About this trial

This is a prospective pilot study, the primary aim of which is to determine whether the presence of 18F FLT imaging signal uptake abnormalities correlate with clinically validated evidence of hematopoietic malignant disease (e.g. MRD, molecular, flow or histology) after immunotherapy and other treatments.

Eligibility criteria

Qualifiers

Aged 4 to 80 years

Evidence of high-risk hematopoietic malignancy with relapsed/refractory disease: acute lymphocytic leukemia, Acute myeloid leukemia, Ambiguous lineage leukemia, myeloma

Karnofsky/Lansky score of ≥ 50

Agree to use contraceptive measures during study protocol participation (when age appropriate)

Disqualifiers

Patients with uncontrolled infections

Pregnancy or lactating

History of prior fluorothymidine allergy or intolerance.

Trial design

Treatments tested in this trial

  • FLT

Treatment groups

60 Participants
are divided into 4 treatment groups

Locations

3
Children's National Health System20010, Washington D.C.District of Columbia, United States
Emory University30322, AtlantaGeorgia, United States
University of Oklahoma Health Sciences Center73117, Oklahoma CityOklahoma, United States

Sponsors and collaborators

University of Oklahoma

Lead sponsor

Emory University

Collaborator