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Assessing Antitumor Activity in Preclinical Tumor Xenograft Model. Department of Biostatistics St. Jude Children’s Research Hospital John(Jianrong) Wu. Tumor Xenograft Model. Tumor xenograft models.
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Assessing Antitumor Activity in Preclinical Tumor Xenograft Model Department of Biostatistics St. Jude Children’s Research Hospital John(Jianrong) Wu
Tumor xenograft models • Subcutaneous tumor model: tumor xenograft is implanted under the skin and typically located on the flank of the mouse. • Orthotopic tumor model: tumor xenograft is either implanted into the equivalent organ from which the cancer originated, or where metastatsese are found in patients.
Challenges • A relative small number of mice (10/per group) were tested. • Missing data issue: due to mice die of toxicity or be sacrificed when tumors grow to certain size. • Skewed distribution of tumor volume data • Various of tumor growth patterns.
Tumor Growth Inhibition (T/C ratio) Relative Tumor volume time t
Skewed tumor volume data Demidenko, 2010
Drawback of separate analysis of tumor volume at each time point • Multiple tests at different time points inflate type I error. • Excluding animals with missing observation is inefficient and could result a biased conclusion. • T-test may be not valid due to skewed distribution of tumor volume data. • Separate analysis at each time point ignores the intra-subject correlation. • Using an arbitrary cut-off point to assess antitumor activity and without any formal statistical inference
Statistical inference for tumor volume data • Inference T/C ratio and its 95% confidence interval –Hothorn (2006), Wu (2009, 2010), Cheng and Wu (2010) • Multivariate analysis – Tan et al (2002) • MANOVA – Heitjian et al (1995) • Nonparametric multivariate analysis – Koziol et al (1981)
Tumor Growth Delay (T-C) 4 Relative Tumor volume time
Example: D456-cisplatin tumor xenograft model Wu J, Confidence intervals for the difference of median failure times applied to censored tumor growth delay data, Statistics in Biopharmaceutical Research, 3:488-496, 2011 The medians of tumor quadrupling times are 8.7 (days) and 24.9 (days) for control and treatment, respectively. TGD=16.2 days with standard error of 1.9 days The 95% confidence bootstrap percentile interval of TGD is (10.8, 21.2).
Log10 cell kill (LCK) • Log10 cell kill is defined as the negative log10 fraction of tumor cells surviving (SF). • We illustrate its quantification with assumptions (a) control tumor growth follows an exponential growth curve (b) treated tumor regrowth after treament approximates untreated controls, then LCK = - log10(SF) = (T – C)/(3.32 DT) where DT is tumor doubling time of control. or -log(SF)=Tumor Growth Delay * Rate of Growth
SAS macro • Macro %long: transform the tumor volume data to be a longitudinal form • Macro %day2event: calculate tumor doubling and quadrupling times. • Macro %lck: calculate tumor growth delay (T-C) and log10 cell kill.
References for T/C ratio • Heitjan DF, Manni A, Santen RJ. Statistical analysis of in vivo tumor growth experiments. Cancer Research 1993;53:6042–6050 • Houghton PJ, Morton CL, et al. (2007). The pediatric preclinical testing program: Description of models and early testing results. Pediatr. Blood Cancer 49:928–940. • Hothorn L (2006). Statistical analysis of in vivo anticancer experiments: Tumor growth inhibition. Drug Inform. J. 40:229–238. • Wu J (2010), Statistical Inference for Tumor Growth Inhibition T/C Ratio, JBS, 20:954-964 • Wu J and Houghton PJ (2009), Interval approach to assessing antitumor activity for tumor xenograft studies, Pharmaceutical Statistics, 9:46-54. • Tan, M., Fang, H. B., Tian, G. L., Houghton, P. J. (2002). Small-sample inference for incomplete longitudinal data with truncation and censoring in tumor xenograft models. Biometrics 58:612–620. • Koziol et al. (1981). A distribution-free test for tumor-growth curve analyses with application to an animal tumor immunotherapy experiment. Biometrics, 37:383-390
References for TGD • Wu J, Confidence intervals for the difference of median failure times applied to censored tumor growth delay data, Statistics in Biopharmaceutical Research, 3:488-496, 2011. • Wu J, Assessment of antitumor activity for tumor xenograft studies using exponential growth models. Journal of Biopharmaceutical Statistics, 21:472-483, May, 2011. • Demidenko E (2010), Three endpoints of in vivo tumor radiobiology and their statistical estimation. 86:164-173. • Corbett, T. H., White, K., Polin, L., Kushner, J., Paluch, J., Shih, C., Grossman, C. S. (2003).Discovery and preclinical antitumor efficacy evaluations of LY32262 and LY33169.Investigational New Drugs 21:33–45.
References for LCK • Demidenko E (2010), Three endpoints of in vivo tumor radiology and their statistical estimation, Int J Radial Biol. 86:164-173 • Lloyd H (1975), Estimation of tumor cell kill from Gompertz growth curves, Cancer Chemother Rep, 59:267-277. • Corbett TH et al (2003), Discovery and preclinical antitumor efficacy evaluations of LY32262 and LY33169. Invest New Drugs 21:33-45. • Wu J (2011), Assessment of antitumor activity for tumor xenograft studies using exponential growth models, JBS, 1:472-483 • Wu J and Houghton PJ (2009), Assessing cytotoxic treatment effects in preclinical tumor xenograft models, JBS,19:755-762