Evidence map›Paper›PMID 35585358›Full record

ArticleInternational journal of colorectal disease2022

Prospective analysis of the expression status of FGFR2 and HER2 in colorectal and gastric cancer populations: DS-Screen Study.

Hisateru Yasui, Atsushi Takeno, Hiroki Hara, Hiroshi Imamura, Hiroki Akamatsu, Kazumasa Fujitani, Minoru Nakane, Chihiro Nakayama Kondoh, Seigo Yukisawa, Junichiro Nasu and 9 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of colorectal disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 31% 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, 10 citations in OpenAlex.

  1. Advancements in targeted therapy for gastric cancer.Therapeutic advances in gastroenterology · 2026
    Review
  2. Article
  3. HER2-targeted therapies beyond breast cancer - an update.Nature reviews. Clinical oncology · 2024
    Review
  4. Article
  5. Targeting FGFR for cancer therapy.Journal of hematology & oncology · 2024
    Review
  6. Review
  7. Chemotherapeutic Activity of Imidazolium-Supported Pd(II)Pharmaceuticals (Basel, Switzerland) · 2023
    Article
  8. Review
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

19 authors at 16 institutions in 1 country.

Hisateru YasuiKobe City Medical Center General Hospital, Hyogo, Japan.
Atsushi TakenoKansai Rosai Hospital, Hyogo, Japan.
Hiroki HaraSaitama Cancer Center, Saitama, Japan.
Hiroshi ImamuraToyonaka Municipal Hospital, Osaka, Japan.
Hiroki AkamatsuOsaka Police Hospital, Osaka, Japan.
Kazumasa FujitaniOsaka General Medical Center, Osaka, Japan.
Minoru NakaneJapanese Red Cross Musashino Hospital, Tokyo, Japan.
Chihiro Nakayama KondohToranomon Hospital, Tokyo, Japan.
Seigo YukisawaTochigi Cancer Center, Tochigi, Japan.
Junichiro NasuOkayama Saiseikai General Hospital, Okayama, Japan.
Yoshinori MiyataSaku Central Hospital Advanced Care Center, Nagano, Japan.
Akitaka MakiyamaJapan Community Healthcare Organization Kyushu Hospital, Fukuoka, Japan.
Hiroyasu IshidaMito Medical Center, Ibaraki, Japan.
Norimasa YoshidaJapanese Red Cross Kyoto Daiichi Hospital, Kyoto, Japan.
Eiji MatsumuraDaiichi Sankyo Co., Ltd, Tokyo, Japan.
Masato IshigamiDaiichi Sankyo Co., Ltd, Tokyo, Japan.
Masahiro SugiharaDaiichi Sankyo Co., Ltd, Tokyo, Japan.
Atsushi OchiaiNational Cancer Center Exploratory Oncology Research & Clinical Trial Center, Tokyo, Japan.
Toshihiko DoiNational Cancer Center Hospital East, Chiba, Japan. tdoi@east.ncc.go.jp.
Daiichi-Sankyo (Japan) · JPGifu University Hospital · JPKansai Rosai Hospital · JPKobe City Medical Center General Hospital · JPKyoto first Red Cross hospital · JPMusashino Red Cross Hospital · JPNational Cancer Center Hospital East · JPNational Hospital Organization Mito Medical Center · JPOkayama Saiseikai General Hospital · JPOsaka Police Hospital · JPOsaka Prefectural Medical Center · JPSaitama Cancer Center · JPSaku Central Hospital · JPTochigi Cancer Center · JPToranomon Hospital · JPToyonaka Municipal Hospital · JP

Funding

AbbVie grants and personal feesAmgen personal feesAstellas Pharma grantsAstellas Pharma Personal feesAstraZeneca grantsBayer Yakuhin grants and personal feesBayer Yakuhin Personal feBeiGene grantsBoehringer Ingelheim grants and personal feesBristol-Myers Squibb grants and personal feesBristol-Myers Squibb honorariaChugai Pharmaceutical grants and personal feesChugai Pharmaceutical Personal feesDaiichi-Sankyo Grant and Personal FeeDaiichi-Sankyo grants and personal feesDaiichi-Sankyo honorariaDaiichi Sankyo Company research fundingDainippon Sumitomo Pharma grants and personal feesEisai grantsElevar Therapeutics grantsEli Lilly Japan grantsEli Lilly Japan honorariaEli Lilly Japan Personal feesGSK grantsIncyte grantsJanssen Pharmaceuticals grants and personal feesKyowa Kirin Personal feesMerck Biopharma grants and personal feesMerck Serono grantsMSD K.K. grants and personal feesNovartis grants and personal feesOncolys BioPharma Personal feesOno Pharmaceutical grants and personal feesOno Pharmaceutical honorariaOno Pharmaceutical Personal feesOtsuka Pharmaceutical Personal feesPfizer grantsPfizer Japan grantsQuintiles (IQVIA) grantsRakuten Medical Personal feesSanofi Personal feesTaiho Pharmaceutical grants and personal feesTaiho Pharmaceutical honorariaTakeda Pharmaceutical Company Personal feesYakult Honsha Personal fees
6 · The paper itself

Abstract

purposeFibroblast growth factor receptor 2 (FGFR2) and human epidermal growth factor receptor 2 (HER2) proteins are both molecular targets for cancer therapy. The objective of this study was to evaluate the expression status of FGFR2 and HER2 in patients with gastric cancer (GC) or colorectal cancer (CRC).

methodsArchived tumor tissue samples from patients with histologically-confirmed GC or CRC suitable for chemotherapy were analyzed for FGFR2 and HER2 expression using immunohistochemistry and fluorescence in situ hybridization (HER2 in CRC only).

resultsA total of 176 GC patients and 389 CRC patients were enrolled. Among patients with GC, 25.6% were FGFR2-positive and 26.1% were HER2-positive. Among patients with CRC, 2.9% were FGFR2-positive and 16.2% were HER2-positive. No clear relationship was found between FGFR2 and HER2 status in either GC or CRC. In GC, FGFR2 and HER2 statuses did not differ between different primary cancer locations, whereas there were some differences between histological types. Based on FGFR2- and/or HER2-positive status, 117 patients were identified as potentially suitable for inclusion in clinical trials of therapeutic agents targeting the relevant protein (GC = 45, CRC = 72; FGFR = 56, HER2 = 62), of whom 7 were eventually enrolled into such clinical trials.

conclusionsThis study indicated the prevalence of FGFR2 and HER2 in GC and CRC in the Japanese population. The screening performed in this study could be useful for identifying eligible patients for future clinical trials of agents targeting these proteins.

trial registrationClinical trial registration Japic CTI No.: JapicCTI-163380.  https://www. CLINICALTRIALS: jp/cti-user/trial/ShowDirect.jsp?directLink=RNlzx1PPCuT.PrVNPxPRwA .

Indexed as

Colorectal NeoplasmsStomach NeoplasmsErb-b2 Receptor Tyrosine KinasesHumansIn Situ Hybridization, FluorescenceReceptor, Fibroblast Growth Factor, Type 2ERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesFGFR2 protein, humanReceptor, Fibroblast Growth Factor, Type 2Colorectal cancerFGFR2Gastric cancerHER2

Identifiers

PMID35585358
PMCPMC9167213
OpenAlexW4280512930

What OpenQuestion holds

Textmetadata
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.