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Benchmarking AI for Clinical Oncology decisioNmaking (BEACON): A Prospective, Multicentre, Blinded Evaluation of Frontier Large Language Models Against Multidisciplinary Tumour Board Recommendations in Oncology Treatment Planning

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

BEACON (Benchmarking AI for Clinical Oncology decisioNmaking) is a prospective, multicentre, comparative, blinded, non-interventional benchmark evaluating the treatment recommendations of five frontier large language models (LLMs) against the recommendations of multidisciplinary tumour boards (RCP) in oncology treatment planning. One hundred standardised synthetic cases (20 per localisation, across breast, lung, urological, digestive and gynaecological cancers) are submitted as identical structured input to two independent tumour boards per localisation and to five frontier LLMs. Each recommendation - human or model - is decomposed into five predefined decision domains (intent, surgery, radiotherapy, systemic therapy, work-up and biomarkers) and scored 0/1/2 for concordance against a two-tier reference: the consensus of the two tumour boards, complemented by an a priori locked guideline matrix (ESMO, NCCN). The primary endpoint is domain-level concordance between LLM and RCP consensus, expressed as a linearly weighted Cohen's kappa. A co-primary safety endpoint captures the proportion of recommendations carrying serious harm potential, because concordance alone can conceal dangerous errors. Because expert boards may disagree with one another on identical cases, model performance is always interpreted against the human consensus. BEACON is designed as reusable, openly licensed, pre-registered infrastructure: all synthetic cases, evaluation rubrics, the locked guideline matrix, scoring algorithms and verbatim prompts are released for full reproducibility.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Synthetic oncology case within one of the five predefined localisations (breast, lung, urological, digestive, gynaecological).

• Complete structured schema: UICC 8th-edition stage, biomarkers, ECOG performance status, comorbidities and a standardised clinical question.

• A clinically answerable treatment-planning question that is mappable to the locked guideline matrix.

Locations
Other Locations
France
Hopital Européen Georges Pompidou
RECRUITING
Paris
Contact Information
Primary
Jean-Emmanuel Bibault, MD PhD
jean-emmanuel.bibault@aphp.fr
01 56 09 34 06
Backup
Jérôme Lambert, MD PhD
jerome.lambert@u-paris.fr
0142499742
Time Frame
Start Date: 2026-05-01
Estimated Completion Date: 2026-10-01
Participants
Target number of participants: 100
Treatments
Breast cancers
Lung cancers
Urological cancers
Digestive cancers
Gynaecological cancers
Sponsors
Leads: Assistance Publique - Hôpitaux de Paris

This content was sourced from clinicaltrials.gov

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