Optimal Biological Dose and Phase I/II Trials
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Publisher
Springer Nature Singapore
Link
https://link.springer.com/content/pdf/10.1007/978-981-19-8176-0_3
Reference20 articles.
1. Fraisse, J., Dinart, D., Tosi, D., Bellera, C., & Mollevi, C. (2021). Optimal biological dose: A systematic review in cancer phase I clinical trials. BMC Cancer, 21(1), 1–10.
2. Guo, B., & Yuan, Y. (2017). Bayesian phase I/II biomarker-based dose finding for precision medicine with molecularly targeted agents. Journal of the American Statistical Association, 112(518), 508–520.
3. Houede, N., Thall, P. F., Nguyen, H., Paoletti, X., & Kramar, A. (2010). Utility-based optimization of combination therapy using ordinal toxicity and efficacy in phase I/II trials. Biometrics, 66(2), 532–540.
4. Iasonos, A., & O’Quigley, J. (2013). Design considerations for dose-expansion cohorts in phase I trials. Journal of Clinical Oncology, 31(31), 4014.
5. Jin, I. H., Liu, S., Thall, P. F., & Yuan, Y. (2014). Using data augmentation to facilitate conduct of phase I-II clinical trials with delayed outcomes. Journal of the American Statistical Association, 109(506), 525–536.
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