Evaluating Treatment Effects with Patient-Response–Related Outcomes in Comparative Clinical Trials
AbstractIn comparative clinical investigations for nearly all disease types, patient responses - signifying clinically meaningful improvements in health or reductions in disease burden - are routinely employed as key end points for assessing treatment activity or efficacy. Trials typically use the response rate to summarize treatment effects, a metric with limitations for investigating the temporal profile of the effect. In this Clinical Trials Workshop, the authors present a novel approach for analyzing time to response and duration of response in clinical trials using, as an example, data from the JAVELIN Renal-101 trial of avelumab and axitinib versus sunitinib for treating renal cell carcinoma.
Authors
- Lü Tian (ORCID: https://orcid.org/0000-0002-5893-0169)
- Lu Mao (ORCID: https://orcid.org/0000-0002-8626-9822)
- Ethan B. Ludmir (ORCID: https://orcid.org/0000-0002-5472-5344)
- Paul Gerard Guy Richardson (ORCID: https://orcid.org/0000-0002-7426-8865)
- L. J. Wei (ORCID: https://orcid.org/0000-0002-8582-920X)
- Bo Huang (ORCID: https://orcid.org/0000-0002-3088-9328)
- Michael D. Hughes (ORCID: https://orcid.org/0000-0001-8562-2316)
Institutions
- The University of Texas MD Anderson Cancer Center (US)
- University of Wisconsin–Madison (US)
- Harvard University (US)
- Pfizer (United States) (US)
- Dana-Farber Cancer Institute (US)
- Stanford University (US)
Publication Details
- Journal
- NEJM Evidence
- Published
- 2025-11-25
- DOI
- https://doi.org/10.1056/evidctw2400349
- Primary Topic
- Renal cell carcinoma treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00