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The Effect of Lenvatinib Combined with Xindilimab on Tumor Marker Levels and Survival in Patients with Advanced Liver Cancer |
Zhou Guohui |
Affiliated Hospital of Putian University,Putian Fujian 351100,China |
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Abstract Objective To investigate the effects of lenvatinib combined with sintilimab on tumor marker levels and survival in patients with advanced liver cancer.Method A retrospective collection of data was conducted on 96 patients with advanced liver cancer.They were divided into a control group(48 cases)and a study group(48 cases)according to different treatment plans;The control group was treated with lenvatinib,while the study group was treated with lenvatinib combined with sildenafil monoclonal antibody for at least 3 cycles;Compare and analyze the treatment efficacy,tumor marker levels,liver function indicators,quality of life,adverse reactions,and survival status between the two groups.The disease control rate of the research group(70.83%)was higher than that of the control group(41.67%)(P<0.05);The research group had lower levels of alpha fetoprotein(AFP),carcinoembryonic antigen(CEA),abnormal prothrombin(PIVKA II),carbohydrate antigen(CA199),total bilirubin(TBIL),aspartate aminotransferase(AST),and alanine aminotransferase(ALT)compared to the control group after three cycles of treatment;The study group had higher scores in all dimensions of the EORTC QLQ-C30 quality of life assessment scale for cancer patients treated for three cycles compared to the control group(P<0.05);There was no statistically significant difference in adverse reactions between the study group(14.58%)and the control group(10.42%)(P>0.05);The survival rate of the study group was higher than that of the control group,and the median survival time was longer than that of group A(P<0.05).Conclusion The combination of lenvatinib and xindilimab is effective in the treatment of advanced liver cancer patients,reducing tumor marker levels,alleviating liver function damage,improving quality of life,and increasing survival rate,with good safety.
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Received: 20 February 2025
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