Hematopathology Send-out Tests to NeoGenomics
UT-Medical School at Houston, Pathology/ Last Revision on: 12/20/2024
Flow Cytometry (T, technical only)
-For new acute leukemia cases: Extended L/L Panel
(31 markers)
-For new cases with suspected diagnosis: Standard
L/L Panel (24 markers) with appropriate Add-on Tubes
(Note that appropriate Add-on Panels may be automatically
added by technical personnel if abnormal cell subsets are detected)
-For samples from Surgical Path/Cytopath: T&B
Tissue Panel with appropriate Add-on Tubes (such as Plasma
Cell)
-For PNH: High Sensitivity PNH
-For MRD in B-ALL: B-ALL MRD (G, only Global option is available)
-Sample pickup by NeoGenomics: twice
daily M-F (noon and 5:45-6:15 pm). Besides these pickups, STAT pickup can be
done by calling 866.776.5907 (option 3, giving client account number: 17336 for
Memorial Hermann-TMC). Put sample in usual flow sample box at lab window.
-Local Houston flow cytometry lab, operating Monday-Sat: 7256 South Sam Houston Parkway West, Suite 300 Houston, TX 77085; phone 866 776 5907
Cytogenetics, FISH, and PCR/NGS (G, global)
NOTES: for patient already in remission, we will just order tests to cover
known positive abnormalities from previous diagnostic bone marrow
(translocations, mutations, etc). Only for patients still refractory or with
relapse we would order all tests as for new cases to cover any genomic
evolution that yield new abnormalities.
1.AML
(a) Sample in dark green-top tube for
-Oncology Chromosome Analysis
-AML Std FISH Panel:
5q-, -5 (5p15, 5q31, 5q33) | 7q-, -7
(Cen 7, 7q22, 7q31) | Trisomy 8 (Cen 8) | MLL (11q23) | 20q- (20q12, 20qter) |
RUNX1/RUNX1T1 (ETO/AML1) t(8;21) | PML/RARA t(15;17) | CBFB inv(16), t(16;16)
-BCR/ABL1 by FISH
(b) Sample in lavender-top tube for:
- Neotype AML Express (NGS):TAT 3-5
days
DNA Sequencing: SNVs/InDels (38 genes): ABL1, ASXL1,
BCOR, BRAF, CALR, CBL, CEBPA, CSF3R, DDX41, DNMT3A, ETV6, EZH2, FLT3, GATA2,
HRAS, IDH1, IDH2, JAK2, KIT, KRAS, MPL, NF1, NPM1, NRAS, PHF6, PPM1D, PRPF8,
PTPN11, RUNX1, SETBP1, SF3B1, SRSF2, STAG2, TET2, TP53, U2AF1, WT1, ZRSR2
RNA Sequencing: Fusions (9 genes): ABL1, KAT6A, KMT2A, MECOM, MYH11, NUP98,
NUP214, RUNX1, RARA
-PML-RARA Translocation, t(15;17) (Quantitative PML/RARA) for follow-up bone marrows with APL cases
-RUNX1-RUNX1T1 (AML1-ETO)
Translocation, t(8;21), quantitative PCR testing. For AML cases with
known t(8;21) or inv(16), typically by FISH from baseline BM
-Note: for
difficult APL cases, call Neogenomics to request for a STAT FISH testing for the PML/RARA component.
It can be done on the same day of Neogenomics
receiving the sample in their lab. The other FISH tests in the AML panel can be
completed later. Note
STAT along with MD contact name and phone number to receive STAT results.
2A. Adult B cell ALL
(a) Sample in green-top tube for
-Oncology Chromosome Analysis
-ALL, Adult FISH Panel [TCF3/PBX1 (E2A/PBX1) t(1;19) | Trisomy or Tetrasomy 4,
6, 10, 17 (Cen 4, Cen 6, Cen 10, Cen 17) | MYC (8q24) | BCR/ABL1/ASS1 t(9;22) |
MLL (11q23) | IgH (14q32) |]
-For bcr-abl1-like ALL: ALL, Ph-like [PDGFRb (5q32), BCR/ABL1-ASS1 t(9;22), JAK2 (9p24.1), EPOR
(19p13.2) and CRLF2 (Xp22.33/Yp11.32)]
Note: STAT FISH testing is
available by request for BCR-ABL1. Note STAT along with MD contact name and
phone number to receive STAT results.
b) Sample in lavender-top
tube:
-BCR/ABL1 Standard p210,p190 (quant PCR for known case with bcr/abl1)
-ClonoSEQ B-cell clonality (ID) for 1st BM; ClonoSEQ B-cell tracking for follow-up BM
2B. Adult T cell ALL
(a) Sample in green-top tube for
-Oncology Chromosome Analysis
-To Mayo for TALPF (pedi FISH, <31 years old) or TALAF (adult FISH,
>/=31 years old).
