The latest promising treatment for aggressive childhood cancer neuroblastoma, an aggressive form of childhood cancer, is the KSP inhibitor. The study was led by researchers at Lund University in Sweden, and is published in the journal Science Translational Medicine.

About 800 children in the US are diagnosed with neuroblastoma annually. Neuroblastoma is an aggressive cancer of the nervous system. It most frequently arises in the adrenal glands. Despite intensive chemotherapy, the disease can be difficult to cure and the prognosis is often poor. Researchers at Lund University have identified and tested a drug shown to be very effective against neuroblastoma.

Initially we conducted a large-scale drug screen where we examined how 500 drugs affected neuroblastoma cells from patients. Most of these medications have never before been used on patients with neuroblastoma” – Karin Hansson, doctoral student and first author of the study.

The researchers then obtained a “short list” of the most effective drugs. One of these was a so-called KSP inhibitor. This was particularly interesting as patients with a high proportion of KSP protein have the more aggressive variant of neuroblastoma.

Treated mice showed how the KSP inhibitor prevented tumor growth and drastically prolonged survival. In some cases, the tumor disappeared completely. KSP inhibitors block the protein in tumor cells, meaning that the cells can no longer divide and therefore eventually die.

This promising treatment for aggressive childhood cancer neuroblastoma, the KSP inhibitor, has not previously been used for neuroblastoma. It was shown to be extra effective against this type of cancer. It also did not affect healthy bone marrow cells. This is important as side effects are a major problem in childhood cancer therapies.

The results were very clear and the treatment is very promising. But even so, there will probably be a need to combine this treatment with other drugs to completely knock out all tumor cells. Fortunately, the drug is already approved for use in humans. Now, of course, we hope that clinical trials for neuroblastoma will be initiated,” concludes Daniel Bexell, associate professor and research group leader at Lund University.

Source: Medical Express.com

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