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Orderable Name APLDF Acute Promyelocytic Leukemia-PML::RARA fusion, Expedited Diagnostic FISH, Varies


Ordering Guidance


This test is intended for diagnostic samples only when PML::RARA fusion is presumed and targeted PML and RARA fluorescence in situ hybridization (FISH) probes are needed to diagnose acute promyelocytic leukemia (APL).

 

Complete acute myeloid leukemia (AML) diagnostic FISH panel tests for adults and pediatric patients are also available. AML panel tests will be automatically prioritized by the laboratory when PML::RARA fusion is present. Most often, AML panel tests found with PML::RARA fusion will be reported the next business day from receipt in the Genomics laboratory. Same day testing is not available for panel testing. If panel testing is warranted, order either AMLFA / Adult Acute Myeloid Leukemia Panel, FISH, Varies or AMLFP / Pediatric Acute Myeloid Leukemia Panel, FISH, Varies, as appropriate based on patient age.

 

This test should not be used to screen for residual AML or when the diagnosis of APL is not strongly suggested. Monitoring patients known to have PML::RARA fusion should be performed by quantitative reverse transcription-polymerase chain reaction (RT-PCR) testing and not FISH testing. If the specimen does not meet the criteria for RT-PCR, follow-up FISH testing for PML::RARA fusion should be ordered as AMLMF / Acute Myeloid Leukemia (AML), Specified FISH, Varies with a PML/RARA specific probe request.

 

If this test is received in the laboratory concurrently with an order for either AMLFA / Adult Acute Myeloid Leukemia Panel, FISH, Varies or AMLFP / Pediatric Acute Myeloid Leukemia Panel, FISH, Varies, panel testing will be held pending the results of this test. Ordering an AML panel test concurrently with this test will result in an approximate 1 business day delay of the panel test reporting. If PML::RARA fusion is detected, the AMLFA or AMLFP panel test will be cancelled by the laboratory. If no fusion is identified, the complete AML FISH panel test will be performed, except for the PML/RARA FISH probe set.

 

If the entire AML FISH panel is preferred for an adult patient (aged 31 years or older), order AMLFA / Adult Acute Myeloid Leukemia panel, FISH, Varies.

 

If the entire AML FISH panel is preferred for a pediatric patient (aged 30 years or younger), order AMLFP / Pediatric Acute Myeloid Leukemia panel, FISH, Varies.

 

If upfront break-apart RARA FISH testing is desired, order AMLMF / Acute Myeloid Leukemia (AML), Specified FISH, Varies. Results will be reported the next business day.

 

For more information see Acute Promyelocytic Leukemia: Guideline to Diagnosis and Follow-up



Additional Testing Requirements


At diagnosis, PMLR / PML::RARA Quantitative, PCR, Varies should be performed in parallel with this test.

At follow-up, only PMLR / PML::RARA Quantitative, PCR, Varies should be performed.



Shipping Instructions


Advise Express Mail or equivalent if not on courier service.



Necessary Information


1. A reason for testing must be provided. If this information is not provided, an appropriate indication for testing may be entered by Mayo Clinic Laboratories.

2. A flow cytometry and/or a bone marrow pathology report should be submitted with each specimen. The laboratory will not reject testing if this information is not provided, but appropriate testing and interpretation may be compromised or delayed.

3. If a result callback by phone is needed after finalized results are released, the ordering healthcare professional must supply the name and direct phone number of a licensed physician (MD or DO) at the time the order is received.

-Result callbacks are only available during regular business hours.

-Preliminary results or exact times the finalized report will be available will not be provided under any circumstances.



Specimen Required


Submit only 1 of the following specimens:

 

Preferred

Specimen Type: Bone marrow

Container/Tube:

Preferred: Yellow top (ACD)

Acceptable: Green top (sodium heparin) or lavender top (EDTA)

Specimen Volume: 2 to 3 mL

Collection Instructions:

1. It is preferable to send the first aspirate from the bone marrow collection.

2. Invert several times to mix bone marrow.

3. Send bone marrow in original tube. Do not aliquot.

 

Acceptable

Specimen Type: Whole blood

Container/Tube:

Preferred: Yellow top (ACD)

Acceptable: Green top (sodium heparin) or lavender top (EDTA)

Specimen Volume: 6 mL

Collection Instructions:

1. Invert several times to mix blood.

2. Send whole blood in original tube. Do not aliquot.


Useful For

Detecting, at diagnosis, acute promyelocytic leukemia (APL)

 

This test should not be used to screen for residual APL.

Reflex Tests

Test ID Reporting Name Available Separately Always Performed
APLDB Probe, Each Additional (APLDF) No, (Bill Only) No

Testing Algorithm

This test includes a charge for the probe application, analysis, and professional interpretation of results for 1 probe set (2 individual fluorescence in situ hybridization [FISH] probes). Additional charges will be incurred for all reflex or additional probe sets performed. Analysis charges will be incurred based on the number of cells analyzed per probe set. If no cells are available for analysis, no analysis charges will be incurred.

 

This test should only be ordered at the time of diagnosis.

 

In the absence of PML::RARA fusion, when an extra RARA FISH signal is identified, reflex testing using the break-apart RARA probe set will be performed to resolve or confirm RARA rearrangement concerns. If additional RARA testing is required, results will be delayed until the next business day.

 

Appropriate ancillary probes may be performed at consultant discretion to render comprehensive assessment. Any additional probes will have the results included within the final report and will be performed at an additional charge.

Method Name

Fluorescence In Situ Hybridization (FISH)

Specimen Type

Varies

Specimen Minimum Volume

Bone marrow: 1 mL; Whole blood: 2 mL

Specimen Stability Information

Specimen Type Temperature Time
Varies Ambient (preferred)
  Refrigerated 

Reject Due To

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

Reference Values

An interpretive report will be provided

Day(s) Performed

Monday through Sunday

Report Available

1 to 3 days

CPT Code Information

88271x2, 88275x1, 88291x1- FISH Probe, Analysis, Interpretation; 1 probe set

88271x2, 88275x1-FISH Probe, Analysis; each additional probe set (if appropriate)