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26465 MayoComplete Acute Myeloid Leukemia, Therapeutic Gene Mutation Panel (FLT3, IDH1, IDH2, TP53), Next-Generation Sequencing, Varies (NGAMT)

MayoComplete Acute Myeloid Leukemia, Therapeutic Gene Mutation Panel (FLT3, IDH1, IDH2, TP53), Next-Generation Sequencing, Varies (NGAMT)
Test Code: NGAMTSO
Synonyms/Keywords

NGS Acute Myeloid Leukemia, Therapeutic Gene Mutation Pnl (FLT3, IDH1, IDH2, TP53), Varies (NGAMT); FLT3; IDH1; IDH2; Next gen sequencing of leukemia (AML); Next Gen Sequencing Test; NGS cancer panel, hematologic; NGS hematologic malignancies; Somatic mutation detection by next generation sequencing (NGS), hematologic; TP53; Enasidenib therapy; Midostaurin therapy; Gilteritinib therapy; Ivosidenib therapy; NGS for Acute Myeloid Leukemia evaluation

Test Components

​This test includes next-generation sequencing to evaluate for the following 4 genes: FLT3, IDH1, IDH2, and TP53.

Useful For

​Evaluation of acute myeloid leukemia (AML) using a focused 4-gene panel at the time of diagnosis, or possibly relapsed or refractory disease, to help determine optimal (eg, targeted) therapeutic approaches

Specimen Requirements
Submit only 1 of the following specimens:  ​ ​ ​ ​ ​ ​ ​
Fasting RequiredSpecimen TypePreferred Container/TubeAcceptable Container/TubeSpecimen VolumeSpecimen Minimum Volume
(allows for 1 repeat)
Pediatric Minimum Volume
(no repeat)
​ ​​​Bone marrow aspirate (preferred)​​EDTA Lavender Top Tube (LTT) or ACD Yellow Top tube (YTT) ​ ​Sodiuum Heparin ​Green Top Tube (GTT)​2 mL ​​1 mL ​​ ​
​ ​​​​Peripheral Blood ​ ​​​​EDTA Lavender Top Tube (LTT)  or ACD Yellow Top tube (YTT) ​ ​​ ​Sodiuum Heparin ​Green Top Tube (GTT) ​​3 mL ​​1 mL ​​ ​
Extracted DNA from blood or bone marrow​​​ ​1.5- to 2-mL tube with indication of volume and concentration of the DNAEntire specimen​100 mcL at 20 ng/mcL concentration
Collection Processing Instructions

Peripheral blood and bone marrow specimens must arrive within 14 days of collection.

 

The following information is required:

1. Clinical diagnosis

2. Pertinent clinical history, including disease phase (diagnostic, remission, relapse/refractory) and therapy status (especially if patient has received a hematopoietic stem cell transplant).

3. Clinical or morphologic suspicion

4. Date of collection

5. Specimen source

 

Bone marrow aspirate (preferred) & Peripheral blood:

1. Invert several times to mix specimen.

2. Send specimen in original tube.  DO NOT aliquot.

3. Label specimen as bone marrow or blood.

 

Specimen Type: Extracted DNA from blood or bone marrow

1. Label specimen as extracted DNA from blood or bone marrow.

2. Indicate volume and concentration of the DNA on specimen.

Specimen Stability Information
Specimen TypeTemperatureTime
Bone marrow aspirate & Pheripheral Blood​​Ambient (preferred)​14 days
​Refrigerated
Extracted DNA from blood or bone marrow​ ​ ​​Frozen (preferred)14 days ​
​Refrigerated
​Ambient
Rejection Criteria

Gross hemolysis, Bone marrow biopsies, Slides, Paraffin shavings or frozen tissues, paraffin-embedded tissues. Paraffin-embedded bone marrow aspirates, and Moderately to severely clotted specimens

Interference

​This test is a targeted next-generation sequencing (NGS) assay that encompasses 4 genes with partial gene region (including select intronic or noncoding regions) or hot spot coverage (depending on specific locus). Therefore, this test will not detect other genetic abnormalities in genes or regions outside the specified target areas. The test detects single base substitutions (ie, point mutations) as well as small insertion or deletion type events, but it does not detect gene rearrangements (ie, translocations), gene fusions, copy number alterations, or large scale (segmental chromosome region) deletions and complex changes.

