Abstract

T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematologic malignancy that affects both children and adults. Optimization of chemotherapy regimens over the last five decades has led to steady improvements in outcome for pediatric patients, who have a long-term survival rate of 80%. For adults, however, the five-year survival rate is only 35–40% and both pediatric and adult patients who suffer relapse have uniformly poor outcomes.1 Further, improvements in outcome will thus require introduction of new approaches and more specific, targeted therapies.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.