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RET (10q11), FISH, Tissue

Test Summary

Identifying RET gene rearrangements in patients with late-stage, lung adenocarcinomas that are negative for EGFR mutations and ALK rearrangements

Aliases

  • Non-small cell lung cancer (NSCLC)

Specimen Collection

Special Instructions

N/A

Preferred Specimen

Formalin-fixed, paraffin-embedded (FFPE) tumor tissue block. Blocks prepared with alternative fixation methods may be acceptable; provide fixation method used. Paraffin-embedded specimens can be from any anatomic location (skin, soft tissue, lymph node, etc). Bone specimens that have been decalcified will be attempted for testing, but the success rate is approximately 50%.

Minimum Volume

Slides: 1 Hematoxylin and eosin stained and 2 unstained

Instructions

A pathology report is required for testing to be performed. If not provided, appropriate testing and/or interpretation may be compromised or delayed. Acceptable pathology reports include working drafts, preliminary pathology, or surgical pathology reports.

Patient Preparation

N/A

Storage

Room temperature: indefinite
Refrigerated: indefinite
Frozen: NA

Transport Temperature

Ambient

Specimen Stability

  • N/A

Limitations

N/A

Other Acceptable Specimens

Tissue slides: 1 Hematoxylin and eosin stained and 4 unstained. Submit 4 consecutive unstained, positively charged, unbaked slides with 5 micron-thick sections of the tumor tissue and 1 slide stained with hematoxylin and eosin.

Unacceptable Specimens

All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.

Order Code

RETF

EPIC (Premier) Code

LAB6472

Includes

N/A

CPT Code

  • 88271x2
  • 88291 – DNA probe
  • each (first probe set)
  • Interpretation and report 88271x2 – DNA probe
  • each additional probe set (if appropriate) 88271x1 – DNA probe
  • each coverage for sets containing 3 probes (if appropriate) 88271x2 – DNA probe
  • each coverage for sets containing 4 probes (if appropriate) 88271x3 – DNA probe
  • each coverage for sets containing 5 probes (if appropriate) 88274 w/modifier 52 – Interphase in situ hybridization < 25 cells
  • each probe set (if appropriate) 88274 – Interphase in situ hybridization 25 to 99 cells
  • each probe set (if appropriate) 88275 – Interphase in situ hybridization 100 to 300 cells
  • each probe set (if appropriate)

Billing Code

  • 671157
  • 671166

CPT Statement

Methodology

Fluorescence In Situ Hybridization (FISH)

FDA Status

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

Mayo Clinic Laboratories
200 First Street SW
Rochester MN, 55905

Reference Range

N/A

Setup Schedule / Expected Turnaround Time

Monday - Friday; Report available: 7 - 10 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

Formalin-fixed, paraffin-embedded (FFPE) tumor tissue block. Blocks prepared with alternative fixation methods may be acceptable; provide fixation method used. Paraffin-embedded specimens can be from any anatomic location (skin, soft tissue, lymph node, etc). Bone specimens that have been decalcified will be attempted for testing, but the success rate is approximately 50%.

Minimum Volume

Slides: 1 Hematoxylin and eosin stained and 2 unstained

Instructions

A pathology report is required for testing to be performed. If not provided, appropriate testing and/or interpretation may be compromised or delayed. Acceptable pathology reports include working drafts, preliminary pathology, or surgical pathology reports.

Patient Preparation

N/A

Storage

Room temperature: indefinite
Refrigerated: indefinite
Frozen: NA

Transport Temperature

Ambient

Specimen Stability

  • N/A

Limitations

N/A

Other Acceptable Specimens

Tissue slides: 1 Hematoxylin and eosin stained and 4 unstained. Submit 4 consecutive unstained, positively charged, unbaked slides with 5 micron-thick sections of the tumor tissue and 1 slide stained with hematoxylin and eosin.

Unacceptable Specimens

All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.

Billing

CPT Code

  • 88271x2
  • 88291 – DNA probe
  • each (first probe set)
  • Interpretation and report 88271x2 – DNA probe
  • each additional probe set (if appropriate) 88271x1 – DNA probe
  • each coverage for sets containing 3 probes (if appropriate) 88271x2 – DNA probe
  • each coverage for sets containing 4 probes (if appropriate) 88271x3 – DNA probe
  • each coverage for sets containing 5 probes (if appropriate) 88274 w/modifier 52 – Interphase in situ hybridization < 25 cells
  • each probe set (if appropriate) 88274 – Interphase in situ hybridization 25 to 99 cells
  • each probe set (if appropriate) 88275 – Interphase in situ hybridization 100 to 300 cells
  • each probe set (if appropriate)

Billing Code

  • 671157
  • 671166

CPT Statement

Result Information

Methodology

Fluorescence In Situ Hybridization (FISH)

Testing Laboratory

N/A

Reference Range

N/A

Setup Schedule / Expected Turnaround Time

Monday - Friday; Report available: 7 - 10 days