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Search by test name, test code, CPT or LOINC code, or a gene to find the panels that cover it. Select a test to see its methodology, specimen requirements, and storage and transport instructions.

Description

A comprehensive genomic profiling test performed on intact circulating tumor cells, not DNA fragments, from a single blood draw. 517-gene panel; reported alterations: single nucleotide variants (SNVs), insertions and deletions (indels), copy number variants (CNVs). Signatures: tumor mutational burden (TMB) and microsatellite instability (MSI). Enumeration: CTC count reported for the entire patient accession. Validated across a range of solid tumors. Laboratory-developed test; not cleared or approved by the U.S. FDA.

Methodology

Next-Generation Sequencing

Days performed

Genes (517)

A1CF
ABCB1
ABL1
ABL2
ABRAXAS1
ACSM2B
ACVR1
ACVR1B
ACVR2A
ADAM18
ADAMTS12
ADAMTS2
+ 505 more

Specimen requirements

Container: CellSave CTC Preservation Tubes (kit supplied)
Volume: Two 10 mL CellSave CTC Preservation Tubes
Collection: Specimen: Peripheral whole blood
Rejection: Streck and EDTA tubes are not accepted.

Storage & transportation

Room temp
Refrigerated
Frozen
Transport: Refrigerated (2–8 °C)

Open full test pageCPT codes are listed for reference; the billing party is responsible for coding accuracy.

Questions about a test or specimen? Contact client services at 888-617-2239 or info@cancercelldx.com.