Evidence map›Paper›PMID 34773974›Full record

ArticleBMC medical research methodology2021

Advancing data science in drug development through an innovative computational framework for data sharing and statistical analysis.

Ann-Marie Mallon, Dieter A Häring, Frank Dahlke, Piet Aarden, Soroosh Afyouni, Daniel Delbarre, Khaled El Emam, Habib Ganjgahi, Stephen Gardiner, Chun Hei Kwok and 15 more

Abstract read
In one paragraph

Article in BMC medical research methodology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. How patients with multiple sclerosis acquire disability.Brain : a journal of neurology · 2022
    Article
  9. Review
  10. Article
  11. Applying Machine Learning Techniques to Predict Drug-Related Side Effect: A Policy Brief.Inquiry : a journal of medical care organization, provision and financing
    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

25 authors.

Ann-Marie MallonMRC Harwell Institute, Harwell Campus, Oxfordshire, OX11 0RD, UK. a.mallon@har.mrc.ac.uk.ORCID 0000-0003-4047-4019
Dieter A HäringNovartis Pharma AG, Basel, Switzerland.
Frank DahlkeNovartis Pharma AG, Basel, Switzerland.
Piet AardenNovartis Pharma AG, Basel, Switzerland.
Soroosh AfyouniBig Data Institute, University of Oxford Li Ka Shing Centre for Health Information and Discovery, Old Road Campus, Oxford, OX3 7LF, UK.
Daniel DelbarreMRC Harwell Institute, Harwell Campus, Oxfordshire, OX11 0RD, UK.
Khaled El EmamChildren's Hospital of Eastern Ontario Research Institute, 401 Smyth Road, Ottawa, Ontario, K1J 8 L1, Canada.
Habib GanjgahiDepartment of Statistics, University of Oxford, 24-29 St Giles', OX1 3LB, Oxford, UK.
Stephen GardinerMRC Harwell Institute, Harwell Campus, Oxfordshire, OX11 0RD, UK.
Chun Hei KwokMRC Harwell Institute, Harwell Campus, Oxfordshire, OX11 0RD, UK.
Dominique M WestMRC Harwell Institute, Harwell Campus, Oxfordshire, OX11 0RD, UK.
Ewan StraitonMRC Harwell Institute, Harwell Campus, Oxfordshire, OX11 0RD, UK.
Sibylle HaemmerleNovartis Pharma AG, Basel, Switzerland.
Adam HuffmanBig Data Institute, University of Oxford Li Ka Shing Centre for Health Information and Discovery, Old Road Campus, Oxford, OX3 7LF, UK.
Tom HofmannNovartis Pharma AG, Basel, Switzerland.
Luke J KellyBig Data Institute, University of Oxford Li Ka Shing Centre for Health Information and Discovery, Old Road Campus, Oxford, OX3 7LF, UK.
Peter KruscheNovartis Pharma AG, Basel, Switzerland.
Marie-Claude LarameeNovartis Pharma AG, Basel, Switzerland.
Karine LheritierNovartis Pharma AG, Basel, Switzerland.
Greg LigozioNovartis Pharma AG, East Hanover, NJ, USA.
Aimee ReadieNovartis Pharma AG, East Hanover, NJ, USA.
Luis SantosMRC Harwell Institute, Harwell Campus, Oxfordshire, OX11 0RD, UK.
Thomas E NicholsBig Data Institute, University of Oxford Li Ka Shing Centre for Health Information and Discovery, Old Road Campus, Oxford, OX3 7LF, UK.
Janice BransonNovartis Pharma AG, Basel, Switzerland.
Chris HolmesDepartment of Statistics, University of Oxford, 24-29 St Giles', OX1 3LB, Oxford, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNovartis and the University of Oxford's Big Data Institute (BDI) have established a research alliance with the aim to improve health care and drug development by making it more efficient and targeted. Using a combination of the latest statistical machine learning technology with an innovative IT platform developed to manage large volumes of anonymised data from numerous data sources and types we plan to identify novel patterns with clinical relevance which cannot be detected by humans alone to identify phenotypes and early predictors of patient disease activity and progression.

methodThe collaboration focuses on highly complex autoimmune diseases and develops a computational framework to assemble a research-ready dataset across numerous modalities. For the Multiple Sclerosis (MS) project, the collaboration has anonymised and integrated phase II to phase IV clinical and imaging trial data from ≈35,000 patients across all clinical phenotypes and collected in more than 2200 centres worldwide. For the "IL-17" project, the collaboration has anonymised and integrated clinical and imaging data from over 30 phase II and III Cosentyx clinical trials including more than 15,000 patients, suffering from four autoimmune disorders (Psoriasis, Axial Spondyloarthritis, Psoriatic arthritis (PsA) and Rheumatoid arthritis (RA)).

resultsA fundamental component of successful data analysis and the collaborative development of novel machine learning methods on these rich data sets has been the construction of a research informatics framework that can capture the data at regular intervals where images could be anonymised and integrated with the de-identified clinical data, quality controlled and compiled into a research-ready relational database which would then be available to multi-disciplinary analysts. The collaborative development from a group of software developers, data wranglers, statisticians, clinicians, and domain scientists across both organisations has been key. This framework is innovative, as it facilitates collaborative data management and makes a complicated clinical trial data set from a pharmaceutical company available to academic researchers who become associated with the project.

conclusionsAn informatics framework has been developed to capture clinical trial data into a pipeline of anonymisation, quality control, data exploration, and subsequent integration into a database. Establishing this framework has been integral to the development of analytical tools.

Indexed as

Data ScienceInformation DisseminationDatabases, FactualDrug DevelopmentHumansResearch DesignClinical trialData anonymisationData managementMachine learning

Identifiers

PMID34773974
PMCPMC8590765

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.