Evidence map›Paper›PMID 36890418›Full record

ArticleSurgical endoscopy2023

Endoscopic resection of gastric low-grade dysplasia with high risk factors is associated with decreased advanced neoplasia: a single-center retrospective cohort study.

Lang Yang, Xian-Zong Ma, Xin Wang, Jun-Feng Xu, Heng Zhang, Yu-Rong Tao, Na Li, Hui Su, Yu-Qi He, Jian-Qiu Sheng and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Surgical endoscopy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Guideline
  2. 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

11 authors at 1 institution in 1 country.

Lang Yang *Department of Gastroenterology, The First Medical Center of Chinese PLA General Hospital, Beijing, 100853, China.
Xian-Zong Ma *Department of Gastroenterology, The Seventh Medical Center of Chinese PLA General Hospital, No. 5 Nan Men Cang, Dong Cheng District, Beijing, 100700, China.
Xin Wang *Department of Gastroenterology, The Seventh Medical Center of Chinese PLA General Hospital, No. 5 Nan Men Cang, Dong Cheng District, Beijing, 100700, China.
Jun-Feng XuDepartment of Gastroenterology, The First Medical Center of Chinese PLA General Hospital, Beijing, 100853, China.
Heng ZhangDepartment of Gastroenterology, The Seventh Medical Center of Chinese PLA General Hospital, No. 5 Nan Men Cang, Dong Cheng District, Beijing, 100700, China.
Yu-Rong TaoDepartment of Gastroenterology, The First Medical Center of Chinese PLA General Hospital, Beijing, 100853, China.
Na LiDepartment of Gastroenterology, The First Medical Center of Chinese PLA General Hospital, Beijing, 100853, China.
Hui SuDepartment of Gastroenterology, The Seventh Medical Center of Chinese PLA General Hospital, No. 5 Nan Men Cang, Dong Cheng District, Beijing, 100700, China.
Yu-Qi HeDepartment of Gastroenterology, The Seventh Medical Center of Chinese PLA General Hospital, No. 5 Nan Men Cang, Dong Cheng District, Beijing, 100700, China.
Jian-Qiu ShengDepartment of Gastroenterology, The First Medical Center of Chinese PLA General Hospital, Beijing, 100853, China. shengjianqiu@301hospital.com.cn.
Peng JinDepartment of Gastroenterology, The First Medical Center of Chinese PLA General Hospital, Beijing, 100853, China. jinpeng@301hospital.com.cn.ORCID 0000-0003-2402-4472
Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe natural course of gastric low-grade dysplasia (LGD) remains unclear, and there are inconsistent management recommendations among guidelines and consensus.

objectiveThis study aimed to investigate the incidence of advanced neoplasia in patients with gastric LGD and identify the related risk factors.

methodsCases of biopsy demonstrated LGD (BD-LGD) at our center from 2010 to 2021 were reviewed retrospectively. Risk factors related to histological progression were identified, and outcomes of patients based on risk stratification were evaluated.

resultsNinety-seven (23.0%) of 421 included BD-LGD lesions were diagnosed as advanced neoplasia. Among 409 superficial BD-LGD lesions, lesion in the upper third of the stomach, H. pylori infection, larger size, and narrow band imaging (NBI)-positive findings were independent risk factors of progression. NBI-positive lesions and NBI-negative lesions with or without other risk factors had 44.7%, 1.7%, and 0.0% risk of advanced neoplasia, respectively. Invisible lesions, visible lesions (VLs) without a clear margin, and VLs with a clear margin and size ≤ 10 mm, or > 10 mm had 4.8%, 7.9%, 16.7%, and 55.7% risk of advanced neoplasia, respectively. In addition, endoscopic resection decreased the risk of cancer (P < 0.001) and advanced neoplasia (P < 0.001) in patients with NBI-positive lesions, but not in NBI-negative patients. Similar results were found in patients with VLs with clear margin and size > 10 mm. Moreover, NBI-positive lesions had higher sensitivity and lower specificity for predicting advanced neoplasia than VLs with a clear margin and size > 10 mm determined by white-light endoscopy (97.6% vs. 62.7%, P < 0.001; and 63.0% vs. 85.6%, P < 0.001, respectively).

conclusionProgression of superficial BD-LGD is associated with NBI-positive lesions, as well as with VLs with a clear margin (size > 10 mm) if NBI is unavailable, and selective resection of those lesions offers benefits for patients by decreasing the risk of advanced neoplasia.

Indexed as

Precancerous ConditionsStomach NeoplasmsEndoscopyHumansNarrow Band ImagingRetrospective StudiesRisk FactorsStomachEndoscopic resectionLow-grade dysplasiaOutcomeRisk factorsStomach neoplasms

Identifiers

PMID36890418
OpenAlexW4323542853

What OpenQuestion holds

Textmetadata
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.