Inverse Bayesian Inference for Extracting Lesion Dynamics from Longitudinal Spectral CT

📅 2026-07-25
📈 Citations: 0
Influential: 0
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🤖 AI Summary
This study addresses the challenge of deciphering the dynamic mechanisms driving lesion evolution from longitudinal spectral CT imaging. It introduces, for the first time in medical image analysis, an interpretable, parameterized framework based on inverse Bayesian inference, decomposing lesion dynamics into intrinsic kinetics, local tumor burden coupling, and microenvironmental state. By integrating differential equation modeling with photon-counting CT data, the method enables mechanistic inference of tumor evolution. Applied to a non-small cell lung cancer (NSCLC) metastatic cohort, it reveals competitive coupling among pulmonary lesions (B = −0.34, p < 0.05) and cooperative coupling in hepatic lesions (C ≈ +1.0, p < 0.05). Parameter recoverability is further validated using synthetic data, establishing a novel paradigm for investigating tumor evolutionary dynamics.
📝 Abstract
Longitudinal medical imaging captures temporal evolution of lesions, yet extracting the underlying dynamical parameters governing this evolution remains challenging. We propose an inverse Bayesian framework for inferring lesion dynamics from longitudinal spectral CT. We decompose spectral feature ($x$) evolution into three components: \begin{equation*} \frac{dx_i}{dt} = A_i x_i + B \cdot n + C \cdot Δx_{\text{sat}} \end{equation*} where $A_i$ captures intrinsic dynamics (lesion-autonomous evolution), $B$ captures local environment tumour burden (organ tumour burden through satellite count coupling), and $C$ captures environment/satellite state change (i.e., whether surrounding lesions move similarly or not). We demonstrate the framework on photon-counting NSCLC CT data from metastases, recovering distinct dynamical regimes: lung lesions exhibit significant satellite count coupling ($B=-0.34$, $p<0.05$) suggesting competitive dynamics, while liver lesions show synergistic satellite behaviour coupling ($C\approx+1.0$, $p<0.05$). Synthetic validation confirms parameter recovery, and cross-coupling analysis validates that our method detects non-zero coupling when present. This work establishes inverse dynamical inference as a principled methodology for extracting interpretable parameters from longitudinal imaging, moving beyond static feature extraction toward mechanistic characterisation of lesion behaviour. The code and data are available at: https://github.com/lukasf98/inverse-bayesian-inference
Problem

Research questions and friction points this paper is trying to address.

lesion dynamics
longitudinal imaging
spectral CT
inverse inference
dynamical parameters
Innovation

Methods, ideas, or system contributions that make the work stand out.

inverse Bayesian inference
lesion dynamics
spectral CT
longitudinal imaging
dynamical modeling
L
Lukas Förner
Dept. of diagnostic and interventional Radiology and Neuroradiology, University Hospital Augsburg, Germany
M
Melina Wördehoff
Dept. of diagnostic and interventional Radiology and Neuroradiology, University Hospital Augsburg, Germany
J
Julian Steffens
Dept. of diagnostic and interventional Radiology and Neuroradiology, University Hospital Augsburg, Germany
M
Maximilian Schmutz
Dept. of Hematology and Oncology, University Hospital Augsburg, Germany
R
Rainer Claus
Dept. of Hematology and Oncology, University Hospital Augsburg, Germany
J
Josua Decker
Dept. of diagnostic and interventional Radiology and Neuroradiology, University Hospital Augsburg, Germany
T
Thomas Kröncke
Dept. of diagnostic and interventional Radiology and Neuroradiology, University Hospital Augsburg, Germany
K
Kartikay Tehlan
Dept. of diagnostic and interventional Radiology and Neuroradiology, University Hospital Augsburg, Germany
Thomas Wendler
Thomas Wendler
Universität Augsburg, Medical Faculty
Medical ImagingMedical Robotics