Evidence map›Paper›PMID 35434933›Full record

ArticleCancer medicine2022

Impact of pre-existing interstitial lung abnormal shadow on lung injury development and severity in patients of non-small cell lung cancer treated with osimertinib.

Ryota Shibaki, Yuichi Ozawa, Susumu Noguchi, Yusuke Murakami, Eri Takase, Yuichiro Azuma, Masaru Maebeya, Takeya Sugimoto, Atsushi Hayata, Takahiro Hayakawa and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2022. 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
1.8field-weighted citation impact, top 14% 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, 13 citations in OpenAlex.

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  6. Is MG53 a potential therapeutic target for cancer?Frontiers in endocrinology · 2023
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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

14 authors at 7 institutions in 1 country.

Ryota ShibakiInternal Medicine III, Wakayama Medical University, Wakayama, Japan.
Yuichi OzawaInternal Medicine III, Wakayama Medical University, Wakayama, Japan.ORCID 0000-0003-3798-3488
Susumu NoguchiRespiratory Medicine, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.
Yusuke MurakamiRespiratory Medicine, National Hospital Organization Minami Wakayama Medical Center, Wakayama, Japan.
Eri TakaseDepartment of Respiratory Medicine, Naga Municipal Hospital, Wakayama, Japan.
Yuichiro AzumaRespiratory Medicine, National Hospital Organization Wakayama Hospital, Wakayama, Japan.
Masaru MaebeyaRespiratory Medicine, Wakayama Rosai Hospital, Wakayama, Japan.
Takeya SugimotoInternal Medicine III, Wakayama Medical University, Wakayama, Japan.
Atsushi HayataInternal Medicine III, Wakayama Medical University, Wakayama, Japan.
Takahiro HayakawaInternal Medicine, Kinan Hospital, Wakayama, Japan.
Shinya TamakiThe Second Department of Internal Medicine, Hidaka General Hospital, Wakayama, Japan.
Masanori NakanishiInternal Medicine III, Wakayama Medical University, Wakayama, Japan.
Shunsuke TeraokaInternal Medicine III, Wakayama Medical University, Wakayama, Japan.
Hiroaki AkamatsuInternal Medicine III, Wakayama Medical University, Wakayama, Japan.
Wakayama Medical University · JPNational Hospital Organization · JPHidaka Hospital · JPJapanese Red Cross Society Wakayama Medical Center · JPKinan Hospital · JPNaga Municipal Hospital · JPWakayama Rosai Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFirst-generation epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) sometimes causes lung injury, thereby affecting survival. Although pre-existing interstitial lung abnormal shadow (pre-ILS) increases the risk of lung injury by EGFR-TKIs, its impact on osimertinib, a third-generation EGFR-TKI, remains unknown. PATIENTS AND

methodsThis retrospective cohort study consecutively enrolled patients of EGFR-mutated non-small cell lung cancer treated with osimertinib. Computed tomography images were obtained and evaluated independently by three pulmonologists in a blinded manner. Factors associated with lung injury were assessed using a logistic regression model. Survival curves were calculated by the Kaplan-Meier method and compared using a log-rank test.

resultsOf the 195 patients, 40 had pre-ILS, and 21 (8 with and 13 without pre-ILS) developed lung injury during the observation period. Multivariate analysis revealed that pre-ILS was independently associated with lung injury (odds ratio, 3.1; 95% confidence interval [CI], 1.1-8.2; p = 0.025). Severe (≥Grade 3) lung injury was observed in eight (4.1%) patients, of whom, two (5%) and six (3.9%) had and did not have pre-ILS (p = 0.67), respectively. Grade 5 lung injury was not observed, and survival curves were similar between the patients who developed lung injury and those who did not (median 11 vs. 12 months; hazard ratio, 1.2; 95% CI, 0.56-2.7; p = 0.60).

conclusionsPre-ILS increased the risk of lung injury in patients of non-small cell lung cancer treated with osimertinib, while the severity of lung injury was not clearly affected by the presence of pre-ILS.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAcrylamidesAniline CompoundsErbB ReceptorsHumansIndolesLungMutationProtein Kinase InhibitorsPyrimidinesRetrospective StudiesAcrylamidesAniline CompoundsErbB ReceptorsIndolesosimertinibProtein Kinase InhibitorsPyrimidinesepidermal growth factor receptorinterstitial lung abnormalitieslung injurynon-small cell lung cancer

Identifiers

PMID35434933
PMCPMC9582680
OpenAlexW4223901505

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.