Investigation | Blood sample requirement | Result / report available |
Myeloid Gene panel analysis by Next Generation Sequencing
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2-3 mL EDTA-anticoagulated bone marrow / or 4 mL EDTA-anticoagulated peripheral blood
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Up to 21 calendar days
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Acute Myeloid Leukaemia (AML) – rapid analysis testing
FLT3 ITD/TKD NPM1
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2-3 mL EDTA-anticoagulated bone marrow / or 4 mL EDTA-anticoagulated peripheral blood |
Up to 5 calendar days for FLT3 Up to 14 calendar days for NPM1
NPM1 screening is usually performed in parallel with FLT3, therefore the TAT may be shorter. |
Acute Myeloid Leukaemia (AML) –fusion detection and MRD monitoring
NPM1 CBFβ-MYH11 inv(16) AML1-ETO t(8;21)
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15-20 mL EDTA-anticoagulated peripheral blood and 2-3 mL EDTA-anticoagulated bone marrow |
Up to 14 calendar days
For clinical urgency based upon priority clinical needs, a request can be made, and a 1 week turn around time arranged with the Lab. |
APL – fusion detection and MRD monitoring
PML-RARA t(15;17) |
15-20 mL EDTA-anticoagulated peripheral blood and 2-3 mL EDTA-anticoagulated bone marrow |
Up to 14 calendar days
For clinical urgency based upon priority clinical needs, a request can be made, and a 1 week turn around time arranged with the Lab |
CML and ALL – fusion detection and MRD monitoring
BCR-ABL t(9;22)
BCR-ABL kinase domain mutation analysis |
15-20 mL EDTA-anticoagulated peripheral blood and / or 2-3 mL EDTA-anticoagulated bone marrow when required
Same as above. Please note: A separate sample is not required if MRD monitoring and AKD analysis are requested together. |
Up to 14 calendar for CML and ALL* For clinical urgency based upon priority clinical needs, a request can be made, and a 1 week turn around time arranged with the Lab. *Please note if BCR-ABL major negative, and where indicated, reflex testing for BCR-ABL minor will be performed. This may increase the quoted TAT .
Up to 21 calendar days For clinical urgency based upon priority clinical needs, a request can be made, and a shorter turn around time arranged with the Lab.
|
Myeloproliferative neoplasms PV, ET and IMF
MPN panel (JAK2, CALR, MPL)
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4 mL EDTA-anticoagulated peripheral blood
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Up to 21 calendar days
For clinical urgency based upon priority clinical needs, a request can be made, and a shorter turn around time arranged with the Lab. |
B and T Cell clonality analysis
Immunoglobulin and T cell receptor clonality analysis |
Formalin fixed parafin embedded tissue (5×10µM scrolls). For peripheral blood screen 4 mL EDTA PB or a bone marrow aspirate screen 2-3 mL EDTA BM
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Up to 14 calendar days |
Lymphoid Gene Panel Analysis by Next Generation Sequencing, including MYD88 for Waldenstrom’s Macroglobulinaemia (WM)
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2-3 mL EDTA-anticoagulated bone marrow / or 4 mL EDTA-anticoagulated peripheral blood
Formalin fixed parafin embedded tissue (5×10µM scrolls).
|
Up to 21 calendar days
|
Chronic Lymphocytic Leukaemia (CLL)
IGH Somatic Hypermutation analysis (IGHV mutation analysis)
CLL gene panel analysis including TP53 |
2-3 mL EDTA-anticoagulated bone marrow / or 4 mL EDTA-anticoagulated peripheral blood
Same as above. Please note: A separate sample is not required if IGHV and gene panel analysis are requested together unless FFPE is sent for lymphoid panel testing. |
Up to 21 calendar days
Up to 21 calendar days
|
Hairy Cell Leukaemia (HCL)
BRAF V600E mutation analysis |
2-3 mL EDTA-anticoagulated bone marrow / or 4 mL EDTA-anticoagulated peripheral blood
|
Up to 21 calendar days |
SNP array testing
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2-3 mL EDTA-anticoagulated bone marrow / or 4 mL EDTA-anticoagulated peripheral blood (note for Manchester patients this should be sent to the GLH at St Mary’s Hospital; for Liverpool patients please send to the genomics dept at Liverpool Women’s Hospital)
|
Up to 21 calendar days |
Whole Genome sequencing (WGS)
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https://mft.nhs.uk/nwglh/test-information/cancer/solid-tumour/whole-genome-sequencing-for-cancer/ |
4 – 6 weeks |
Please note that for a few specialist tests, samples will be referred to one of the other GLH laboratories but sample referral and reporting will be handled by the NW-GLH via the HMDS service with the exception of ALL MRD samples (adult and paediatric) which should continue to be sent according to current pathways until further notice.
Samples from AML patients whose MRD analysis was previously undertaken elsewhere should be sent to the same external centre for the duration of the patient’s management.
As the test directory will be regularly updated there may be some new or rare targets not currently available. If this is the case the laboratory will contact you to discuss testing options.