Evidence map›Paper›PMID 31558980›Full record

ArticleWorld journal of gastrointestinal oncology2019

Gallbladder cancer harboring

Chiaki Inagaki, Daichi Maeda, Akie Kimura, Toru Otsuru, Yoshifumi Iwagami, Naohiro Nishida, Daisuke Sakai, Ryo Shitotsuki, Shinichi Yachida, Yuichiro Doki and 1 more

Open access · hybridAbstract readCase Reports
In one paragraph

Article in World journal of gastrointestinal oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Overview of current targeted therapy in gallbladder cancer.Signal transduction and targeted therapy · 2020
    Review
  5. 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 2 institutions in 1 country.

Chiaki InagakiDepartment of Frontier Science for Cancer and Chemotherapy, Osaka University Graduate School of Medicine, Suita 5650871, Osaka, Japan.
Daichi MaedaDepartment of Clinical Genomics, Osaka University Graduate School of Medicine, Suita 5650871, Osaka, Japan.
Akie KimuraDepartment of Frontier Science for Cancer and Chemotherapy, Osaka University Graduate School of Medicine, Suita 5650871, Osaka, Japan.
Toru OtsuruDepartment of Frontier Science for Cancer and Chemotherapy, Osaka University Graduate School of Medicine, Suita 5650871, Osaka, Japan.
Yoshifumi IwagamiDepartment of Gastroenterological Surgery, Osaka University Graduate School of Medicine, Suita 5650871, Osaka, Japan.
Naohiro NishidaDepartment of Frontier Science for Cancer and Chemotherapy, Osaka University Graduate School of Medicine, Suita 5650871, Osaka, Japan.
Daisuke SakaiDepartment of Frontier Science for Cancer and Chemotherapy, Osaka University Graduate School of Medicine, Suita 5650871, Osaka, Japan.
Ryo ShitotsukiCenter for Cancer Genomics and Personalized Medicine, Osaka University Graduate School of Medicine, Suita 5650871, Osaka, Japan.
Shinichi YachidaDepartment of Cancer Genome Informatics, Osaka University Graduate School of Medicine, Suita 5650871, Osaka, Japan.
Yuichiro DokiDepartment of Gastroenterological Surgery, Osaka University Graduate School of Medicine, Suita 5650871, Osaka, Japan.
Taroh SatohDepartment of Frontier Science for Cancer and Chemotherapy, Osaka University Graduate School of Medicine, Suita 5650871, Osaka, Japan. taroh@cfs.med.osaka-u.ac.jp.
The University of Osaka · JPOsaka Gakuin University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBile duct cancer constitutes gallbladder cancer (GBC), intrahepatic cholangiocarcinoma (ICA), and extrahepatic cholangiocarcinoma (ECA). These three entities show morphological and immunohistochemical resemblance so that it is difficult to differentiate between primary ICA and liver metastasis of GBC, which sometimes becomes a point of discussion in clinical practice. Although these cancers demonstrate significant differences in their mutational landscape, several reports demonstrated shared genomic alteration in paired primary and metastatic site aids in distinguishing metastatic recurrence from second primary cancers. CASE SUMMARY: We present a 73-year-old female patient who underwent curative resection for GBC harboring epidermal growth factor receptor 2 (ERBB2) activating mutation on next-generation sequencing (NGS)-based genomic testing. One year later, a hepatic lesion was observed on follow-up imaging and she underwent surgical resection for a pathological diagnosis. The histological findings of the hepatic lesion were similar to those of the primary lesion. Additionally, using NGS panel testing, the hepatic lesion was found to have

conclusionThis case illustrated NGS panel usefulness in distinguishing GBC recurrence from second primary cancer and

Indexed as

Bile duct cancerCase reportERBB2 mutationGall bladder cancerMutation-driven targeted treatmentPrecision medicine

Identifiers

PMID31558980
PMCPMC6755105
OpenAlexW2972418573

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.