Evidence map›Paper›PMID 33625533›Full record

ArticleCancer immunology, immunotherapy : CII2021

Comparative assessment of manual chart review and ICD claims data in evaluating immunotherapy-related adverse events.

Andrew Nashed, Shijun Zhang, Chien-Wei Chiang, M Zitu, Gregory A Otterson, Carolyn J Presley, Kari Kendra, Sandip H Patel, Andrew Johns, Mingjia Li and 4 more

Abstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Role for Artificial Intelligence in the Detection of Immune-Related Adverse Events.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
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  17. 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

14 authors.

Andrew NashedDepartment of Internal Medicine, The Ohio State University, A450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA. Andrew.Nashed@osumc.edu.ORCID http://orcid.org/0000-0002-0120-1504
Shijun ZhangDepartment of Biomedical Informatics and Center for Biostatistics, The Ohio State University, A450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA.
Chien-Wei ChiangDepartment of Biomedical Informatics and Center for Biostatistics, The Ohio State University, A450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA.
M ZituDepartment of Biomedical Informatics and Center for Biostatistics, The Ohio State University, A450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA.
Gregory A OttersonDivision of Medical Oncology, The Ohio State University, A450B Starling Loving Hall ColumbusA450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA.
Carolyn J PresleyDivision of Medical Oncology, The Ohio State University, A450B Starling Loving Hall ColumbusA450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA.
Kari KendraDivision of Medical Oncology, The Ohio State University, A450B Starling Loving Hall ColumbusA450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA.
Sandip H PatelDivision of Medical Oncology, The Ohio State University, A450B Starling Loving Hall ColumbusA450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA.
Andrew JohnsDepartment of Internal Medicine, The Ohio State University, A450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA.
Mingjia LiDepartment of Internal Medicine, The Ohio State University, A450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA.
Madison GroganDivision of Medical Oncology, The Ohio State University, A450B Starling Loving Hall ColumbusA450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA.
Gabrielle LopezDivision of Medical Oncology, The Ohio State University, A450B Starling Loving Hall ColumbusA450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA.
Dwight H OwenDivision of Medical Oncology, The Ohio State University, A450B Starling Loving Hall ColumbusA450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA.
Lang LiDepartment of Biomedical Informatics and Center for Biostatistics, The Ohio State University, A450B Starling Loving Hall Columbus, Columbus, OH, 43210, USA.

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
The OSU Center for Clinical and Translational Science: Advancing Today's Discoveries to Improve HealthUL1TR002733 · NCATS · OHIO STATE UNIVERSITY · PI RINGEL, MATTHEW D · 2018 to 2022
$28.9M
Translational Training Grant in Experimental TherapeuticsK12CA133250 · NCI · OHIO STATE UNIVERSITY · PI WILLIAM E. CARSON, Rosa Lapalombella · 2008 to 2026
$15.0M
NCATS NIH HHS UL1 TR002733NCI NIH HHS K12 CA133250NCI NIH HHS P30 CA016058
6 · The paper itself

Abstract

backgroundThe aim of this retrospective study was to demonstrate that irAEs, specifically gastrointestinal and pulmonary, examined through International Classification of Disease (ICD) data leads to underrepresentation of true irAEs and overrepresentation of false irAEs, thereby concluding that ICD claims data are a poor approach to electronic health record (EHR) data mining for irAEs in immunotherapy clinical research.

methodsThis retrospective analysis was conducted in 1,063 cancer patients who received ICIs between 2011 and 2017. We identified irAEs by manual review of medical records to determine the incidence of each of our endpoints, namely colitis, hepatitis, pneumonitis, other irAE, or no irAE. We then performed a secondary analysis utilizing ICD claims data alone using a broad range of symptom and disease-specific ICD codes representative of irAEs.

results16% (n = 174/1,063) of the total study population was initially found to have either pneumonitis 3% (n = 37), colitis 7% (n = 81) or hepatitis 5% (n = 56) on manual review. Of these patients, 46% (n = 80/174) did not have ICD code evidence in the EHR reflecting their irAE. Of the total patients not found to have any irAEs during manual review, 61% (n = 459/748) of patients had ICD codes suggestive of possible irAE, yet were not identified as having an irAE during manual review. DISCUSSION: Examining gastrointestinal and pulmonary irAEs through the International Classification of Disease (ICD) data leads to underrepresentation of true irAEs and overrepresentation of false irAEs.

Indexed as

HumansImmune Checkpoint InhibitorsImmunotherapyInternational Classification of DiseasesMiddle AgedNeoplasmsProspective StudiesRetrospective StudiesImmune Checkpoint InhibitorsAdverse drug events (ADEs)Data-miningICD codesImmune checkpoint inhibitors (ICI)Immune-related adverse events (irAE)Immunotherapy

Identifiers

PMID33625533
PMCPMC10992210

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.