Researchers have developed a new strategy to personalized medicine in advanced cancer patients with a poor prognosis. This calls for new tools to filter relevant genetic information.

The new study has been published in the journal Clinical Cancer Research. Applying this new tool, the treatments induced clinical responses in up to 77% of patients, either through the stabilization of their condition or through a partial clinical response.
During the first phase, the authors analyzed the genetic signature of the tumors –specifically, the hundreds of millions of letters that make up the exome; the part of the genome whose information produces proteins– in 23 patients suffering from advanced cancers, such as pancreatic adenocarcinomas and colon cancer. By using whole exome sequencing and bioinformatics analyses, researchers picked out mutations that could play an important role in the growth and spread of tumors.
The second part of the study involved the use of Avatar mice to study potentially effective treatments according to the patient's genetic signature. As Elena Garralda, predoctoral researcher from Hidalgo's Group, points out, avatar mice are "one of the key aspects of our research."
AVATAR MICE: A TESTING GROUND FOR DRUGS
Avatar mice are used as a testing ground, with each patient having their own equivalent animal, in order to study the effectiveness of drugs under real conditions: if the drug works in the avatar, the likelihood of it also working in the patient is very high.
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"We have demonstrated that it is possible to apply our personalized cancer treatment strategy to the clinic", says Garralda, adding: "as we learn more about the genetic information obtained from cancer exome sequencing, future clinical trials will allow for the inclusion of patients with specific genetic alterations, and therefore a better access to cancer drugs."
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Currently, one the main objectives for the team is to study the efficiency of the procedures in a larger number of patients with advanced pancreatic cancer, thereby comparing them to standard treatments.
Pancreatic cancer often has a poor prognosis, with survival rates of less than 1 year. It is a complex and heterogeneous disease, meaning that the personalized study of the most relevant mutations in tumor growth (driver mutations) could be a promising strategy in the search for new treatments.
Source-Eurekalert