Overview
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.
Description
BEACON is a prospective, multicentre, blinded benchmark using automated, criteria-based scoring. It is built on three design decisions that distinguish it from the existing literature: (i) synthetic, standardised cases remove the record-completeness variability that confounds retrospective comparisons and allow the identical input to be given to every board and every model; (ii) two independent tumour boards per localisation let human-human agreement be measured rather than assumed; and (iii) a guideline matrix, locked a priori, provides an objective anchor applied identically to human and model recommendations.
Reference standard. For each case-domain, a guideline matrix (guideline-recommended / acceptable / unsupported options per case-domain; ESMO, NCCN), locked and time-stamped before data collection, is applied identically to boards and models.
Five decision domains. Every recommendation is decomposed into D1 Intent, D2 Surgery, D3 Radiotherapy, D4 Systemic therapy (class + line), and D5 Work-up \& biomarkers before any comparison.
Eligibility
Inclusion Criteria:
- 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.
Exclusion Criteria:
- Case outside the five predefined localisations.
- Incomplete, internally inconsistent or ambiguous schema.
- Duplicate or near-duplicate of an existing case in the set.
- Question not resolvable by current guidelines.
