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Genome-wide association and other genetic studies hint at variants increasing subsequent neoplasm risk in individuals treated for cancer during childhood.

Tumor infiltrating cell adoptive cell therapy success in metastatic melanoma patients was associated with DNA methylation and histone acetylation changes.

Using blood samples from more than 15,000 individuals with advanced cancer, researchers identified somatic mutation patterns similar to those in TCGA's database.

Researchers compared precision and non-precision approaches in 346 Phase I studies, and found that personalized medicine improves patient outcomes.

The new rule is aimed at women with early-stage invasive breast cancer and known hormone and HER2 receptor status.

SAP has released products for integrating and analyzing structured and unstructured clinical and genomic datasets, and supporting patient cohort analysis.

The three organizations are inviting comment from health professionals on the recommendations.

In developing the recommendations, the expert panel attempted to keep up with the fast-moving advances in oncology.

The recommendations address incidental findings from next-generation sequencing tests, physician education, as well as test regulation and reimbursement.

Data presented at the meeting helped better define the potential benefits and risks of broad panel-based tests for hereditary cancer genes.

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