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 Content is derived from published guidelines and regulatory sources and may contain errors or outdated information.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 · Diffuse Large B-Cell Lymphoma (DLBCL)

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.

4 test recommendations across 1 clinical indication

At Diagnosis

Stage I DLBCL at initial diagnosis. Full molecular workup required — DHL/THL identifies patients needing DA-EPOCH-R regardless of stage.

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 DLBCL regardless of stage. DHL (MYC + BCL2) is ~10% of DLBCL and requires DA-EPOCH-R. Must complete before starting any systemic therapy.

Specimen

FFPE tumorFresh/frozen tissue
Required

Cell-of-Origin Gene Expression Profiling

COO / GEP

LOINC 81538-8

Gene expression profiling to classify DLBCL cell-of-origin (COO) as GCB or ABC/non-GCB. GCB DLBCL has superior outcomes with R-CHOP; ABC/non-GCB benefits from pola-R-CHP (POLARIX) and novel regimens. Lymph2Cx (NanoString) is the validated clinical platform; Hans IHC algorithm is less accurate.

Ordering Note

Required for all DLBCL. COO (GCB vs. ABC/non-GCB) provides prognostic information and guides pola-R-CHP vs. R-CHOP selection.

Specimen

FFPE tumor

Recommended 1 test

Recommended

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

Routinely reported with lymphoma pathology. Ki-67 >90% suggests aggressive biology; combined with MYC IHC overexpression raises DHL suspicion even before FISH.

Specimen

FFPE tumor

Evidence

NCCN
NCCN DLBCL v5.2024
NCCN Cat. 2A

Optional 1 test

OptionalFDA Companion Dx

Comprehensive Solid Tumor NGS Panel

Comprehensive NGS

LOINC 81445-4

Next-generation sequencing panel covering ≥300 cancer-relevant genes, including all major NSCLC drivers (EGFR, ALK, ROS1, BRAF, KRAS, MET, RET, NTRK, HER2, FGFR), plus tumor mutational burden (TMB) and microsatellite instability (MSI). Examples include FoundationOne CDx, Tempus xT, Caris MI Transcriptome, and equivalent institutional panels. Preferred over single-gene sequential testing for efficiency and cost-effectiveness.

Ordering Note

Optional. NGS identifies EZH2, MYD88, CD79B, and other mutations relevant for R/R treatment. Consider at diagnosis for comprehensive molecular profiling.

Specimen

FFPE tumor tissue (≥20% tumor)Liquid biopsy (ctDNA)Fresh/frozen tumor tissue

Evidence

NCCN
NCCN DLBCL v5.2024
NCCN Cat. 2B

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
COO / GEPPrior AuthPrior AuthPrior AuthInvestigationalPrior AuthPrior Auth
Ki-67CoveredCoveredCoveredUnknownUnknownUnknown
Comprehensive NGSCoveredCoveredCoveredPrior 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.