Chemotherapy drugs for liver cancer and possible side effects

Share This Post

Effective drugs in liver cancer

The most effective drugs in liver cancer chemotherapy are doxorubicin (doxorubicin), 5-fluorouracil and cisplatin. But usually these drugs can only shrink the tumor, and the response usually does not last long, and has little effect on the life extension of patients.

Due to the poor response of systemic chemotherapy, doctors tried to inject chemotherapy drugs directly into the hepatic artery and directly into the liver. This technique is called hepatic artery infusion (HAI). But a healthy liver will decompose most drugs. Compared with systemic chemotherapy, this pair of chemotherapy methods is better and does not increase side effects. The most commonly used drugs include fluorouridine (FUDR), cisplatin, mitomycin C and doxorubicin. Early research found that HAI can effectively control tumors, but more research is still needed. However, this technique is not useful for all patients because it requires surgery to insert the catheter into the hepatic artery, which is not feasible for many patients with liver cancer who cannot tolerate the operation.

Side effects of chemotherapy in liver cancer

The side effects of chemotherapy mainly depend on the dosage of medication and the time of taking the medication. Common side effects include: hair loss, mouth ulcers, loss of appetite, nausea and vomiting, diarrhea, increased risk of infection (low white blood cell count), easy bruising or bleeding (low platelet count), and fatigue (low red blood cell count). These side effects usually do not last very long and usually disappear after treatment. Doctors will also give patients appropriate medicines according to the actual situation to help them prevent or reduce side effects such as nausea and vomiting. In some cases, it may be necessary to reduce the dose of chemotherapy drugs, or it may be necessary to delay or stop treatment to avoid serious side effects.

Subscribe To Our Newsletter

Get updates and never miss a blog from Cancerfax

More To Explore

Targeting FGFR4 and CD276 with CAR T-cells demonstrates a strong antitumor impact against children rhabdomyosarcoma
CAR T-Cell therapy

Targeting FGFR4 and CD276 with CAR T-cells demonstrates a strong antitumor impact against children rhabdomyosarcoma

Chimeric antigen receptor (CAR) T-cells that specifically target Fibroblast Growth Factor Receptor 4 (FGFR4), a surface tyrosine receptor that is extensively expressed in rhabdomyosarcoma (RMS), are now undergoing clinical research. However, the effectiveness of these CAR T-cells may be hindered by tumor heterogeneity and inadequate activation. In this study, we present a method to enhance the co-stimulatory and targeting characteristics of a FGFR4 CAR through an optimization process. We substituted the hinge and transmembrane domain of CD8 as well as the 4-1BB co-stimulatory domain with the corresponding domains of CD28. The CARs produced exhibit heightened anti-tumor efficacy in multiple RMS xenograft models, with the exception of the RMS559 cell line, which is known for its aggressive nature.

Need help? Our team is ready to assist you.

We wish a speedy recovery of your dear and near one.

Start chat
We Are Online! Chat With Us!
Scan the code
Hello,

Welcome to CancerFax !

CancerFax is a pioneering platform dedicated to connecting individuals facing advanced-stage cancer with groundbreaking cell therapies like CAR T-Cell therapy, Gene therapy, TIL therapy, and clinical trials worldwide.

Let us know what we can do for you.

1) CAR T-Cell therapy
2) Gene therapy
3) Gamma-Delta T Cell therapy
4) TIL therapy
5) NK Cell therapy