Aventa Lymphoma
Replace multiple FISH panels for fusion and rearrangement detection with a single, comprehensive test
Whole-genome | Reports on 417 genes
The Aventa Lymphoma test gives you an integrated approach for evaluating all clinically relevant rearrangements in B- and T-cell lymphomas so that you can:
Accurately diagnose disease and classify subtypes | Refine patient risk assessment to inform treatment decisions | Choose the most effective therapy to optimize outcomes
~35%
FISH testing misses ~35% of diagnosis-, prognosis- and treatment-informing fusions and rearrangements
Find them with Aventa Lymphoma
FISH vs Aventa Lymphoma
Conventional FISH:
narrow in scope
Although commonly used to detect fusions and rearrangements in lymphoma, FISH has key limitations:
Assay is not highly multiplexable, must probe each target individually, often done sequentially, consuming additional time and tissue
Requires anticipation of relevant targets — incorrect initial diagnosis can lead to appropriate targets remaining untested
May fail to detect clinically significant variants involving atypical breakpoints or noncanonical partner genes or other rare biomarkers
Aventa Lymphoma: single-assay, genome-wide coverage
The Aventa Lymphoma test overcomes these constraints through a comprehensive, one-step approach:
All-in-one testing — Assesses 417 genes at once, reducing time and tissue requirements
Diagnosis-agnostic detection of all rearrangements, ensuring even the rarest are found
Technology is robust to cryptic breakpoints and detects rearrangements regardless of partner
Enhanced sensitivity — Delivers a 100- to 1000-fold higher signal than FISH
Ordering Aventa tests is easy
We handle specimen retrieval and return, and results are returned in about 10 business days.
We are committed to making our tests accessible and affordable
Aventa Assist offers programs to help patients whose costs for Aventa tests are not fully covered by insurance.