Evidence map›Paper›PMID 41348986›Full record

ArticleJCO precision oncology2025

Presenting Features and Causes of Diagnostic Delays: A Report From the NUT Carcinoma Registry.

Sara A Walton, Justin J Kim, Francesco Paoloni, Jean W Liew, Danielle Haradon, Jessica Haradon, Kathryn W Miller, Paul K Paik, Jamie E Chaft, Mark G Kris and 11 more

Abstract read
In one paragraph

Article in JCO precision oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

21 authors.

Sara A WaltonLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0009-0007-3755-0451
Justin J KimLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0009-0000-7393-3758
Francesco PaoloniLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, MA.
Jean W LiewBoston University Chobanian and Avedisian School of Medicine, Boston, MA.ORCID 0000-0002-8104-2450
Danielle HaradonLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0009-0006-2613-3866
Jessica HaradonLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, MA.
Kathryn W MillerLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, MA.
Paul K PaikThoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, Memorial Sloan Kettering Cancer Center, and Weill Cornell Medical College, New York, NY.ORCID 0000-0002-9464-3984
Jamie E ChaftThoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, Memorial Sloan Kettering Cancer Center, and Weill Cornell Medical College, New York, NY.ORCID 0000-0002-5838-9982
Mark G KrisThoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, Memorial Sloan Kettering Cancer Center, and Weill Cornell Medical College, New York, NY.
Robert HsuDivision of Medical Oncology, Department of Internal Medicine, University of Southern California/Norris Comprehensive Cancer Center, Los Angeles, CA.ORCID 0000-0003-3957-6106
Sarina A Piha-PaulDepartment of Investigational Cancer Therapeutics, University of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-9455-1660
Julia K RotowLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, MA.
Pasi A JänneLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-7821-4928
David A BarbieLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, MA.
Lynette M ShollDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.ORCID 0000-0002-9532-9735
Steven G DuBoisDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.ORCID 0000-0003-0882-738X
Glenn J HannaDepartment of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.ORCID 0000-0002-9969-2523
Geoffrey I ShapiroDepartment of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.ORCID 0000-0002-3331-4095
Christopher A FrenchDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.ORCID 0000-0002-7434-4987
Jia LuoLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0003-3606-827X

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Michael Jason de la Cruz · 1985 to 2026
$347.4M
Pathogenesis of NUT-Rearranged CarcinomaR01CA124633 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Christopher A French · 2007 to 2026
$7.0M
CTSA K12 Program at Harvard Medical SchoolK12TR004381 · NCATS · HARVARD MEDICAL SCHOOL · PI Karen K Miller · 2023 to 2026
$6.5M
NCATS NIH HHS K12 TR004381NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA124633
6 · The paper itself

Abstract

purposeDiagnostic delays are common for patients with NUT carcinoma (NC), a cancer driven by NUT fusion oncoprotein. Rapid diagnosis is crucial for the best outcomes. We investigated NC's presenting features and associations with diagnostic delays.

methodsWe manually reviewed medical records from US participants in the NC Registry (2007-2024). Baseline features were analyzed descriptively, and multivariable logistic regression was used to examine odds ratios for delays.

resultsWe analyzed 132 patients (median age 37 years). At presentation, 55% had metastatic disease and 64% had a thoracic primary. The median interval from symptom onset to diagnosis was 10 weeks (range, 1-165 weeks). The initial histopathologic diagnosis was poorly differentiated/squamous cell cancer in 52%, insufficient malignant cells in 14%, carcinoma in 12%, and NC in 22%. Immunohistochemistry (IHC) testing revealed NUT in 100%; 93% were keratin+, 88% p63+, 89% p40+, and 72% had Ki-67 ≥50%. IHC was used to diagnose NC in 79%. Nonthoracic primaries were associated with a longer time between symptom onset and NC diagnosis (odds ratio, 3.25). Of 32 patients who started treatment before diagnosis, 78% were on agents appropriate for NC. After a diagnosis of NC, 33% participated in clinical trials.

conclusionNC almost always presents as squamous/poorly differentiated non-small cell lung or head and neck cancer. Overall, 78% of patients were initially diagnosed as non-NC. Efforts to raise awareness, recognition, and rapid diagnosis of NC by both oncologists and pathologists are critical if we are to improve outcomes.

Indexed as

CarcinomaDelayed DiagnosisAdultAgedFemaleHumansMaleMiddle AgedNeoplasm ProteinsNuclear ProteinsRegistriesYoung AdultNeoplasm ProteinsNuclear ProteinsNUTM1 protein, human

Identifiers

PMID41348986
PMCPMC12695031

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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.