Evidence map›Paper›PMID 42021926›Full record

ArticleESMO real world data and digital oncology2026

Accelerating real-world data collection using large language models in rare neoplasms: a bone sarcoma example.

P Teterycz, S Rynkun, B Szostakowski, M Wągrodzki, P Rutkowski, M Rosińska

Abstract read
In one paragraph

Article 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

6 authors.

P TeteryczDigital Medicine Center, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
S RynkunDigital Medicine Center, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
B SzostakowskiDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
M WągrodzkiDepartment of Pathology and Laboratory Diagnostics, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
P RutkowskiDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
M RosińskaDigital Medicine Center, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Real-world data collection in oncology remains a challenge due to the complex and unstructured format of medical notes. Recently, large language models (LLMs) have demonstrated success in extracting information from free-text data across various domains. This study evaluates the performance of multiple small LLMs as information extractors on Polish medical notes. Materials and methods: Electronic health records (EHRs) of 302 bone sarcoma patients treated in a reference center between 2016 and 2022 were selected. Five variables-pathology type, tumor size, localization, grade, and primary resection-were annotated by an experienced oncologist. Multiple prompting techniques and four LLMs were used to query the models with the task of returning the value for each variable using an XML tag. Additionally, among non-concordant values we distinguished valid results, i.e. of expected format and containing a key word/phrase from a per-variable, expert-devised list. An ensemble voting approach was applied, selecting values appearing in the majority of valid outputs. Results: Single-model accuracy was modest (17.5%-30.3%) and highly prompt-dependent. The tumor localization values turned out to be the easiest to assess with an accuracy of up to 36.2%. The majority of non-concordant values were non-valid. The voting strategy improved performance significantly, with 83.6% overall accuracy, peaking at 90.0% for the resection type variable. Conclusions: Our study highlights the potential of using lightweight LLMs in the automation of data extraction from medical notes, which could significantly accelerate clinical research. A singular small LLM is not yet sufficient for real use cases in non-English settings; however, prompt engineering and ensemble methods can greatly improve performance.

Indexed as

artificial intelligencebone sarcomadata extractionLLMs

Identifiers

PMID42021926
PMCPMC13098454

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.