survival rate versus pemetrexed plus cisplatin.

Conclusion: Osimertinib could inhibit the expression of serum CEA and VEGF in patients with advanced non-small cell lung cancer and reduce the adverse events with significant efficacy, so it is worthy of clinical promotion and application.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9159882PMC
http://dx.doi.org/10.1155/2022/3032087DOI Listing

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