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Analysis of alkaline phosphatase and γ-glutamyltransferase after radiofrequency ablation of primary liver cancer: A retrospective study. | LitMetric

AI Article Synopsis

  • The study investigates how changes in alkaline phosphatase (ALP) and γ-glutamyltransferase (GGT) levels affect the prognosis of patients with primary liver cancer (PLC) after they undergo radiofrequency ablation (RFA).
  • Data was collected from 165 patients treated with RFA between 2018 and 2023, utilizing statistical methods like chi-square tests and Cox regression to analyze survival outcomes.
  • Results indicated that both normal ALP and GGT levels correlated with significantly better survival rates compared to abnormal levels, with ALP and GGT identified as key independent prognostic factors for overall survival in PLC patients post-treatment.

Article Abstract

Background: Changes in alkaline phosphatase (ALP) and γ-glutamyltransferase (GGT) levels in patients with primary liver cancer (PLC) after radiofrequency ablation (RFA). Hepatocellular carcinoma is a malignant tumor with high incidence worldwide. As a common local treatment, RFA has attracted much attention for its efficacy and influence on liver function.

Aim: To investigate the effect of serum ALP and GGT levels on the prognosis of patients with PLC treated by RFA.

Methods: The preoperative clinical data of 165 patients who were pathologically or clinically diagnosed with PLC and who received RFA in our hospital between October 2018 and June 2023 were collected. The chi-square test was used to compare the data between groups. The Kaplan-Meier method and Cox regression were used to analyze the associations between serum ALP and GGT levels and overall survival, progression-free survival (PFS) and clinical characteristics of patients before treatment.

Results: The 1-year survival rates of patients with normal (≤ 135 U/L) and abnormal (> 135 U/L) serum ALP before treatment were 91% and 79%, respectively; the 2-year survival rates were 90% and 68%, respectively; and the 5-year survival rates were 35% and 18%, respectively. The difference between the two groups was statistically significant ( = 0.01). Before treatment, the 1-year survival rates of patients with normal serum GGT levels (≤ 45 U/L) and abnormal serum GGT levels (> 45 U/L) were 95% and 87%, the 2-year survival rates were 85% and 71%, and the 5-year survival rates were 37% and 21%, respectively. The difference between the two groups was statistically significant ( < 0.001). Serum ALP [hazard ratio (HR) = 1.766, 95% confidence interval (95%CI): 1.068-2.921, = 0.027] and GGT (HR = 2. 312, 95%CI: 1.367-3.912, = 0.002) is closely related to the overall survival of PLC patients after RF ablation and is an independent prognostic factor. The 1-year PFS rates were 72% and 50%, the 2-year PFS rates were 52% and 21%, and the 5-year PFS rates were 14% and 3%, respectively. The difference between the two groups was statistically significant ( < 0001). The 1-year PFS rates were 81% and 56% in patients with normal and abnormal serum GGT levels before treatment, respectively; the 2-year PFS rates were 62% and 35%, respectively; and the 5-year PFS rates were 18% and 7%, respectively, with statistical significance between the two groups ( < 0.001). The serum ALP concentration (HR = 1. 653, 95%CI: 1.001-2.729, = 0.049) and GGT (HR = 1.949, 95%CI: 1.296-2.930, = 0.001) was closely associated with PFS after RFA in patients with PLC. The proportion of male patients with abnormal ALP levels is high, the Child-Pugh grade of liver function is poor, and the incidence of ascites is high. Among GGT-abnormal patients, the Child-Pugh grade of liver function was poor, the tumor stage was late, the proportion of patients with tumors ≥ 5 cm was high, and the incidence of hepatic encephalopathy was high.

Conclusion: Serum ALP and GGT levels before treatment can be used to predict the prognosis of patients with PLC after RFA, and they have certain guiding significance for the long-term survival of patients with PLC after radiofrequency therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11438821PMC
http://dx.doi.org/10.4240/wjgs.v16.i9.2860DOI Listing

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