This assay does not distinguish between somatic and germline alterations in analyzed gene regions, particularly with variant allele frequencies near 50% or 100%. If nucleotide alterations in genes associated with germline variant syndromes are present and there is a strong clinical suspicion or family history of malignant disease predisposition, additional genetic testing and appropriate counseling may be indicated. A low incidence of gene mutations associated with myeloid neoplasms can be detected in nonmalignant hematopoietic cells in individuals with advancing age (clonal hematopoiesis of indeterminate potential), and these may not be clearly distinguishable from tumor-associated mutations. Some apparent mutations classified as variants of uncertain significance may represent rare or low-frequency polymorphisms.

Prior treatment for hematologic malignancy could affect the results obtained in this assay. In particular, a prior allogeneic hematopoietic stem cell transplant may cause difficulties in resolving somatic or polymorphic alterations or assigning variant calls correctly to donor and recipient fractions, if pertinent clinical or laboratory information (eg, chimerism engraftment status) is not provided.

The finding of a genetic alteration does not necessarily indicate the presence of a myeloid neoplasm. Correlation with clinical, histopathologic, and additional laboratory findings is required for final interpretation of NGS results and is the responsibility of the managing physician.Detailed variant assessment and interpretive comments will be provided for all reportable genetic alterations.

Performing Laboratory Information
Performing LocationDay(s) Test PerformedReport AvailableMethodology/Instrumentation
Mayo Clinic Laboratories​​Monday through Friday​16 to 21 daysNext-Generation Sequencing (NGS)
Reference Lab
Test Information

Ordering Guidance:

This test is a subset of the NGSHM / OncoHeme Next-Generation Sequencing for Myeloid Neoplasms test and focuses more specifically on the gene mutations that are most utilized for therapeutic management of acute myeloid leukemias (AML). If a wider gene mutation analysis is desired, or the indication is for a myeloid malignancy other than AML, then NGSHM / OncoHeme Next-Generation Sequencing (NGS), Hematologic Neoplasms should be considered.

 

Next-generation sequencing (NGS) is a comprehensive molecular diagnostic methodology that can interrogate multiple regions of genomic tumor DNA in a single assay. Many hematologic neoplasms, including acute myeloid leukemia (AML), are characterized by morphologic or phenotypic similarities, but can have characteristic somatic mutations in many genes. In addition, many cases of AML lack a clonal cytogenetic finding at diagnosis (normal karyotype) and can be better classified according to gene mutation profile. The presence and pattern of gene mutations in AML can provide critical prognostic information and may help in guiding therapeutic management decisions by physicians, particularly if targeted therapies are available.

Reference Range Information

An interpretive report will be provided.

Interpretation

Detailed variant assessment and interpretive comments will be provided for all reportable genetic alterations.

Outreach CPTs
CPTModifier
(if needed)
QuantityDescriptionComments
​81120​1​IDH1 common variants
​81121​1​IDH2 common variants
​81245​1​FLT3 gene analysis
​81246​1​TKD variants
​81352​1​targeted sequence analysis
Synonyms/Keywords

NGS Acute Myeloid Leukemia, Therapeutic Gene Mutation Pnl (FLT3, IDH1, IDH2, TP53), Varies (NGAMT); FLT3; IDH1; IDH2; Next gen sequencing of leukemia (AML); Next Gen Sequencing Test; NGS cancer panel, hematologic; NGS hematologic malignancies; Somatic mutation detection by next generation sequencing (NGS), hematologic; TP53; Enasidenib therapy; Midostaurin therapy; Gilteritinib therapy; Ivosidenib therapy; NGS for Acute Myeloid Leukemia evaluation

Test Components

​This test includes next-generation sequencing to evaluate for the following 4 genes: FLT3, IDH1, IDH2, and TP53.

Ordering Applications
Ordering ApplicationDescription
​Cerner​NGS Acute Myeloid Leukemia, Therapeutic Gene Mutation Pnl (FLT3,IDH1,IDH2, TP53) Varies (NGAMT)
​COM​NGS Acute Myeloid Leukemia (NGAMT)
If the ordering application you are looking for is not listed, contact your local laboratory for assistance.
Specimen Requirements
Submit only 1 of the following specimens:  ​ ​ ​ ​ ​ ​ ​
Fasting RequiredSpecimen TypePreferred Container/TubeAcceptable Container/TubeSpecimen VolumeSpecimen Minimum Volume
(allows for 1 repeat)
Pediatric Minimum Volume
(no repeat)
​ ​​​Bone marrow aspirate (preferred)​​EDTA Lavender Top Tube (LTT) or ACD Yellow Top tube (YTT) ​ ​Sodiuum Heparin ​Green Top Tube (GTT)​2 mL ​​1 mL ​​ ​
​ ​​​​Peripheral Blood ​ ​​​​EDTA Lavender Top Tube (LTT)  or ACD Yellow Top tube (YTT) ​ ​​ ​Sodiuum Heparin ​Green Top Tube (GTT) ​​3 mL ​​1 mL ​​ ​
Extracted DNA from blood or bone marrow​​​ ​1.5- to 2-mL tube with indication of volume and concentration of the DNAEntire specimen​100 mcL at 20 ng/mcL concentration
Collection Processing

Peripheral blood and bone marrow specimens must arrive within 14 days of collection.

