Evidence map›Paper›PMID 40591070›Full record

ArticleBulletin of mathematical biology2025

Pattern Formation as a Resilience Mechanism in Cancer Immunotherapy.

Molly Brennan, Andrew L Krause, Edgardo Villar-Sepúlveda, Christopher B Prior

Abstract read
In one paragraph

Article in Bulletin of mathematical biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. 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

4 authors.

Molly BrennanDepartment of Mathematics, University College London, 25 Gordon Street, London, WC1H 0AY, United Kingdom.
Andrew L KrauseMathematical Sciences Department, Durham University, Upper Mountjoy Campus, Stockton Rd, Durham, DH1 3LE, United Kingdom. andrew.krause@durham.ac.uk.ORCID http://orcid.org/0000-0001-9638-7278
Edgardo Villar-SepúlvedaSchool of Engineering Mathematics and Technology, University of Bristol, Ada Lovelace Building, Tankard's Cl, University Walk, Bristol, BS8 1TW, United Kingdom.
Christopher B PriorMathematical Sciences Department, Durham University, Upper Mountjoy Campus, Stockton Rd, Durham, DH1 3LE, United Kingdom.

Funding

Agencia Nacional de Investigación y Desarrollo 72210071
6 · The paper itself

Abstract

Mathematical and computational modelling in oncology has played an increasingly important role in not only understanding the impact of various approaches to treatment on tumour growth, but in optimizing dosing regimens and aiding the development of treatment strategies. However, as with all modelling, only an approximation is made in the description of the biological and physical system. Here we show that tissue-scale spatial structure can have a profound impact on the resilience of tumours to immunotherapy using a classical model incorporating IL-2 compounds and effector cells as treatment parameters. Using linear stability analysis, numerical continuation, and direct simulations, we show that diffusing cancer cell populations can undergo pattern-forming (Turing) instabilities, leading to spatially-structured states that persist far into treatment regimes where the corresponding spatially homogeneous systems would uniformly predict a cancer-free state. These spatially-patterned states persist in a wide range of parameters, as well as under time-dependent treatment regimes. Incorporating treatment via domain boundaries can increase this resistance to treatment in the interior of the domain, further highlighting the importance of spatial modelling when designing treatment protocols informed by mathematical models. Counter-intuitively, this mechanism shows that increased effector cell mobility can increase the resilience of tumours to treatment. We conclude by discussing practical and theoretical considerations for understanding this kind of spatial resilience in other models of cancer treatment, in particular those incorporating more realistic spatial transport. This paper belongs to the special collection: Problems, Progress and Perspectives in Mathematical and Computational Biology.

Indexed as

ImmunotherapyModels, BiologicalModels, ImmunologicalNeoplasmsComputational BiologyComputer SimulationHumansInterleukin-2Mathematical ConceptsTumor MicroenvironmentInterleukin-2ImmunotherapyPattern FormationResilienceSolid Tumours

Identifiers

PMID40591070
PMCPMC12214011

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Registered trials

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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.