Evidence map›Paper›PMID 41930309›Full record

ReviewESMO real world data and digital oncology2026

How to bring generative AI to oncology practice.

D Truhn, J N Kather

Abstract readReview
In one paragraph

Review in ESMO real world data and digital oncology, 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

2 authors.

D TruhnDiagnostic and Interventional Radiology, University Hospital Aachen, Aachen, Germany.
J N KatherElse Kroener Fresenius Center for Digital Health, Faculty of Medicine, TUD Dresden University of Technology, Dresden, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Generative artificial intelligence (AI) is entering oncology. Large language models are the near-term workhorse because oncology runs on narrative text and structured tables. We review current adoption and outline a practical path from stand-alone chat models to retrieval-augmented systems and, ultimately, agentic assistants that plan tasks, call domain tools, and integrate multimodal data within the electronic health record. Concrete uses include molecular tumor board synthesis with transparent evidence, grading along guidelines, synoptic radiology and pathology drafting, and computable trial matching. We also map the constraints: fragmented hospital information technology, privacy and provenance requirements, domain shift across sites, and persistent hallucinations. We envision that evaluation must move beyond leaderboards toward multicenter, prospective designs with endpoints that reflect clinical utility, such as faithfulness to cited sources, extraction accuracy, time to task completion, plan correctness, recovery after tool failure, and silent clinical studies before exposure. Finally, we sketch an adoption trajectory. Institutions will replace

Indexed as

artificial intelligencegenerative AIlarge language modelsoncology

Identifiers

PMID41930309
PMCPMC13040884

What OpenQuestion 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 OpenQuestion graph.