Test Code PCPRO Plasma Cell DNA Content and Proliferation, Bone Marrow
Reporting Name
Plasma Cell Proliferation, MarrowUseful For
Establishing a diagnosis of a plasma cell proliferative disorder
Providing prognostic information for newly diagnosed multiple myeloma and other plasma cell proliferative disorders
Assessing response to therapy and detecting disease relapse and progression in treated plasma cell proliferative disorder patients
Determining plasma cell DNA content and proliferation
Additional Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
FCINT | Flow Cytometry Interp, 2-8 Markers | No, (Bill Only) | Yes |
Testing Algorithm
When this test is ordered, flow cytometry interpretation will always be performed at an additional charge.
For more information see:
Method Name
Flow Cytometry/DNA Content/Cell Cycle Analysis
Performing Laboratory
Mayo Clinic Laboratories in RochesterSpecimen Type
Bone MarrowOrdering Guidance
This test can be ordered at diagnosis or follow-up of a plasma cell neoplasm (plasma cell proliferative disorder).
If CSMRT / mSMART Plasma Cell Proliferative Disorder, Pre-Analysis Cell Sorting, Bone Marrow or MPCDS / mSMART, Plasma Cell Proliferative Disorder, FISH, Bone Marrow is desired to be performed at Mayo, order MSMRT / Mayo Algorithmic Approach for Stratification of Myeloma and Risk-Adapted Therapy Report, Bone Marrow.
The Multiple Myeloma: Laboratory Screening algorithm will allow plasma cell fluorescence in situ hybridization (FISH) testing to be added, based on this test's flow cytometry results.
Necessary Information
1. Include patient's disease state (untreated, treated, monoclonal gammopathy of undetermined significance, stable).
2. Indicate if patient is on anti-CD38 therapy.
Specimen Required
Specimen Type: Redirected bone marrow
Preferred: Yellow top (ACD solution A or B)
Acceptable: Lavender top (EDTA) or green top (sodium heparin)
Specimen Volume: 4 mL
Specimen Stability Information: 3 days
Specimen Minimum Volume
2 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Bone Marrow | Ambient (preferred) | ||
Refrigerated |
Reject Due To
Gross hemolysis | Reject |
Fully clotted | Reject |
Special Instructions
Reference Values
Plasma Cell Clonality:
Normal bone marrow
No monotypic clonal plasma cells detected
DNA Index:
Normal polytypic plasma cells
DNA index (G0/G1 cells): Diploid 0.95-1.05
Day(s) Performed
Preanalytical processing: Monday through Saturday
Results reported: Monday through Friday
CPT Code Information
88182-Flow cytometry, cell cycle or DNA analysis
88184-Flow cytometry; first cell surface, cytoplasmic or nuclear marker
88185 x 5-Flow cytometry; additional cell surface, cytoplasmic or nuclear marker (each)
88187-Flow cytometry interpretation, 2 to 8 Markers (added as FCINT)
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
PCPRO | Plasma Cell Proliferation, Marrow | 93363-0 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
CK056 | Monotypic Plasma Cells: | 93362-2 |
CK057 | Monotypic PC per Total Events | 93021-4 |
CK058 | Monotypic Plasma Cells S-phase | 93361-4 |
CK059 | Monotypic Plasma Cells DNA Index | 93360-6 |
CK060 | Monotypic Plasma Cells DNA Ploidy | 93359-8 |
CK061 | Polytypic PC per Total Events | 93358-0 |
CK062 | Polytypic PC per All Plasma Cells | 93020-6 |
CK063 | Final Diagnosis | 50398-7 |
Clinical Information
Plasma cell proliferative disorders are a group of plasma cell derived clonal hematologic neoplasms that exhibit a wide range of biologic activity ranging from monoclonal gammopathy of uncertain significance (MGUS), a usually indolent disorder with a low rate of disease progression, to multiple myeloma (MM), a disease that is often aggressive with poor long-term survival. Detecting plasma cell clonality through demonstrating immunoglobulin (Ig) light chain restriction (ie, the presence of either predominately kappa or predominately lambda light chains), supplemented by the plasma cell immunophenotype and DNA index, is an important element in establishing the diagnosis.
It is important to correctly classify patients with plasma cell proliferative disorders as the various disease entities are treated differently. A number of factors are used for this classification including the proportions of clonal bone marrow plasma cells, the DNA index of the clonal plasma cells, and their proliferative activity. The plasma cell DNA index and proliferation assessment by flow cytometry are rapid and reliable. This information can be used to distinguish patients with overt active MM from less aggressive diseases such as MGUS and smoldering MM.
Furthermore, in combination with other laboratory data, the results of these studies can be used as a measure of disease aggressiveness in newly diagnosed MM and to determine therapeutic efficacy and detect disease relapse in treated MM patients.
The following algorithms are available:
Specimen Retention Time
14 daysTest 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 US Food and Drug Administration.Report Available
1 to 4 daysForms
If not ordering electronically, complete, print, and send a Hematopathology/Cytogenetics Test Request (T726) with the specimen.