ctDNA-Based MRD Testing
Precise MRD Detection. Confident Decisions on Treatment and Surveillance.
LymphoVista delivers ctDNA results at the milestones that shape your clinical decisions — end of treatment, mid-cycle, and follow-up. Validated panels for B-cell and Hodgkin lymphoma.
Presented at ASH 2024 · EHA 2024
93.86%
Sensitivity (B-Cell)
99.999%
Specificity
HR 6.9
Hazard Ratio — Hodgkin (p<0.0001)
Two Specialized Panels
LymphoVista offers disease-specific ctDNA assays optimized for B-cell lymphomas and Hodgkin lymphoma respectively. Select a variant to view its specifications and clinical evidence.
LymphoVista
For B-Cell Lymphomas
Limit of Detection (LoD): 6.69 × 10⁻⁶
18-month OS: 77% (MRD-neg) vs 33% (MRD-pos) — HR 4.61, p<0.0001
18-month PFS: 51% (MRD-neg) vs 5% (MRD-pos) — HR 4.32, p<0.0001
326 samples from 88 patients
See published survival data ↓Four Decisions Enabled
Three Steps. Zero Complexity.
Genotyping
Send 20 ml blood in cfDNA tubes. We create a patient-specific mutation profile.
MRD Monitoring
Longitudinal ctDNA monitoring tracks disease burden over your treatment timeline.
Report & Interpretation
Receive a clear clinical report within 2–4 weeks. MRD status, trend, and clinical context included.
"Lymphoma patients deserve better than waiting for imaging to confirm what ctDNA can already tell you. That is why we built LymphoVista."
Detect relapse. Earlier.
LymphoVista delivers clinical-grade MRD monitoring for lymphoma — contact us to discuss your patient cases.
Contact Our Team →References
- Mattlener et al. Presentation at American Society of Hematology (ASH) Annual Meeting 2024.
- Schleifenbaum et al. Presentation at European Hematology Association (EHA) Annual Meeting 2024.