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Robust EM Continual Reassessment Method in Oncology Dose Finding

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  • Yuan, Ying
  • Yin, Guosheng

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  • Yuan, Ying & Yin, Guosheng, 2011. "Robust EM Continual Reassessment Method in Oncology Dose Finding," Journal of the American Statistical Association, American Statistical Association, vol. 106(495), pages 818-831.
    • Handle: RePEc:bes:jnlasa:v:106:i:495:y:2011:p:818-831
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    File URL: http://pubs.amstat.org/doi/abs/10.1198/jasa.2011.ap09476
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    Cited by:

    1. Thomas M. Braun, 2018. "Motivating sample sizes in adaptive Phase I trials via Bayesian posterior credible intervals," Biometrics, The International Biometric Society, vol. 74(3), pages 1065-1071, September.
    2. Yifei Zhang & Sha Cao & Chi Zhang & Ick Hoon Jin & Yong Zang, 2021. "A Bayesian adaptive phase I/II clinical trial design with late‐onset competing risk outcomes," Biometrics, The International Biometric Society, vol. 77(3), pages 796-808, September.
    3. Chunyan Cai & Ying Yuan & Yuan Ji, 2014. "A Bayesian dose finding design for oncology clinical trials of combinational biological agents," Journal of the Royal Statistical Society Series C, Royal Statistical Society, vol. 63(1), pages 159-173, January.
    4. Beibei Guo & Ying Yuan, 2017. "Bayesian Phase I/II Biomarker-Based Dose Finding for Precision Medicine With Molecularly Targeted Agents," Journal of the American Statistical Association, Taylor & Francis Journals, vol. 112(518), pages 508-520, April.

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