A modified weighted log-rank test for confirmatory trials with a high proportion of treatment switching
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Le résumé fourni par la source
In confirmatory cancer clinical trials, overall survival (OS) is normally a primary endpoint in the intention-to-treat (ITT) analysis under regulatory standards. After the tumor progresses, it is common that patients allocated to the control group switch to the experimental treatment, or another drug in the same class. Such treatment switching may dilute the relative efficacy of the new drug compared to the control group, leading to lower statistical power. It would be possible to decrease the estimation bias by shortening the follow-up period but this may lead to a loss of information and power. Instead we propose a modified weighted log-rank test (mWLR) that aims at balancing these factors by down-weighting events occurring when many patients have switched treatment. As the weighting should be pre-specified and the impact of treatment switching is unknown, we predict the hazard ratio function and use it to compute the weights of the mWLR. The method may incorporate information from previous trials regarding the potential hazard ratio function over time. We are motivated by the RECORD-1 trial of everolimus against placebo in patients with metastatic renal-cell carcinoma where almost 80% of the patients in the placebo group received everolimus after disease progression. Extensive simulations show that the new test gives considerably higher efficiency than the standard log-rank test in realistic scenarios.
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Le contrôle bibliographique ouvert
DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.
- Titre Crossref
- A modified weighted log-rank test for confirmatory trials with a high proportion of treatment switching
- Date Crossref
- 15/11/2021
- Éditeur
- Public Library of Science (PLoS)
- Type
- journal-article
Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.
Où se fait cette recherche
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Novartis (Switzerland) pays non établi dans la noticeEntreprise
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AstraZeneca (Sweden) pays non établi dans la noticeEntreprise
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Global Drug Development pays non établi dans la noticeInstitution
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Statistical Innovation pays non établi dans la noticeInstitution
Novartis (Switzerland), AstraZeneca (Sweden) et Global Drug Development, avec 1 autre affiliation.
Une affiliation ne permet pas de déduire la nationalité d’un auteur.