ArticlePharmaceutical statistics
Great Wall: A Generalized Dose Optimization Design for Drug Combination Trials Maximizing Survival Benefit.
Article in Pharmaceutical statistics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Great Wall: A Generalized Dose Optimization Design for Drug Combination Trials Maximizing Survival Benefit.Pharmaceutical statisticsArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
Most phase I-II drug-combination trial designs assume that selecting the optimal dose combination based on early outcomes will also lead to maximum long-term survival benefits. However, this assumption is often violated in many clinical studies, generally due to high rates of relapse following the initial response. To address this problem, we propose the Great Wall design, a general dose optimization design for drug-combination trials. The Great Wall design employs a "divide-and-conquer" algorithm to address the issue of partial order of toxicity and uses early outcomes to eliminate dose combinations that are excessively toxic or less efficacious. It utilizes a dose randomization approach to construct a candidate set of the promising dose combinations balancing the toxicity and early efficacy outcomes. The patients assigned to the candidate set are followed to collect the survival outcomes and the final optimal dose combination is then selected to maximize the survival benefit. The simulation studies confirm the desirable operating characteristics of the Great Wall design under various clinical settings. R codes are also provided to facilitate the application. The Great Wall design is modular and practically useful in settings where investigators plan to follow patients long enough to assess survival outcomes.
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Registered trials
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