Three Models. One Probability.
Every Nodule.
A 3D Vision Transformer nodule encoder, a Sybil-derived whole-scan encoder, and a longitudinal decoder, working together to score malignancy risk from a single LDCT.
Vision Transformer
patients trained
vs Lung-RADS 0.88
in CADe viewer
M · 67 · 38 PY
10/10/2025
1.25 mm
0.32 mGy
✓ registered
✓ 20+ PY
✓ Age 50-80
L: -600
Where Rule-Based Scoring Reaches Its Limit
Lung-RADS is the clinical standard, and it should be. LungAI doesn't replace it. It fills the gap between what a size threshold can see and what a 100-million-parameter model can.
A Malignancy Score That Goes Beyond the Diameter
LungAI is a CADx medical device that reads the full DICOM image, not just the nodule's size, and returns a continuous 0–100 malignancy probability inside your existing workflow.
LungAI accepts a low-dose CT scan as input and outputs a continuous malignancy score from 0 to 100 for each pre-selected pulmonary nodule. A higher score means a higher probability that the nodule is cancerous.
Unlike Lung-RADS, which uses categorical size thresholds, LungAI uses a 100-million-parameter vision transformer that operates on the full DICOM image. It incorporates nodule morphology, surrounding tissue, patient age, sex, and smoking history, and when available, a prior scan for longitudinal comparison.
The score is delivered inside your existing PACS workflow as a PDF report alongside the CT, with no separate platform to log in to.
per nodule, not just a category
Three Dimensions Lung-RADS Cannot See
LungAI incorporates nodule type, change over time, and patient demographics as explicit model inputs. Each one shifts the malignancy probability in ways a size threshold alone never could.
LungAI distinguishes between nodule types and weights malignancy probability differently for each. Ground-glass and part-solid nodules carry different risk profiles than solid nodules of the same diameter.
When a prior LDCT is available, LungAI automatically registers the nodule across scans and incorporates interval change into the malignancy score. No manual comparison required.
Age, sex, and pack-years smoked are explicit model inputs. A 6mm nodule in a 72-year-old with 40 pack-years is scored differently than the same nodule in a 51-year-old with 20 pack-years.
A Number That Tells You What a Category Cannot
Every nodule gets a 0–100 malignancy score delivered directly in PACS. No new login, no separate platform. Just a probability that sits next to the image you're already reading.
The Numbers Behind The Score
In our internal study on the NLST held-out dataset, LungAI demonstrated strong sensitivity and specificity, an AUROC of 0.96, and read times under 3 minutes when paired with a CADe platform.
In our internal study, LungAI demonstrated 94% sensitivity and approximately 88% specificity, an AUROC of 0.96, and a read time of 1.5 to 3 minutes when paired with a CADe platform.
Learn more about the DataFits Into What You Already Have, Billable From Day One
LungAI plugs into your existing CADe and PACS environment with no new workstation or workflow changes, and every screened patient generates a new CPT 0721T billing event.
LungAI Scores the Nodule. LungIQ Finds the Patient.
High-quality screening starts before the scan. LungIQ uses large language models to identify USPSTF-eligible patients who have never been offered screening, so every scanner slot is filled with the right patient.
Ready to See LungAI in Your Workflow?
Whether you want a live demo in your CADe viewer or want to build a full lung screening program, the next step takes less than 30 minutes.
Request a live demo showing how LungAI appears inside your CADe viewer, what the 0–100 score looks like per nodule, and how the PDF report is delivered into PACS. Less than 30 minutes.
Request a workflow demoTalk to our partnerships team about how Oatmeal Health drives scan referrals to your center, integrates LungAI into your CADe workflow, and enables your radiologists to bill CPT 0721T on eligible scans.
Talk to our team