Count data and recurrent events in clinical trials, such as the number of lesions in magnetic resonance imaging in multiple sclerosis, the number of relapses in multiple sclerosis, the number of hospitalizations in heart failure, and the number of exacerbations in asthma or in chronic obstructive pulmonary disease (COPD) are often modeled by negative binomial distributions. In this manuscript, we study planning and analyzing clinical trials with group sequential designs for negative binomial outcomes. We propose a group sequential testing procedure for negative binomial outcomes based on Wald statistics using maximum likelihood estimators. The asymptotic distribution of the proposed group sequential test statistics is derived. The finite sample size properties of the proposed group sequential test for negative binomial outcomes and the methods for planning the respective clinical trials are assessed in a simulation study. The simulation scenarios are motivated by clinical trials in chronic heart failure and relapsing multiple sclerosis, which cover a wide range of practically relevant settings. Our research assures that the asymptotic normal theory of group sequential designs can be applied to negative binomial outcomes when the hypotheses are tested using Wald statistics and maximum likelihood estimators. We also propose two methods, one based on Student’s t-distribution and one based on resampling, to improve type I error rate control in small samples. The statistical methods studied in this manuscript are implemented in the R package gscounts, which is available for download on the Comprehensive R Archive Network (CRAN).

1. Jennison C and Turnbull BW. Group sequential designs with applications to clinical trials. Boca Raton, Florida, USA: Chapman & Hall/CRC, 2000.
Google Scholar
2. Shoben, AB, Emerson, SS. Violations of the independent increment assumption when using generalized estimating equation in longitudinal group sequential trials. Stat Med 2014; 33: 50415056.
Google Scholar | Crossref | Medline
3. Whitehead, J . The design and analysis of sequential clinical trials, West Sussex, England: John Wiley & Sons, 1997.
Google Scholar | Crossref
4. Wassmer G and Brannath W. Group sequential and confirmatory adaptive designs in clinical trials. Heidelberg, Germany: Springer, 2016.
Google Scholar
5. Sormani, MP, Bruzzi, P, Miller, DH, et al. Modelling MRI enhancing lesion counts in multiple sclerosis using a negative binomial model: implications for clinical trials. J Neurol Sci 1999; 163: 7480.
Google Scholar | Crossref | Medline | ISI
6. Keene, ON, Jones, MRK, Lane, PW, et al. Analysis of exacerbation rates in asthma and chronic obstructive pulmonary disease: example from the TRISTAN study. Pharmaceut Stat 2007; 6: 8997.
Google Scholar | Crossref | Medline
7. Keene, ON, Calverley, PMA, Jones, PW, et al. Statistical analysis of exacerbation rates in COPD: TRISTAN and ISOLDE revisited. Eur Respir J 2008; 32: 1724.
Google Scholar | Crossref | Medline
8. Keene, ON, Vestbo, J, Anderson, J, et al. Methods for therapeutic trials in COPD: lessons from the TORCH trial. Eur Respir J 2009; 34: 10181023.
Google Scholar | Crossref | Medline
9. Rodés-Cabau, J, Horlick, E, Ibrahim, R, et al. Effect of clopidogrel and aspirin vs aspirin alone on migraine headaches after transcatheter atrial septal defect closure: the CANOA randomized clinical trial. J Am Med Assoc 2015; 314: 21472154.
Google Scholar | Crossref
10. Schlesinger, N, Mysler, E, Lin, HY, et al. Canakinumab reduces the risk of acute gouty arthritis flares during initiation of allopurinol treatment: results of a double-blind, randomised study. Ann Rheumat Dis 2011; 70: 12641271.
Google Scholar | Crossref | Medline | ISI
11. Rogers, JK, Pocock, SJ, McMurray, JJV, et al. Analysing recurrent hospitalizations in heart failure: a review of statistical methodology, with application to CHARM-Preserved. Eur J Heart Failure 2014; 16: 3340.
Google Scholar | Crossref | Medline
12. Cook, RJ, Lawless, JF. Interim monitoring of longitudinal comparative studies with recurrent event responses. Biometrics 1996; 52: 13111323.
Google Scholar | Crossref | Medline
13. Cook, RJ, Farewell, VT. Incorporating surrogate endpoints into group sequential trials. Biometric J 1996; 38: 119130.
Google Scholar | Crossref
