Example
We will perform the analysis from Williamson et al. (2008) to the SANAD (Standard And New Antiepileptic Drugs) study data – the largest trial of AEDs to date (Marson et al., 2007).
Background
The time to withdrawal of a randomized drug or addition of another, has been recommended by the International League Against Epilepsy to be one of the primary endpoints for clinical trials of anti-epileptic drugs (AEDs) (Commission on Antiepileptic Drugs, 1998). Patients may decide to switch to an alternative AED because of inadequate seizure control (ISC) or to withdraw from a treatment because of unacceptable adverse effects (UAE). Overall analysis of treatment failures may miss differential effects of AEDs on the reasons for withdrawal, which may differ in terms of their relative importance for patients (Williamson et al., 2007).
The primary SANAD analysis of patients with partial epilepsy concluded that the newer drug lamotrigine (LTG) was preferable in terms of treatment failure to carbamazepine (CBZ), which had been the standard for many years (Williamson et al., 2006). LTG was significantly better in terms of withdrawal for UAE and not significantly worse in terms of withdrawal for poor seizure control. Subsequent correspondence after the trial results were published indicated that some readers were concerned that differential titration rates may have been to the disadvantage of CBZ (Cross et al., 2007). An AED that is titrated more quickly may bring benefits in terms of seizure control but be more likely to cause adverse effects. This criticism has also been leveled at previous AED trials (O’Donoghue & Sander, 1995).
Data
SANAD was an unblinded randomized trial recruiting patients with epilepsy for whom CBZ was considered to be standard treatment and they were randomized to CBZ, gabapentin, LTG, oxcarbazepine or topiramate (Marson et al., 2007). Time to treatment failure was a primary outcome with the analysis of competing risks, i.e. treatment failure due to either ISC or UAE, an important secondary objective. Although LTG appeared to be superior to CBZ in the main analysis, concerns were raised that the results were biased in favor of the newer drug. CBZ was considered to have been titrated more quickly bringing benefits in terms of seizure control but being more likely to cause adverse effects. The data set analysed here, comparing CBZ and LTG, includes 605 patients. During the trial, 94 patients withdrew from the randomized drug due to UAE while 120 withdrew due to ISC. In order to compare the two AEDs after adjusting for titration rate, dose calibration was first undertaken by standardizing the dose of both drugs relative to the midpoint of the maintenance dose range for each particular drug. The maintenance dose recommended in the SANAD trial was independently deemed to be reasonable (Faught, 2007) and the approach to calibration considered sensible. These calibrated doses are taken to be the longitudinal measurements in the competing-risks joint model.
The data is available in the joineR package by
running
library(joineR)## Loading required package: survivaldata(epileptic)
head(epileptic)## id dose time with.time with.status with.status2 with.status.uae
## 1 1 2.00 86 2400 0 0 0
## 2 1 2.00 119 2400 0 0 0
## 3 1 2.00 268 2400 0 0 0
## 4 1 2.67 451 2400 0 0 0
## 5 1 2.67 535 2400 0 0 0
## 6 1 2.67 770 2400 0 0 0
## with.status.isc treat age gender learn.dis
## 1 0 CBZ 75.67 M No
## 2 0 CBZ 75.67 M No
## 3 0 CBZ 75.67 M No
## 4 0 CBZ 75.67 M No
## 5 0 CBZ 75.67 M No
## 6 0 CBZ 75.67 M NoIn the analysis, Williamson et al. (2008) considered an interaction term between time and treatment in the longitudinal data submodel. Therefore, we will manually code this term using
epileptic$interaction <- with(epileptic, time * (treat == "LTG"))A jointdata object is first constructed using the
jointdata() function. Note that there are several status
columns: with.status is a composite event status (treatment
failure or censored), with.status.uae is a binary event
status for UAE (with failure due to ISC treated as censoring),
with.status.isc is a binary event status for ISC (with
failure due to UAE treated as censoring), and with.status2
is a vector taking values 0, 1, and 2, with 0 denoting censoring and 1
and 2 denoting dropout due to ISC and UAE, respectively.
longitudinal <- epileptic[, c(1:3, 13)]
survival <- UniqueVariables(epileptic, c(4, 6), "id")
baseline <- UniqueVariables(epileptic, "treat", "id")
data <- jointdata(longitudinal = longitudinal,
survival = survival,
baseline = baseline,
id.col = "id", time.col = "time")
summary(data)## $subjects
## [1] "Number of subjects: 605"
##
## $longitudinal
## class
## dose numeric
## time integer
## interaction integer
##
## $survival
##
## Number of subjects that fail due to cause 1: 120
## Number of subjects that fail due to cause 2: 94
## Number of subjects censored: 391
##
## $baseline
## class
## treat factor
##
## $times
## [1] "Unbalanced longitudinal study or more than twenty observation times"jointplot(data, Y.col = "dose", Cens.col = "with.status2")## Warning in jointplot(data, Y.col = "dose", Cens.col = "with.status2"): jointplot
## does not display profiles for different failure events
Model
To fit the joint model, we use the usual joint()
function as
fit2 <- joint(data = data, long.formula = dose ~ time + treat + interaction,
surv.formula = Surv(with.time, with.status2) ~ treat,
longsep = FALSE, survsep = FALSE, gpt = 3)## Competing risks detectedsummary(fit2)##
## Call:
## joint(data = data, long.formula = dose ~ time + treat + interaction,
## surv.formula = Surv(with.time, with.status2) ~ treat, longsep = FALSE,
## survsep = FALSE, gpt = 3)
##
## Random effects joint model
## Data: data
## Log-likelihood: -4056.936
##
## Longitudinal sub-model fixed effects: dose ~ time + treat + interaction
## (Intercept) 1.9730179636
## time 0.0003545439
## treatLTG -0.1380959688
## interaction 0.0006185222
##
## Competing risks sub-model effects: Surv(with.time, with.status2) ~ treat
## Failure cause 1:
## treatLTG 0.02721022
## Failure cause 2:
## treatLTG -0.6601433
##
## Latent association:
## gamma_1 0.5894143
## gamma_2 -0.9258597
##
## Variance components:
## U_0 U_1 Residual
## 7.321131e-01 1.211086e-06 1.964523e-01
##
## Convergence at iteration: 19
##
## Number of observations: 2797
## Number of groups: 605To estimate standard errors, we use the jointSE()
function as follows. However, we do not run the code in this vignette
due to computational time required.
fit2.se <- jointSE(fit2, n.boot = 100)
fit2.seConclusion
Significant \(\gamma\) estimates in the model suggests that calibrated dose is associated with time to treatment failure for both particular causes. It is observed that these estimates have opposite signs for the two failure reasons. This was a situation anticipated previously in this application, since side effects are more likely at higher doses, whereas seizure control is poorer at low doses (Williamson et al., 2006). Thus, patients on higher doses may be more likely to be withdrawn from treatment due to poor seizure control since the reason they are on higher doses is that they are having continued seizures. Patients on higher doses may also be less likely to be withdrawn from treatment due to UAE since the reason a required dose increase is possible is because no such events have occurred
The results from all models fitted suggest that if LTG is titrated at the same rate as CBZ, the beneficial effect of LTG on UAE would still be evident and the two drugs still appear to provide similar seizure control. Thus, the conclusion from the original simpler analysis of the cause-specific hazards is found to be robust to the variation in titration between the drugs in the trial.