Evidence map›Paper›PMID 30278037›Full record

ArticlePLoS biology2018

Is adaptive therapy natural?

Frédéric Thomas, Emmanuel Donnadieu, Guillaume M Charriere, Camille Jacqueline, Aurélie Tasiemski, Pascal Pujol, François Renaud, Benjamin Roche, Rodrigo Hamede, Joel Brown and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
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

15 citing papers in PubMed, 28 citations in OpenAlex.

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  10. Exploiting evolutionary trade-offs for posttreatment management of drug-resistant populations.Proceedings of the National Academy of Sciences of the United States of America · 2020
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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

12 authors at 6 institutions in 4 countries.

Frédéric ThomasCentre de Recherches Ecologiques et Evolutives sur le Cancer/Maladies Infectieuses et Vecteurs: Ecologie, Génétique, Evolution, et Contrôle, CNRS, Université de Montpellier, Montpellier, France.ORCID 0000-0003-2238-1978
Emmanuel DonnadieuInserm, Unité 1016, Institut Cochin, Paris, France.
Guillaume M CharriereInteractions Host Pathogen Environment, University of Montpellier, Centre National de la Recherche Scientifique, Institut français de recherche pour l'exploitation de la mer, University of Perpignan Via Domitia, Montpellier, France.
Camille JacquelineCentre de Recherches Ecologiques et Evolutives sur le Cancer/Maladies Infectieuses et Vecteurs: Ecologie, Génétique, Evolution, et Contrôle, CNRS, Université de Montpellier, Montpellier, France.
Aurélie TasiemskiUniversité de Lille-sciences et technologies, UMR 8198 Evo-Eco-Paleo, Villeneuve d'Ascq/CNRS/INSERM/CHU Lille, Institut Pasteur de Lille, U1019-Unité Mixte de Recherche 8204, Lille, France.
Pascal PujolService de génétique médicale et chromosomique, Unité d'oncogénétique, centre hospitalier régional et universitaire de Montpellier, Hôpital Arnaud de Villeneuve, Montpellier, France.
François RenaudCentre de Recherches Ecologiques et Evolutives sur le Cancer/Maladies Infectieuses et Vecteurs: Ecologie, Génétique, Evolution, et Contrôle, CNRS, Université de Montpellier, Montpellier, France.
Benjamin RocheCentre de Recherches Ecologiques et Evolutives sur le Cancer/Maladies Infectieuses et Vecteurs: Ecologie, Génétique, Evolution, et Contrôle, CNRS, Université de Montpellier, Montpellier, France.
Rodrigo HamedeSchool of Natural Sciences, University of Tasmania, Hobart, Tasmania, Australia.
Joel BrownDepartment of Radiology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida, United States of America.
Robert GatenbyDepartment of Radiology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida, United States of America.
Beata UjvariSchool of Natural Sciences, University of Tasmania, Hobart, Tasmania, Australia.
Centre National de la Recherche Scientifique · FRMoffitt Cancer Center · USUniversity of Tasmania · AUDélégation Paris 5 · FRHôpital Arnaud de Villeneuve · FRUniversité de Perpignan · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Research suggests that progression-free survival can be prolonged by integrating evolutionary principles into clinical cancer treatment protocols. The goal is to prevent or slow the proliferation of resistant malignant cell populations. The logic behind this therapy relies on ecological and evolutionary processes. These same processes would be available to natural selection in decreasing the probability of an organism's death due to cancer. We propose that organisms' anticancer adaptions include not only ones for preventing cancer but also ones for directing and retarding the evolution of life-threatening cancer cells. We term this last strategy natural adaptive therapy (NAT). The body's NAT might include a lower than otherwise possible immune response. A restrained immune response might forego maximum short-term kill rates. Restraint would forestall immune-resistant cancer cells and produce long-term durable control of the cancer population. Here, we define, develop, and explore the possibility of NAT. The discovery of NAT mechanisms could identify new strategies in tumor prevention and treatments. Furthermore, we discuss the potential risks of immunotherapies that force the immune system to ramp up the short-term kill rates of malignant cancer cells in a manner that undermines the body's NAT and accelerates the evolution of immune resistance.

Indexed as

Adaptive ImmunityAnimalsBiological EvolutionCell ProliferationDrug Resistance, NeoplasmHumansImmunity, InnateImmunotherapyModels, BiologicalNeoplasms

Identifiers

PMID30278037
PMCPMC6168119
OpenAlexW2894708343

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.