Evidence map›Paper›PMID 33822966›Full record

Observational studyJapanese journal of clinical oncology2021

Fibroblast growth factor receptor 2 (FGFR2) fusions in Japanese patients with intrahepatic cholangiocarcinoma.

Masanori Tsujie, Tomohisa Iwai, Shoji Kubo, Takashi Ura, Etsuro Hatano, Daisuke Sakai, Yutaka Takeda, Masaki Kaibori, Tomoe Kobayashi, Akio Katanuma and 2 more

Erratum issuedOpen access · hybridAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Japanese journal of clinical oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Observational
  7. Article
  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 16 institutions in 1 country.

Masanori TsujieDepartment of Surgery, Osaka Rosai Hospital, Osaka, Japan.ORCID 0000-0002-1265-3397
Tomohisa IwaiDepartment of Gastroenterology, Kitasato University Hospital, Sagamihara, Japan.
Shoji KuboDepartment of Hepato-Biliary-Pancreatic Surgery, Osaka City University Hospital, Osaka.
Takashi UraDepartment of Clinical Oncology, National Hospital Organization Kyoto Medical Center, Kyoto, Japan.
Etsuro HatanoDepartment of Gastroenterological Surgery, Hyogo College of Medicine, Nishinomiya, Japan.
Daisuke SakaiDepartment of Gastroenterological Surgery, Osaka University Hospital, Suita, Japan.
Yutaka TakedaDepartment of Gastroenterological Surgery, Kansai Rosai Hospital, Amagasaki, Japan.
Masaki KaiboriDepartment of Surgery, Kansai Medical University, Osaka, Japan.
Tomoe KobayashiDepartment of Gastroenterology and Hematology, Tomakomai City Hospital, Tomakomai, Japan.
Akio KatanumaCenter for Gastroenterology, Teine-Keijinkai Hospital, Sapporo, Japan.
Yu KatayoseDepartment of Hepato-Biliary Pancreatic Surgery, Tohoku Medical and Pharmaceutical University Hospital, Sendai, Japan.
Koji FukaseDepartment of Surgery, Japanese Red Cross Ishinomaki Hospital, Ishinomaki, Japan.
Hyogo Medical University · JPJapanese Red Cross Medical Center · JPKansai Medical University · JPKansai Rosai Hospital · JPKasugai Municipal Hospital · JPKitasato University Hospital · JPKyoto Medical Center · JPNational Institute of Technology, Tomakomai College · JPOgaki Municipal Hospital · JPOsaka City University Hospital · JPOsaka Hospital · JPOsaka Rosai Hospital · JPOsaka University Hospital · JPTeine Keijinkai Hospital · JPTohoku Medical and Pharmaceutical University Hospital · JPYamagata Prefectural Central Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveFibroblast growth factor receptor gene alterations have emerged as promising drug targets for intrahepatic cholangiocarcinoma, a rare cancer that has a poor prognosis. This study evaluated the frequency of fibroblast growth factor receptor 2 fusions in clinical specimens from Japanese patients with iCCA.

methodsThis study enrolled 116 patients who had histologically or cytologically confirmed adenocarcinoma and been diagnosed as relapsing after resection or with unresectable intrahepatic cholangiocarcinoma. We evaluated the frequency of fibroblast growth factor receptor 2 fusions-positive cells in their specimens using break-apart fluorescent in situ hybridization 'for 114 patients who met the study protocol'.

resultsOf a total of 114 cases, six (5.3%) were identified as fibroblast growth factor receptor 2 fusions-positive with a high frequency (87% or more) of fibroblast growth factor receptor 2 fusions-positive tumour cells whereas the remainder, with the exception of three cases with indeterminate results, were identified as fibroblast growth factor receptor 2 fusions-negative. The patients' baseline characteristics as well as their objective response rates, disease control rates, times to progression, and times to treatment failure with previous or ongoing first-line chemotherapy did not have any obvious relationship to the proportion of fibroblast growth factor receptor 2 fusions-positive case.

conclusionsFurther detailed elucidation of fibroblast growth factor receptor 2 fusion status is expected to contribute to the development of promising therapeutic options for patients suffering from recurrent or unresectable intrahepatic cholangiocarcinoma.

Indexed as

AdultAgedAged, 80 and overBile Duct NeoplasmsBile Ducts, IntrahepaticCholangiocarcinomaFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHumansIn Situ Hybridization, FluorescenceJapanMaleMiddle AgedNeoplasm Recurrence, LocalFGFR2 protein, humanOncogene Proteins, FusionReceptor, Fibroblast Growth Factor, Type 2break-apart fluorescent in situ hybridizationFGFR2 fusionsintrahepatic cholangiocarcinoma

Identifiers

PMID33822966
PMCPMC8448429
OpenAlexW3151233975

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.