14. Jiang, W . Group sequential procedures for repeated events data with frailty. J Biopharmaceut Stat 1999; 9: 379399.
Google Scholar | Crossref | Medline
15. Xia, Q, Hoover, DR. A procedure for group sequential comparative Poisson trials. J Biopharmaceut Stat 2007; 16: 869881.
Google Scholar | Crossref
16. Cook, RJ, Grace, YY, Lee, KA. Sequential testing with recurrent events over multiple treatment periods. Stat Biosci 2010; 2: 137153.
Google Scholar | Crossref
17. Ponikowski, P, Voors, AA, Anker, SD, et al. 2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure. Eur J Heart Failure 2016; 18: 891975.
Google Scholar | Crossref | Medline | ISI
18. Committee for Medicinal Products for Human Use (CHMP). Guideline on clinical investigation of medicinal products for the treatment of chronic heart failure, https://goo.gl/HHgONb (accessed 20 October 2016).
Google Scholar
19. Rogers, JK, McMurray, JJV, Pocock, SJ, et al. Eplerenone in patients with systolic heart failure and mild symptoms analysis of repeat hospitalizations. Circulation 2012; 126: 23172323.
Google Scholar | Crossref | Medline
20. Rogers, JK, Jhund, PS, Perez, AC, et al. Effect of rosuvastatin on repeat heart failure hospitalizations: the CORONA Trial (Controlled Rosuvastatin Multinational Trial in Heart Failure). JACC: Heart Failure 2014; 2: 289297.
Google Scholar | Crossref | Medline
21. Udelson, JE . Heart failure with preserved ejection fraction. Circulation 2011; 124: 540543.
Google Scholar | Crossref | Medline | ISI
22. Redfield, MM . Heart failure with preserved ejection fraction. New Engl J Med 2016; 375: 18681877.
Google Scholar | Crossref | Medline
23. Yusuf, S, Pfeffer, MA, Swedberg, K, et al. Effects of candesartan in patients with chronic heart failure and preserved left-ventricular ejection fraction: the CHARM-Preserved Trial. Lancet 2003; 362: 777781.
Google Scholar | Crossref | Medline | ISI
24. Mehta, C, Gao, P, Bhatt, DL, et al. Optimizing trial design: sequential, adaptive, and enrichment strategies. Circulation 2009; 119: 597605.
Google Scholar | Crossref | Medline | ISI
25. Jackson, N, Atar, D, Borentain, M, et al. Improving clinical trials for cardiovascular diseases: a position paper from the Cardiovascular Round Table of the European Society of Cardiology. Eur Heart J 2016; 37: 747754.
Google Scholar | Crossref | Medline
26. Cohen, JA, Rudick, RA. Multiple sclerosis therapeutics, Cambridge, England: Cambridge University Press, 2011.
Google Scholar | Crossref
27. Selmaj, K, Li, SKB, Hartung, HP, et al. Siponimod for patients with relapsing-remitting multiple sclerosis (BOLD): an adaptive, dose-ranging, randomised, phase 2 study. Lancet Neurol 2013; 12: 756767.
Google Scholar | Crossref | Medline | ISI
28. Cook, RJ, Lawless, J. The statistical analysis of recurrent events, New York, NY, USA: Springer Science & Business Media, 2007.
Google Scholar
29. Lawless, JF . Negative binomial and mixed Poisson regression. Can J Stat 1987; 15: 209225.
Google Scholar | Crossref | ISI
30. Gallo, P, Mao, L, Shih, VH. Alternative views on setting clinical trial futility criteria. J Biopharmaceut Stat 2014; 24: 976993.
Google Scholar | Crossref | Medline
31. Scharfstein, DO, Tsiatis, AA, Robins, JM. Semiparametric efficiency and its implication on the design and analysis of group-sequential studies. J Am Stat Assoc 1997; 92: 13421350.
Google Scholar | Crossref
32. Jennison, C, Turnbull, BW. Group-sequential analysis incorporating covariate information. J Am Stat Assoc 1997; 92: 13301341.
Google Scholar | Crossref | ISI
33. Lan, KKG, DeMets, DL. Discrete sequential boundaries for clinical trials. Biometrika 1983; 70: 659663.
Google Scholar | Crossref | ISI
34. Proschan, MA, Follmann, DA, Waclawiw, MA. Effects of assumption violations on type I error rate in group sequential monitoring. Biometrics 1992; 48: 11311143.
Google Scholar | Crossref | ISI
35. Aban, IB, Cutter, GR, Mavinga, N. Inferences and power analysis concerning two negative binomial distributions with an application to MRI lesion counts data. Computat Stat Data Analys 2009; 53: 820833.
Google Scholar | Crossref | ISI
36. Farrington, CP, Manning, G. Test statistics and sample size formulae for comparative binomial trials with null hypothesis of non-zero risk difference or non-unity relative risk. Stat Med 1990; 9: 14471454.
