Evidence map›Paper›PMID 28913766›Full record

ReviewCurrent hematologic malignancy reports2017

Computational Modeling and Treatment Identification in the Myelodysplastic Syndromes.

Leylah M Drusbosky, Christopher R Cogle

Abstract readReview
In one paragraph

Review in Current hematologic malignancy reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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.

Leylah M DrusboskyDivision of Hematology and Oncology, Department of Medicine, College of Medicine, University of Florida, 1600 SW Archer Road, Box 100278, Gainesville, FL, 32610-0278, USA.
Christopher R CogleDivision of Hematology and Oncology, Department of Medicine, College of Medicine, University of Florida, 1600 SW Archer Road, Box 100278, Gainesville, FL, 32610-0278, USA. christopher.cogle@medicine.ufl.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewThis review discusses the need for computational modeling in myelodysplastic syndromes (MDS) and early test results. RECENT

findingsAs our evolving understanding of MDS reveals a molecularly complicated disease, the need for sophisticated computer analytics is required to keep track of the number and complex interplay among the molecular abnormalities. Computational modeling and digital drug simulations using whole exome sequencing data input have produced early results showing high accuracy in predicting treatment response to standard of care drugs. Furthermore, the computational MDS models serve as clinically relevant MDS cell lines for pre-clinical assays of investigational agents. MDS is an ideal disease for computational modeling and digital drug simulations. Current research is focused on establishing the prediction value of computational modeling. Future research will test the clinical advantage of computer-informed therapy in MDS.

Indexed as

Computer SimulationModels, BiologicalHumansMyelodysplastic SyndromesBiomarkersComputational biologyIn silicoMyelodysplastic syndromes

Identifiers

PMID28913766
PMCPMC5670191

What OpenQuestion holds

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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.