Evidence map›Paper›PMID 22896655›Full record

SynthesisClinical cancer research : an official journal of the American Association for Cancer Research2012

Clinicopathologic features and long-term outcomes of NUT midline carcinoma.

Daniel E Bauer, Chelsey M Mitchell, Kelly M Strait, Christopher S Lathan, Edward B Stelow, Sonja C Lüer, Somala Muhammed, Andrew G Evans, Lynette M Sholl, Juan Rosai and 7 more

2 registry-linked trialsAbstract readMeta-Analysis
In one paragraph

Synthesis in Clinical cancer research : an official journal of the American Association for Cancer Research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 201 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
201citing papers in PubMed, 3 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.

NCT03976518 phase2completednot on this mapstarted 2019, after this paper: background citation

Phase II, Open-label Study of Atezolizumab in a Cohort of Pretreated, Advanced Non-small Cell Lung Cancer (NSCLC) Patients With Rare Histological Subtypes (CHANCE Trial).

TypeinterventionalSponsorGruppo Oncologico Italiano di Ricerca ClinicaRan2019 to 2024Enrolled43ConditionsNon-Small Cell Lung CancerArmsAtezolizumab
NCT07459127 active not recruitingnot on this mapstarted 2023, after this paper: background citation

A Multicenter Retrospective Real-World Cohort Study of Pulmonary NUT Carcinoma With Integrated Clinical, Pathologic, and Imaging Analyses

TypeobservationalSponsorThree Gorges Hospital of Chongqing UniversityRan2023 to 2026Enrolled150ConditionsNUT CarcinomaArmsStandard-of-care anticancer treatment (retrospective)
3 · Its place in the literature

Who cites it

201 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Patterns of care and impact of prognostic factors in the outcome of NUT midline carcinoma: a systematic review and individual patient data analysis of 119 cases.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2018
    Pooled it
  4. Trial
  5. Head and neck NUT carcinoma-radiotherapy dose, chemotherapy choice, and outcomes: lessons from a 7-year complete remission.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Shared PRAME epitopes are T-cell targets in NUT carcinoma.Journal for immunotherapy of cancer · 2026
    Article
  16. Article
  17. Article
  18. An Early-Stage Nuclear Protein in Testis Carcinoma of the Lung in an Older Woman.Interdisciplinary cardiovascular and thoracic surgery · 2026
    Article
  19. Review
  20. Article

141 more citing papers are in PubMed but not listed here.

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

17 authors.

Daniel E BauerDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, and Division of Hematology/Oncology, Children's Hospital Boston, Harvard Medical School, Boston, Massachusetts 02115, USA.
Chelsey M Mitchell
Kelly M Strait
Christopher S Lathan
Edward B Stelow
Sonja C Lüer
Somala Muhammed
Andrew G Evans
Lynette M Sholl
Juan Rosai
Eugenia Giraldi
Richard P Oakley
Carlos Rodriguez-Galindo
Wendy B London
Stephen E Sallan
James E Bradner
Christopher A French

Funding

Pathogenesis of NUT-Rearranged CarcinomaR01CA124633 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Christopher A French · 2007 to 2026
$7.0M
Racial disparities in the treatment of lung cancer in African AmericansK01CA124581 · NCI · DANA-FARBER CANCER INST · PI LATHAN, CHRISTOPHER S. · 2007 to 2011
$823k
NCI NIH HHS 1R01CA124633NCI NIH HHS 3K01CA124581-03S1NCI NIH HHS 3R01CA124633-04S1NCI NIH HHS K01 CA124581NCI NIH HHS R01 CA124633
6 · The paper itself

Abstract

purposeNUT midline carcinoma (NMC) is a poorly differentiated squamous cancer characterized by rearrangement of the NUT gene. Research advances have provided opportunities for targeted therapy in NMC, yet the clinical features of this rare disease have not been systematically characterized. We report on a large population of such patients to identify the disease characteristics and treatments, correlate them with outcome, and to consider clinical recommendations. EXPERIMENTAL

designA clinical database was established using retrospective demographic and outcomes data available on all known cases of NMC. Questionnaires were completed by treating physicians. Pathologic, demographic, and clinical variables were assessed for 63 patients, the largest cohort of patients with NMC studied to date. Outcome data from 54 patients were available for survival analyses.

resultsThe diagnosis of NMC has increased annually since 2007. Since 2009, there has been an observed increase in the age at diagnosis (P < 0.05). Geographic distribution of patients with NMC has been concentrated in the United States (n = 41, 65%). The median overall survival for patients with NMC was 6.7 months. The 2-year progression-free survival (PFS) was 9% with a 95% confidence interval (CI) of 1% to 17% [1-year PFS 15% (5-24%) and 2-year overall survival (OS) was 19% with a 95% CI of 7%-31% (1-year OS: 30% (27-34%)]. Multivariate analysis suggested that extent of surgical resection and initial radiotherapy were independent predictors of PFS and OS. Notably, no chemotherapeutic regimen was associated with improved outcome.

conclusionsNMC portends a poor prognosis among all squamous cell neoplasms and seems to be frequently unrecognized. The finding that conventional chemotherapy has been inadequate indicates a pressing need for the development of targeted therapeutics. Intensive local therapies such as gross total resection and radiotherapy might be associated with enhanced survival.

Indexed as

Carcinoma, Squamous CellAdolescentAdultAgedChildChild, PreschoolChromosome AberrationsDisease-Free SurvivalFemaleHumansInfantKaplan-Meier EstimateMaleMiddle AgedNeoplasm ProteinsNuclear ProteinsNeoplasm ProteinsNuclear ProteinsNUTM1 protein, humanOncogene Proteins

Identifiers

PMID22896655
PMCPMC3473162

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.