Robust EM continual reassessment method in oncology dose finding
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Publication:3111177
Recommendations
- Bayesian Model Averaging Continual Reassessment Method in Phase I Clinical Trials
- Continual reassessment and related dose-finding designs
- A note on the robustness of the continual reassessment method
- A note on continual reassessment method
- Bayesian data augmentation dose finding with continual reassessment method and delayed toxicity
Cited in
(10)- Review of Statistical Treatment for Oncology Dose-Escalation Trial with Prolonged Evaluation Window or Fast Enrollment
- Adaptive clinical trial designs for phase I cancer studies
- A Bayesian adaptive phase I/II clinical trial design with late‐onset competing risk outcomes
- Biomarker-based precision dose finding for immunotherapy combined with radiotherapy
- Statistical frameworks for oncology dose-finding designs with late-onset toxicities: a review
- Application of gamma process to two-agent combinations with delayed toxicity
- Time-to-event continual reassessment method incorporating treatment cycle information with application to an oncology phase I trial
- Bayesian data augmentation dose finding with continual reassessment method and delayed toxicity
- Surv-CRM-12: a Bayesian phase I/II survival CRM for right-censored toxicity endpoints with competing disease progression
- BIPSE: a biomarker-based phase I/II design for immunotherapy trials with progression-free survival endpoint
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