Evidence map›Paper›PMID 39540676›Full record

ArticleCancer reports (Hoboken, N.J.)2024

A Case of Advanced Biliary Tract Cancer With EGFR Amplification That Responded to Necitumumab.

Makoto Sugimori, Masaki Nishimura, Kazuya Sugimori, Sho Tsuyuki, Akane Hirotani, Haruo Miwa, Takashi Kaneko, Haruka Hirose, Yoshiaki Inayama, Akito Nozaki and 3 more

Abstract readCase Reports
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Makoto SugimoriDivision of Cancer Genome Medicine, Yokohama City University Medical Center, Yokohama, Japan.ORCID 0000-0001-5272-5167
Masaki NishimuraGastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
Kazuya SugimoriGastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
Sho TsuyukiDivision of Cancer Genome Medicine, Yokohama City University Medical Center, Yokohama, Japan.
Akane HirotaniDivision of Cancer Genome Medicine, Yokohama City University Medical Center, Yokohama, Japan.
Haruo MiwaGastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
Takashi KanekoGastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
Haruka HiroseDivision of Genomics Laboratory, Yokohama City University Medical Center, Yokohama, Japan.
Yoshiaki InayamaDivision of Genomics Laboratory, Yokohama City University Medical Center, Yokohama, Japan.
Akito NozakiGastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
Kazushi NumataGastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
Chikara KunisakiDivision of Cancer Genome Medicine, Yokohama City University Medical Center, Yokohama, Japan.
Shin MaedaDepartment of Gastroenterology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

Funding

Kihara memorial Yokohama Foundation for the Advancement of Life Science 2022,1046-28Yokohama City University Research Grant for the Promotion of Advanced Medicine
6 · The paper itself

Abstract

backgroundRecent advances in cancer genome analysis and the practice of precision medicine have made it possible to identify fractions with rare genetic alterations. Among biliary tract cancers, EGFR-amplified cancers are known to be rare fractions across organs and have a poor prognosis. The use of anti-EGFR antibody for EGFR-amplified cancers has been promising; however, the evidence is not yet clear. CASE: In this report, we describe the case of a 48-year-old man diagnosed with advanced gallbladder cancer. The patient was administered gemcitabine plus cisplatin, followed by S-1 monotherapy; however, disease progression was observed after two cycles of each regimen. Comprehensive genomic profiling test revealed EGFR-amplification, and the patient was treated with combination therapy with the anti-EGFR antibody necitumumab, gemcitabine, and cisplatin. After two cycles of treatment, tumor size reduced, and the treatment response was evaluated as partial response. On Day 90, after five cycles of treatment, tumor progression was confirmed. In addition, after disease progression, liquid biopsy revealed acquired pathogenic gene alterations suggesting anti-EGFR antibody resistance.

conclusionThis report supports the clinical benefit of anti-EGFR antibodies for EGFR-amplified biliary tract cancers and the importance of genomic analysis in personalized therapy and drug resistance research.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsErbB ReceptorsGene AmplificationBiliary Tract NeoplasmsCisplatinDeoxycytidineGallbladder NeoplasmsGemcitabineHumansMaleMiddle AgedTreatment OutcomeAntibodies, Monoclonal, HumanizedCisplatinDeoxycytidineEGFR protein, humanErbB ReceptorsGemcitabinenecitumumabbiliary tract cancercase reportdrug resistanceEGFRliquid biopsy

Identifiers

PMID39540676
PMCPMC11561843

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.