Google Scholar | Crossref | Medline | ISI
37. Tang, NS, Tang, ML, Wang, SF. Sample size determination for matched-pair equivalence trials using rate ratio. Biostatistics 2006; 8: 625631.
Google Scholar | Crossref | Medline
38. Mütze, T, Munk, A, Friede, T. Design and analysis of three-arm trials with negative binomially distributed endpoints. Stat Med 2016; 35: 505521.
Google Scholar | Crossref | Medline
39. Pocock, SJ . Group sequential methods in the design and analysis of clinical trials. Biometrika 1977; 64: 191199.
Google Scholar | Crossref | ISI
40. Mütze, T, Konietschke, F, Munk, A, et al. A studentized permutation test for three-arm trials in the ‘gold standard’ design. Stat Med 2017; 36: 883898.
Google Scholar | Crossref | Medline
41. Spiessens, B, Debois, M. Adjusted significance levels for subgroup analyses in clinical trials. Contemporary Clin Trials 2010; 31: 647656.
Google Scholar | Crossref | Medline
42. Placzek M and Friede T. Clinical trials with nested subgroups: analysis, sample size determination and internal pilot. Stat Meth Med Res 2017; 27: 3286–3303.
Google Scholar
43. Graf AC, Wassmer G, Friede T, et al. Robustness of testing procedures for confirmatory subpopulation analyses based on a continuous biomarker. Stat Meth Med Res 2017 (submitted).
Google Scholar
44. Jennison C. Bootstrap tests and confidence intervals for a hazard ration when the number of observed failures is small, with applications to group sequential survival studies. In: Proceedings of the 22nd interface conference on computing science and statistics, Michigan, USA, May 1990, pp.89–97.
Google Scholar
45. Mütze T. R package gscounts, https://cran.r-project.org/web/packages/gscounts/index.html (2017).
Google Scholar
46. Kieser, M, Hauschke, D. Assessment of clinical relevance by considering point estimates and associated confidence intervals. Pharmaceut Stat 2005; 4: 101107.
Google Scholar | Crossref
47. Fisch, R, Jones, I, Jones, J, et al. Bayesian design of proof-of-concept trials. Therapeut Innovat Regulat Sci 2015; 49: 155162.
Google Scholar | SAGE Journals | ISI
48. Gsponer, T, Gerber, F, Bornkamp, B, et al. A practical guide to Bayesian group sequential designs. Pharmaceut Stat 2014; 13: 7180.
Google Scholar | Crossref | Medline | ISI
49. Asendorf T, Henderson R, Schmidli H, et al. Modelling and sample size reestimation for longitudinal count data with incomplete follow up. (Submitted for publication).
Google Scholar
50. Committee for Medicinal Products for Human Use (CHMP). Guideline on adjustment for baseline covariates in clinical trials, https://goo.gl/YIJHEh (accessed 20 November 2016).
Google Scholar
51. McCullagh, P, Nelder, JA. Generalized linear models, Boca Raton, Florida, USA: Chapman & Hall, 1989.
Google Scholar | Crossref
52. Scharfstein, DO, Tsiatis, AA. The use of simulation and bootstrap in information-based group sequential studies. Stat Med 1998; 17: 7587.
Google Scholar | Crossref | Medline
53. Mehta CR and Tsiatis AA. Flexible sample size considerations using information-based interim monitoring. Drug Inform J 2001; 35: 1095–1112.
Google Scholar
54. Parmar, MKB, Griffiths, GO, Spiegelhalter, DJ, et al. Monitoring of large randomised clinical trials: a new approach with Bayesian methods. Lancet 2001; 358: 375381.
Google Scholar | Crossref | Medline | ISI
55. Friede, T, Schmidli, H. Blinded sample size reestimation with count data: methods and applications in multiple sclerosis. Stat Med 2010; 29: 11451156.
Google Scholar | Medline | ISI
56. Friede, T, Schmidli, H. Blinded sample size reestimation with negative binomial counts in superiority and non-inferiority trials. Meth Inform Med 2010; 49: 618624.
Google Scholar | Crossref | Medline | ISI
Access Options

My Account

Welcome
You do not have access to this content.



Chinese Institutions / 中国用户

Click the button below for the full-text content

请点击以下获取该全文

Institutional Access

does not have access to this content.

Purchase Content

24 hours online access to download content

Research off-campus without worrying about access issues. Find out about Lean Library here

Your Access Options


Purchase

SMM-article-ppv for $41.50
Single Issue 24 hour E-access for $543.66

Cookies Notification

This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more.
Top