Evidence map›Paper›PMID 42414222›Full record

SynthesisThoracic cancer2026

EGFR Mutations and Recurrence Outcomes in Resected Non-Small Cell Lung Cancer: An Updated 2015-2025 Systematic Review and Meta-Analysis.

Soo Han Kim, Hayoung Seong, Hyojin Jang, Saerom Kim, Wanho Yoo, Jeongha Mok, Kwangha Lee, Ki Uk Kim, Min Ki Lee, Mi-Hyun Kim and 1 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Thoracic cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Soo Han KimDepartment of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.
Hayoung SeongDepartment of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.
Hyojin JangDepartment of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.
Saerom KimDepartment of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.
Wanho YooDepartment of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.
Jeongha MokDepartment of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.
Kwangha LeeDepartment of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.
Ki Uk KimDepartment of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.
Min Ki LeeDepartment of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.
Mi-Hyun KimDepartment of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.ORCID https://orcid.org/0000-0002-6527-6804
Jung Seop EomDepartment of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.ORCID https://orcid.org/0000-0002-0832-1314

Funding

Korea Health Industry Development Institute HR20C0026National Research Foundation of Korea RS-2023-00223764Pusan National University Hospital 2025
6 · The paper itself

Abstract

backgroundThe prognostic significance of EGFR mutations in resected non-small cell lung cancer (NSCLC) remains uncertain despite their established predictive value in advanced disease. We assessed the prognostic impact of EGFR mutation status on recurrence and disease-free survival (DFS) in resected stage I-III NSCLC.

methodsIn this systematic review and meta-analysis, we searched PubMed, Embase, and Cochrane Library to identify studies of resected stage I-III NSCLC reporting recurrence or DFS according to EGFR status. Pooled recurrence rates, risk ratio (RR), and hazard ratio (HR) were calculated using random-effects models. Subgroup analyses were conducted by stage, recurrence site, mutation subtype, and adjuvant treatment.

resultsA total of 20 studies (4 randomized controlled trials and 16 retrospective observational studies), comprising 12 123 patients (7203 EGFR-mutant and 4920 wild-type), were included. Four studies focused on stage I disease, five on stage II-III, and eleven across stage I-III. The pooled recurrence RR comparing EGFR-mutant and wild-type tumors was 1.04 (95% CI, 0.88-1.23), and the pooled DFS HR was 1.07 (95% CI, 0.84-1.37), indicating no significant difference. Recurrence patterns were comparable, with no differences in local or distant relapse and only a modest, non-significant increase in central nervous system recurrence. Among EGFR-mutant tumors, adjuvant EGFR-TKIs improved DFS (HR 0.45, 95% CI, 0.29-0.71) unlike chemotherapy (HR 1.05, 95% CI, 0.67-1.66).

conclusionEGFR mutation status is not associated with recurrence, DFS, or recurrence patterns in resected NSCLC. Adjuvant EGFR-TKIs, but not chemotherapy, confer significant DFS benefit, supporting their use as standard postoperative therapy.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsMutationNeoplasm Recurrence, LocalErbB ReceptorsHumansPrognosisEGFR protein, humanErbB Receptorsdisease‐free survivalEGFR mutationmeta‐analysisnon‐small cell lung cancerprognosisrecurrence

Identifiers

PMID42414222
PMCPMC13341228

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.