Evidence map›Paper›PMID 35670186›Full record

ArticleThoracic cancer2022

Lymphovascular invasion: A non-sized T descriptor for stage IA non-small cell lung cancer.

Jing-Sheng Cai, Xun Wang, Fei Yang, Yun Li, Man-Tang Qiu

Abstract read
In one paragraph

Article in Thoracic cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

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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

5 authors.

Jing-Sheng CaiDepartment of Thoracic Surgery, Peking University People's Hospital, Beijing, People's Republic of China.ORCID 0000-0003-3859-7159
Xun WangDepartment of Thoracic Surgery, Peking University People's Hospital, Beijing, People's Republic of China.
Fei YangDepartment of Pathology, Peking University People's Hospital, Beijing, People's Republic of China.
Yun LiDepartment of Thoracic Surgery, Peking University People's Hospital, Beijing, People's Republic of China.
Man-Tang QiuDepartment of Thoracic Surgery, Peking University People's Hospital, Beijing, People's Republic of China.ORCID 0000-0002-0419-9139

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLymphovascular invasion (LVI) has not been included in the tumor-node-metastasis (TNM) staging manual of non-small-cell lung cancer (NSCLC). We aimed to investigate the predictive value of LVI on stage IA NSCLC and proposed a method of incorporating LVI into the T category based on the latest TNM staging manual.

methodsThe least absolute shrinkage and selection operator (LASSO)-penalized Cox multivariable regression model was performed to identify prognostic factors. The Kaplan-Meier method was used to compare overall survival (OS) and disease-free survival (DFS) between groups. Propensity score matching (PSM) was used to minimize bias.

resultsA total of 1452 eligible stage I NSCLC cases (stage IA without LVI, 1022 cases; stage IA with LVI, 120 cases; stage IB, 310 cases) were included. LASSO-penalized multivariable Cox analysis revealed that LVI was an independent prognostic factor for both OS and DFS. Survival analysis demonstrated that the survivals of stage IA NSCLCs without LVI were better than those of stage IA with LVI and stage IB NSCLCs. In the matched cohort, the survivals of stage IA NSCLCs with LVI were comparable to those of stage IB NSCLCs.

conclusionsStage IA NSCLCs with LVI and stage IB NSCLCs had similar survivals, and we proposed that LVI might be a non-sized T descriptor that upstaged stage IA diseases to stage IB.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsHumansNeoplasm InvasivenessNeoplasm StagingPrognosisRetrospective Studieslymphovascular invasionnon-small-cell lung cancerTNM stageupstage

Identifiers

PMID35670186
PMCPMC9436680

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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.