Paper detail

Using Targeted Maximum Likelihood Estimation to Estimate Treatment Effect with Longitudinal Continuous or Binary Data: A Systematic Evaluation of 28 Diabetes Clinical Trials

The primary analysis of clinical trials in diabetes therapeutic area often involves a mixed-model repeated measure (MMRM) approach to estimate the average treatment effect for longitudinal continuous outcome, and a generalized linear mixed model (GLMM) approach for longitudinal binary outcome. In this paper, we considered another estimator of the average treatment effect, called targeted maximum likelihood estimator (TMLE). This estimator can be a one-step alternative to model either continuous or binary outcome. We compared those estimators by simulation studies and by analyzing real data from 28 diabetes clinical trials. The simulations involved different missing data scenarios, and the real data sets covered a wide range of possible distributions of the outcome and covariates in real-life clinical trials for diabetes drugs with different mechanisms of action. For all the settings, adjusted estimators tended to be more efficient than the unadjusted one. In the setting of longitudinal continuous outcome, the MMRM approach with visits and baseline variables interaction appeared to dominate the performance of the MMRM considering the main effects only for the baseline variables while showing better or comparable efficiency to the TMLE estimator in both simulations and data applications. For modeling longitudinal binary outcome, TMLE generally outperformed GLMM in terms of relative efficiency, and its avoidance of the cumbersome covariance fitting procedure from GLMM makes TMLE a more advantageous estimator.

preprint2022arXivOpen access
0citations
0reviews
0saves
Nocode
Nodataset
0institutions

Next steps

Decide what to do with this paper

Use like or dislike for the fast social read. The more specific scholarly feedback stays available below when needed.

Log in to curate

Reading frame

Keep the important context close to the paper

Keep the important signals around this paper in one place: votes, save state, collection context, reviews and the metadata you need before deciding what to do next.

Institutions

Add specific reaction

Move through the context

Research map

Open full explorer

Move through nearby people, institutions, topics and adjacent work without leaving the paper page.

Building this graph slice

BZPEER is loading the nearby papers, people, topics and institutions for this page.

Structured reviews

0 review(s)

ContributeLeave structured feedbackUse the review template when you have a concrete strength, concern or method question.Open review form

No structured reviews yet. High-signal critique starts here.

Work discussion

0 comment(s)

DiscussAdd a high-signal commentKeep quick notes, caveats and replication pointers separate from formal reviews.Open comment form

No discussion yet. The first strong comment sets the tone.