Evidence map›Paper›PMID 31406302›Full record

ReviewNature reviews. Cancer2019

Co-occurring genomic alterations in non-small-cell lung cancer biology and therapy.

Ferdinandos Skoulidis, John V Heymach

3 registry-linked trialsAbstract readReview
In one paragraph

Review in Nature reviews. Cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 636 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
636citing papers in PubMed, 1 pooled it
77.8field-weighted citation impact, top 1% 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.

NCT06876402 active not recruitingnot on this map

Assessment of the Prevalence and Prognostic Value of Gene Molecular Alterations and Association With Clinicopathological Factors in Patients With Non-small Cell Lung Cancer (NSCLC)

TypeobservationalSponsorHellenic Cooperative Oncology GroupRan2013 to 2025Enrolled367ConditionsNSCLC (Non-small Cell Lung Cancer)
NCT06959173 recruitingnot on this mapstarted 2025, after this paper: background citation

Organoid-guided Personalized Treatment of Pleural Effusion

TypeobservationalSponsorHenan Cancer HospitalRan2025 to 2027Enrolled20ConditionsLung Cancer
NCT07303218 active not recruitingnot on this mapstarted 2025, after this paper: background citation

The HER Project: Homologous Recombination Deficiency in EGFR-Mutated NSCLC, a Retrospective and Prospective Translational Single-center Study

TypeobservationalSponsorIRCCS San RaffaeleRan2025 to 2032Enrolled100ConditionsEGFR, Non Small Cell Lung Cancer, Homologous Recombination Deficiency, PARP InhibitorArmsNo Intervention: Observational Cohort
3 · Its place in the literature

Who cites it

636 citing papers in PubMed, 1 synthesis or guideline pooled it, 972 citations in OpenAlex.

  1. Pooled it
  2. LRP1b Loss Predicts Sensitivity to Immunotherapy in Patients with NSCLC: An Analysis of the Phase III CheckMate-026 Randomized Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Real-world evolution of first-line ALK-positive NSCLC management in Spain.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  8. SSX1 and TRIM58 expression stratifies lung squamous cell carcinoma by tumor immune microenvironment characteristics and informs potential immunotherapy responsiveness.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  9. Article
  10. Review
  11. Article
  12. Lessons from Cohort Studies of Targetable Metabolic Deficiencies in Lung Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Ultra-rare TP53 and KRAS variants predict survival in ICI-treated solid tumours.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  19. Article
  20. Review

576 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

2 authors at 1 institution in 1 country.

Ferdinandos SkoulidisDepartment of Thoracic and Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. fskoulidis@mdanderson.org.ORCID http://orcid.org/0000-0002-4676-4503
John V HeymachDepartment of Thoracic and Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HEYMACH, JOHN V., MINNA, JOHN D. · 1996 to 2024
$57.4M
Therapeutic approaches for LKB1-deficient non-small cell lung cancerR01CA205150 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HEYMACH, JOHN V., WONG, KWOK KIN · 2016 to 2020
$3.0M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA070907NCI NIH HHS R01 CA205150
6 · The paper itself

Abstract

The impressive clinical activity of small-molecule receptor tyrosine kinase inhibitors for oncogene-addicted subgroups of non-small-cell lung cancer (for example, those driven by activating mutations in the gene encoding epidermal growth factor receptor (EGFR) or rearrangements in the genes encoding the receptor tyrosine kinases anaplastic lymphoma kinase (ALK), ROS proto-oncogene 1 (ROS1) and rearranged during transfection (RET)) has established an oncogene-centric molecular classification paradigm in this disease. However, recent studies have revealed considerable phenotypic diversity downstream of tumour-initiating oncogenes. Co-occurring genomic alterations, particularly in tumour suppressor genes such as TP53 and LKB1 (also known as STK11), have emerged as core determinants of the molecular and clinical heterogeneity of oncogene-driven lung cancer subgroups through their effects on both tumour cell-intrinsic and non-cell-autonomous cancer hallmarks. In this Review, we discuss the impact of co-mutations on the pathogenesis, biology, microenvironmental interactions and therapeutic vulnerabilities of non-small-cell lung cancer and assess the challenges and opportunities that co-mutations present for personalized anticancer therapy, as well as the expanding field of precision immunotherapy.

Indexed as

Genome, HumanAlgorithmsAMP-Activated Protein Kinase KinasesAnimalsCarcinoma, Non-Small-Cell LungDisease-Free SurvivalErbB ReceptorsHumansImmunotherapyLung NeoplasmsMiceMutationOncogenesPhenotypePrognosisProtein Serine-Threonine KinasesAMP-Activated Protein Kinase KinasesEGFR protein, humanErbB ReceptorsKRAS protein, humanMAS1 protein, humanProtein Serine-Threonine KinasesProto-Oncogene MasProto-Oncogene Proteins p21(ras)STK11 protein, humanTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID31406302
PMCPMC7043073
OpenAlexW2967210753

What OpenQuestion holds

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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.