Multiple Myeloma Enriched Microarray and Multiple Myeloma FISH

CPT: 81277
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Synonyms

  • Monoclonal Gammopathy of Undetermined Significance (MGUS)
  • Oncology Array
  • Plasma Cell Leukemia
  • Reveal® MM Enrich CMA

Test Includes

Fluorescence in situ hybridization (FISH) for multiple myeloma (MM); IgH-CCDN1; FGFR3/IgH; CMAF/IgH; SNP microarray (Reveal®)


Special Instructions

Indicate pertinent clinical diagnosis and previous cytogenetics studies on the test request form.


Expected Turnaround Time

10 - 14 days



Specimen Requirements


Specimen

Bone marrow


Volume

1 to 3 mL bone marrow


Minimum Volume

1 mL bone marrow


Container

Green-top (sodium heparin) tube with bone marrow aspirate.


Storage Instructions

Maintain specimen at room temperature.


Causes for Rejection

Whole blood; broken tube. For SNP microarray, quantity not sufficient for analysis, gel-separator tubes, microtainer tubes, fixed cell pellets.


Test Details


Use

Diagnostic test for multiple myeloma. Plasma cell enrichment diagnosis increased as much as 50% to 100%. The FISH results on the enriched assay should not be used as a quantitative assay, since the abnormal cells do not represent the percentage of abnormal cells in the aspirate. The SNP assay will detect chromosomal imbalance that may be present in neoplastic disorders and clonal evolution. It provides detection of copy-neutral loss of heterozygosity of any chromosome, and the percent and location of homozygosity, that may be associated with cancer gene mutations.


Limitations

The SNP assay does not detect balanced rearrangements, low-level mosaicism (<10%), marker chromosomes that only contain heterochromatin or tetraploidy.

This test was developed and its performance characteristics determined by LabCorp. It has not been cleared or approved by the Food and Drug Administration.


Methodology

Fluorescence in situ hybridization (FISH) and plasma cell enrichment. SNP microarray analysis is performed using the Cytoscan® HD platform, which uses more than 743,000 SNP probes and 1,953,000 NPCN probes with a median spacing of 0.88 kb.


References

Fonseca R, Barlogie B, Bataille R, et al. Genetics and cytogenetics of multiple myeloma: A workshop report. Cancer Res. 2004 Feb 15;64:1546-1558.14989251
Fonseca R, Bergsagel PL, Drach J, et al. International Myeloma Working Group molecular classification of multiple myeloma: Spotlight review. Leukemia. 2009 Dec;23(12):2210-2221.19798094
Pozdnyakova O, Crowley-Larsen P, Zota V, Wang SA, Miron PM. Interphase FISH in plasma cell dyscrasia: Increased in abnormality detection with plasma cell enrichment. Cancer Genet Cytogenet. 2009 Mar;189(2):112-117.19215792

LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
510904 MM Enrich CMA + MM Trans FISH 511435 Specimen Type 31208-2
510904 MM Enrich CMA + MM Trans FISH 510189 # of Genotyping Targets N/A
510904 MM Enrich CMA + MM Trans FISH 510190 Diagnosis 62357-9
510904 MM Enrich CMA + MM Trans FISH 510191 Interpretation 62365-2
510904 MM Enrich CMA + MM Trans FISH 510192 Director Review: 48672-0
510904 MM Enrich CMA + MM Trans FISH 512123 PDF 51967-8
510904 MM Enrich CMA + MM Trans FISH 510816 Specimen Type 31208-2
510904 MM Enrich CMA + MM Trans FISH 510817 Cells Counted 62361-1
510904 MM Enrich CMA + MM Trans FISH 510818 Cells Analyzed 62360-3
510904 MM Enrich CMA + MM Trans FISH 510819 FISH Result 62357-9
510904 MM Enrich CMA + MM Trans FISH 510964 Interpretation 62365-2
510904 MM Enrich CMA + MM Trans FISH 510973 Director Review: 48672-0

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