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Test Code ALLM B-ALL Monitoring, MRD Detection, Bone Marrow

Useful For

Aids in monitoring a previously confirmed diagnosis of B-cell lymphoblastic leukemia

Additional Tests

Test ID Reporting Name Available Separately Always Performed
FIRST Flow Cytometry, Cell Surface, First No, (Bill Only) Yes
ADD1 Flow Cytometry, Cell Surface, Addl No, (Bill Only) Yes

Testing Algorithm

When this test is ordered, flow cytometry interpretation, 2 to 8 markers will always be performed at an additional charge.

Reporting Name

B-ALL Monitoring, MRD Detection, BM

Specimen Type

Bone Marrow


Additional Testing Requirements


If cytogenetic tests are also desired an additional specimen should be submitted. It is important that the specimen be obtained, processed, and transported according to instructions for the other required test.



Shipping Instructions


Specimens must be received within 72 hours.



Necessary Information


If cytogenetic tests are also desired an additional specimen should be submitted. It is important that the specimen be obtained, processed, and transported according to instructions for the other required test.



Specimen Required


Container/Tube:

Preferred: Yellow top (ACD)
Acceptable: EDTA, heparin
Specimen Volume: 3 mL

Slides: Include 5- to 10-unstained bone marrow aspirate smears, if possible.
Collection Instructions:
1. Submission of bilateral specimens is not required.
2. Label specimen appropriately (bone marrow).


Specimen Minimum Volume

1 mL

Specimen Stability Information

Specimen Type Temperature Time
Bone Marrow Ambient

Clinical Information

B-cell lymphoblastic leukemia/lymphoma (B-ALL) is a neoplasm of precursor cells (lymphoblasts) committed to B-cell lineage. B-ALL is the most common acute leukemia in children and adolescents, and also occurs in adults. Patients with B-ALL typically present with a high blast count in the peripheral blood, and bone marrow replacement with the disease. The diagnosis of B-ALL is based on a combination of morphologic features showing primarily small blasts with open chromatin and high N:C ratio, and an immunophenotype showing immaturity (CD34 and/or TdT expression) associated with B-cell lineage markers (CD19, CD22, and CD79a).

 

New therapeutic approaches in B-ALL have been increasingly successful. One of the most important predictors of the disease relapse is the ability to detect minimal residual disease (MRD) in the bone marrow specimens following induction phase of the therapy (day 28). Immunophenotyping studies are necessary as morphologic features are not sufficient to detect MRD. The absence of MRD (at 0.01% sensitivity) is an important prognostic indicator in these patients.

 

This test is used to establish an antigen footprint of tumor cells at diagnosis to monitor minimal residual disease in these patients after treatments and/or transplants.

Reference Values

An interpretive report will be provided. This test will be processed as a laboratory consultation. An interpretation of the immunophenotypic findings and correlation with the morphologic features will be provided by a hematopathologist for every case.

Day(s) and Time(s) Performed

Specimens are processed and reported Monday through Saturday

Analytic Time

1 day

Performing Laboratory

Mayo Medical Laboratories in Rochester

CPT Code Information

88184-Flow cytometry; first cell surface, cytoplasmic or nuclear marker
88185 x 7-Flow cytometry; additional cell surface, cytoplasmic or nuclear marker (each)
88187-Flow cytometry interpretation, 2 to 8 markers

LOINC Code Information

Test ID Test Order Name Order LOINC Value
ALLM B-ALL Monitoring, MRD Detection, BM In Process

 

Result ID Test Result Name Result LOINC Value
CK085 ALLM Result In Process
CK088 Final Diagnosis 22637-3
CK089 Special Studies 22635-7
CK090 Microscopic Description 22635-7

NY State Approved

Yes

Method Name

Immunophenotyping

Test Classification

This test was developed using an analyte specific reagent. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.

Reflex Tests

Test ID Reporting Name Available Separately Always Performed
FCINT Flow Cytometry Interp, 2-8 Markers No, (Bill Only) No

Forms

If not ordering electronically, complete, print, and send a Hematopathology/Cytogenetics Test Request Form (T726) with the specimen (http://www.mayomedicallaboratories.com/it-mmfiles/hematopathology-request-form.pdf)