PAIN
Volume 151, Issue 3 , Pages 592-597, December 2010

Numbers-needed-to-treat analyses – Do timing, dropouts, and outcome matter? Pooled analysis of two randomized, placebo-controlled chronic low back pain trials

  • R. Andrew Moore

      Affiliations

    • Pain Research and Nuffield Department of Anaesthetics, University of Oxford, Oxford, UK
    • Corresponding Author InformationCorresponding author. Address: Pain Research and Nuffield Department of Anaesthetics, University of Oxford, John Radcliffe Hospital, Level 6 West Wing, Oxford, OX3 9DU, UK. Tel.: +44 1865 231512; fax: +44 1865 234539.
  • ,
  • Steven S. Smugar

      Affiliations

    • Merck Research Laboratories, Rahway, NJ, USA
  • ,
  • Hongwei Wang

      Affiliations

    • Merck Research Laboratories, Rahway, NJ, USA
  • ,
  • Paul M. Peloso

      Affiliations

    • Merck Research Laboratories, Rahway, NJ, USA
  • ,
  • Arnold Gammaitoni

      Affiliations

    • Merck Research Laboratories, Rahway, NJ, USA

Received 29 October 2009; received in revised form 14 June 2010; accepted 14 July 2010. published online 01 September 2010.

Abstract 

Numbers-needed-to-treat (NNT) are useful for presenting treatment response, conveying the clinical relevance of results. NNTs are typically calculated at a landmark endpoint (end of trial), but often using the last observation carried forward (LOCF), which ignores patient discontinuations. We compared NNTs in chronic low back pain (CLBP) using three separate imputation methods, using data from two identical 12-week trials comparing etoricoxib 60mg (N=210), 90mg (N=212), and placebo (N=217). We calculated the number of patients with improvements in pain intensity from baseline of ⩾15%, ⩾30%, ⩾50%, and ⩾70% at 2, 4, 8, and 12weeks of treatment. For longitudinal response over time, patient discontinuations were assigned a 0% improvement from dropout forward. Landmark response at week 12 was assessed using LOCF and completer approaches, using only observed (non-missing) data. The longitudinal approach was most conservative; after 12weeks 65% of patients taking etoricoxib had ⩾15% improvement, 60% had ⩾30% improvement, 45% had ⩾50%, improvement, and 30% had ⩾70% improvement, with placebo rates approximately 55%, 45%, 30%, and 15%, respectively. Response rates were higher with landmark analyses. Landmark NNTs at week 12 were generally similar or slightly lower (better) than those from a longitudinal approach, but results were inconsistent. Landmark analyses provide no information on response variability, as is obtained with longitudinal analysis. Outcome, imputation method, and reporting method are intimately connected and need to be considered alongside trial quality and validity to make sensible comparisons between treatments.

Keywords: Analgesia, Low back pain, NNT, NSAID, Responder, Back pain, Outcome, Imputation methods

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PII: S0304-3959(10)00426-4

doi:10.1016/j.pain.2010.07.013

Refers to article:

  • Dropouts and sub-groups – statistics can help but not cure , 14 September 2010

    P. Croft, R. Froud, A.M. Lewis
    PAIN December 2010 (Vol. 151, Issue 3, Pages 563-564)

PAIN
Volume 151, Issue 3 , Pages 592-597, December 2010