Evidence map›Paper›PMID 40429725›Full record

ArticleInternational journal of molecular sciences2025

Incongruence Between Prerequisite Molecular Testing and Treatment with Personalized Therapies for Non-Small Cell Lung Cancer: A Surveillance, Epidemiology and End Results-Medicare Study.

Wiley M Turner, Stephanie Tuminello, Matthew Untalan, Raja Flores, Emanuela Taioli

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Wiley M TurnerInstitute for Translational Epidemiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.ORCID 0009-0004-4633-0897
Stephanie TuminelloInstitute for Translational Epidemiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Matthew UntalanInstitute for Translational Epidemiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.ORCID 0009-0006-4616-2744
Raja FloresDepartment of Thoracic Surgery, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Emanuela TaioliInstitute for Translational Epidemiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

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
The Tisch Cancer Institute (TCI) Paul Calabresi K12 Career Development Award for Clinical OncologyK12CA270375 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Nina Bhardwaj, JAMES L. M. FERRARA · 2022 to 2026
$2.5M
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
NCI NIH HHS HHSN261201800009CNCI NIH HHS HHSN261201800009INCI NIH HHS HHSN261201800015CNCI NIH HHS HHSN261201800015INCI NIH HHS K12 CA270375NCI NIH HHS P20 CA264076NCI NIH HHS P20CA264076NCI NIH HHS P30 CA196521NCI NIH HHS P30CA196521
6 · The paper itself

Abstract

Personalized medicine, including targeted and immunotherapy, has substantially changed the landscape of non-small cell lung cancer (NSCLC). About 30% of NSCLC tumors have targetable mutations, like EGFR, and 28% of tumors will have a PD-L1 score or tumor mutation burden high enough to warrant immunotherapy; a molecular test prior to therapy assesses eligibility. However, the congruence between testing and treatment, and the effect of treatment without testing on outcomes, is understudied. We extracted a cohort of NSCLC patients from the Surveillance, Epidemiology and End Results (SEER)-Medicare-linked data. The primary outcome was survival. Demographic and clinical characteristics of those receiving vs. not receiving a molecular test were compared, and a Kaplan-Meier curve along with a multivariable Cox proportional hazards regression assessed the association of survival with the receipt of molecular diagnostic testing, adjusting for sex, race, age, income tract, metro/urban/rural region, histology, and stage. There were 911 NSCLC patients treated with personalized therapy, of which 513 (56.3%) had received prior molecular testing. Black patients were less likely than White patients to receive testing (36.4% vs. 59.9%;

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsPrecision MedicineAgedAged, 80 and overErbB ReceptorsFemaleHumansImmunotherapyMaleMedicareMutationSEER ProgramUnited StatesEGFR protein, humanErbB Receptorsimmunotherapymolecular diagnostic testingnon-small cell lung cancer (NSCLC)personalized medicinetargeted therapy

Identifiers

PMID40429725
PMCPMC12111554

What OpenQuestion holds

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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.