Evidence map›Paper›PMID 40372142›Full record

ArticleStatistical methods in medical research2025

A model-free phase I/II dose optimization design for immunotherapy trials.

Yingjie Qiu, Mengyi Lu, Yan Han, Wenxian Zhou, Yi Zhao, Leng Han, Yong Zang

Abstract read
In one paragraph

Article in Statistical methods in medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Yingjie QiuPeter O'Donnell Jr. School of Public Health, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0009-0009-9429-2131
Mengyi LuDepartment of Biostatistics, Nanjing Medical University, Nanjing, Jiangsu, China.
Yan HanDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN, USA.
Wenxian ZhouDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN, USA.
Yi ZhaoDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN, USA.
Leng HanDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN, USA.
Yong ZangDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID 0000-0001-5036-5815

Funding

Curve-free phase I/II clinical trial designs for molecularly targeted agents and immunotherapyR21CA264257 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI ZANG, YONG · 2021 to 2022
$277k
NCI NIH HHS R21 CA264257
6 · The paper itself

Abstract

We present a model-free phase I/II clinical trial design, referred to as the UFO design, to optimize the dose of immunotherapy by jointly modeling toxicity, efficacy, and immune response outcomes. Instead of relying on complex parametric modeling approaches, we propose a model-free approach that uses the inherent correlations among different types of outcomes in immunotherapy and the constrained dose-outcome order to facilitate information sharing across different doses. This approach ensures the efficiency and transparency of the UFO design to be implemented in clinical practice. The UFO design is also extended to accommodate the delayed outcomes. It demonstrates favorable operating characteristics through simulation studies. The R Shniy app for simulation and trial implementation using the UFO design is also provided at iusccc.shinyapps.io/smartdesign.

Indexed as

Clinical Trials, Phase I as TopicClinical Trials, Phase II as TopicImmunotherapyResearch DesignComputer SimulationHumansModels, Statisticaladmissible setdelayed outcomesdose optimizationimmunotherapyisotonic regressionmodel-freePhase I/II clinical trialsutility

Identifiers

PMID40372142
PMCPMC13275141

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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.