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| Efficacy of Huisheng Oral Liquid Combined with Osimertinib in the Treatment of Patients with Advanced Non-Small Cell Lung Cancer |
| CHEN Qingpo |
| Department of Oncology Ⅱ, Xuchang Beihai Hospital, Xuchang Henan 461000 |
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Abstract 【Objective】 To evaluate the efficacy of Huisheng Oral Liquid combined with osimertinib in the treatment of patients with advanced non-small cell lung cancer (NSCLC). 【Methods】 A total of 72 patients with advanced NSCLC admitted from May 2020 to August 2022 were randomly divided into a control group and an observation group, with 36 cases in each group. The control group received oral osimertinib alone, while the observation group received Huisheng Oral Liquid in addition to osimertinib. Clinical efficacy, tumor marker levels [cyto-keratin 19 fragment antigen 21-1(CYFRA21-1), neuron-specific enolase (NSE), and squamous cell carcinoma antigen (SCCAg)], immune function indices (CD4+ T cells, CD8+ T cells, CD3+ T cells), and adverse drug reactions were compared between the two groups before and after treatment. Patients were followed up for 3 years, and overall survival (OS) and progression-free survival (PFS) were compared between the two groups. 【Results】 After treatment, the objective response rate and overall response rate in the observation group were significantly higher than those in the control group (P<0.05). The levels of CYFRA21-1, NSE, and SCCAg in the observation group were significantly lower than those in the control group (P<0.05). The observation group showed higher CD4+ and CD3+ levels and lower CD8+ levels compared to the control group (P<0.05). The overall incidence of adverse reactions was lower in the observation group than in the control group (P<0.05). The median OS and PFS were significantly longer in the observation group than in the control group (P<0.05). 【Conclusion】 Huisheng Oral Liquid combined with osimertinib can significantly improve the efficacy in patients with advanced NSCLC, reduce tumor marker levels, enhance immune function, alleviate side effects, and improve survival outcomes.
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Received: 31 October 2025
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