genoCDS

Medical Disclaimer

genoCDS is a clinical reference tool for qualified healthcare professionals only. Content is derived from published guidelines and regulatory sources and may contain errors or outdated information. It is not a substitute for professional medical judgment, institutional protocols, or individual patient assessment. Always verify recommendations against current primary sources before making clinical decisions. Full disclaimer →

B-Cell Lymphomas · Follicular Lymphoma (FL)

Stage Stage I

Involvement of a single lymph node region (I) or single extralymphatic organ/site (IE). Limited disease — often treated with combined modality or abbreviated systemic therapy.

3 test recommendations across 1 clinical indication

At Diagnosis

Limited-stage FL (Stages I–II). Ki-67 and pathologic grade distinguish Grade 1–2 FL (indolent) from Grade 3B (DLBCL-like).

Required 2 tests

Required

BCL2/BCL6/MYC FISH Panel

Double/Triple-Hit FISH

LOINC 81239-0

FISH panel detecting rearrangements of MYC (8q24), BCL2 (18q21), and BCL6 (3q27). MYC + BCL2 rearrangements define double-hit lymphoma (DHL); MYC + BCL2 + BCL6 define triple-hit lymphoma (THL). Both are reclassified as High-Grade B-Cell Lymphoma (HGBL) per WHO 2022 and require intensified induction (DA-EPOCH-R). Required for all newly diagnosed DLBCL.

Ordering Note

Required for all FL at diagnosis. BCL2 FISH confirms t(14;18). MYC rearrangement in FL mandates urgent re-evaluation for DLBCL transformation. BCL6 rearrangement may indicate Grade 3B.

Specimen

FFPE tumorFresh/frozen tissue

Evidence

NCCN
NCCN FL v3.2024
NCCN Cat. 1
Required

Ki-67 Proliferation Index (IHC)

Ki-67

LOINC 85319-2

IHC measurement of MKI67 nuclear antigen, reflecting proliferating cell fraction. In MCL: Ki-67 ≥30% = MIPI-b high risk; ≥50% = blastoid/pleomorphic variant. In FL: Ki-67 >20% raises concern for Grade 3B or transformation. In DLBCL: Ki-67 >90% suggests very aggressive biology.

Ordering Note

Required. Ki-67 is central to grade determination. Ki-67 >20% at Grade 1–2 histology suggests sampling error or focal transformation.

Specimen

FFPE tumor

Evidence

NCCN
NCCN FL v3.2024
NCCN Cat. 1

Recommended 1 test

Recommended

TP53 Mutation Analysis

TP53

LOINC 81433-9

Sequencing of TP53 (17p13.1) for somatic mutations and copy number loss. In MCL: TP53 mutation (~15–20%) is the strongest adverse prognostic factor, predicting chemotherapy resistance and inferior BTK inhibitor outcomes. TP53-mutant MCL requires novel approaches (venetoclax, CAR-T, clinical trial). In FL: TP53 mutation increases transformation risk.

Ordering Note

Recommended for risk stratification. TP53 mutation in limited-stage FL is associated with early relapse and transformation — may influence treat vs. observe decision.

Specimen

FFPE tumorPeripheral blood

Evidence

NCCN
NCCN FL v3.2024
NCCN Cat. 2A

Payer Coverage

Payer Coverage Summary

Coverage status as of last policy review. Prior authorization requirements and coverage criteria may change. Verify directly with each payer before ordering.

TestMedicare (CMS)UnitedHealthAnthem BCBSHumanaCignaAetna
Double/Triple-Hit FISHCoveredCoveredCoveredCoveredCoveredCovered
Ki-67CoveredCoveredCoveredUnknownUnknownUnknown
TP53CoveredCoveredCoveredPrior AuthCoveredCovered

Coverage data last verified via automated policy research. Always confirm current policies with each payer.

Reference only. Testing guidance shown is derived from published clinical guidelines and regulatory sources. It does not constitute a clinical recommendation for any individual patient. Payer coverage information is a general summary and may not reflect current policy or individual benefit design. Full disclaimer

Recommendations on this page are derived from publicly available guidelines (NCCN, ASCO, ESMO, FDA, OncoKB) and are paraphrased for reference. They do not constitute medical advice. Evidence levels reflect the grading systems of each respective organization and should be interpreted in clinical context. This reference is updated periodically but may not reflect the most recent guideline revisions.