Evidence map›Paper›PMID 37331495›Full record

ArticleJournal of biomedical informatics2023

Semi-supervised calibration of noisy event risk (SCANER) with electronic health records.

Chuan Hong, Liang Liang, Qianyu Yuan, Kelly Cho, Katherine P Liao, Michael J Pencina, David C Christiani, Tianxi Cai

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical informatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Deep learning with noisy labels in medical prediction problems: a scoping review.Journal of the American Medical Informatics Association : JAMIA · 2024
    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

8 authors at 3 institutions in 1 country.

Chuan HongDuke University, Durham, NC, USA; Harvard Medical School, Boston, MA, USA.
Liang LiangHarvard T.H. Chan School of Public Health, Boston, MA, USA.
Qianyu YuanHarvard T.H. Chan School of Public Health, Boston, MA, USA.
Kelly ChoHarvard Medical School, Boston, MA, USA; VA Boston Healthcare System, Boston, MA, USA; Brigham and Women's Hospital, Boston, MA, USA.
Katherine P LiaoHarvard Medical School, Boston, MA, USA; VA Boston Healthcare System, Boston, MA, USA; Brigham and Women's Hospital, Boston, MA, USA.
Michael J PencinaDuke University, Durham, NC, USA.
David C ChristianiHarvard T.H. Chan School of Public Health, Boston, MA, USA; Massachusetts General Hospital, Boston, MA, USA.
Tianxi CaiHarvard T.H. Chan School of Public Health, Boston, MA, USA; Massachusetts General Hospital, Boston, MA, USA. Electronic address: tcai@hsph.harvard.edu.
Harvard University · USBrigham and Women's Hospital · USDuke University · US

Funding

The Boston Lung Cancer Survival CohortU01CA209414 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI David C Christiani · 2017 to 2026
$12.2M
Statistical Methods for Analysis of Massive Genetic and Genomic Data in Cancer ResearchR35CA197449 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI XIHONG LIN · 2015 to 2026
$10.9M
Statistical Methods for Optimizing Personalized Treatment SelectionR01HL089778 · NHLBI · STANFORD UNIVERSITY · PI LU TIAN · 2008 to 2026
$4.8M
Bridging clinical trial and real-world data via machine learning to advance rheumatoid arthritis treatment strategiesR01AR080193 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI CAI, TIANXI, LIAO, KATHERINE PHOENIX · 2022 to 2025
$2.7M
NCI NIH HHS R35 CA197449NCI NIH HHS U01 CA209414NHLBI NIH HHS R01 HL089778NIAMS NIH HHS R01 AR080193
6 · The paper itself

Abstract

objectiveElectronic health records (EHR), containing detailed longitudinal clinical information on a large number of patients and covering broad patient populations, open opportunities for comprehensive predictive modeling of disease progression and treatment response. However, since EHRs were originally constructed for administrative purposes not for research, in the EHR-linked studies, it is often not feasible to capture reliable information for analytical variables, especially in the survival setting, when both accurate event status and event times are needed for model building. For example, progression-free survival (PFS), a commonly used survival outcome for cancer patients, often involves complex information embedded in free-text clinical notes and cannot be extracted reliably. Proxies of PFS time such as time to the first mention of progression in the notes are at best good approximations to the true event time. This leads to difficulty in efficiently estimating event rates for an EHR patient cohort. Estimating survival rates based on error-prone outcome definitions can lead to biased results and hamper the power in the downstream analysis. On the other hand, extracting accurate event time information via manual annotation is time and resource intensive. The objective of this study is to develop a calibrated survival rate estimator using noisy outcomes from EHR data. MATERIALS AND

methodsIn this paper, we propose a two-stage semi-supervised calibration of noisy event rate (SCANER) estimator that can effectively overcome censoring induced dependency and attains more robust performance (i.e., not sensitive to misspecification of the imputation model) by fully utilizing both a small-labeled set of gold-standard survival outcomes annotated via manual chart review and a set of proxy features automatically captured via EHR in the unlabeled set. We validate the SCANER estimator by estimating the PFS rates for a virtual cohort of lung cancer patients from one large tertiary care center and the ICU-free survival rates for COVID patients from two large tertiary care centers.

resultsIn terms of survival rate estimates, the SCANER had very similar point estimates compared to the complete-case Kaplan Meier estimator. On the other hand, other benchmark methods for comparison, which fail to account for the induced dependency between event time and the censoring time conditioning on surrogate outcomes, produced biased results across all three case studies. In terms of standard errors, the SCANER estimator was more efficient than the KM estimator, with up to 50% efficiency gain.

conclusionThe SCANER estimator achieves more efficient, robust, and accurate survival rate estimates compared to existing approaches. This promising new approach can also improve the resolution (i.e., granularity of event time) by using labels conditioning on multiple surrogates, particularly among less common or poorly coded conditions.

Indexed as

COVID-19Lung NeoplasmsCalibrationElectronic Health RecordsHumansSurvival Analysis

Identifiers

PMID37331495
PMCPMC10478159
OpenAlexW4380894269

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.