2017 Dec 18;1(27):2724-2728. doi: 10.1182/bloodadvances.2017010470. eCollection 2017 Dec 26.

Author information

1
Department of Pathology and Laboratory Medicine and.
2
Department of Pharmacy, Children's of Alabama, Birmingham, AL; and.
3
Institute for Cancer Outcomes and Survivorship, School of Medicine, University of Alabama at Birmingham, Birmingham, AL.

Abstract

A 19-year-old ataxia-telangiectasia patient with T-cell prolymphocytic leukemia harbored 2 JAK3-activating hotspot mutations.The patient suffered toxicities with chemotherapy, but demonstrated a clinical response to novel use of a JAK3 inhibitor (tofacitinib).