Evidence map›Paper›PMID 28147447›Full record

ArticleStatistics in medicine2017

Patient subgroup identification for clinical drug development.

Xin Huang, Yan Sun, Paul Trow, Saptarshi Chatterjee, Arunava Chakravartty, Lu Tian, Viswanath Devanarayan

Abstract read
In one paragraph

Article in Statistics in medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. MOSIC: Model-Agnostic Optimal Subgroup Identification with Multi-Constraint for Improved Reliability.KDD : proceedings. International Conference on Knowledge Discovery & Data Mining · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Predicting clinical progression trajectories of early Alzheimer's disease patients.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
  10. Review
  11. A reference-free R-learner for treatment recommendation.Statistical methods in medical research · 2023
    Article
  12. Article
  13. A Computational Framework for Identifying Age Risks in Drug-Adverse Event Pairs.AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science · 2022
    Article
  14. BCL2 Family Inhibitors in the Biology and Treatment of Multiple Myeloma.Blood and lymphatic cancer : targets and therapy · 2021
    Review
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

7 authors.

Xin HuangAbbVie, Inc., North Chicago, IL, U.S.A.
Yan SunAbbVie, Inc., North Chicago, IL, U.S.A.
Paul TrowAbbVie, Inc., North Chicago, IL, U.S.A.
Saptarshi ChatterjeeAbbVie, Inc., North Chicago, IL, U.S.A.
Arunava ChakravarttyAbbVie, Inc., North Chicago, IL, U.S.A.
Lu TianStanford University School of Medicine, Palo Alto, CA, U.S.A.
Viswanath DevanarayanAbbVie, Inc., North Chicago, IL, U.S.A.

Funding

Statistical Methods for Optimizing Personalized Treatment SelectionR01HL089778 · NHLBI · STANFORD UNIVERSITY · PI LU TIAN · 2008 to 2026
$4.8M
NHLBI NIH HHS R01 HL089778
6 · The paper itself

Abstract

Causal mechanism of relationship between the clinical outcome (efficacy or safety endpoints) and putative biomarkers, clinical baseline, and related predictors is usually unknown and must be deduced empirically from experimental data. Such relationships enable the development of tailored therapeutics and implementation of a precision medicine strategy in clinical trials to help stratify patients in terms of disease progression, clinical response, treatment differentiation, and so on. These relationships often require complex modeling to develop the prognostic and predictive signatures. For the purpose of easier interpretation and implementation in clinical practice, defining a multivariate biomarker signature in terms of thresholds (cutoffs/cut points) on individual biomarkers is preferable. In this paper, we propose some methods for developing such signatures in the context of continuous, binary and time-to-event endpoints. Results from simulations and case study illustration are also provided. Copyright © 2017 John Wiley & Sons, Ltd.

Indexed as

Drug TherapyBiomarkersClinical Trials as TopicEndpoint DeterminationHumansModels, StatisticalStatistics as TopicTreatment OutcomeBiomarkersclinical trialcross-validationcutoff estimationprecision medicinepredictive modelingpredictive significancesubgroup identificationvariable selection

Identifiers

PMID28147447
PMCPMC7704099

What OpenQuestion holds

Textmetadata
LicenceTDM
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.