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Delfi Diagnostics

High-risk lung cancer patients (smokers)

Variable
Not FDA approved
Detects: Lung cancer
Sample: Blood draw
Results: 10-14 days

Test Performance

Sensitivity

80% sensitivity

Specificity

58% specificity

Detection Method

Fragmentomics

Turnaround

10-14 days

Key Features

Lung cancer screening • Fragmentomics technology • Complements LDCT • High-risk patients

Who It's For

Important Notes

Novel fragmentomics approach - applies machine learning to whole-genome sequencing of cfDNA fragmentation patterns. Complements rather than replaces low-dose CT screening. 99.8% negative predictive value;an elevated result raises the likelihood of finding lung cancer on LDCT by 5.2x. For adults 50-80 with a 20 pack-year smoking history. CLIA LDT, not FDA approved. Now authorised in all 50 states following its New York State permit in 2026.

Learn more about Delfi Diagnostics

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