Evidence map›Paper›PMID 32295332›Full record

ArticleGut and liver2021

Clinicopathologic Features of Submucosal Papillary Gastric Cancer Differ from Those of Other Differentiated-Type Histologies.

Seung Yong Shin, Jie-Hyun Kim, Myeong-Cherl Kook, Do Youn Park, Keun Won Ryu, Il Ju Choi, Sung Hoon Noh, Hyunki Kim, Yong Chan Lee

Open access · diamondAbstract read
In one paragraph

Article in Gut and liver, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 17% 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, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
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  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Seung Yong ShinDepartment of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID 0000-0001-8970-2444
Jie-Hyun KimDepartment of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID 0000-0002-9198-3326
Myeong-Cherl KookDepartment of Pathology, Center for Gastric Cancer, National Cancer Center, Goyang, Korea.ORCID 0000-0002-3435-3301
Do Youn ParkDepartment of Pathology, Pusan National University Hospital, Pusan National University School of Medicine, Busan, Korea.ORCID 0000-0001-7641-1509
Keun Won RyuDepartment of Surgery, Center for Gastric Cancer, National Cancer Center, Goyang, Korea.ORCID 0000-0002-5935-9777
Il Ju ChoiDepartment of Internal Medicine, Center for Gastric Cancer, National Cancer Center, Goyang, Korea.ORCID 0000-0002-8339-9824
Sung Hoon NohDepartment of Surgery, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID 0000-0003-4386-6886
Hyunki KimDepartment of Pathology, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID 0000-0003-2292-5584
Yong Chan LeeDepartment of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID 0000-0001-8800-6906
Yonsei University · KRNational Cancer Center · KRNational Cancer Center · USPusan National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aims: Papillary gastric cancer (GC) is classified as differentiated adenocarcinoma, together with well-differentiated (WD) and moderately differentiated (MD) adenocarcinoma. This study evaluated the risk of lymph node metastasis (LNM) in submucosal (SM) invasive papillary GC compared with other differentiated early GC types. Methods: This retrospective study involved three tertiary hospitals and enrolled 1,798 lesions with differentiated SM invasive GC treated with curative gastrectomy between March 2001 and December 2012. All pathology slides were reviewed, and clinicopathologic findings associated with LNM, including tumor size, location, gross type, ulceration, depth and width of SM invasion, and lymphovascular invasion (LVI), were analyzed. Results: The proportion of SM papillary GC was 2.8% (n=51). SM papillary GC was associated with larger tumor size and deeper and wider SM invasion than other differentiated GC types. LNM was significantly higher in the papillary type than in the MD and WD types. LNM was found in 27.5% of SM papillary GC patients (WD: 9.0%, MD: 21.2%). LVI was the only significant risk factor for LNM in SM papillary GC. The depth or width of SM invasion was not associated with LNM in papillary GC. Lower third location or elevated gross appearance was significantly associated with LVI. Conclusions: SM papillary GC had the highest LNM rate, with features different from those of other differentiated SM invasive GCs. The treatment strategy for SM papillary GC should be carefully approached, especially for lesions located in the lower third or of the elevated gross type.

Indexed as

Stomach NeoplasmsGastrectomyGastric MucosaHumansLymph Node ExcisionNeoplasm InvasivenessRetrospective StudiesRisk FactorsAdenocarcinomaLymphatic metastasispapillaryRisk factorsStomach neoplasm

Identifiers

PMID32295332
PMCPMC7817937
OpenAlexW3017096772

What OpenQuestion holds

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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.