Literature DB >> 9620807

Intention-to-treat vs. on-treatment analyses of clinical trial data: experience from a study of pyrimethamine in the primary prophylaxis of toxoplasmosis in HIV-infected patients. ANRS 005/ACTG 154 Trial Group.

G Chêne1, P Morlat, C Leport, R Hafner, L Dequae, I Charreau, J P Aboulker, B Luft, J Aubertin, J L Vildé, R Salamon.   

Abstract

Randomized clinical trials analyzed by the intent-to-treat approach provide unbiased comparisons among treatment groups. To avoid dilution of treatment effect, many people also perform an analysis by treatment actually received, although this method may introduce bias into the results. This paper presents several approaches used for analyzing data of a recent trial and the difficulties encountered in interpreting the results of each approach. The ANRS 005/ACTG 154 Study was a double-blind, placebo-controlled, randomized, international (French, U.S., and Spanish) multicenter trial designed to assess the effectiveness of pyrimethamine for the primary prophylaxis of cerebral toxoplasmosis (CT) in HIV-infected patients with advanced immunodeficiency. In the intention-to-treat analysis, the cumulative probability of CT at 1 year did not differ significantly between the pyrimethamine arm (11.9%) and the placebo arm (13.1%), Hazard Ratio (HR) = 0.94 (95% Confidence Interval (CI) = 0.62-1.42), whereas an on-treatment analysis resulted in a significant difference: 4.2% in the pyrimethamine arm and 12.4% in the placebo arm, HR = 0.44 (95% CI = 0.24-0.80). The data showed a significant interaction between compliance and treatment outcome; and side effects were more frequently cited as reasons for compliance violations in the pyrimethamine group. Several different analytic approaches (censoring data at the time patients discontinued the study medication only for selected reasons) failed to explain the disparity between the estimation of effect of pyrimethamine by the intention-to-treat and on-treatment analyses. This experience led us to believe that comparing the results of both analyses was the best method to convince clinicians that intention-to-treat was the only interpretable analysis. We were concerned that even if pyrimethamine had a beneficial effect, it was very difficult (1) to quantify and (2) to apply to clinical practice unless one could predict the occurrence of study drug discontinuation for each patient at the time of treatment assignment. Although exploratory analyses may yield clinically relevant information and useful clarifications in the evaluation of treatments, intention-to-treat remains the only interpretable analysis of clinical trials.

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Year:  1998        PMID: 9620807     DOI: 10.1016/s0197-2456(97)00145-1

Source DB:  PubMed          Journal:  Control Clin Trials        ISSN: 0197-2456


  9 in total

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4.  Modified intention to treat reporting in randomised controlled trials: systematic review.

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Journal:  BMJ       Date:  2010-06-14

5.  Opening the "Black Box": family check-up intervention effects on self-regulation that prevents growth in problem behavior and substance use.

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Journal:  Trials       Date:  2015-08-17       Impact factor: 2.279

7.  Second-line glucose-lowering drugs added to metformin and the risk of hospitalization for heart failure: A nationwide cohort study.

Authors:  Su Jin Lee; Kyoung Hwa Ha; Jung Hyun Lee; Hokyou Lee; Dae Jung Kim; Hyeon Chang Kim
Journal:  PLoS One       Date:  2019-02-11       Impact factor: 3.240

8.  Randomised controlled trials and clinical maternity care: moving on from intention-to-treat and other simplistic analyses of efficacy.

Authors:  A W Welsh
Journal:  BMC Pregnancy Childbirth       Date:  2013-01-17       Impact factor: 3.007

Review 9.  A commentary on randomized clinical trials: How to produce them with a good level of evidence.

Authors:  Olga Dumont Flecha; Dhelfeson Willya Douglas de Oliveira; Leandro Silva Marques; Patricia Furtado Gonçalves
Journal:  Perspect Clin Res       Date:  2016 Apr-Jun
  9 in total

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