Evidence map›Paper›PMID 40402308›Full record

ArticleJournal of mathematical biology2025

A stochastic modelling framework for cancer patient trajectories: combining tumour growth, metastasis, and survival.

Vincent Wieland, Jan Hasenauer

Abstract read
In one paragraph

Article in Journal of mathematical biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Vincent WielandLife and Medical Science Institute, University of Bonn, Bonn, Germany.
Jan HasenauerLife and Medical Science Institute, University of Bonn, Bonn, Germany. jan.hasenauer@uni-bonn.de.ORCID 0000-0002-4935-3312

Funding

Bundesministerium für Bildung und Forschung 031L0292FDeutsche Forschungsgemeinschaft EXC 2047-390685813Deutsche Forschungsgemeinschaft EXC 2151-390873048European Research Council 101126146Rheinische Friedrich-Wilhelms-Universität Bonn Schlegel Professur
6 · The paper itself

Abstract

Cancer is a major burden of disease around the globe and one of the leading causes of premature death. The key to improve patient outcomes in modern clinical cancer research is to gain insights into dynamics underlying cancer evolution in order to facilitate the search for effective therapies. However, most cancer data analysis tools are designed for controlled trials and cannot leverage routine clinical data, which are available in far greater quantities. In addition, many cancer models focus on single disease processes in isolation, disregarding interaction. This work proposes a unified stochastic modelling framework for cancer progression that combines (stochastic) processes for tumour growth, metastatic seeding, and patient survival to provide a comprehensive understanding of cancer progression. In addition, our models aim to use non-equidistantly sampled data collected in clinical routine to analyse the whole patient trajectory over the course of the disease. The model formulation features closed-form expressions of the likelihood functions for parameter inference from clinical data. The efficacy of our model approach is demonstrated through a simulation study involving four exemplary models, which utilise both analytic and numerical likelihoods. The results of the simulation studies demonstrate the accuracy and computational efficiency of the analytic likelihood formulations. We found that estimation can retrieve the correct model parameters and reveal the underlying data dynamics, and that this modelling framework is flexible in choosing the precise parameterisation. This work can serve as a foundation for the development of combined stochastic models for guiding personalized therapies in oncology.

Indexed as

Models, BiologicalNeoplasmsComputational BiologyComputer SimulationDisease ProgressionHumansLikelihood FunctionsMathematical ConceptsNeoplasm MetastasisStochastic ProcessesCancer modellingMathematical oncologyStochastic modelling

Identifiers

PMID40402308
PMCPMC12098478

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.