Conference Coverage

cfDNA reveals targetable mutations in pediatric neuroblastoma, sarcoma


 

REPORTING FROM ASPHO 2018

The investigators have used the data from this study to create a genome-wide z score derived from shallow whole genome sequencing profiles and cfDNA, and found that a high genomewide z score, compared with a low score was significantly associated a more than four-fold greater risk for worse survival (hazard ratio, 4.42; P = .049).

“Establishing a platform using cfDNA to identify molecular profiles of these tumors can serve as a powerful tool for guiding treatment and monitoring response to treatment,” the investigators concluded.

The study was supported by Cycle for Survival and the Kristen Ann Carr Fund. The investigators reported having no conflicts of interest.

SOURCE: Kothari P et al. ASPHO 2018. Abstract #809.

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