Tumor Marker Tests in Common Use

A tumor marker is anything present in or produced by cancer cells or other cells of the body in response to cancer or certain benign (noncancerous) conditions that provides information about a cancer, such as how aggressive it is, whether it can be treated with a targeted therapy, or whether it is responding to treatment. See the Tumor Markers page for more information.

Listed below are tumor marker tests that are in common use, mainly to determine treatment or to help make a diagnosis of cancer. This list is not comprehensive; in particular, new tumor markers frequently become available and may not be included.

This list also does not include the many tumor markers that are tested by immunophenotyping and immunohistochemistry to help diagnose cancer and to distinguish between different types of cancer.

Some tumor markers listed below are targets for targeted therapy in multiple cancers but serve as tumor markers for only a subset of cancers. For each test, the main cancer types that it is used for are listed. Some markers may be used for other cancer types that are not listed. 

ALK gene rearrangements and overexpression

Alpha-fetoprotein(AFP)

B-cell immunoglobulin gene rearrangement

BCL2 gene rearrangement

BCR-ABL fusion gene (Philadelphia chromosome)

Beta-2-microglobulin (B2M)

Beta-human chorionic gonadotropin (Beta-hCG)

Bladder Tumor Antigen (BTA)

BRAF V600 mutations

BRCA1 and BRCA2 gene mutations

CA15-3/CA27.29

CA19-9

CA-125

CA 27.29

Calcitonin

Carcinoembryonic antigen (CEA)

CD19

CD20

CD22

CD25

CD30

CD33

Chromogranin A (CgA)

Chromosome 17p deletion

Chromosomes 3, 7, 17, and 9p21

Circulating tumor cells of epithelial origin (CELLSEARCH)

C-kit/CD117

Cyclin D1 (CCND1) gene rearrangement or expression

Cytokeratin fragment 21-1

Des-gamma-carboxy prothrombin (DCP)

DPD gene mutation

EGFR 

ESR1 gene mutation

Estrogen receptor (ER)/progesterone receptor (PR)

FGFR2 and FGFR3 gene mutations

Fibrin/fibrinogen

5-HIAA

5-Protein signature (OVA1)

FLT3 gene mutations

46-Gene signature (Prolaris)

FoundationOne CDx (F1CDx) genomic test

FoundationOne Liquid CDx 

Gastrin

Guardant360 CDx genomic test

HE4

HER2/neu (ERBB2) gene amplification, mutations, protein overexpression

IDH1 and IDH2 gene mutations

Immunoglobulins

IRF4 gene rearrangement

JAK2 gene mutation

KRAS gene mutation

Lactate dehydrogenase

Microsatellite instability (MSI) and/or mismatch repair deficiency (dMMR) 

MYC gene expression

MYD88 gene mutation

Myeloperoxidase (MPO)

Neuron-specific enolase (NSE)

NTRK gene fusion

Nuclear matrix protein 22

PCA3 mRNA

PIK3CA gene mutation status

PML/RARα fusion gene

Programmed death ligand 1 (PD-L1)

Prostate-specific antigen (PSA)

Prostatic Acid Phosphatase (PAP)

RET gene fusions and mutations

ROS1 gene rearrangement

17-Gene signature (Oncotype DX GPS test)

70-Gene signature (Mammaprint)

Soluble mesothelin-related peptides (SMRP)

Somatostatin receptor

T-cell receptor gene rearrangement

Terminal transferase (TdT)

Thiopurine S-methyltransferase (TPMT) enzyme activity or TPMT genetic test

Thyroglobulin

TP53 gene mutations

Tumor mutational burden (TMB)

21-Gene signature (Oncotype DX)

UGT1A1*28 variant homozygosity

Urine catecholamines: VMA and HVA

Urokinase plasminogen activator (uPA) and plasminogen activator inhibitor (PAI-1)