(b) Sample in purple top to:
-NeoGenomics for NOTCH1 mutation
analysis
-ClonoSEQ T-cell clonality (ID) for 1st BM; ClonoSEQ T-cell tracking for follow-up BM
2C. Pediatric B cell ALL
(a) Sample in green-top tube for
-Oncology Chromosome Analysis
-ALL, Pediatric FISH Panel [TCF3/PBX1 (E2A/PBX1) t(1;19) | Trisomy or Tetrasomy 4,
6, 10, 17 (Cen 4, Cen 6, Cen 10, Cen 17) | MYC (8q24) | BCR/ABL1/ASS1 t(9;22) |
MLL (11q23) | ETV6/RUNX1 (TEL/AML1) t(12;21) | IgH
(14q32)]. Note that we need to write down name of this test in request slip.
-For bcr-abl1-like ALL: ALL, Ph-like [PDGFRb (5q32), BCR/ABL1-ASS1 t(9;22), JAK2 (9p24.1), EPOR
(19p13.2) and CRLF2 (Xp22.33/Yp11.32)]
Note: STAT FISH testing is
available by request for BCR-ABL1. Note STAT along with MD contact name and
phone number to receive STAT results.
b) Sample in lavender-top tube for
-BCR/ABL1 Standard p210,p190 (quant PCR for known case with bcr/abl1)
-ClonoSEQ B-cell clonality (ID) for 1st BM; ClonoSEQ B-cell tracking for follow-up BM
-NeoTYPE ALL Profile
-B cell ALL MRD by flow cytometry (global) for follow-up
BM
2D. Pediatric T cell ALL
(a) Sample in green-top tube for
-Oncology Chromosome Analysis
-To Mayo for TALPF (pedi FISH, <31 years old)
(b) Sample in purple top
-To NeoGenomics for NOTCH1 mutation analysis
-ClonoSEQ T-cell clonality (ID) for 1st BM; ClonoSEQ T-cell tracking for follow-up BM
-MRD T cell ALL by
flow cytometry to PhenoPath (Requisitions
are in the hemepath signout room)
3. CML
(a) Sample in green-top tube for
-Oncology Chromosome Analysis
(b) Sample in lavender-top tube for quantitative PCR testing:
-BCR/ABL1 Standard p210,p190 (diagnostic and
follow-up bone marrows)
(c) For detection of resistance to Imatinib Mesylate if clinically
indicated: Abl1 Kinase Domain (Gleevec Resistance), sample in purple-top
tube for PCR
4. PV
(a) Sample in green-top tube for
-Oncology Chromosome Analysis
(b) Sample in lavender tube for PCR: JAK2 V617F
qualitative (check box if negative reflex to JAK2 Exon 12-14 mutation )
5. ET, PM, MPN-NOS, MPN/MDS
(a) Sample in green-top tube for
-Oncology Chromosome Analysis
-MPN FISH panel: PDGFRa,
CHIC2, FIP1L1 (4q12) | PDGFRb (5q33) | FGFR1 (8p11) |
BCR/ABL1 t(9;22) including ASS1 (9q34)
(b) Sample in lavender tube for MPN Extended Reflex Panel:
JAK2 V617F, JAK2 Exon
12-14, CALR exon 9, and MPL exon 10.
