Evidence map›Paper›PMID 30007404›Full record

ArticleWorld journal of surgical oncology2018

Therapeutic and prophylactic gastrectomy in a family with hereditary diffuse gastric cancer secondary to a CDH1 mutation: a case series.

Olsi Gjyshi, Pankaj Vashi, Laura Seewald, Mitra Kohan, Elham Abboud, Eric Fowler, Revathi Suppiah, Hatem Halabi

Open access · goldAbstract readCase Reports
In one paragraph

Article in World journal of surgical oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Prophylactic laparoscopic total gastrectomy for gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS): the first report in Asia.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2022
    Article
  7. Cancers · 2021
    Article
  8. Article
  9. First report of a Mexican family with mutation in the CDH1 gene.Molecular genetics & genomic medicine · 2020
    Article
  10. Review
  11. 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

8 authors at 4 institutions in 1 country.

Olsi GjyshiPresence Saint Joseph Hospital, Chicago, IL, USA.
Pankaj VashiCancer Treatment Centers of America, Zion, IL, USA.
Laura SeewaldUniversity of Michigan, Ann Arbor, MI, USA.
Mitra KohanChicago Medical School, North Chicago, IL, USA.
Elham AbboudCancer Treatment Centers of America, Zion, IL, USA.
Eric FowlerCancer Treatment Centers of America, Zion, IL, USA.
Revathi SuppiahCancer Treatment Centers of America, Zion, IL, USA.
Hatem HalabiCancer Treatment Centers of America, Zion, IL, USA. hatem.halabi@ctca-hope.com.ORCID http://orcid.org/0000-0001-7261-558X
Cancer Treatment Centers of America · USPresence Saint Joseph Hospital · USRosalind Franklin University of Medicine and Science · USUniversity of Michigan · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastric cancer is the fifth most prevalent and the third most lethal cancer worldwide, causing approximately 720,000 deaths annually. Although most cases of gastric cancers are sporadic, one of its inherited forms, hereditary diffuse gastric cancer (HDGC), constitutes about 1-3% of cases. Interestingly, females in families with HDGC are also predisposed to developing lobular breast cancer (LBC). Recent analyses have identified loss-of-function germline mutations in cadherein-1 (CDH1) as a culprit in HDGC and LBC. This discovery fueled several sequencing analyses and case series reports analyzing the pattern of inheritance of CDH1 and its propensity to induce HDGC. In 2015, a multinational and multidisciplinary task force updated the guidelines and criteria for screening, diagnosing, and managing HDGC. CASE PRESENTATION: Here, we present a case series of three siblings with family history of HDGC who tested positive for the CDH1 mutation and describe their surgical treatment course, post-operative management, and follow-up as they pertain to the updated guidelines.

conclusionsDespite recent updates in guidelines in the diagnosis and management of HDGC, the disease remains challenging to address with patients given the high level of uncertainty and the comorbidities associated with prophylactic intervention. We strongly recommend that an interdisciplinary team inclusive of clinical and surgical oncologists, along with geneticists, social work, and psychological support, should follow the patients in a longitudinal and comprehensive manner in order to achieve full recovery and return to normalcy, as with our patients.

Indexed as

AdultAntigens, CDCadherinsCarcinoma, Signet Ring CellFemaleGastrectomyGenetic Predisposition to DiseaseGerm-Line MutationHumansLoss of Function MutationMaleNeoplastic Syndromes, HereditaryPrognosisProphylactic Surgical ProceduresStomach NeoplasmsYoung AdultAntigens, CDCadherinsCDH1 protein, humanCadherin-1 (CDH1)Hereditary diffuse gastric cancer (HDGC)Lobular breast cancer (LBC)

Identifiers

PMID30007404
PMCPMC6046101
OpenAlexW2883336789

What OpenQuestion holds

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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.