» Articles » PMID: 37485037

The Synergy of Gene Targeting Drug Icaritin Soft Capsule with Immunomodulator and TACE Brings New Hope for Drug Combination in Patients with Advanced Liver Cancer: A Case Report and Literature Review

Overview
Publisher Dove Medical Press
Specialty Oncology
Date 2023 Jul 24
PMID 37485037
Authors
Affiliations
Soon will be listed here.
Abstract

At present, the average five-year survival rate of liver cancer in China is only 12.1%. The reason for this association lies in the diagnosis at its middle or/and advanced stage of liver cancer for lacking special clinical symptoms in almost 70% of patients without the chance of effective surgical resection. Epidemiological studies have shown that there are only 30% of patients with an initial diagnosis of liver cancer have the opportunity to undergo radical surgery. Therefore, systematic and comprehensive treatment would play an important role in liver cancer treatment at its middle or/and advanced stage, and the related therapeutic schedule still needs further improvement and optimization. We applied a gene-targeted drug of Icaritin soft capsule in the treatment of a liver cancer patient at its advanced stage. And the level of AFP was found to decrease to 6.4ng/mL from 10.86ng/mL; meanwhile, MRI showed that the primary tumor significantly reduced in size, with shrinking of the hepatogastric space, hepatic aortic side, and renal artery side lymph nodes. After treatment with TACE and Icaritin, the patient had no discomfort and no longer experienced abdominal pain and bloating and gained three kilograms of weight. The therapeutic effect of Icaritin-targeted drugs was completely demonstrated during the later treatment follow-up. That is to say, the multiple anti-tumor characteristics of Icaritin with good safety were fully displayed in this case, and it can be used in combination with other drugs to treat hepatocellular carcinoma in the clinical setting. The results show that Icaritin can put some effects on the combined treatment of patients with liver cancer.

Citing Articles

COE targets EphA2 to inhibit vasculogenic mimicry formation induced by hypoxia in hepatocellular carcinoma.

Chen J, Dai S, Wu S, Wu M, Yu K, Liu J Front Pharmacol. 2024; 15:1421470.

PMID: 39050762 PMC: 11266089. DOI: 10.3389/fphar.2024.1421470.


Advancements in the Biotransformation and Biosynthesis of the Primary Active Flavonoids Derived from .

Zhang X, Tang B, Wen S, Wang Y, Pan C, Qu L Molecules. 2023; 28(20).

PMID: 37894651 PMC: 10609448. DOI: 10.3390/molecules28207173.

References
1.
Jin L, Miao J, Liu Y, Li X, Jie Y, Niu Q . Icaritin induces mitochondrial apoptosis by up-regulating miR-124 in human oral squamous cell carcinoma cells. Biomed Pharmacother. 2016; 85:287-295. DOI: 10.1016/j.biopha.2016.11.023. View

2.
Kudo M . A New Treatment Option for Intermediate-Stage Hepatocellular Carcinoma with High Tumor Burden: Initial Lenvatinib Therapy with Subsequent Selective TACE. Liver Cancer. 2019; 8(5):299-311. PMC: 6872999. DOI: 10.1159/000502905. View

3.
Xu B, Jiang C, Han H, Liu H, Tang M, Liu L . Icaritin inhibits the invasion and epithelial-to-mesenchymal transition of glioblastoma cells by targeting EMMPRIN via PTEN/AKt/HIF-1α signalling. Clin Exp Pharmacol Physiol. 2015; 42(12):1296-307. DOI: 10.1111/1440-1681.12488. View

4.
Li Y, Chen G, Han Z, Cheng H, Qiao L, Li Y . IL-6/STAT3 Signaling Contributes to Sorafenib Resistance in Hepatocellular Carcinoma Through Targeting Cancer Stem Cells. Onco Targets Ther. 2020; 13:9721-9730. PMC: 7533247. DOI: 10.2147/OTT.S262089. View

5.
Wang S, Wang Q, Wang H, Qin C, Cui X, Li L . Induction of ROS and DNA damage-dependent senescence by icaritin contributes to its antitumor activity in hepatocellular carcinoma cells. Pharm Biol. 2019; 57(1):424-431. PMC: 8871611. DOI: 10.1080/13880209.2019.1628073. View