4.4 Article

Effect of decoction of Fuzheng Jiedu Xiaoji formula (???????) plus chemoembolization on primary liver cancer in patients

Journal

JOURNAL OF TRADITIONAL CHINESE MEDICINE
Volume 42, Issue 3, Pages 446-450

Publisher

JOURNAL TRADITIONAL CHINESE MED
DOI: 10.19852/j.cnki.jtcm.2022.03.011

Keywords

liver neoplasms; ATP binding cassette transporter; subfamily B; member 1; chemoembolization; therapeutic; Fuzheng Jiedu Xiaoji formula

Funding

  1. Beijing Municipal Administration of Hospitals Incubating Program [pz2017029]

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This study investigated the effect and underlying mechanism of Fuzheng Jiedu Xiaoji formula (FJXF) combined with chemoembolization (TACE) on primary liver cancer (PLC) patients. The combination therapy showed a better short-term clinical effect compared to TACE alone, possibly by alleviating multidrug resistance. Additionally, FJXF did not increase the risk of liver damage.
OBJECTIVE: To investigate the effect of the decoction of Fuzheng Jiedu Xiaoji formula (??? ?????? ??? ?????????, FJXF) plus chemoembolization (TACE) on primary liver cancer (PLC) in patients, and study the underlying mechanism. METHODS: Patients with PLC who met the inclusion criteria were randomized into case group and control group. The case group was treated with FJXF combined with TACE. The control group was treated with TACE alone. The short-term clinical effect was evaluated; liver biochemistry, liver function index and multidrug resistance-associated indicators were detected. RESULTS: FJXF combined with TACE in the case group significantly increased the disease control rate than TACE alone in the control group (83.3% vs 61.1%). There was a reduction in the serum alpha-fetoprotein at 8 weeks after treatment in each group, while no difference between the two groups. The same trend can be observed for transaminase and direct bilirubin in both groups. In the case group, it showed a significant increase for albumin at 8 weeks after treatment, while no change in the control group. Multidrug resistance-associated indicators for multidrug resistance protein 1 and p-glycoprotein were upregulated in the case group but remained stable in the control group. CONCLUSIONS: FJXF combined TACE had a better short-term effect than TACE alone in patients with PLC. The potential mechanism was probably associated with alleviated multidrug resistance induced by FJXF. Additionally, FJXF didn't increase the risk of liver damage in the combined therapy.

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