Evidence map›Paper›PMID 40688855›Full record

ArticleCureus2025

Successful Treatment of BRAF V600E-Mutant Intrahepatic Cholangiocarcinoma With Encorafenib, Binimetinib, and Cetuximab.

Toshifumi Yamaguchi, Yoshinobu Hirose, Yasutaka Nakazawa, Akiko Kagotani, Hiroyuki Kodama, Hiroki Yukami, Shin Kameishi, Nanako Matsuo, Elham Fakhrejahani, Hiroki Nishikawa

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. 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.

Toshifumi YamaguchiCancer Chemotherapy Center, Osaka Medical and Pharmaceutical University Hospital, Osaka, JPN.
Yoshinobu HiroseDepartment of Pathology, Osaka Medical and Pharmaceutical University Hospital, Osaka, JPN.
Yasutaka NakazawaDepartment of Pathology, Osaka Medical and Pharmaceutical University Hospital, Osaka, JPN.
Akiko KagotaniDepartment of Pathology, Osaka Medical and Pharmaceutical University Hospital, Osaka, JPN.
Hiroyuki KodamaCancer Chemotherapy Center, Osaka Medical and Pharmaceutical University Hospital, Osaka, JPN.
Hiroki YukamiCancer Chemotherapy Center, Osaka Medical and Pharmaceutical University Hospital, Osaka, JPN.
Shin KameishiCancer Chemotherapy Center, Osaka Medical and Pharmaceutical University Hospital, Osaka, JPN.
Nanako MatsuoCancer Chemotherapy Center, Osaka Medical and Pharmaceutical University Hospital, Osaka, JPN.
Elham FakhrejahaniDepartment of Oncology, Kyoto Breast Cancer Research Network, Kyoto, JPN.
Hiroki NishikawaDepartment of Second Internal Medicine, Osaka Medical and Pharmaceutical University Hospital, Osaka, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BRAF mutations, particularly BRAF V600E, are rare but clinically significant molecular alterations in intrahepatic cholangiocarcinoma (IHCC), often linked to aggressive disease and poor prognosis. While targeted therapies have shown efficacy in BRAF-mutant colorectal cancer, their role in IHCC remains uncertain. This report describes the case of a 59-year-old woman with advanced BRAF V600E-mutated IHCC (cT3N3M1c, stage IVc) treated with encorafenib, binimetinib, and cetuximab. The BRAF V600E mutation was identified through next-generation sequencing. Initially, the patient was given gemcitabine, cisplatin, and durvalumab as first-line chemotherapy; however, her metastatic lesions progressed rapidly within one month. Due to the lack of response, second-line treatment with encorafenib, binimetinib, and cetuximab was started, resulting in a favorable initial response. Unfortunately, the disease progressed five months after initiating this regimen. This case highlights the potential benefit of combined BRAF/MEK/EGFR inhibition in BRAF V600E-mutated IHCC and underscores the need for further research to optimize treatment strategies for this patient population.

Indexed as

billiary tract cancerbinimetinibbraf v600 mutationencorafenibnext generation sequencing (ngs)

Identifiers

PMID40688855
PMCPMC12272295

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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.