Evidence map›Paper›PMID 31859066›Full record

ArticleClinical lung cancer2020

Clinicopathologic Characteristics, Treatment Outcomes, and Acquired Resistance Patterns of Atypical EGFR Mutations and HER2 Alterations in Stage IV Non-Small-Cell Lung Cancer.

Tejas Patil, Rao Mushtaq, Sydney Marsh, Christine Azelby, Miheer Pujara, Kurtis D Davies, Dara L Aisner, William T Purcell, Erin L Schenk, Jose M Pacheco and 3 more

Open access · greenAbstract read
In one paragraph

Article in Clinical lung cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Non-small cell lung cancer withFrontiers in oncology · 2023
    Pooled it
  3. Review
  4. Article
  5. Amivantamab Plus Lazertinib in AtypicalJournal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Exploring the correlation between HER2 alterations andJournal of cancer research and clinical oncology · 2023
    Article
  11. Real-World Clinical Outcomes for Patients withCurrent oncology (Toronto, Ont.) · 2023
    Article
  12. [Advances in Diagnosis and Treatment of HER2-positive Non-small Cell Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

13 authors at 2 institutions in 1 country.

Tejas PatilDivision of Medical Oncology, University of Colorado School of Medicine, Aurora, CO. Electronic address: tejas.patil@cuanschutz.edu.
Rao MushtaqDivision of Medical Oncology, University of Colorado School of Medicine, Aurora, CO.
Sydney MarshDepartment of Internal Medicine, University of Colorado School of Medicine, Aurora, CO.
Christine AzelbyDepartment of Internal Medicine, University of Colorado School of Medicine, Aurora, CO.
Miheer PujaraDepartment of Internal Medicine, University of Colorado School of Medicine, Aurora, CO.
Kurtis D DaviesDepartment of Pathology, University of Colorado School of Medicine, Aurora, CO.
Dara L AisnerDepartment of Pathology, University of Colorado School of Medicine, Aurora, CO.
William T PurcellDivision of Medical Oncology, University of Colorado School of Medicine, Aurora, CO.
Erin L SchenkDivision of Medical Oncology, University of Colorado School of Medicine, Aurora, CO.
Jose M PachecoDivision of Medical Oncology, University of Colorado School of Medicine, Aurora, CO.
Paul A BunnDivision of Medical Oncology, University of Colorado School of Medicine, Aurora, CO.
D Ross CamidgeDivision of Medical Oncology, University of Colorado School of Medicine, Aurora, CO.
Robert C DoebeleDivision of Medical Oncology, University of Colorado School of Medicine, Aurora, CO.
University of Colorado Denver · USUniversity of Colorado Anschutz Medical Campus · US

Funding

NIH Prior Approval Process ProfessionalUL1TR002535 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2018 to 2022
$51.1M
Tissue Bank and Biomarkers CoreP50CA058187 · NCI · UNIVERSITY OF COLORADO DENVER · PI KEITH, ROBERT · 1992 to 2018
$43.8M
Paul Calabresis Award in Clinical Oncology ResearchK12CA086913 · NCI · UNIVERSITY OF COLORADO DENVER · PI VIRGINIA F. BORGES, Jill E Slansky · 2000 to 2026
$17.8M
NCATS NIH HHS UL1 TR002535NCI NIH HHS K12 CA086913NCI NIH HHS P50 CA058187
6 · The paper itself

Abstract

backgroundThe clinicopathologic characteristics, acquired resistance patterns, and outcomes among patients with atypical EGFR mutations and HER2 alterations remain underexplored. PATIENTS AND

methodsA single-center retrospective review was conducted. Oncogenes assessed include typical EGFR (t-EGFR; exon 19 del and L858R), atypical EGFR (a-EGFR; G719X, exon 20, L861Q), HER2 (exon 19, exon 20, amplifications), gene fusions (ALK, ROS1, RET), RAS (KRAS, NRAS), and RAF (BRAF V600E). Progression-free survival (PFS), overall survival (OS), disease control rate, and objective response rate (Response Evaluation Criteria in Solid Tumors 1.1) were collected.

resultsAmong 570 patients, we found 55 a-EGFR mutations (13 G719X, 38 exon 20, 4 L861Q) and 31 HER2 alterations (2 exon 19 mutations, 27 exon 20 insertions, 2 amplifications). Patients with EGFR and HER2 alterations had increased lung and bone metastases relative to patients with gene fusions, RAS/RAF mutations, and no identified driver oncogenes (P < .001). Patients with EGFR exon 20 insertions had a median PFS to EGFR tyrosine kinase inhibitors (TKIs) of 5 months and an OS of 16 months-significantly worse than exon 19 del and L858R (Bonferroni correction; P < .001), but not G719X or L861Q. Relative to t-EGFR mutations, T790M and MET amplification occurred less frequently as acquired resistance mechanisms among a-EGFR samples (P < .001). Ten patients with a-EGFR mutations and HER2 alterations received single-agent immune checkpoint inhibitors (ICIs) with no radiographic responses and a median PFS of 2 months.

conclusionEGFR and HER2-mutated NSCLC have a high rate of synchronous lung and bone metastases. Patients with a-EGFR mutations have inferior responses to EGFR-directed therapies with lower rates of acquired T790M and MET amplification. Responses to ICIs are uniformly poor. Novel therapeutic approaches are needed.

Indexed as

MutationAdenocarcinoma of LungAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorCarcinoma, Non-Small-Cell LungCarcinoma, Squamous CellDrug Resistance, NeoplasmErb-b2 Receptor Tyrosine KinasesErbB ReceptorsFemaleFollow-Up StudiesGene AmplificationHumansBiomarkers, TumorEGFR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesErbB ReceptorsBone metastasesERBB2Exon 20 insertionImmune checkpoint inhibitorTyrosine kinase inhibitor

Identifiers

PMID31859066
PMCPMC7442280
OpenAlexW2990223332

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.