Evidence map›Paper›PMID 42799834›Full record

ArticleClinical journal of gastroenterology2026

Response to pembrolizumab after progression on durvalumab in cholangiocarcinoma: a case report of immune checkpoint inhibitor switching.

Akito Furuta, Masatoshi Murakami, Katsuhito Teramatsu, Satoru Kinjo, Kazuhide Matsumoto, Keijiro Ueda, Takeo Yamamoto, Yoshinao Oda, Nao Fujimori, Yoshihiro Ogawa

Abstract read
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In one paragraph

Article in Clinical journal of gastroenterology, 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.

Akito FurutaDepartment of Medicine and Bioregulatory Science, Kyushu University Hospital, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Masatoshi MurakamiDepartment of Medicine and Bioregulatory Science, Kyushu University Hospital, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. murakami.masatoshi.589@m.kyushu-u.ac.jp.ORCID http://orcid.org/0000-0002-8791-0052
Katsuhito TeramatsuDepartment of Gastroenterology, Kyushu Rosai Hospital, Kitakyushu, Japan.
Satoru KinjoDepartment of Medicine and Bioregulatory Science, Kyushu University Hospital, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Kazuhide MatsumotoDepartment of Medicine and Bioregulatory Science, Kyushu University Hospital, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Keijiro UedaDepartment of Medicine and Bioregulatory Science, Kyushu University Hospital, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Takeo YamamotoDepartment of Anatomic Pathology, Pathological Sciences, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Yoshinao OdaDepartment of Anatomic Pathology, Pathological Sciences, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Nao FujimoriDepartment of Medicine and Bioregulatory Science, Kyushu University Hospital, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Yoshihiro OgawaDepartment of Medicine and Bioregulatory Science, Kyushu University Hospital, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Currently, combination therapy incorporating immune checkpoint inhibitors (ICIs) is the standard first-line treatment for advanced biliary tract cancer (BTC). However, the relative efficacy of anti-PD-1 and -L1 antibodies remains unclear, and evidence regarding ICI switching after treatment failure is limited. Here, we report a case of advanced distal cholangiocarcinoma in which pembrolizumab demonstrated clinical efficacy after durvalumab failure, with partial response maintained for six months. Pembrolizumab treatment was discontinued because of interstitial pneumonitis requiring corticosteroid therapy. Immunohistochemical analysis demonstrated staining for PD-L1 and -L2 in the tumor cells. Anti-PD-1 antibodies inhibit interactions between PD-L1 and -L2, whereas anti-PD-L1 antibodies do not affect PD-L2. Although the mechanisms underlying the response remain unclear, blockade of the PD-L2-PD-1 axis may have contributed to the clinical response to pembrolizumab after durvalumab failure. This case suggests that switching from anti-PD-L1 to anti-PD-1 therapy may represent an individualized therapeutic option in selected patients with BTC.

Indexed as

Biliary tract cancerImmune checkpoint inhibitor switchingPD-L2Pembrolizumab

Identifiers

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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.