Evidence map›Paper›PMID 41964727›Full record

ReviewCurrent oncology reports2026

Updates in the Management of EGFR-Mutated Non-small Cell Lung Cancer (NSCLC).

Abhinav Vyas, Won Jin Jeon, Sanad Alhushki, Eric Singhi, Fawzi Abu Rous, Rajat Thawani, Aakash Desai

Abstract readReview
In one paragraph

Review in Current oncology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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.

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

2 citing papers in PubMed.

  1. Article
  2. Comparing Real-Time PCR and Amplicon-Based NGS for RoutineDiagnostics (Basel, Switzerland) · 2026
    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.

Abhinav VyasDivision of Medical Oncology and Hematology, Loma Linda University, Loma Linda, CA, USA.
Won Jin JeonDivision of Medical Oncology and Hematology, Loma Linda University, Loma Linda, CA, USA.
Sanad AlhushkiO'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA.
Eric SinghiDepartment of General Oncology, Division of Cancer, Medicine, MD Anderson Cancer Center, Houston, TX, USA.
Fawzi Abu RousMedical Oncology, Henry Ford Health, Detroit, MI, USA.
Rajat ThawaniDivision of Hematology/Medical Oncology, Oregon Health & Science University, Portland, OR, USA. thawani@ohsu.edu.ORCID 0000-0002-5378-9434
Aakash DesaiO'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA. aakashdesai@uabmc.edu.ORCID 0000-0002-2943-3817

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewWith the approvals of various targeted therapies including tyrosine kinase inhibitors to antibody–drug conjugates, the treatment landscape of patients with EGFR-mutant non-small cell lung cancer has drastically improved. The use of EGFR-targeted therapies has shifted to include not only advanced/ metastatic disease but also to early-stage non-small cell lung cancer. RECENT

findingsNovel therapy options have sought to address the need for effective agents against acquired resistance mechanisms in EGFR mutations. Further, the role of tyrosine kinase inhibitors against EGFR mutation in the perioperative setting has been most recently evaluated. With early outcomes, clinicians are met with the need to guide patients through various treatment regimens, and mature survival results are anticipated for several key trials. Of import, the growing focus on personalized treatment options based on outcomes, quality-of-life, toxicity, tolerability, and various disease-related factors warrants consideration. This review comprehensively describes frontline and subsequent-line therapy options for patients with early stage, unresectable/ locally advanced, and advanced/ metastatic stages of EGFR-mutant non-small cell lung cancer, including unprecedented therapeutic agents.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAntineoplastic AgentsErbB ReceptorsHumansMolecular Targeted TherapyMutationProtein Kinase InhibitorsAntineoplastic AgentsEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsEGFR-mutantNon-small cell lung cancerTargeted therapy

Identifiers

PMID41964727
PMCPMC13070087

What OpenQuestion holds

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LicenceCC BY
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.