ALL Adult FISH Panel

  • FISH

This FISH panel is designed to detect key genetic abnormalities associated with B-cell acute lymphoblastic leukemia (B-ALL) and B lymphoblastic lymphoma (LBL) in adults. It includes the following probes:

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)

Test Customization: Probes may be ordered separately, except that Centromeres 4 and 17 are paired, as are Centromeres 6 and 10. CDKN2A (p16) deletion testing is available to be ordered separately.

STAT Processing (upon request): Available for BCR/ABL1/ASS1 t(9;22). Include "STAT" along with the requesting physician's name and contact information for expedited results.

Turnaround time
3-5 Days
STAT BCR-ABL1 (upon request):
12-24 hours from receipt in the NeoGenomics laboratory

Level of Service

  • Global
  • Tech Only
New York Approved: Yes

Clinical Significance

The ALL Adult FISH Panel is used to detect recurrent chromosome abnormalities in adults with B-cell acute lymphoblastic leukemia (B-ALL) and B lymphoblastic lymphoma (LBL). Identifying specific abnormalities helps predict disease aggressiveness and response to therapy, guiding both risk stratification and treatment decisions.

This panel includes key targets relevant to adult disease biology, including the Philadelphia chromosome (BCR-ABL1) and other translocations and copy number changes linked to prognosis and therapy selection. A positive result for BCR-ABL1, for example, indicates Philadelphia-positive ALL, which can be treated with tyrosine kinase inhibitors (TKIs) (Fielding et al., 2014; Jabbour et al., 2015). Similarly, detecting MYC or MLL rearrangements can signal more aggressive disease and the need for alternative treatment approaches (Arber et al., 2017). Trisomies and tetrasomies of chromosomes 4, 6, 10, and 17 can provide additional prognostic information and influence treatment intensity (Moorman et al., 2007).

This panel is designed specifically for adults and excludes probes for ETV6/RUNX1 t(12;21), which are more common in pediatric ALL (Pui et al., 2011). The insights provided by this panel support both initial diagnosis and ongoing management, helping oncologists tailor therapy to each patient’s genetic profile.

Specimen Requirements

Bone Marrow Aspirate: 1-2 mL in sodium heparin tube. EDTA tube is acceptable.
Peripheral Blood: 2-5 mL in sodium heparin tube. EDTA tube is acceptable.
Fresh, Unfixed Tissue: Tissue in RPMI.
Bone Marrow/Peripheral Blood Smear or Fresh Tissue Touch Preparation Slides: Minimum 7 slides, labeled with specimen type.
Fluids: Mix in equal parts with RPMI (specimen volume to RPMI ratio of 1:1).
Fixed Cell Suspension: A client-prepared fixed cell suspension is acceptable if received in 3:1 Methanol:Glacial Acetic Acid.

Storage and Transportation

Storage & Transportation: Use cold pack for transport, making sure cold pack is not in direct contact with specimen. For fresh samples: refrigerate before shipping and ship same day as drawn whenever possible. Do not freeze. NYS clients please provide date and time of Collection.

CPT Code(s)*

88374x7 automated. Codes may differ if manual analysis is performed.

*The CPT codes provided with our test descriptions are based on AMA guidelines and are for informational purposes only. Correct CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed.

Last Updated: October 02, 2025

Get in touch

Our Client Services team is on hand to help. Please call us at 866.776.5907, Option 3.