Evidence map›Paper›PMID 42238457›Full record

ArticlemedRxiv : the preprint server for health sciences2026

BUDS: Benchmark Uncertainty Design Selection for Two-Stage Single-Arm Phase II Trials.

Rebecca Irlmeier, Zhuoli Jin, Fei Ye

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Rebecca IrlmeierBiostatistics and Bioinformatics Shared Resource, Sylvester Comprehensive Cancer Center, Miami, Florida.ORCID 0000-0001-8210-9584
Zhuoli JinSylvester Comprehensive Cancer Center, Miami, Florida.ORCID 0009-0007-6360-4855
Fei YeBiostatistics and Bioinformatics Shared Resource, Sylvester Comprehensive Cancer Center, Miami, Florida.ORCID 0000-0001-6472-5076

Funding

Tumor Biology Research ProgramP30CA240139 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI George S. Grills · 2019 to 2026
$24.1M
NCI NIH HHS P30 CA240139
6 · The paper itself

Abstract

Background: Simon two-stage designs for binary endpoints and their time-to-event analogues, including the restricted-Kwak and Jung method, rely on a fixed historical benchmark. In practice, historical benchmarks are often uncertain due to small samples, population heterogeneity, changing eligibility criteria, and evolving standards of care. When the clinically relevant benchmark exceeds the value used to calibrate the design, Type I error rates can be substantially inflated, leading to costly advancement of ineffective treatments. Existing design-selection criteria generally optimize efficiency at a single benchmark without accounting for this uncertainty. Methods: We propose Benchmark Uncertainty Design Selection (BUDS), a framework for selecting two-stage designs for both binary and time-to-event (TTE) endpoints. Rather than relying on a single planning benchmark, BUDS addresses benchmark uncertainty by specifying a plausible range of response rates for binary endpoints or survival probabilities at a prespecified timepoint for TTE endpoints. Among feasible designs that satisfy both Type I error ( Results: Across representative scenarios, the Type I error rate increases substantially when true benchmarks exceed their planning values using single-benchmark objectives, reaching 0.407 for Simon Optimal design (response rates: 0.10 vs. 0.15; Conclusions: BUDS provides a transparent framework for selecting designs when historical benchmarks are uncertain. It makes the trade-off between robustness and efficiency explicit while controlling Type I error across the plausible benchmark range. The framework applies to both binary and time-to-event endpoints in two-stage single-arm Phase II trial planning and is implemented in the open-source

Indexed as

benchmark uncertaintybinary endpointdesign-selection objectivesmisspecificationsingle-arm two-stage phase II trialtime-to-event endpointType I error

Identifiers

PMID42238457
PMCPMC13228699

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.