Evidence map›Paper›PMID 32917914›Full record

ArticleScientific reports2020

The efficacy of first-line tyrosine kinase inhibitors combined with co-medications in Asian patients with EGFR mutation non-small cell lung cancer.

Vincent Yi-Fong Su, Kuang-Yao Yang, Ting-Yu Huang, Chia-Chen Hsu, Yuh-Min Chen, Jiin-Cherng Yen, Yueh-Ching Chou, Yuh-Lih Chang, Chien-Hui He

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
3.2field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it, 32 citations in OpenAlex.

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  16. State-of-the-Art Molecular Oncology of Lung Cancer in Taiwan.International journal of molecular sciences · 2022
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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 4 institutions in 1 country.

Vincent Yi-Fong Su *Department of Internal Medicine, Taipei City Hospital, Taipei, Taiwan.
Kuang-Yao Yang *Department of Chest Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Ting-Yu HuangDepartment and Institute of Pharmacology, National Yang-Ming University, Taipei, Taiwan.
Chia-Chen HsuDepartment of Pharmacy, Taipei Veterans General Hospital, Taipei, Taiwan.
Yuh-Min ChenDepartment of Chest Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Jiin-Cherng YenDepartment and Institute of Pharmacology, National Yang-Ming University, Taipei, Taiwan.
Yueh-Ching ChouDepartment of Pharmacy, Taipei Veterans General Hospital, Taipei, Taiwan. ycchou@vghtpe.gov.tw.
Yuh-Lih ChangDepartment of Pharmacy, Taipei Veterans General Hospital, Taipei, Taiwan. ylchang@vghtpe.gov.tw.
Chien-Hui HeDepartment of Chest Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
National Yang Ming Chiao Tung University · TWTaipei Veterans General Hospital · TWNational Yang Ming Chiao Tung University · TWNational Yang Ming University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The real-world efficacy of epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) in patients with advanced non-small cell lung cancer (NSCLC) harboring EGFR-activating mutations remains unclear. We conducted a retrospective cohort study using data from the claims database of Taipei Veterans General Hospital to perform direct comparisons of these three EGFR-TKIs (gefitinib, erlotinib, and afatinib) combined with co-medications (metformin, statins, antacids, and steroids). Stage IIIB and IV NSCLC patients with EGFR mutations receiving EGFR-TKIs as first-line treatment for > 3 months between 2011 and 2016 were enrolled. The primary endpoint was time to treatment failure (TTF). Patients who had received co-medications (≥ 28 defined daily doses) in the first 3 months of EGFR-TKI therapy were assigned to co-medications groups. A total of 853 patients treated with gefitinib (n = 534), erlotinib (n = 220), and afatinib (n = 99) were enrolled. The median duration of TTF was 11.5 months in the gefitinib arm, 11.7 months in the erlotinib arm, and 16.1 months in the afatinib arm (log-rank test, P < 0.001). After adjustments, afatinib showed lower risk of treatment failure compared with gefitinib (hazard ratio [HR] 0.54, 95% confidence interval [CI] 0.41-0.71) and erlotinib (HR 0.62, 95% CI 0.46-0.83). The risk of treatment failure in patients treated with EGFR-TKIs who received concomitant systemic glucocorticoid therapy was higher than in those treated with EGFR-TKI monotherapy (HR 1.47, 95% CI 1.08-2.01). Afatinib or erlotinib use was associated with a lower risk of treatment failure in patients with advanced NSCLC harboring EGFR mutations compared to gefitinib use. Concurrent use of systemic glucocorticoids was linked to higher risk of treatment failure.

Indexed as

Asian PeopleCarcinoma, Non-Small-Cell LungLung NeoplasmsAfatinibAgedAged, 80 and overAntacidsAntineoplastic Combined Chemotherapy ProtocolsErbB ReceptorsErlotinib HydrochlorideFemaleGefitinibHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMaleMetforminAfatinibAntacidsEGFR protein, humanErbB ReceptorsErlotinib HydrochlorideGefitinibHydroxymethylglutaryl-CoA Reductase InhibitorsMetforminNeoplasm ProteinsProtein Kinase InhibitorsSteroids

Identifiers

PMID32917914
PMCPMC7486374
OpenAlexW3086847943

What OpenQuestion holds

Textmetadata
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.