Evidence map›Paper›PMID 42089553›Full record

ArticleJournal of hepato-biliary-pancreatic sciences2026

Feasibility of Comprehensive Genomic Profiling for Biliary Tract Cancer Using Transpapillary Biopsy Samples: A Prospective Study.

Kazuya Miyamoto, Kazuyuki Matsumoto, Toshiaki Ohara, Masayoshi Fujisawa, Hirohumi Inoue, Ryosuke Sato, Akihiro Matsumi, Yuki Fujii, Daisuke Uchida, Motoyuki Otsuka

Abstract readClinical Study
In one paragraph

Article in Journal of hepato-biliary-pancreatic sciences, 2026. 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

10 authors.

Kazuya MiyamotoDepartment of Gastroenterology and Hepatology, Okayama University Hospital, Okayama, Japan.
Kazuyuki MatsumotoDepartment of Endoscopy, Okayama University Hospital, Okayama, Japan.ORCID https://orcid.org/0000-0002-5102-7452
Toshiaki OharaDepartment of Pathology and Experimental Medicine, Okayama University Hospital, Okayama, Japan.
Masayoshi FujisawaDepartment of Pathology and Experimental Medicine, Okayama University Hospital, Okayama, Japan.
Hirohumi InoueDepartment of Medical Support, Okayama University Hospital, Okayama, Japan.
Ryosuke SatoDepartment of Gastroenterology and Hepatology, Okayama University Hospital, Okayama, Japan.ORCID https://orcid.org/0000-0002-5368-6347
Akihiro MatsumiDepartment of Endoscopy, Okayama University Hospital, Okayama, Japan.
Yuki FujiiDepartment of Endoscopy, Okayama University Hospital, Okayama, Japan.
Daisuke UchidaDepartment of Gastroenterology and Hepatology, Okayama University Hospital, Okayama, Japan.
Motoyuki OtsukaDepartment of Gastroenterology and Hepatology, Okayama University Hospital, Okayama, Japan.ORCID https://orcid.org/0000-0003-2869-2881

Funding

JSPS KAKENHI 24K21142
6 · The paper itself

Abstract

backgroundPatients with biliary tract cancer (BTC) often have actionable mutations, and comprehensive genomic profiling (CGP) plays an important role. However, the feasibility of CGP using transpapillary biopsy (TPB) samples remains unclear.

methodsThirty patients with suspected BTC based on radiographic imaging were enrolled. Pre-analytical criteria for CGP suitability were based on the OncoGuide NCC Oncopanel System (NCCOP) and FoundationOne CDx (F1CDx). Each patient underwent six biopsies using an endoscopic introducer: five biopsy samples were preserved as formalin-fixed paraffin-embedded (FFPE) samples and one as a fresh frozen (FF) sample. DNA quality indicators were compared between the two groups.

resultsMalignancy was confirmed in 29 patients, and one had a benign biliary stricture. Suitability rate was 31% (9/29) for NCCOP and 3.4% (1/29) for F1CDx. Compared to FFPE samples, FF samples demonstrated significantly higher DNA concentration [ng/μL, interquartile range (IQR)], [0.34 (0.16-0.95) vs. 37.8 (11.6-67.6), p < 0.001] and DNA integrity number (IQR) [7.1 (6.8-7.3) vs. 8.9 (8.3-9), p = 0.021].

conclusionsIntroducer-assisted multipass TPB may increase the rate of obtaining adequate CGP specimens, but its suitability remains limited and strongly panel dependent. Since FF samples have better DNA quality, establishing a system detailing their use is desirable.

trial registrationClinicalTrials.gov identifier: UMIN 000049826.

Indexed as

Biliary Tract NeoplasmsGene Expression ProfilingAgedBiopsyFeasibility StudiesFemaleHumansMaleMiddle AgedProspective Studiesbiliary tract cancerbiopsyDNAendoscopic retrograde cholangiopancreatographygenetic profile

Identifiers

PMID42089553
PMCPMC13485206

What OpenQuestion holds

Textmetadata
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.