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FISH, p53, Deletion 17p13.1
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Test Code
P53FSH
CPT Codes
88271 (x2), 88275
Preferred Specimen
3 mL bone marrow or 5 mL whole blood collected in sodium heparin (green-top) tube
Minimum Volume
1 mL bone marrow • 3 mL whole blood
Other Acceptable Specimens
Bone marrow or whole blood collected in: sodium heparin (royal blue-top) tube, or sodium heparin lead-free (tan-top) tube • Bone marrow submitted in culture transport media • 5x5mm fresh lymph node, or fresh biopsy in culture transport media
Instructions
Clinical history/reason for referral is required with test order. Prior therapy and transplant history should be provided with test order.
Please specify if this test is run for plasma cell neoplasms.
Submit 1 to 3 mL of bone marrow or 3 to 5 mL whole blood in a sodium heparin (green-top) tube. Bone marrow transport medium is available upon request.
Specimen viability decreases during transit. Send specimen to testing lab for viability determination. Do not freeze. Do not reject.
Note: If results are not possible, the test order may be canceled and replaced with a Cytogenetics Communication.
Please specify if this test is run for plasma cell neoplasms.
Submit 1 to 3 mL of bone marrow or 3 to 5 mL whole blood in a sodium heparin (green-top) tube. Bone marrow transport medium is available upon request.
Specimen viability decreases during transit. Send specimen to testing lab for viability determination. Do not freeze. Do not reject.
Note: If results are not possible, the test order may be canceled and replaced with a Cytogenetics Communication.
Transport Temperature
Fresh lymph node: Refrigerated (cold packs)
All other specimens: Room temperature
All other specimens: Room temperature
Specimen Stability
Room temperature: See instructions
Refrigerated: See instructions
Frozen: See instructions
Refrigerated: See instructions
Frozen: See instructions
Methodology
Fluorescence in situ Hybridization (FISH)
FDA Status
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Setup Schedule
Monday-Sunday Morning Report available: 5 Days
Reference Range
See Laboratory Report
Clinical Significance
Loss of the p53 gene, located in chromosome 17p13.1, is a common occurrence in neoplastic disorders, including hematologic disorders. FISH studies for deletion p53 are performed in addition to G-banding analysis of bone marrow, hematologic blood, lymph nodes, and solid tumors. This probe may be useful in detecting loss of p53 in complex karyotypes. Deletion of p53 is an adverse prognostic marker in CLL and follicular lymphoma.
Performing Laboratory
Quest Diagnostics Nichols Institute
14225 Newbrook Dr
Chantilly, VA 20153
Last Updated: November 29, 2021