Evidence map›Paper›PMID 30646854›Full record

ArticleBMC cancer2019

Programmed cell death ligand 1 (PD-L1, CD274) in cholangiocarcinoma - correlation with clinicopathological data and comparison of antibodies.

Mark Kriegsmann, Stephanie Roessler, Katharina Kriegsmann, Marcus Renner, Rémi Longuespée, Thomas Albrecht, Moritz Loeffler, Stephan Singer, Arianeb Mehrabi, Monika Nadja Vogel and 6 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04211168 (Toripalimab Plus Lenvatinib as Second-line Treatment in Advanced Biliary Tract Cancers), which is not on this map. Cited by 26 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 4 pooled it
6.8field-weighted citation impact, top 3% of its field
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.

NCT04211168 phase2unknown statusnot on this mapstarted 2020, after this paper: background citation

Toripalimab Plus Lenvatinib as Second-line Treatment in Advanced Biliary Tract Cancers: a Single-arm, Non-randomized, Single-center Clinical Trial and Biomarker Study

TypeinterventionalSponsorPeking Union Medical College HospitalRan2020 to 2024Enrolled44ConditionsAdvanced Biliary Tract CancerArmsToripalimab plus Lenvatinib
3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 4 syntheses or guidelines pooled it, 38 citations in OpenAlex.

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  18. Progress toward improving outcomes in patients with cholangiocarcinoma.Current treatment options in gastroenterology · 2021
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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

16 authors at 2 institutions in 1 country.

Mark KriegsmannInstitute of Pathology, University Heidelberg, Im Neuenheimer Feld 224, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-7319-3646
Stephanie RoesslerInstitute of Pathology, University Heidelberg, Im Neuenheimer Feld 224, Heidelberg, Germany.
Katharina KriegsmannDepartment of Rheumatology, Oncology and Hematology, University of Heidelberg, Heidelberg, Germany.
Marcus RennerInstitute of Pathology, University Heidelberg, Im Neuenheimer Feld 224, Heidelberg, Germany.
Rémi LonguespéeInstitute of Pathology, University Heidelberg, Im Neuenheimer Feld 224, Heidelberg, Germany.
Thomas AlbrechtInstitute of Pathology, University Heidelberg, Im Neuenheimer Feld 224, Heidelberg, Germany.
Moritz LoefflerInstitute of Pathology, University Heidelberg, Im Neuenheimer Feld 224, Heidelberg, Germany.
Stephan SingerInstitute of Pathology, University Heidelberg, Im Neuenheimer Feld 224, Heidelberg, Germany.
Arianeb MehrabiDepartment of General Visceral and Transplantation Surgery, University Hospital Heidelberg, Im Neuenheimer Feld 110, Heidelberg, Germany.
Monika Nadja VogelDiagnostic and Interventional Radiology, Thoraxklinik at University Hospital of Heidelberg, Heidelberg, Germany.
Anita PathilDepartment of Internal Medicine IV, Gastroenterology and Hepatology, University Hospital Heidelberg, Im Neuenheimer Feld 410, Heidelberg, Germany.
Bruno KöhlerDepartment of Medical Oncology, University Hospital Heidelberg, National Center for Tumor Diseases, Heidelberg, Germany.
Christoph SpringfeldDepartment of Medical Oncology, University Hospital Heidelberg, National Center for Tumor Diseases, Heidelberg, Germany.
Christian RuppDepartment of Internal Medicine IV, Gastroenterology and Hepatology, University Hospital Heidelberg, Im Neuenheimer Feld 410, Heidelberg, Germany.
Karl Heinz WeissDepartment of Internal Medicine IV, Gastroenterology and Hepatology, University Hospital Heidelberg, Im Neuenheimer Feld 410, Heidelberg, Germany.
Benjamin GoeppertInstitute of Pathology, University Heidelberg, Im Neuenheimer Feld 224, Heidelberg, Germany. Benjamin.goeppert@med.uni-heidelberg.de.
Heidelberg University · DEGerman Cancer Research Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCholangiocarcinoma (CCA) may arise in the intra- or extrahepatic biliary tract and is associated with a poor prognosis. Despite recent advances, to date there is still no established targeted therapeutic approach available. Non-surgical therapeutic agents are urgently needed, as most patients are non-eligible to surgical resection. Anti-PD-L1 therapy prevents cancer cells from evading the immune system and has emerged as a new treatment option in several cancer entities. Recently, PD-L1 expression has been analyzed in comparably small CCA patient cohorts. However, a systematic validation of different PD-L1 antibodies has not been performed in CCA so far.

methodsWe stained a tissue microarray consisting of 170 patients, including 72 intrahepatic cholangiocarcinomas (iCCAs), 57 perihilar cholangiocarcinomas (pCCAs) and 41 distal cholangiocarcinomas (dCCAs) by immunohistochemistry and evaluated PD-L1 positivity in tumor and stromal cells. We analyzed three different PD-L1 antibodies (clones 28-8, SP142, and SP263) that are frequently used and recommended for predictive diagnostic testing in other cancer types.

resultsFor PD-L1 antibody clone SP263, 5% of iCCAs, 4% of pCCAs and 3% of dCCAs exhibited PD-L1 expression on tumor cells, thereby showing the highest frequencies of PD-L1 positivity. Accordingly, highest PD-L1 positivity rates of stromal cells with 31% in iCCA, 40% in pCCA and 61% in dCCA were detected for clone SP263. Agreement of PD-L1 positivity in tumor cells was moderate for clone 28-8 and SP263 (κ = 0.44) and poor between 28-8 and SP142 (κ = 0.13), as well as  SP142 and SP263 (κ = 0.11), respectively. Statistical analyses of PD-L1 expression (clone SP263) on tumor cells with clinicopathological data revealed a positive correlation with shortened overall survival in CCA patients.

conclusionsSelection of appropriate PD-L1 antibodies and careful evaluation of immunohistochemical staining patterns have a significant impact on PD-L1 testing in CCA. Clinical trials are necessary to investigate the putative beneficial effects of PD-L1 targeted immunotherapy in CCA patients.

Indexed as

AdultAgedAged, 80 and overAntibodiesB7-H1 AntigenBile Duct NeoplasmsBile Ducts, IntrahepaticCohort StudiesFemaleHumansImmunohistochemistryKlatskin TumorMaleMiddle AgedNeoplasm StagingStaining and LabelingAntibodiesB7-H1 AntigenCD274 protein, human28–8CD274CholangiocarcinomaPD-L1SP142SP263

Identifiers

PMID30646854
PMCPMC6332835
OpenAlexW2914163382

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Registered trials

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.