Evidence map›Paper›PMID 39254646›Full record

ArticleJournal of the National Cancer Institute2025

Racial and socioeconomic disparities in non-small cell lung cancer molecular diagnostics uptake.

Stephanie Tuminello, Wiley M Turner, Matthew Untalan, Tara Ivic-Pavlicic, Raja Flores, Emanuela Taioli

Abstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

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

  1. Pooled it
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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

6 authors.

Stephanie TuminelloInstitute for Translational Epidemiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Wiley M TurnerInstitute for Translational Epidemiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID 0009-0004-4633-0897
Matthew UntalanInstitute for Translational Epidemiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Tara Ivic-PavlicicInstitute for Translational Epidemiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Raja FloresDepartment of Thoracic Surgery, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Emanuela TaioliInstitute for Translational Epidemiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID 0000-0001-5734-4806

Funding

THE TISCH CANCER INSTITUTE - CANCER CENTER SUPPORT GRANTP30CA196521 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Ramon E Parsons · 2015 to 2026
$35.4M
Disparities in molecular testing among non-small cell lung cancer patientsP20CA264076 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI TAIOLI, EMANUELA · 2021 to 2024
$1.2M
California Department of Public HealthCalifornia Health and Safety Code Section 103885CDC HHSCenters for Disease Control and Prevention's National Program of Cancer Registries 1NU58D007156NCI NIH HHS HHSN261201800009CNCI NIH HHS HHSN261201800009INCI NIH HHS HHSN261201800015CNCI NIH HHS HHSN261201800015INCI NIH HHS HHSN26120180032INCI NIH HHS P20 CA264076NCI NIH HHS P30 CA196521NIH HHS #P30CA196521University of California
6 · The paper itself

Abstract

backgroundPrecision therapies, such as targeted and immunotherapies, have substantially changed the landscape of late-stage non-small cell lung cancer (NSCLC). Yet, utilization of these therapies is disproportionate across strata defined by race and socioeconomic status, possibly because of disparities in molecular diagnostic testing (or biomarker testing), which is a prerequisite to treatment.

methodsWe extracted a cohort of NSCLC patients from the Surveillance, Epidemiology, and End Results-Medicare linked data. The primary outcome was receipt of a molecular diagnostic test, based on claims data. The primary predictors were race and socioeconomic status. Likelihood of receiving a molecular diagnostic test and overall survival were investigated using logistic and Cox proportional hazards regression, adjusted for sex, age, residence, histology, marital status, and comorbidity.

resultsOf the 28 511 NSCLC patients, 11 209 (39.3%) received molecular diagnostic testing. Compared with White patients, fewer Black patients received a molecular diagnostic test (40.4% vs 27.9%; P < .001). After adjustment, Black patients (adjusted odds ratio [OR] = 0.64, 95% confidence interval [CI] = 0.58 to 0.71) and those living in areas with greater poverty (adjusted OR = 0.85, 95% CI = 0.80 to 0.89) had statistically significant decreased likelihood of molecular diagnostic testing. Patients who did receive testing had a statistically significant decreased risk of death (adjusted hazard ratio [HR] = 0.74, 95% CI = 0.72 to 0.76). These results held in the stratified analysis of stage IV NSCLC patients.

conclusionDisparities exist in comprehensive molecular diagnostics, which is critical for clinical decision making. Addressing barriers to molecular testing could help close gaps in cancer care and improve patient outcomes.

Indexed as

Carcinoma, Non-Small-Cell LungHealthcare DisparitiesLung NeoplasmsSEER ProgramAgedAged, 80 and overBiomarkers, TumorFemaleHumansMaleMedicareMolecular Diagnostic TechniquesSocial ClassSocioeconomic Disparities in HealthSocioeconomic FactorsUnited StatesBiomarkers, Tumor

Identifiers

PMID39254646
PMCPMC11717419

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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.