Evidence map›Paper›PMID 28934846›Full record

ArticleCancer research and treatment2018

EGFR Mutation Status in Lung Adenocarcinoma-Associated Malignant Pleural Effusion and Efficacy of EGFR Tyrosine Kinase Inhibitors.

Jiyoul Yang, Ok-Jun Lee, Seung-Myoung Son, Chang Gok Woo, Yusook Jeong, Yaewon Yang, Jihyun Kwon, Ki Hyeong Lee, Hye Sook Han

Open access · diamondAbstract read
In one paragraph

Article in Cancer research and treatment, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.3field-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

24 citing papers in PubMed, 39 citations in OpenAlex.

  1. OsimertinibTranslational lung cancer research · 2026
    Article
  2. Review
  3. Integrating pleural PD-1Frontiers in immunology · 2026
    Article
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  7. Article
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  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Advances in pleural infection and malignancy.European respiratory review : an official journal of the European Respiratory Society · 2021
    Article
  17. Article
  18. Article
  19. Article
  20. 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

9 authors at 2 institutions in 1 country.

Jiyoul YangDepartment of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea.
Ok-Jun LeeDepartment of Pathology, Chungbuk National University Hospital, Cheongju, Korea.
Seung-Myoung SonDepartment of Pathology, Chungbuk National University Hospital, Cheongju, Korea.
Chang Gok WooDepartment of Pathology, Chungbuk National University Hospital, Cheongju, Korea.
Yusook JeongDepartment of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea.
Yaewon YangDepartment of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea.
Jihyun KwonDepartment of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea.
Ki Hyeong LeeDepartment of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea.
Hye Sook HanDepartment of Internal Medicine, Chungbuk National University Hospital, Cheongju, Korea.
Chungbuk National University Hospital · KRChungbuk National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMalignant pleural effusions (MPEs) are often observed in lung cancer, particularly adenocarcinoma. The aim of this study was to investigate epidermal growth factor receptor (EGFR) mutation status in lung adenocarcinoma-associated MPEs (LA-MPEs) and its correlation with efficacy of EGFR tyrosine kinase inhibitor (TKI) therapy. MATERIALS AND

methodsSamples comprised 40 cell blocks of pathologically-confirmed LA-MPEs collected before the start of EGFR TKI therapy. EGFR mutation status was re-evaluated by peptide nucleic acid clamping and the clinical outcomes of EGFR TKI‒treated patients were analyzed retrospectively.

resultsEGFR mutations were detected in 72.5% of LA-MPE cell blocks (29/40). The median progression-free survival for patients with EGFR mutations in LA-MPEs was better than that for patients with wild-type EGFR (7.33 months vs. 2.07 months; hazard ratio, 0.486; 95% confidence interval, 0.206 to 1.144; p=0.032). The objective response rate (ORR) of 26 patients with EGFR mutations in LA-MPEs among the 36 patients with measurable lesions was 80.8%, while the ORR of the 10 patients with wild-type EGFR in LA-MPEs was 10% (p < 0.001). Among the 26 patients with EGFR mutations in LA-MPEs, the ORR of target lesions and LA-MPEs were 88.5% and 61.5%, respectively (p=0.026).

conclusionEGFR mutation status in cell blocks of LA-MPEs confirmed by pathologic diagnosis is highly predictive of EGFR TKI efficacy. For patients with EGFR mutations in LA-MPEs, the response to EGFR TKIs seems to be worse for pleural effusions than for solid tumors.

Indexed as

MutationAdenocarcinomaAdenocarcinoma of LungAdultAgedAged, 80 and overDisease ProgressionErbB ReceptorsFemaleHumansLung NeoplasmsMaleMiddle AgedPleural Effusion, MalignantProtein Kinase InhibitorsRetrospective StudiesEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsEpidermal growth factor receptorLung adenocarcinomaPleural effusionTyrosine kinase inhibitor

Identifiers

PMID28934846
PMCPMC6056963
OpenAlexW2756163907

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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.