Evidence map›Paper›PMID 34255071›Full record

ArticleJournal of the National Cancer Institute2022

Development and Validation of a Risk Prediction Model for Second Primary Lung Cancer.

Eunji Choi, Nilotpal Sanyal, Victoria Y Ding, Rebecca M Gardner, Jacqueline V Aredo, Justin Lee, Julie T Wu, Thomas P Hickey, Brian Barrett, Thomas L Riley and 10 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 12% 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, 16 citations in OpenAlex.

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  9. Optimizing Lung Cancer Screening With Risk Prediction: Current Challenges and the Emerging Role of Biomarkers.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 8 institutions in 2 countries.

Eunji ChoiQuantitative Sciences Unit, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0003-1315-1433
Nilotpal SanyalQuantitative Sciences Unit, Stanford University School of Medicine, Stanford, CA, USA.
Victoria Y DingQuantitative Sciences Unit, Stanford University School of Medicine, Stanford, CA, USA.
Rebecca M GardnerQuantitative Sciences Unit, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0001-5292-3219
Jacqueline V AredoStanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0003-0559-3565
Justin LeeQuantitative Sciences Unit, Stanford University School of Medicine, Stanford, CA, USA.
Julie T WuStanford University School of Medicine, Stanford, CA, USA.
Thomas P HickeyInformation Management Services, Rockville, MD, USA.
Brian BarrettInformation Management Services, Rockville, MD, USA.
Thomas L RileyInformation Management Services, Rockville, MD, USA.
Lynne R WilkensCancer Epidemiology Program, University of Hawaii Cancer Center, Honolulu, HI, USA.
Ann N LeungDepartment of Radiology, Stanford University School of Medicine, Stanford, CA, USA.
Loïc Le MarchandCancer Epidemiology Program, University of Hawaii Cancer Center, Honolulu, HI, USA.ORCID 0000-0001-5013-980X
Martin C TammemägiDepartment of Health Sciences, Brock University, St Catharines, Ontario, Canada.
Rayjean J HungProsserman Centre for Population Health Research, Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.ORCID 0000-0002-4486-7496
Christopher I AmosDepartment of Medicine, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0002-8540-7023
Neal D FreedmanDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Iona ChengDepartment of Epidemiology and Biostatistics, University of California, San Francisco, CA, USA.
Heather A WakeleeStanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0003-1136-980X
Summer S HanQuantitative Sciences Unit, Stanford University School of Medicine, Stanford, CA, USA.
Stanford University · USInformation Management Services · USUniversity of Hawaiʻi at Mānoa · USBaylor College of Medicine · USBrock University · CALunenfeld-Tanenbaum Research Institute · CANational Institutes of Health · USUniversity of California, San Francisco · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Melinda L. Telli · 2007 to 2026
$71.4M
PLCO Trial Etiologic and Early Marker StudyZIACP010152 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI MOORE, STEVEN · 2009 to 2025
$29.9M
Evaluation of genetic, clinical, and environmental risk factors to establish effective screening strategies for second primary lung cancerR37CA226081 · NCI · STANFORD UNIVERSITY · PI HAN, SUMMER S · 2018 to 2024
$4.3M
NCI NIH HHS P30 CA124435NCI NIH HHS R37 CA226081
6 · The paper itself

Abstract

backgroundWith advancing therapeutics, lung cancer (LC) survivors are rapidly increasing in number. Although mounting evidence suggests LC survivors have high risk of second primary lung cancer (SPLC), there is no validated prediction model available for clinical use to identify high-risk LC survivors for SPLC.

methodsUsing data from 6325 ever-smokers in the Multiethnic Cohort (MEC) study diagnosed with initial primary lung cancer (IPLC) in 1993-2017, we developed a prediction model for 10-year SPLC risk after IPLC diagnosis using cause-specific Cox regression. We evaluated the model's clinical utility using decision curve analysis and externally validated it using 2 population-based data-Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (PLCO) and National Lung Screening Trial (NLST)-that included 2963 and 2844 IPLC (101 and 93 SPLC cases), respectively.

resultsOver 14 063 person-years, 145 (2.3%) ever-smoking IPLC patients developed SPLC in MEC. Our prediction model demonstrated a high predictive accuracy (Brier score = 2.9, 95% confidence interval [CI] = 2.4 to 3.3) and discrimination (area under the receiver operating characteristics [AUC] = 81.9%, 95% CI = 78.2% to 85.5%) based on bootstrap validation in MEC. Stratification by the estimated risk quartiles showed that the observed SPLC incidence was statistically significantly higher in the 4th vs 1st quartile (9.5% vs 0.2%; P < .001). Decision curve analysis indicated that in a wide range of 10-year risk thresholds from 1% to 20%, the model yielded a larger net-benefit vs hypothetical all-screening or no-screening scenarios. External validation using PLCO and NLST showed an AUC of 78.8% (95% CI = 74.6% to 82.9%) and 72.7% (95% CI = 67.7% to 77.7%), respectively.

conclusionsWe developed and validated a SPLC prediction model based on large population-based cohorts. The proposed prediction model can help identify high-risk LC patients for SPLC and can be incorporated into clinical decision making for SPLC surveillance and screening.

Indexed as

Lung NeoplasmsNeoplasms, Second PrimaryEarly Detection of CancerHumansLungMaleSmoking

Identifiers

PMID34255071
PMCPMC8755509
OpenAlexW3183089822

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.