Evidence map›Paper›PMID 37121400›Full record

ArticleAnnals of oncology : official journal of the European Society for Medical Oncology2023

Molecular markers of metastatic disease in KRAS-mutant lung adenocarcinoma.

D Boiarsky, C A Lydon, E S Chambers, L M Sholl, M Nishino, F Skoulidis, J V Heymach, J Luo, M M Awad, P A Janne and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Annals of oncology : official journal of the European Society for Medical Oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Immune checkpoint inhibitors have limited efficacy inTranslational lung cancer research · 2025
    Article
  9. Article
  10. Article
  11. Prognostic Impact ofBiomedicines · 2025
    Article
  12. Article
  13. Review
  14. The role of SMARCA4 in lung cancer.Scientific reports · 2025
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. MVASA-HGN: multi-view adaptive semantic-aware heterogeneous graph network forQuantitative imaging in medicine and surgery · 2025
    Article
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

13 authors at 6 institutions in 1 country.

D BoiarskyDepartment of Medicine, Tufts Medical Center, Boston.
C A LydonDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston.
E S ChambersLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston.
L M ShollCenter for Advanced Molecular Diagnostics, Brigham & Women's Hospital & Harvard Medical School, Boston.
M NishinoDepartment of Radiology, Brigham and Women's Hospital, Boston.
F SkoulidisDepartment of Thoracic/Head and Neck Medical Oncology, University of Texas M.D. Anderson Cancer Center, Houston.
J V HeymachDepartment of Thoracic/Head and Neck Medical Oncology, University of Texas M.D. Anderson Cancer Center, Houston.
J LuoDepartment of Medicine, Dana-Farber Cancer Institute, Boston.
M M AwadDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston.
P A JanneLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston.
E M Van AllenDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston; Broad Institute of Harvard & MIT, Cambridge; Center for Cancer Precision Medicine, Dana-Farber Cancer Institute, Boston.
D A BarbieLowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston.
N I VokesDepartment of Thoracic/Head and Neck Medical Oncology, University of Texas M.D. Anderson Cancer Center, Houston; Department of Genomic Medicine, University of Texas M.D. Anderson Cancer Center, Houston, USA. Electronic address: nvokes@mdanderson.org.
Dana-Farber Cancer Institute · USThe University of Texas MD Anderson Cancer Center · USBrigham and Women's Hospital · USBroad Institute · USHarvard University · USTufts Medical Center · US

Funding

UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GIBBONS, DON LYNN · 1996 to 2024
$57.4M
Physician Scientist Training in Cancer ResearchT32CA009172 · NCI · DANA-FARBER CANCER INSTITUTE · PI Jennifer R Brown, James A. DeCaprio · 1985 to 2026
$17.1M
Project 3P50CA265826 · NCI · DANA-FARBER CANCER INST · PI David A Barbie, Lecia V. Sequist · 2022 to 2026
$13.7M
The Boston Lung Cancer Survival CohortU01CA209414 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI David C Christiani · 2017 to 2026
$12.2M
Development of Combination Therapies to Delay/Prevent Acquired Drug ResistanceR35CA220497 · NCI · DANA-FARBER CANCER INST · PI JANNE, PASI A · 2018 to 2024
$7.2M
Targeting the cytokine circuitry of KRAS-driven lung cancerR01CA190394 · NCI · DANA-FARBER CANCER INST · PI David A Barbie · 2015 to 2026
$4.5M
Novel therapeutic approaches for enhancing anti-tumor immunity in SCLCU01CA213273 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BYERS, LAUREN AVERETT, HEYMACH, JOHN V. · 2017 to 2021
$3.0M
Automated in vivo analysis of tumor growth rate as a guide for therapeutic decisions to advance personalized cancer treatmentR01CA203636 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI NISHINO, MIZUKI · 2017 to 2021
$2.9M
Integrative Somatic and Germline Computational Biology to Redefine Clinical Actionability in Solid TumorsR01CA227388 · NCI · DANA-FARBER CANCER INST · PI VAN ALLEN, ELIEZER M · 2018 to 2022
$2.0M
NCI NIH HHS P50 CA070907NCI NIH HHS P50 CA265826NCI NIH HHS R01 CA190394NCI NIH HHS R01 CA203636NCI NIH HHS R01 CA227388NCI NIH HHS R35 CA220497NCI NIH HHS T32 CA009172NCI NIH HHS U01 CA209414NCI NIH HHS U01 CA213273
6 · The paper itself

Abstract

backgroundPrior studies characterized the association of molecular alterations with treatment-specific outcomes in KRAS-mutant (KRAS PATIENTS AND

methodsWe analyzed clinicogenomic data from 1817 patients with KRAS

resultsKEAP1 (DFCI: OR = 2.3, q = 0.04; MSKCC: OR = 2.2, q = 0.00027) and SMARCA4 mutations (DFCI: OR = 2.5, q = 0.06; MSKCC: OR = 2.6, q = 0.0021) were enriched in M1 versus M0 tumors. On integrative modeling, NRF2 activation was the genomic feature most associated with OS. KEAP1 mutations were enriched in M1 versus M0 tumors independent of STK11 status (KEAP1

conclusionsMutations in KEAP1 and SMARCA4, but not STK11, were associated with metastatic disease and poor OS. Functional STK11 loss, however, may contribute to poor outcomes in KEAP1

Indexed as

Adenocarcinoma of LungLung NeoplasmsBiomarkers, TumorDNA HelicasesHumansKelch-Like ECH-Associated Protein 1MutationNF-E2-Related Factor 2Nuclear ProteinsPrognosisProtein Serine-Threonine KinasesProto-Oncogene Proteins p21(ras)Transcription FactorsBiomarkers, TumorDNA HelicasesKelch-Like ECH-Associated Protein 1KRAS protein, humanNF-E2-Related Factor 2Nuclear ProteinsProtein Serine-Threonine KinasesProto-Oncogene Proteins p21(ras)SMARCA4 protein, humanTranscription FactorsKEAP1KRASlung adenocarcinomametastaticSTK11

Identifiers

PMID37121400
PMCPMC10425882
OpenAlexW4367301236

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.