Evidence map›Paper›PMID 42761668›Full record

ArticleExploration of targeted anti-tumor therapy2026

Significance of next-generation sequencing in the era of targeted therapy for biliary tract cancer: an analysis at a single institution.

Kei Nakagawa, Hideaki Sato, Masahiro Iseki, Daisuke Douchi, Shuichi Aoki, Michiaki Unno

Abstract read
In one paragraph

Article in Exploration of targeted anti-tumor therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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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

6 authors.

Kei NakagawaDepartment of Surgery, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.ORCID https://orcid.org/0000-0002-3058-5674
Hideaki SatoDepartment of Surgery, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.ORCID https://orcid.org/0009-0006-9688-4956
Masahiro IsekiDepartment of Surgery, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.ORCID https://orcid.org/0000-0002-4954-3810
Daisuke DouchiDepartment of Surgery, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.ORCID https://orcid.org/0000-0003-4582-6589
Shuichi AokiDepartment of Surgery, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.ORCID https://orcid.org/0000-0003-4221-0236
Michiaki UnnoDepartment of Surgery, Tohoku University Graduate School of Medicine, Sendai 980-8574, Japan.ORCID https://orcid.org/0000-0002-2145-6416

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: Treatment approaches for biliary tract cancer (BTC) vary widely. Genomic profiling through next-generation sequencing (NGS) has made it possible to apply precision medicine in the management of BTC. This retrospective observational study aimed to evaluate the implementation of treatments based on identified genomic mutations and their clinical significance in patients with BTC in Japan, where NGS is covered by health insurance. Methods: We conducted a retrospective analysis of 65 patients with unresectable or recurrent BTC who underwent comprehensive genomic profiling at a single institution between November 2019 and October 2024. Genomic mutations were classified according to the ESMO Scale for Clinical Actionability of molecular Targets (ESCAT) scale. Overall survival (OS) was estimated using the Kaplan-Meier method and compared using the log-rank test. Results: Among the 65 patients, clinically relevant genomic mutations classified using the ESCAT scale were identified in 47 patients, and clinically treatable genomic mutations were identified in 13 patients. Six patients ultimately received mutation-guided therapy, including fibroblast growth factor receptor inhibitors and pembrolizumab. The median time from specimen submission to review by the expert panel was 26 (range, 16-40) days. No significant difference in OS was observed based on the site of the primary tumor (log-rank test, Conclusions: Although clinically actionable genomic mutations were identified in one-fifth of patients, < 10% ultimately received treatment based on those findings, highlighting a gap between genomic profiling and treatment implementation. In contrast, with the increasing number of available therapies, access to precision treatment for patients with BTC may improve in the future through a combination of early adoption of NGS and the complementary use of liquid biopsy when tissue is unavailable.

Indexed as

biliary tract cancerESCATmolecular target drugsnext-generation sequencingprecision medicinetargeted therapy

Identifiers

PMID42761668
PMCPMC13586963

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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.