Evidence map›Paper›PMID 26606521›Full record

ArticlePloS one2015

Merging Children's Oncology Group Data with an External Administrative Database Using Indirect Patient Identifiers: A Report from the Children's Oncology Group.

Yimei Li, Matt Hall, Brian T Fisher, Alix E Seif, Yuan-Shung Huang, Rochelle Bagatell, Kelly D Getz, Todd A Alonzo, Robert B Gerbing, Lillian Sung and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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  5. Leveraging Clinical Trial Populations and Data from the Children's Oncology Group for Cancer Survivorship Research.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2022
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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

13 authors at 6 institutions in 2 countries.

Yimei LiDepartment of Biostatistics and Epidemiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.
Matt HallChildren's Hospital Association, Overland Park, Kansas, United States of America.
Brian T FisherDivision of Infectious Disease, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
Alix E SeifDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
Yuan-Shung HuangCenter for Pediatric Clinical Effectiveness, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
Rochelle BagatellDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
Kelly D GetzDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
Todd A AlonzoDepartment of Preventive Medicine, University of Southern California, Los Angeles, California, United States of America.
Robert B GerbingChildren's Oncology Group, Monrovia, California, United States of America.
Lillian SungDepartment of Hematology/Oncology, The Hospital for Sick Children, University of Toronto, Toronto, Canada.
Peter C AdamsonDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
Alan GamisChildren's Oncology Group, Monrovia, California, United States of America.
Richard AplencDepartment of Biostatistics and Epidemiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.
Children's Hospital of Philadelphia · USChildren's Oncology Group · USUniversity of Pennsylvania · USChildren's Hospital Association · USSickKids Foundation · CAUniversity of Southern California · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Robert H. Vonderheide · 1985 to 2026
$222.3M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
Developing MBSR for Application in Alcoholism TreatmentR01AA016527 · NIAAA · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI CONNORS, GERARD J · 2007 to 2010
$1.9M
Toxicity Monitoring on Phase III Trials with Administrative DataR01CA165277 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI APLENC, RICHARD · 2012 to 2015
$1.8M
NCI NIH HHS 1R01 CA16527NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180899NCI NIH HHS U10 CA180899-02NCI NIH HHS U10 CA98543-08NIAAA NIH HHS R01 AA016527
6 · The paper itself

Abstract

purposeClinical trials data from National Cancer Institute (NCI)-funded cooperative oncology group trials could be enhanced by merging with external data sources. Merging without direct patient identifiers would provide additional patient privacy protections. We sought to develop and validate a matching algorithm that uses only indirect patient identifiers.

methodsWe merged the data from two Phase III Children's Oncology Group (COG) trials for de novo acute myeloid leukemia (AML) with the Pediatric Health Information Systems (PHIS). We developed a stepwise matching algorithm that used indirect identifiers including treatment site, gender, birth year, birth month, enrollment year and enrollment month. Results from the stepwise algorithm were compared against the direct merge method that used date of birth, treatment site, and gender. The indirect merge algorithm was developed on AAML0531 and validated on AAML1031.

resultsOf 415 patients enrolled on the AAML0531 trial at PHIS centers, we successfully matched 378 (91.1%) patients using the indirect stepwise algorithm. Comparison to the direct merge result suggested that 362 (95.7%) matches identified by the indirect merge algorithm were concordant with the direct merge result. When validating the indirect stepwise algorithm using the AAML1031 trial, we successfully matched 157 out of 165 patients (95.2%) and 150 (95.5%) of the indirectly merged matches were concordant with the directly merged matches.

conclusionsThese data demonstrate that patients enrolled on COG clinical trials can be successfully merged with PHIS administrative data using a stepwise algorithm based on indirect patient identifiers. The merged data sets can be used as a platform for comparative effectiveness and cost effectiveness studies.

Indexed as

Databases, FactualInformation Storage and RetrievalMedical OncologyPediatricsAlgorithmsClinical Trials, Phase III as TopicHumansLeukemia, Myeloid, AcuteReproducibility of Results

Identifiers

PMID26606521
PMCPMC4659568
OpenAlexW2177945213

What OpenQuestion holds

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LicenceCC BY
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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.