Those with TP53 mutation and/or recurrent CNAs without an STAG2 mutation had a directionally increased risk of RFS event relative to those with no molecular lesion (79.6%; 95% CI, 72.0% to 88.1%), but this did not reach statistical significance (BH-corrected log-rank P = .096; Fig 3 A).
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Molecular Characterization Informs Prognosis in Patients With Localized Ewing Sarcoma: A Report From the Children's Oncology Group.
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0.0960