Atezolizumab real-world population PK
Reference paper ↗A two-compartment population PK model representing atezolizumab concentration and exposure with body weight, albumin, sex, and anti-therapeutic-antibody covariates.
- Therapeutic
- Atezolizumab
- Modality
- Monoclonal antibody
- Target
- PD-L1 / CD274
- Disease
- Advanced or recurrent non-small cell lung cancer
- Model type
- PopPK, Exposure-response
Complete model workspace
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- Parameters
- 23
- States
- 3
- Equations
- 3
- Derived outputs
- 10
Explore this model
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Article median
How do real-world patient covariates change atezolizumab concentration and exposure? Explore this intervention regimen through Central atezolizumab concentration, Peripheral atezolizumab concentration, Cumulative atezolizumab exposure.
Starting result
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Starting configuration
Time: 0–82 day; step 0.05
| Input | Default | Available range |
|---|---|---|
| Population systemic clearance | 0.2 L/day | 0.1–0.3 L/day |
| Population central distribution volume | 3.28 L | 1.64–4.92 L |
| Population intercompartmental clearance | 0.546 L/day | 0.273–0.819 L/day |
| Population peripheral distribution volume | 3.63 L | 1.815–5.445 L |
| Body weight | 58.6 kg | 29.3–87.9 kg |
Expected readouts
Central atezolizumab concentration · Peripheral atezolizumab concentration · Exposure (AUC)
Adjustable model parameters
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More key parameters (1)
How the model represents the biology
A two-compartment population PK model representing atezolizumab concentration and exposure with body weight, albumin, sex, and anti-therapeutic-antibody covariates.
Solid arrows show modeled movement or change; two-headed arrows show reversible exchange; dashed arrows show modulation without material transfer.
Model scope: PD-L1 binding, receptor occupancy, immune activation, tumor response, efficacy, target-mediated disposition, and time-varying clearance are not represented.
Modeled relationships (7)
- IV atezolizumab → Central exposure: IV input (flow)
- Central exposure ↔ Peripheral pool: distribution (reversible exchange)
- Central exposure → Linear clearance: linear CL (loss)
- Clinical covariates → Linear clearance: scales CL (modulation)
- Clinical covariates → Central exposure: scales V1 (modulation)
- Clinical covariates → Peripheral pool: scales V2 (modulation)
- Central exposure → Cumulative exposure: integrates C (production)
Modeled relationships: IV atezolizumab to Central exposure: IV input (flow); Central exposure reversibly exchanges with Peripheral pool: distribution (reversible exchange); Central exposure to Linear clearance: linear CL (loss); Clinical covariates to Linear clearance: scales CL (modulation); Clinical covariates to Central exposure: scales V1 (modulation); Clinical covariates to Peripheral pool: scales V2 (modulation); Central exposure to Cumulative exposure: integrates C (production).
Primary readouts: Central atezolizumab concentration; Peripheral concentration; Cumulative exposure.
Related models
Research use only — not for patient-specific prediction or dosing advice.