6. Myeloid and Lymphoid Neoplasms with Eosinophilia
Sample in green-top tube for
-Oncology Chromosome Analysis
-Eosinophilia FISH profile: PDGFRa,
CHIC2, FIP1L1 (4q12) | PDGFRb (5q33) | FGFR1 (8p11) |
CBFB inv(16), t(16;16) |
7. PLASMA CELL MYELOMA
Sample in green top tube for
-Oncology Chromosome Analysis
-Plasma cell myeloma FISH panel [1p-, 1q+, iso(1q): CDKN2C
(1p32), CKS1B (1q21) | +5, hyperdiploidy (5p15) | +9, hyperdiploidy (9q22) | +15, hyperdiploidy
(15q22) | 13q- (13q14, 13q34) | IgH (14q32) | 17p-
(TP53 17p13.1, NF1 17q11.2)]; check with reflex to IgH
Complex if positive [FGFR3/IgH
t(4;14) | CCND1/IgH t(11;14) | IgH/MAF
t(14;16) | IgH/MAFB t(14;20)],
8. CLL
(a) Sample in green top tube for
-Oncology Chromosome Analysis
-CLL FISH Profile: 6q- [SEC63 (6q21), MYB (6q23)] | ATM (11q22.3) | p53
(17p13.1) | Trisomy 12 (Cen 12) | 13q-/-13 (13q14, 13q34) | CCND1/IgH t(11;14)
(b) Sample in lavender-top (baseline bone marrow only) for
-IgVH Hypermutation
analysis
9. MDS (incl Cytopenia)
Sample in green top tube for
-Oncology Chromosome Analysis
-MDS extended FISH panel: RPN1, MECOM (3q21, 3q26.2) | 5q-, -5 (5p15, 5q31,
5q33) | 7q-, -7 (Cen 7, 7q22, 7q31) | Trisomy 8 (Cen 8) | MLL (11q23) | ETV6
(12p13) | 17p- (TP53 17p13.1, NF1 17q11.2) | +19 (19p13.2, 19q13) | 20q-
(20q12, 20qter)
Sample in lavender-top
-Neotype MDS/CMML
Profile (NGS):
ASXL1,
BCOR, BCORL1, BRAF, CALR, CBL, CEBPA, CUX1, DDX41, DNMT3A, ETNK1, ETV6, EZH2,
FLT3, GATA2, GNB1, HRAS, IDH1, IDH2, JAK2, KIT, KRAS, MPL, NF1, NPM1, NRAS,
PDGFRA, PHF6, PIGA, PPM1D, PTEN, PTPN11, RUNX1, SETBP1, SF3B1, SRSF2, STAG2,
STAT3, STAT5B, TET2, TP53, U2AF1, WT1, and ZRSR2
10. B cell Non-Hodgkin Lymphoma FISH Panel, if needed for
diagnosis
(bone marrow aspirate or unstained slides of bone marrow clot)
-Low grade B cell: Low grade/small B
cell lymphoma FISH panel: BCL6
(3q27) | CCND1/IgH t(11;14) IgH/BCL2
t(14;18) | MALT1 (18q21)
-High grade B cell: High grade/large B cell lymphoma FISH panel: BCL6 (3q27) | MYC (8q24) | BCL2 (18q21) |. Note
that this B-NHL High Grade FISH profile is needed for large B cell lymphoma
that meets one or more of the following criteria:
11. LPL
Sample in lavender-top tube for PCR testing: MYD88
12. HCL
(a) Sample in green top tube for
-Oncology Chromosome Analysis
(b) Sample in lavender-top for PCR
-BRAF
++++++++++++++++++++++++++++++++++++++++++++++
SOLID TISSUE (lymph node, bone marrow clot)
Note that decalcified bone marrow biopsy is not accepted
(A) FISH sample for solid tissue:
-Unstained slides at 5 micron thickness
-Minimum 2 slides for each probe; add 2 extra slides
(B) PCR sample for solid tissue:
-Unstained slides at 10 micron thickness
-Minimum 2 slides for each probe; add 2 extra slides
+++++++++++++++++++++++++++++++++++++++++++++
NEOGENOMICS
Account Number: 17336
Account Name: Memorial
Hermann Texas Medical Center
Client Service
Phone: 866.776.5907, option 3 and email: client.services@neogenomics.com
Client Service Fax: 239.690.4237
NeoLink
Online Portal Access: https://neolink.neogenomics.com/APvX/security/login.aspx
Test Menu Link: www.neogenomics.com/test-menu
Requisition Forms:
o Heme: https://www.neogenomics.com/sites/default/files/Requisition/Neo-Hematopathology-Requisition.pdf
o Solid Tumor: https://www.neogenomics.com/sites/default/files/2020-06/Neo_Solid-Tumor-Req_062620_Final_FF.pdf
o IHC: https://www.neogenomics.com/sites/default/files/2019-07/Neo-IHC-Req.PDF