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Large Language Models for Supporting Clear Writing and Detecting Spin in Randomized Controlled Trials in Oncology:
Carole Koechli1,2, Fabio Dennstädt2, Christina Schröder1,2
1Department of Radiation Oncology, Kantonsspital Winterthur, Brauerstrasse 15, Winterthur, Switzerland, 41 52 266 26 53.
Large language models (LLMs) can detect reporting spin in oncology randomized controlled trials (RCTs). By comparing conclusions to full abstracts, LLMs help identify misleading efficacy presentations, enhancing scientific transparency.
Area of Science:
- Oncology
- Medical Informatics
- Scientific Publishing
Background:
- Randomized controlled trials (RCTs) are crucial for oncology intervention evaluation.
- Reporting "spin" in RCTs can mislead readers about true efficacy, particularly in conclusions.
Purpose of the Study:
- To investigate the capability of large language models (LLMs) in detecting spin within oncology RCT reports.
- To assess LLMs' performance in identifying spin, especially in the conclusions section.
Main Methods:
- 250 oncology RCTs were randomly sampled from major medical journals.
- Three commercial LLMs classified trials as positive/negative using varying text inputs (conclusions only to full abstract).
- LLM performance was evaluated against human annotations using accuracy, precision, recall, and F1-score.
Main Results:
- The GPT-o1 model achieved high F1-scores across all input conditions, with the highest at 0.98 when provided with methods, results, and conclusions.
- Analysis of misclassified trials revealed patterns indicative of spin, such as absent primary endpoint results or emphasis on subgroup analyses.
- These spin patterns were rarely present in correctly classified negative trials.
Conclusions:
- LLMs can effectively detect potential spin in oncology RCT reporting by identifying discrepancies between conclusions and full abstracts.
- This LLM-based approach can serve as a supplementary tool to improve transparency in scientific reporting.
- Further development is needed to address more complex trial designs.
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