Evidence map›Paper›PMID 39358611›Full record

ArticleCancer immunology, immunotherapy : CII2024

Exploring the impact of durvalumab on biliary tract cancer: insights from real-world clinical data.

Patrick Reimann, Ilektra-Antonia Mavroeidi, Jonathan Burghofer, Hossein Taghizadeh, Gerald Webersinke, Stefan Kasper, Georg Schreil, Darius Morariu, Andreas Reichinger, Hideo Andreas Baba and 10 more

Abstract readMulticenter Study
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 3 pooled it
–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

9 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Advances in Immunotherapy for Intrahepatic Cholangiocarcinoma.International journal of molecular sciences · 2026
    Review
  7. Review
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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

20 authors.

Patrick ReimannDepartment of Internal Medicine II, Academic Teaching Hospital Feldkirch, Feldkirch, Austria.
Ilektra-Antonia MavroeidiDepartment of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.
Jonathan BurghoferLaboratory for Molecular Genetic Diagnostics, Ordensklinikum Linz, Linz, Austria.
Hossein TaghizadehDepartment of Internal Medicine I, Universitätsklinikum St. Pölten, St. Pölten, Austria.
Gerald WebersinkeLaboratory for Molecular Genetic Diagnostics, Ordensklinikum Linz, Linz, Austria.
Stefan KasperDepartment of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.
Georg SchreilDepartment of Internal Medicine, State Hospital Pyhrn Eisenwurzen, Steyr, Austria.
Darius MorariuDepartment of Internal Medicine, State Hospital Wiener Neustadt, Wiener Neustadt, Austria.
Andreas ReichingerDepartment of Internal Medicine I for Hematology With Stem Cell Transplantation, Hemostaseology, and Medical Oncology, Ordensklinikum Linz, Linz, Austria.
Hideo Andreas BabaGerman Cancer Consortium (DKTK), Partner Site Essen, a partnership between German Cancer Research Center (DKFZ) and University Hospital Essen, Essen, Germany.
Patrick KirchwegerMedical Faculty, Johannes Kepler University Linz, Linz, Austria.
Martin SchulerDepartment of Medical Oncology, West German Cancer Center, University Hospital Essen, Essen, Germany.
Angela DjananiDepartment of Internal Medicine, Medical University of Innsbruck, Innsbruck, Austria.
Gerald W PragerDepartment of Medicine I, Division of Oncology, Medical University Vienna, Vienna, Austria.
Holger RumpoldDepartment of Internal Medicine I for Hematology With Stem Cell Transplantation, Hemostaseology, and Medical Oncology, Ordensklinikum Linz, Linz, Austria.
Magdalena BendaDepartment of Internal Medicine II, Academic Teaching Hospital Feldkirch, Feldkirch, Austria.
Eva-Maria SchneiderDepartment of Internal Medicine II, Academic Teaching Hospital Feldkirch, Feldkirch, Austria.
Sylvia MinkPrivate University of the Principality of Liechtenstein, Triesen, Principality of Liechtenstein.
Thomas WinderDepartment of Internal Medicine II, Academic Teaching Hospital Feldkirch, Feldkirch, Austria.
Bernhard DoleschalDepartment of Internal Medicine I for Hematology With Stem Cell Transplantation, Hemostaseology, and Medical Oncology, Ordensklinikum Linz, Linz, Austria. bernhard.doleschal@ordensklinikum.at.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThis study assesses the effectiveness of durvalumab with platinum and gemcitabine for biliary tract cancers (BTC). It aims to confirm the TOPAZ-1 trial results in a real-world context and explore the link between BTC molecular profiles and patient outcomes.

methodsA retrospective analysis was conducted on 102 BTC patients treated with durvalumab, platinum, and gemcitabine at five cancer centers in Austria and one in Germany from 2022 to 2024. Molecular profiling used targeted DNA and RNA assays. Clinical endpoints, including progression-free survival (PFS) and overall survival (OS), were assessed using log-rank tests and Cox regression, with correlations to second-line molecular-targeted therapies.

resultsAmong 102 patients, 60.8% had intrahepatic cholangiocarcinoma. The treatment achieved a disease control rate of 71.57% and an overall response rate of 35.11%. Median PFS was 6.51 months, and OS was 13.61 months. Patients under 65 had significantly better OS. Alterations in chromatin remodeling or homologous recombination repair genes were not predictive of survival benefit (HR: 0.45; p = 0.851 and HR: 1.63; p = 0.26, respectively). Patients with molecular-informed second-line therapy showed a trend toward survival benefit (HR: 0.23; p = 0.052).

conclusionThis study confirms the phase 3 trial results of durvalumab with platinum and gemcitabine, providing a substantial real-world dataset with detailed molecular characterization. No specific patient subgroup showed a markedly better response to durvalumab based on conventional NGS panels. Further research is needed to explore the link between immunotherapy responses and molecular subgroups.

Indexed as

Antibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsBiliary Tract NeoplasmsAdultAgedAged, 80 and overDeoxycytidineFemaleGemcitabineHumansMaleMiddle AgedRetrospective StudiesAntibodies, MonoclonalDeoxycytidinedurvalumabGemcitabineBiliary tract cancerChromatin remodelingDurvalumabHomologous recombination repair (HRR)Molecular-informed therapyPrecision oncology

Identifiers

PMID39358611
PMCPMC11447177

What OpenQuestion holds

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Registered trials

None linked

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.