Evidence map›Paper›PMID 40840958›Full record

ArticleBMJ open gastroenterology2025

Precision oncology for advanced-stage adenocarcinoma of the appendix: comprehensive molecular characterisation identifies actionable lesions and potential predictive biomarkers.

Sebastian Lange, Hannah Lisiecki, Simon Kreutzfeldt, Christoph Heining, Lena Weiss, Christoph Benedikt Westphalen, Albrecht Stenzinger, Daniel Hübschmann, Moritz Jesinghaus, Hanno Glimm and 3 more

Abstract read
In one paragraph

Article in BMJ open gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

13 authors.

Sebastian Lange *Department of Internal Medicine II, Klinikum Rechts der Isar, TUM School of Medicine and Health, Technical University of Munich, Munich, Bavaria, Germany.ORCID http://orcid.org/0000-0003-0406-1401
Hannah Lisiecki *Institute of Pathology, TUM School of Medicine and Health, Technical University of Munich, Munich, Bavaria, Germany.
Simon KreutzfeldtDivision of Translational Medical Oncology, German Cancer Research Center (DKFZ), Heidelberg, Baden-Würrtemberg, Germany.
Christoph HeiningDepartment for Translational Medical Oncology, National Center for Tumor Diseases (NCT) Dresden and German Cancer Research Center (DKFZ), Dresden, Saxony, Germany.
Lena WeissDepartment of Medicine III, LMU Klinikum, Munich, Bavaria, Germany.
Christoph Benedikt WestphalenGerman Cancer Consortium (DKTK), Heidelberg, Baden-Württemberg, Germany.
Albrecht StenzingerInstitute of Pathology, University Hospital Heidelberg, Heidelberg, Baden-Württemberg, Germany.
Daniel HübschmannGerman Cancer Consortium (DKTK), Heidelberg, Baden-Württemberg, Germany.
Moritz JesinghausInstitute of Pathology, University Hospital Marburg, Marburg, Hesse, Germany.
Hanno GlimmDepartment for Translational Medical Oncology, National Center for Tumor Diseases (NCT) Dresden and German Cancer Research Center (DKFZ), Dresden, Saxony, Germany.
Stefan FröhlingDivision of Translational Medical Oncology, German Cancer Research Center (DKFZ), Heidelberg, Baden-Würrtemberg, Germany.
Nicole PfarrInstitute of Pathology, TUM School of Medicine and Health, Technical University of Munich, Munich, Bavaria, Germany.
Anna Melissa SchlitterInstitute of Pathology, TUM School of Medicine and Health, Technical University of Munich, Munich, Bavaria, Germany melissa.schlitter@web.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAppendiceal adenocarcinoma is a rare cancer with very limited therapeutic options. We aimed to determine whether molecular profiling of advanced appendiceal adenocancer can identify actionable therapeutic alterations.

methodsWe retrospectively analysed cohorts from two large German precision oncology programmes. Patient records and pathology reports from 19 patients with advanced appendiceal adenocarcinoma who were enrolled between 2015 and 2021 were included in this study. We report the molecular features, the resulting molecular tumour board recommendations and their clinical implementation.

resultsIn 95% of the tumours, at least one potentially actionable alteration was identified, including mutations in

conclusionMolecular profiling of appendiceal adenocarcinomas revealed potentially actionable alterations in a number of cases.

Indexed as

AdenocarcinomaAppendiceal NeoplasmsPrecision MedicineAdultAgedAged, 80 and overAtaxia Telangiectasia Mutated ProteinsBiomarkers, TumorClass I Phosphatidylinositol 3-KinasesFemaleGermanyHumansMaleMiddle AgedMutationNeoplasm StagingAtaxia Telangiectasia Mutated ProteinsATM protein, humanBiomarkers, TumorClass I Phosphatidylinositol 3-KinasesPIK3CA protein, humanProto-Oncogene Proteins c-aktCANCERCOLORECTAL NEOPLASIAMOLECULAR PATHOLOGY

Identifiers

PMID40840958
PMCPMC12374629

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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.