Genetic Testing Combined With Personalized Drug Screening On Tumor Samples to Revolutionize Cancer Treatment

However, the disease’s inherent variability means that a one-size-fits-all approach often falls short. Individual responses to the same drug can vary dramatically. Personalized cancer treatment, which outperforms traditional treatment methods, increasingly relies on genomics—DNA profiling of a patient's cancer—to tailor therapy. Current genomic profiling processes can analyze thousands of genes but might take weeks to deliver results and still fail to provide complete clarity on the optimal treatment strategy. For the first time, researchers have combined genetic testing with personalized drug screening directly on tumor samples to identify the right treatment for children with relapsed cancers, offering a timelier and effective approach.

The functional precision medicine approach to target cancer has been developed by researchers at Florida International University (Miami, FL, USA) combines genetic testing with a new method of testing individual drugs on tumor samples. The combined approach offers advantages over the current precision medicine processes by speeding up results and broadening treatment possibilities. This innovative method involves taking a blood or tumor sample, enriching and processing the cancer cells in the lab to mimic natural growth in the body, and then testing these cells against a library of over 120 FDA-approved drugs, which includes both oncological and non-oncological treatments. These drugs are tested individually and in combinations suggested by the clinical team to identify the most effective treatment options. The entire process is completed in about a week.

This new approach was successfully implemented to guide treatment for children with relapsed cancers, showing improvement in 83% of cases. Ongoing larger trials for both children and adults aim to validate and expand these findings. Furthermore, this research opens new avenues for addressing health disparities; it explores how minority populations uniquely respond to FDA-approved drugs and aims to identify biomarkers and more effective targeted therapies for these groups.

“The results are exciting because cancer that comes back is much harder to treat. Seeing improvement in 83 percent of patients is incredibly promising,” said Florida International University cancer researcher Diana Azzam who led the study. “This could be the way we turn cancer into a manageable disease.”

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