Pith. sign in

REVIEW 1 cited by

An Executable Specification of Oncology Dose-Escalation Protocols with Prolog

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 2402.08334 v1 pith:UZIQVCZU submitted 2024-02-13 cs.PL

classification cs.PL
keywords protocolspecificationprogramprologtrialusedclinicallydose-escalation
verification ladder T0 review T1 audit T2 compute T3 formal
0 comments
read the original abstract

We present, as a pure Prolog program, the first executable specification of the 3 + 3 dose-escalation protocol commonly used in early-phase oncology drug development. In this program, the imperative operations of the protocol emerge as consequences of clinically meaningful anticipatory-regret scenarios that are declared as CLP(Z) constraints. This 'regret-constrained' (RC) specification yields a robust formulation which can be used to prove clinically meaningful safety and liveness properties of the protocol before incorporating it into a trial, and then as an on-line decision support system while the trial is underway. Our RC specification also readily accommodates certain pragmatic modifications to trial enrollment which severely strain traditionally imperative formulations. The features of modern Prolog systems let us describe the 3 + 3 protocol with a short and general program that has desirable algebraic properties and can therefore be used, tested and reasoned about in several different ways.

Discussion (0). Continue with ORCID to comment.

Forward citations

Cited by 1 Pith paper

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. Dose-Escalation Trial Protocols that Extend Naturally to Admit Titration

    math.CT 2025-07 conditional novelty 7.0 of 10

    A categorical preorder on trial tallies reveals a new monotonicity flaw in the 3+3 dose-escalation design and yields right Kan and Galois extensions that support titration.

Pith tools