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Incorporating Individual and Collective Ethics into Phase I Cancer Trial Designs

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  • Jay Bartroff
  • Tze Leung Lai

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  • Jay Bartroff & Tze Leung Lai, 2011. "Incorporating Individual and Collective Ethics into Phase I Cancer Trial Designs," Biometrics, The International Biometric Society, vol. 67(2), pages 596-603, June.
    • Handle: RePEc:bla:biomet:v:67:y:2011:i:2:p:596-603
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    File URL: http://hdl.handle.net/10.1111/j.1541-0420.2010.01471.x
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    References listed on IDEAS

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    1. Peter F. Thall & John D. Cook, 2004. "Dose-Finding Based on Efficacy–Toxicity Trade-Offs," Biometrics, The International Biometric Society, vol. 60(3), pages 684-693, September.
    2. Linda M. Haines & Inna Perevozskaya & William F. Rosenberger, 2003. "Bayesian Optimal Designs for Phase I Clinical Trials," Biometrics, The International Biometric Society, vol. 59(3), pages 591-600, September.
    3. Zacks, S. & Rogatko, A. & Babb, J., 1998. "Optimal Bayesian-feasible dose escalation for cancer phase I trials," Statistics & Probability Letters, Elsevier, vol. 38(3), pages 215-220, June.
    4. Ying Kuen Cheung, 2005. "Coherence principles in dose-finding studies," Biometrika, Biometrika Trust, vol. 92(4), pages 863-873, December.
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    Cited by:

    1. Azriel, David, 2014. "Optimal sequential designs in phase I studies," Computational Statistics & Data Analysis, Elsevier, vol. 71(C), pages 288-297.
    2. Graham M. Wheeler, 2018. "Incoherent dose-escalation in phase I trials using the escalation with overdose control approach," Statistical Papers, Springer, vol. 59(2), pages 801-811, June.

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