 

The following information is required:

1. Clinical diagnosis

2. Pertinent clinical history, including disease phase (diagnostic, remission, relapse/refractory) and therapy status (especially if patient has received a hematopoietic stem cell transplant).

3. Clinical or morphologic suspicion

4. Date of collection

5. Specimen source

 

Bone marrow aspirate (preferred) & Peripheral blood:

1. Invert several times to mix specimen.

2. Send specimen in original tube.  DO NOT aliquot.

3. Label specimen as bone marrow or blood.

 

Specimen Type: Extracted DNA from blood or bone marrow

1. Label specimen as extracted DNA from blood or bone marrow.

2. Indicate volume and concentration of the DNA on specimen.

Specimen Stability Information
Specimen TypeTemperatureTime
Bone marrow aspirate & Pheripheral Blood​​Ambient (preferred)​14 days
​Refrigerated
Extracted DNA from blood or bone marrow​ ​ ​​Frozen (preferred)14 days ​
​Refrigerated
​Ambient
Rejection Criteria

Gross hemolysis, Bone marrow biopsies, Slides, Paraffin shavings or frozen tissues, paraffin-embedded tissues. Paraffin-embedded bone marrow aspirates, and Moderately to severely clotted specimens

Interference

​This test is a targeted next-generation sequencing (NGS) assay that encompasses 4 genes with partial gene region (including select intronic or noncoding regions) or hot spot coverage (depending on specific locus). Therefore, this test will not detect other genetic abnormalities in genes or regions outside the specified target areas. The test detects single base substitutions (ie, point mutations) as well as small insertion or deletion type events, but it does not detect gene rearrangements (ie, translocations), gene fusions, copy number alterations, or large scale (segmental chromosome region) deletions and complex changes.

This assay does not distinguish between somatic and germline alterations in analyzed gene regions, particularly with variant allele frequencies near 50% or 100%. If nucleotide alterations in genes associated with germline variant syndromes are present and there is a strong clinical suspicion or family history of malignant disease predisposition, additional genetic testing and appropriate counseling may be indicated. A low incidence of gene mutations associated with myeloid neoplasms can be detected in nonmalignant hematopoietic cells in individuals with advancing age (clonal hematopoiesis of indeterminate potential), and these may not be clearly distinguishable from tumor-associated mutations. Some apparent mutations classified as variants of uncertain significance may represent rare or low-frequency polymorphisms.

Prior treatment for hematologic malignancy could affect the results obtained in this assay. In particular, a prior allogeneic hematopoietic stem cell transplant may cause difficulties in resolving somatic or polymorphic alterations or assigning variant calls correctly to donor and recipient fractions, if pertinent clinical or laboratory information (eg, chimerism engraftment status) is not provided.

The finding of a genetic alteration does not necessarily indicate the presence of a myeloid neoplasm. Correlation with clinical, histopathologic, and additional laboratory findings is required for final interpretation of NGS results and is the responsibility of the managing physician.Detailed variant assessment and interpretive comments will be provided for all reportable genetic alterations.

Useful For

​Evaluation of acute myeloid leukemia (AML) using a focused 4-gene panel at the time of diagnosis, or possibly relapsed or refractory disease, to help determine optimal (eg, targeted) therapeutic approaches

Test Components

​This test includes next-generation sequencing to evaluate for the following 4 genes: FLT3, IDH1, IDH2, and TP53.

Reference Range Information

An interpretive report will be provided.

Interpretation

Detailed variant assessment and interpretive comments will be provided for all reportable genetic alterations.

For more information visit:
Performing Laboratory Information
Performing LocationDay(s) Test PerformedReport AvailableMethodology/Instrumentation
Mayo Clinic Laboratories​​Monday through Friday​16 to 21 daysNext-Generation Sequencing (NGS)
Reference Lab
For billing questions, see Contacts
Outreach CPTs
CPTModifier
(if needed)
QuantityDescriptionComments
​81120​1​IDH1 common variants
​81121​1​IDH2 common variants
​81245​1​FLT3 gene analysis
​81246​1​TKD variants
​81352​1​targeted sequence analysis
For most current information refer to the Marshfield Laboratory online reference manual.