Evidence map›Paper›PMID 41761754›Full record

ArticleCancer reports (Hoboken, N.J.)2026

Successful Management of Suspected Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis in BRAF-Mutant Cholangiocarcinoma Following Treatment With Immune Checkpoint Inhibitors and BRAF/MEK Inhibitors: A Case Report.

Akira Shibata, Michihiro Ono, Shutaro Oiwa, Atsushi Uesugi, Seiya Saito, Makoto Usami, Tomoyuki Abe, Masahiro Yoshida, Masahiro Maeda, Kohichi Takada

Abstract readCase Reports
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Akira ShibataDepartment of Residency and Clinical Training, Steel Memorial Muroran Hospital, Hokkaido, Japan.ORCID 0009-0001-4394-7857
Michihiro OnoDepartment of Pancreatobiliary Medicine, Steel Memorial Muroran Hospital, Hokkaido, Japan.ORCID 0009-0004-9346-6738
Shutaro OiwaDepartment of Gastroenterology, Steel Memorial Muroran Hospital, Hokkaido, Japan.
Atsushi UesugiDepartment of Gastroenterology, Steel Memorial Muroran Hospital, Hokkaido, Japan.
Seiya SaitoDepartment of Gastroenterology, Steel Memorial Muroran Hospital, Hokkaido, Japan.
Makoto UsamiDepartment of Medical Oncology, Steel Memorial Muroran Hospital, Hokkaido, Japan.
Tomoyuki AbeDepartment of Gastroenterology, Steel Memorial Muroran Hospital, Hokkaido, Japan.
Masahiro YoshidaDepartment of Hematology, Steel Memorial Muroran Hospital, Hokkaido, Japan.
Masahiro MaedaDepartment of Gastroenterology, Steel Memorial Muroran Hospital, Hokkaido, Japan.
Kohichi TakadaDivision of Medical Oncology, Department of Internal Medicine, Sapporo Medical University School of Medicine, Japan.ORCID 0000-0002-1393-9442

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe BRAF V600E mutation is a rare genetic alteration in cholangiocarcinoma for which sequential therapy with immune checkpoint inhibitors (ICIs) and BRAF/MEK inhibitors may be effective. However, the full spectrum of adverse events associated with the sequential use of these agents remains unclear. Hemophagocytic lymphohistiocytosis (HLH) is a fatal cytokine release syndrome that can be triggered by a cytokine storm. CASE: A 49-year-old man underwent left lateral hepatectomy and adjuvant chemotherapy for cholangiocarcinoma and subsequently developed lymph node recurrence. The patient initially received systemic chemotherapy with gemcitabine, cisplatin, and S-1; however, due to disease progression, the regimen was switched to gemcitabine, cisplatin, and durvalumab. After these treatments, a BRAF V600E mutation was identified through comprehensive gene panel testing, leading to the initiation of BRAF and MEK inhibitors. However, 3 months later, the patient presented to the emergency department of Steel Memorial Muroran Hospital with fever and fatigue in June 2024. He was initially diagnosed with septic shock but was unresponsive to broad-spectrum antibiotics. Laboratory tests revealed elevated ferritin levels, elevated soluble interleukin-2 receptor levels, and Epstein-Barr Virus (EBV)-DNA. HLH was diagnosed, and multidisciplinary treatment, including steroid pulse therapy, was initiated. The patient's condition improved dramatically, and he survived.

conclusionWe report a rare case of cholangiocarcinoma with suspected EBV-associated HLH that developed after sequential therapy with an ICI and BRAF/MEK inhibitors. Clinicians should consider HLH as a differential diagnosis in patients with a history of ICI therapy who present with severe unexplained inflammation or shock. Prompt diagnosis and multidisciplinary management are crucial to prevent death.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBile Duct NeoplasmsCholangiocarcinomaEpstein-Barr Virus InfectionsImmune Checkpoint InhibitorsLymphohistiocytosis, HemophagocyticProtein Kinase InhibitorsHerpesvirus 4, HumanHumansMaleMiddle AgedMutationProto-Oncogene Proteins B-rafBRAF protein, humanImmune Checkpoint InhibitorsProtein Kinase InhibitorsProto-Oncogene Proteins B-rafBRAF/MEK inhibitorcholangiocarcinomaEpstein–Barr virushemophagocytic lymphohistiocytosisimmune checkpoint inhibitor

Identifiers

PMID41761754
PMCPMC12949388

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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.