A modified weighted log-rank test for confirmatory trials with a high proportion of treatment switching

05/19/2020
by   Jose L Jimenez, et al.
0

In confirmatory cancer clinical trials, overall survival (OS) is normally a primary endpoint in the intention-to-treat (ITT) analysis under regulatory standards. After the tumor progresses, it is common that patients allocated to the control group switch to the experimental treatment, or another drug in the same class. Such treatment switching may dilute the relative efficacy of the new drug compared to the control group, leading to lower statistical power. It would be possible to decrease the estimation bias by shortening the follow-up period but this may lead to a loss of information and power. Instead we propose a modified weighted log-rank test (mWLR) that aims at balancing these factors by down-weighting events occurring when many patients have switched treatment. As the weighting should be pre-specified and the impact of treatment switching is unknown, we predict the hazard ratio function and use it to compute the weights of the mWLR. The method may incorporate information from previous trials regarding the potential hazard ratio function over time. We are motivated by the RECORD-1 trial of everolimus against placebo in patients with metastatic renal-cell carcinoma where almost 80% of the patients in the placebo group received everolimus after disease progression. Extensive simulations show that the new test gives considerably higher efficiency than the standard log-rank test in realistic scenarios.

READ FULL TEXT

page 1

page 2

page 3

page 4

research
08/01/2019

Teasing out the overall survival benefit with adjustment for treatment switching to other therapies

In oncology clinical trials, characterizing the long-term overall surviv...
research
02/27/2020

Assessing causal effects in the presence of treatment switching through principal stratification

Clinical trials focusing on survival outcomes often allow patients in th...
research
03/10/2023

Adjusting for time-varying treatment switches in randomized clinical trials: the danger of extrapolation and how to avoid it

When choosing estimands and estimators in randomized clinical trials, ca...
research
09/25/2020

A novel estimand to adjust for rescue treatment in clinical trials

The interpretation of randomised clinical trial results is often complic...
research
03/26/2020

A Machine Learning alternative to placebo-controlled clinical trials upon new diseases: A primer

The appearance of a new dangerous and contagious disease requires the de...
research
06/27/2020

Impact of the adjustment of stratification factors on time-to-event analyses

In a stratified clinical trial design with time to event end points, str...
research
12/06/2018

Adaptive multicenter designs for continuous response clinical trials in the presence of an unknown sensitive subgroup

The partial effectiveness of drugs is of importance to the pharmaceutica...

Please sign up or login with your details

Forgot password? Click here to reset