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While the majority of children, adolescents, and young adults with B-cell acute lymphoblastic leukemia (B-ALL) can be cured by risk-adapted multi-agent chemotherapy regimens optimized during the past 50 years, long-term survival has remained elusive for pediatric patients with the rare (<1% of cases), but to date universally-fatal, t(17;19) subtype harboring TCF3::HLF (formerly E2A-HLF) fusions first identified and reported in 1991.
Sarah K. Tasian (Sat,) studied this question.
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