Evidence map›Paper›PMID 41646477›Full record

ArticleESMO gastrointestinal oncology2025

A stratified two-stage tumor molecular profiling algorithm to identify clinically actionable molecular alterations in pancreatic cancer.

S Hussung, D Akhoundova, C Pistoni, D Lenggenhager, A Töpfer, C Pauli, B Pestalozzi, C Britschgi, M Zoche, M Rechsteiner and 3 more

Abstract read
In one paragraph

Article in ESMO gastrointestinal oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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.

S HussungUniversity Hospital Zurich, Department of Medical Oncology and Hematology, Zurich, Switzerland.
D AkhoundovaDepartment of Medical Oncology, Inselspital, University Hospital of Bern, Bern, Switzerland.
C PistoniUniversity Hospital Zurich, Department of Medical Oncology and Hematology, Zurich, Switzerland.
D LenggenhagerFaculty of Medicine, University of Zurich, Zurich, Switzerland.
A TöpferUniversity Hospital Zurich, Department of Pathology and Molecular Pathology, Zurich, Switzerland.
C PauliFaculty of Medicine, University of Zurich, Zurich, Switzerland.
B PestalozziUniversity Hospital Zurich, Department of Medical Oncology and Hematology, Zurich, Switzerland.
C BritschgiUniversity Hospital Zurich, Department of Medical Oncology and Hematology, Zurich, Switzerland.
M ZocheUniversity Hospital Zurich, Department of Pathology and Molecular Pathology, Zurich, Switzerland.
M RechsteinerUniversity Hospital Zurich, Department of Pathology and Molecular Pathology, Zurich, Switzerland.
H MochFaculty of Medicine, University of Zurich, Zurich, Switzerland.
A WeberUniversity Hospital Zurich, Department of Pathology and Molecular Pathology, Zurich, Switzerland.
R FritschUniversity Hospital Zurich, Department of Medical Oncology and Hematology, Zurich, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Tumor molecular profiling (TMP) for pancreatic cancer (PC) is recommended by current international guidelines, yet no testing standards exist. Moreover, the magnitude of benefit and the cost-effectiveness of comprehensive next-generation sequencing panels for PC are under debate. Materials and methods: We implemented a stratified two-stage TMP algorithm for advanced PC. Stage 1 comprised immunohistochemistry for mismatch repair deficiency and targeted sequencing employing a 33-gene next-generation sequencing panel covering common PC drivers and DNA damage response genes. Based on pre-specified events ( Results: A total of 94 PC patients were included in the study. Some 63/94 (67.0%) patients underwent TMP according to the algorithm, of which 5/63 (7.9%) fulfilled criteria for subsequent stage 2 comprehensive testing. A total of 31/94 (33%) patients underwent upfront comprehensive molecular testing outside the algorithm based on referring physician's request. Compared with algorithm testing, upfront comprehensive testing detected a higher number of pathogenic molecular alterations/patient (median: five versus three, Conclusions: Stratified two-stage TMP reliably identifies actionable alterations in PC patients, with potential therapeutic benefit. The proposed TMP algorithm might be as effective, yet more feasible and economic compared with comprehensive upfront testing.

Indexed as

molecular tumor boardpancreatic cancerpersonalized treatmentprecision oncologytumor molecular profiling

Identifiers

PMID41646477
PMCPMC12836705

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.