- Joint model for continuous PK and categorical PD data
- Joint model for continuous PK and count PD data
- Joint model for continuous PK and time-to-event data

**Objectives:** learn how to implement a joint model for continuous and non continuous data.

**Projects:** warfarin_cat_project, PKcount_project, PKrtte_project

## Joint model for continuous PK and categorical PD data

**warfarin_cat_project**(data = ‘warfarin_cat_data.txt’, model = ‘PKcategorical1_model.txt’)

In this example, the original continuous PD data has been recoded as 1 (Low), 2 (Medium) and 3 (High).

**More details about the data**

International Normalized Ratio (INR) values are commonly used in clinical practice to target optimal warfarin therapy. Low INR values (<2) are associated with high blood clot risk and high ones (>3) with high risk of bleeding, so the targeted value of INR, corresponding to optimal therapy, is between 2 and 3.

Prothrombin complex activity is inversely proportional to the INR. We can therefore associate the three ordered categories for the INR to three ordered categories for PCA: Low PCA values if PCA is less than 33% (corresponding to INR>3), medium if PCA is between 33% and 50% (INR between 2 and 3) and high if PCA is more than 50% (INR<2).

The column `dv` contains both the PK and the new categorized PD measurements. Instead of modeling the original continuous PD data, we can model the probabilities of each of these categories, which have direct clinical interpretations. The model is still a joint PKPD model since this probability distribution is expected to depend on exposure, i.e., the plasmatic concentration predicted by the PK model. We introduce an effect compartment to mimic the effect delay. Let be the PCA level for patient *i* at time . We can then use a proportional odds model for modeling this categorical data:

$$\begin{array}{ccl}\text{logit} \left(\mathbb{P}(y_{ij}^{(2)} \leq 1 | \psi_i)\right) &= &\alpha_{i} + \beta_{i} Ce(t_{ij}^{(2)},\phi_i^{(1)}) \\ \text{logit} \left(\mathbb{P}(y_{ij}^{(2)} \leq 2 | \psi_i)\right) &=& \alpha_{i} + \gamma_{i} + \beta_{i}Ce(t_{ij}^{(2)},\phi_i^{(1)}) \\ \text{logit} \left(\mathbb{P}(y_{ij}^{(2)} \leq 3 | \psi_i)\right) &= & 1,\end{array}$$

where is the predicted concentration of warfarin in the effect compartment at time t for patient *i* with PK parameters . This model defines a probability distribution for if .

If , the probability of low PCA at time () increases along with the predicted concentration . The joint model is implemented in the model file `PKcategorical1_model.txt`

[LONGITUDINAL] input = {Tlag, ka, V, Cl, ke0, alpha, beta, gamma} EQUATION: {Cc,Ce} = pkmodel(Tlag,ka,V,Cl,ke0) lp1 = alpha + beta*Ce lp2 = lp1+ gamma ; gamma >= 0 DEFINITION: Level = {type=categorical, categories={1,2,3} logit(P(Level<=1)) = lp1 logit(P(Level<=2)) = lp2 } OUTPUT: output = {Cc, Level}

See Categorical data model for more details about categorical data models.

## Joint model for continuous PK and count PD data

**PKcount_project**(data = ‘PKcount_data.txt’, model = ‘PKcount1_model.txt’)

The data file used for this project is `PKcount_data.txt` where the PK and the count PD data are simulated data. We use a Poisson distribution for the count data, assuming that the Poisson parameter is function of the predicted concentration. For any individual *i*, we have

$$\lambda_i(t) = \lambda_{0,i} \left( 1 – \frac{Cc_i(t)}{Cc_i(t) + IC50_i} \right)$$

where is the predicted concentration for individual *i* at time t and

$$ \log\left(P(y_{ij}^{(2)} = k)\right) = -\lambda_i(t_{ij}) + k\,\log(\lambda_i(t_{ij})) – \log(k!)$$

The joint model is implemented in the model file `PKcount1_model.txt`

[LONGITUDINAL] input = {ka, V, Cl, lambda0, IC50} EQUATION: Cc = pkmodel(ka,V,Cl) lambda=lambda0*(1 - Cc/(IC50+Cc)) DEFINITION: Seizure = {type = count, log(P(Seizure=k)) = -lambda + k*log(lambda) - factln(k) } OUTPUT: output = {Cc,Seizure}

See Count data model for more details about count data models.

## Joint model for continuous PK and time-to-event data

**PKrtte_project**(data = ‘PKrtte_data.txt’, model = ‘PKrtteWeibull1_model.txt’)

The data file used for this project is `PKrtte_data.txt` where the PK and the time-to-event data are simulated data. We use a Weibull model for the events count data, assuming that the baseline is function of the predicted concentration. For any individual *i*, we define the hazard function as

$$h_i(t) = \gamma_{i} Cc_i(t) t^{\beta-1}$$

where is the predicted concentration for individual *i* at time **t**. The joint model is implemented in the model file `PKrtteWeibull1_model.txt`

[LONGITUDINAL] input = {ka, V, Cl, gamma, beta} EQUATION: Cc = pkmodel(ka, V, Cl) if t<0.1 haz = 0 else haz = gamma*Cc*(t^(beta-1)) end DEFINITION: Hemorrhaging = {type=event, hazard=haz} OUTPUT: output = {Cc, Hemorrhaging}

See Time-to-event data model for more details about time-to-event data models.