Evidence map›Paper›PMID 29232915›Full record

ArticleMedical sciences (Basel, Switzerland)2017

Histologic Grade Is Predictive of Incidence of Epidermal Growth Factor Receptor Mutations in Metastatic Lung Adenocarcinoma.

Michelle Levy, Liisa Lyon, Erika Barbero, John Wong, Marie Suga, Danny Sam, Minggui Pan

Open access · goldAbstract read
In one paragraph

Article in Medical sciences (Basel, Switzerland), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Differential expression of PD-L1 and IDO1 in association with the immune microenvironment in resected lung adenocarcinomas.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2019
    Article
  5. Article
  6. Article
  7. 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

7 authors at 2 institutions in 1 country.

Michelle LevyInternal Medicine Residency Program, Kaiser Permanente, Santa Clara, CA 95051, USA. michellealevy@gmail.com.
Liisa LyonDivision of Research, Kaiser Permanente, 2000 Broadway, Oakland, CA 94612, USA. liisa.l.lyon@kp.org.
Erika BarberoInternal Medicine Residency Program, Kaiser Permanente, Santa Clara, CA 95051, USA. Erika.m.barbero@kp.org.
John WongInternal Medicine Residency Program, Kaiser Permanente, Santa Clara, CA 95051, USA. jowong@llu.edu.
Marie SugaDivision of Oncology and Hematology, Kaiser Permanente, Vallejo, CA 94589, USA. Jennifer.m.suga@kp.org.
Danny SamInternal Medicine Residency Program, Kaiser Permanente, Santa Clara, CA 95051, USA. Danny.sam@kp.org.
Minggui PanInternal Medicine Residency Program, Kaiser Permanente, Santa Clara, CA 95051, USA. minggui.pan@kp.org.ORCID 0000-0002-8368-6524
Kaiser Permanente · USKaiser Permanente Vallejo Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activating epidermal growth factor receptor (EGFR) mutations in metastatic non-small cell lung cancer (NSCLC) are associated with a high response rate to EGFR tyrosine kinase inhibitor (TKI). The current guidelines recommend routine EGFR mutational analysis prior to initiating first line systemic therapy. The clinical characteristics including smoking status, histologic type, sex and ethnicity are known to be associated with the incidence of EGFR mutations. We retrospectively analyzed 277 patients with metastatic NSCLC within Kaiser Permanente Northern California (KPNC); among these patients, 83 were positive for EGFR mutations. We performed both univariate and multivariable logistic regressions to identify predictors of EGFR mutations. We found that histologic grade was significantly associated with the incidence of EGFR mutation, regardless of ethnicity, sex and smoking status. In grade I (well differentiated) and II (moderately differentiated), histology was associated with significantly higher incidence of EGFR mutations compared to grade II-III (moderate-to-poorly differentiated) and III (poorly differentiated). Ever-smokers with grade III lung adenocarcinoma had 1.8% incidence of EGFR mutations. This study indicates that histologic grade is a predictive factor for the incidence of EGFR mutations and suggests that for patients with grade II-III or III lung adenocarcinoma, prompt initiation of first-line chemotherapy or immunotherapy is appropriate while awaiting results of EGFR mutational analysis, particularly for patients with history of smoking.

Indexed as

EGFR mutationerlotinibHistologic gradeLung adenocarcinomaNSCLC

Identifiers

PMID29232915
PMCPMC5753663
OpenAlexW2771500922

What OpenQuestion holds

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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.