ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2018
Interim Futility Monitoring Assessing Immune Therapies With a Potentially Delayed Treatment Effect.
Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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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.
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Who cites it
12 citing papers in PubMed, 28 citations in OpenAlex.
- Adaptive Design with Bayesian Informed Interim Decisions: Application To a Randomized Trial of Mechanical Circulatory Support.Therapeutic innovation & regulatory science · 2025Article
- The clinical journey of belantamab mafodotin in relapsed or refractory multiple myeloma: lessons in drug development.Blood cancer journal · 2025Review
- Article
- Futility monitoring for randomized clinical trials with non-proportional hazards: An optimal conditional power approach.Clinical trials (London, England) · 2023Article
- Review
- Efficacy and safety of anti-PD-1 antibody plus chemoradiotherapy in locally advanced esophageal squamous cancer.Frontiers in oncology · 2023Article
- Statistical considerations in long-term efficacy evaluation of anti-cancer therapies.Frontiers in pharmacology · 2023Review
- Delayed treatment effects, treatment switching and heterogeneous patient populations: How to design and analyze RCTs in oncology.Pharmaceutical statistics · 2021Article
- TOP: Time-to-Event Bayesian Optimal Phase II Trial Design for Cancer Immunotherapy.Journal of the National Cancer Institute · 2020Article
- Methods for Accommodating Nonproportional Hazards in Clinical Trials: Ready for the Primary Analysis?Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2019Article
- Advancing Drug Development in Gynecologic Malignancies.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019Review
- Maximum Somatic Allele Frequency in Combination With Blood-Based Tumor Mutational Burden to Predict the Efficacy of Atezolizumab in Advanced Non-small Cell Lung Cancer: A Pooled Analysis of the Randomized POPLAR and OAK Studies.Frontiers in oncology · 2019Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Purpose Introduction of new immune therapies that may have a delayed beneficial effect necessitates re-evaluation of traditional clinical trial designs in oncology. A key design feature of randomized trials is interim futility monitoring, which allows stopping early if the accruing data convincingly demonstrate that the experimental treatment is detrimental or is unlikely to be shown superior to the standard treatment. The appropriateness of futility monitoring is frequently questioned when the effect of the experimental treatment may be delayed (eg, in trials of many immune agents). We examine the advisability of using futility monitoring when there is potential for a delayed treatment effect and make recommendations concerning its use. Methods We evaluated the loss of statistical power when using some common futility interim monitoring rules and a new proposed conservative rule via simulation under varying amounts of treatment-effect delay and varying accrual periods. We also considered scenarios where the experimental treatment starts out being worse than the standard treatment but ends up being better, as may sometimes be the case when an immune therapy is compared with an active standard therapy. Results Some standard methods of futility monitoring can result in an unacceptable loss of power when there is a delayed treatment effect, especially if the accrual period is rapid or the experimental treatment is initially worse. The proposed conservative futility rule has a negligible loss of power in the situations considered. Conclusion Although care must be taken with the choice of futility monitoring when there is a delayed treatment effect, inclusion of appropriate rules can reduce the exposure of patients to ineffective therapies without reducing the probability of correctly identifying effective treatments.
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