This clinical study will demonstrate the accuracy of the chromosomal aberration and gene mutation markers of the AMLProfiler molecular diagnostic assay and generate clinical performance data to support a Pre-Market Approval (PMA) submission to the Food and Drug Administration for in vitro diagnostic use within the United States of America. The objective is to demonstrate the positive and negative percent agreement of each marker by comparing AMLProfiler results from multiple clinical participating sites with data generated using a laboratory developed bi-directional sequencing method generated at the molecular diagnostic reference lab. The AMLProfiler assay is a qualitative in vitro diagnostic test for the detection of AML or APL specific chromosomal aberrations (specific recurrent translocations and inversions), as well as expression of specific genetic markers in RNA extracted from bone marrow aspirates of patients with Acute Myeloid Leukemia.
Study Type
OBSERVATIONAL
Enrollment
264
Memorial Sloan Kettering Cancer Center
New York, New York, United States
James Cancer Hospital
Columbus, Ohio, United States
University Hospital Ulm
Ulm, Germany
Erasmus Medical Center
Rotterdam, Netherlands
Cardiff University
Cardiff, Heath Park, United Kingdom
Acceptance Criteria
The acceptance criteria based on lower level of the 95% CI of the positive or negative percent agreement for all markers.
Time frame: Sample taken at initial visit with no follow up (Day 1)
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