Evidence map›Paper›PMID 31419182›Full record

SynthesisJCO clinical cancer informatics2019

Validation of a Semiautomated Natural Language Processing-Based Procedure for Meta-Analysis of Cancer Susceptibility Gene Penetrance.

Zhengyi Deng, Kanhua Yin, Yujia Bao, Victor Diego Armengol, Cathy Wang, Ankur Tiwari, Regina Barzilay, Giovanni Parmigiani, Danielle Braun, Kevin S Hughes

Abstract readMeta-Analysis
In one paragraph

Synthesis in JCO clinical cancer informatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 5 pooled it
–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

15 citing papers in PubMed, 5 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Meta-Analysis of Breast Cancer Risk for Individuals with PALB2 Pathogenic Variants.medRxiv : the preprint server for health sciences · 2024
    Article
  7. Review
  8. Article
  9. Translational NLP: A New Paradigm and General Principles for Natural Language Processing Research.Proceedings of the conference. Association for Computational Linguistics. North American Chapter. Meeting · 2021
    Article
  10. Disease spectrum of gastric cancer susceptibility genes.Medical oncology (Northwood, London, England) · 2021
    Article
  11. Article
  12. Article
  13. Intelligent, Autonomous Machines in Surgery.The Journal of surgical research · 2020
    Article
  14. Article
  15. Extracting Concepts for Precision Oncology from the Biomedical Literature.AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science
    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

10 authors.

Zhengyi DengMassachusetts General Hospital, Boston, MA.
Kanhua YinMassachusetts General Hospital, Boston, MA.
Yujia BaoMassachusetts Institute of Technology, Boston, MA.
Victor Diego ArmengolMassachusetts General Hospital, Boston, MA.
Cathy WangHarvard TH Chan School of Public Health, Boston, MA.
Ankur TiwariMassachusetts General Hospital, Boston, MA.
Regina BarzilayMassachusetts Institute of Technology, Boston, MA.
Giovanni ParmigianiHarvard TH Chan School of Public Health, Boston, MA.
Danielle BraunHarvard TH Chan School of Public Health, Boston, MA.
Kevin S HughesMassachusetts General Hospital, Boston, MA.

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI Irene M. Ghobrial · 1985 to 2026
$330.6M
Training Grant in Quantitative Sciences for Cancer ResearchT32CA009337 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI QUACKENBUSH, JOHN, TRIPPA, LORENZO · 1986 to 2025
$12.3M
NCI NIH HHS P30 CA006516NCI NIH HHS T32 CA009337
6 · The paper itself

Abstract

purposeQuantifying the risk of cancer associated with pathogenic mutations in germline cancer susceptibility genes-that is, penetrance-enables the personalization of preventive management strategies. Conducting a meta-analysis is the best way to obtain robust risk estimates. We have previously developed a natural language processing (NLP) -based abstract classifier which classifies abstracts as relevant to penetrance, prevalence of mutations, both, or neither. In this work, we evaluate the performance of this NLP-based procedure. MATERIALS AND

methodsWe compared the semiautomated NLP-based procedure, which involves automated abstract classification and text mining, followed by human review of identified studies, with the traditional procedure that requires human review of all studies. Ten high-quality gene-cancer penetrance meta-analyses spanning 16 gene-cancer associations were used as the gold standard by which to evaluate the performance of our procedure. For each meta-analysis, we evaluated the number of abstracts that required human review (workload) and the ability to identify the studies that were included by the authors in their quantitative analysis (coverage).

resultsCompared with the traditional procedure, the semiautomated NLP-based procedure led to a lower workload across all 10 meta-analyses, with an overall 84% reduction (2,774 abstracts

conclusionWe demonstrated that an NLP-based procedure can significantly reduce the review workload without compromising the ability to identify relevant studies. NLP algorithms have promising potential for reducing human efforts in the literature review process.

Indexed as

Biomarkers, TumorGenetic Predisposition to DiseaseNatural Language ProcessingPenetranceAlgorithmsComputational BiologyHumansNeoplasmsReproducibility of ResultsWorkflowBiomarkers, Tumor

Identifiers

PMID31419182
PMCPMC6873944

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.