Evidence map›Paper›PMID 26598946›Full record

ReviewNature reviews. Clinical oncology2016

Computational oncology--mathematical modelling of drug regimens for precision medicine.

Dominique Barbolosi, Joseph Ciccolini, Bruno Lacarelle, Fabrice Barlési, Nicolas André

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Clinical oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed
13.9field-weighted citation impact, top 1% 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

98 citing papers in PubMed, 221 citations in OpenAlex.

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  18. Nucleic acid-based drugs for patients with solid tumours.Nature reviews. Clinical oncology · 2024
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38 more citing papers are in PubMed but not listed here.

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

5 authors at 3 institutions in 1 country.

Dominique BarbolosiSMARTc Unit, Aix Marseille Université, INSERM, CRO2 UMR_S 911, Marseille 13005, France.
Joseph CiccoliniSMARTc Unit, Aix Marseille Université, INSERM, CRO2 UMR_S 911, Marseille 13005, France.
Bruno LacarelleSMARTc Unit, Aix Marseille Université, INSERM, CRO2 UMR_S 911, Marseille 13005, France.
Fabrice BarlésiSMARTc Unit, Aix Marseille Université, INSERM, CRO2 UMR_S 911, Marseille 13005, France.
Nicolas AndréAix Marseille Université, INSERM, CRO2 UMR_S 911, Marseille 13005, France.
Centre de Recherche en Cancérologie de Marseille · FRAix-Marseille Université · FRHôpital de la Timone · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Computational oncology is a generic term that encompasses any form of computer-based modelling relating to tumour biology and cancer therapy. Mathematical modelling can be used to probe the pharmacokinetics and pharmacodynamics relationships of the available anticancer agents in order to improve treatment. As a result of the ever-growing numbers of druggable molecular targets and possible drug combinations, obtaining an optimal toxicity-efficacy balance is an increasingly complex task. Consequently, standard empirical approaches to optimizing drug dosing and scheduling in patients are now of limited utility; mathematical modelling can substantially advance this practice through improved rationalization of therapeutic strategies. The implementation of mathematical modelling tools is an emerging trend, but remains largely insufficient to meet clinical needs; at the bedside, anticancer drugs continue to be prescribed and administered according to standard schedules. To shift the therapeutic paradigm towards personalized care, precision medicine in oncology requires powerful new resources for both researchers and clinicians. Mathematical modelling is an attractive approach that could help to refine treatment modalities at all phases of research and development, and in routine patient care. Reviewing preclinical and clinical examples, we highlight the current achievements and limitations with regard to computational modelling of drug regimens, and discuss the potential future implementation of this strategy to achieve precision medicine in oncology.

Indexed as

Models, TheoreticalPrecision MedicineAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsDrug MonitoringHumansMedical InformaticsNeoplasmsAntineoplastic Agents

Identifiers

PMID26598946
OpenAlexW2263360618

What OpenQuestion holds

Textmetadata
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.