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SatIR addresses the limitations of semantic similarity in high-stakes domains by integrating formal constraint satisfaction methods with large language models to handle complex eligibility criteria. This hybrid approach significantly boosts recall for relevant and eligible clinical trials while maintaining low latency, offering a robust framework for applications requiring executable and inspectable logic.
SatIR: Scalable High-Recall Constraint-Satisfaction-Based Information Retrieval for Clinical Trials Matching
arXiv:2604.08849v2 Announce Type: replace Abstract: Many important retrieval problems are not merely problems of semantic similarity, but problems of constraint satisfaction: a retrieved item should be topically relevant to a query and satisfy explicit requirements involving negation, temporal conditions, numeric thresholds, exceptions, ontological relations, and incomplete evidence. We study this challenge in clinical trial matching, a high-stakes test bed where a useful trial must both address a patient's medical needs and satisfy complex eligibility criteria. We propose SatIR, a scalable constraint-based retrieval method for clinical trial matching. SatIR converts trial eligibility criteria and summaries into formal constraints, then retrieves patient--trial pairs by executing these constraints over a database. The system combines Satisfiability Modulo Theories (SMT), relational algebra, medical ontology grounding, and large language models (LLMs): formal methods provide executable and inspectable matching, while LLMs convert ambiguous, incomplete, and implicit clinical information into explicit, controllable constraint representations. Across the SIGIR 2016 patient--trial collection and TREC-2022-RetrievalSubset, a benchmark derived from TREC 2022, SATIR consistently improves eligibility-aware retrieval over similarity-based baselines. Relative to TrialGPT-style retrieval, SATIR retrieves 32%--72% more relevant-and-eligible trials per patient on SIGIR 2016 and achieves $1.8$--$3.2\times$ higher eligible-trial recall on TREC-2022-RetrievalSubset. Retrieval is fast, requiring only 146 milliseconds per patient over 3,621 SIGIR trials.
Abstract:Many important retrieval problems are not merely problems of semantic similarity, but problems of constraint satisfaction: a retrieved item should be topically relevant to a query and satisfy explicit requirements involving negation, temporal conditions, numeric thresholds, exceptions, ontological relations, and incomplete evidence. We study this challenge in clinical trial matching, a high-stakes test bed where a useful trial must both address a patient's medical needs and satisfy complex eligibility criteria. We propose SatIR, a scalable constraint-based retrieval method for clinical trial matching. SatIR converts trial eligibility criteria and summaries into formal constraints, then retrieves patient--trial pairs by executing these constraints over a database. The system combines Satisfiability Modulo Theories (SMT), relational algebra, medical ontology grounding, and large language models (LLMs): formal methods provide executable and inspectable matching, while LLMs convert ambiguous, incomplete, and implicit clinical information into explicit, controllable constraint representations. Across the SIGIR 2016 patient--trial collection and TREC-2022-RetrievalSubset, a benchmark derived from TREC 2022, SATIR consistently improves eligibility-aware retrieval over similarity-based baselines. Relative to TrialGPT-style retrieval, SATIR retrieves 32%--72% more relevant-and-eligible trials per patient on SIGIR 2016 and achieves $1.8$--$3.2\times$ higher eligible-trial recall on TREC-2022-RetrievalSubset. Retrieval is fast, requiring only 146 milliseconds per patient over 3,621 SIGIR trials.
Computation and Language (cs.CL); Artificial Intelligence (cs.AI); Databases (cs.DB); Multiagent Systems (cs.MA); Symbolic Computation (cs.SC)
arXiv:2604.08849 [cs.CL]
(or arXiv:2604.08849v2 [cs.CL] for this version)
https://doi.org/10.48550/arXiv.2604.08849 Focus to learn more arXiv-issued DOI via DataCite
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