Introduction to DynForest methodology

DynForest is a random forest methodology which can include both time-fixed predictors of any nature and time-dependent predictors possibly measured at irregular times. The purpose of DynForest is to predict an outcome which can be categorical, continuous or survival (with possibly competing events).

The random forest should first be built on a learning dataset of N subjects including: Y the outcome; x an ensemble of P time-fixed predictors; z an ensemble of Q time-dependent predictors. The random forest consists of an ensemble of B trees which are grown as detailed below.

Figure 1: Overall scheme of the tree building in DynForest with (A) the tree structure, (B) the node-specific treatment of time-dependent predictors to obtain time-fixed features, (C) the dichotomization of the time-fixed features, (D) the splitting rule.

Figure 1: Overall scheme of the tree building in DynForest with (A) the tree structure, (B) the node-specific treatment of time-dependent predictors to obtain time-fixed features, (C) the dichotomization of the time-fixed features, (D) the splitting rule.

The tree building

The tree building process, summarized in Figure 1, aims to recursively partition the subjects into groups/nodes that are the most homogeneous regarding the outcome Y.

For each tree b (b = 1, ..., B), we first draw a bootstrap sample from the original dataset of N subjects (N draws among the N subjects with replacement). The subjects excluded by the bootstrap constitute the out-of-bag (OOB) sample, noted OOBb for tree b. At each node d ∈ 𝒟b of the tree, we recursively repeat the following steps using the N(d) subjects located at node d:

  1. An ensemble of (d) = {ℳx(d), ℳz(d)} candidate predictors are randomly selected among {ℳx, ℳz} (see Figure 1B). The size of (d) is defined by the hyperparameter mtry.

  2. For each time-dependent predictor in z(d):

    1. We independently model the trajectory of the predictor using a flexible linear mixed model (Laird and Ware 1982) according to time (the specification of the model is defined by the user). It is defined as: Zij = X1ij(tij)β + X2ij(tij)bi + ϵij where Zij is the value of predictor Z for subject i at occasion j, X1ij and X2ij are vectors of time functions and covariates to be specified by the user and tij is the time at occasion j for subject i. Beta are population effects, and bi individual random effects which follow a multivariate normal distribution. ϵij are the zero-mean independent Gaussian errors of measurement.
    2. We predict the vector of random-effects i using the available information of individual i = 1, ..., N(d). i constitute time-independent features summarizing each time-dependent predictors. We thus derive the ensemble z(d) for all the variables in z(d).
  3. We define (d) = {ℳx(d), ℳz(d)} our new ensemble of candidate features.

  4. For each candidate feature W ∈ ℳ(d):

    1. We build a series of splits cW(d) according to the feature values if continuous, or subsets of categories otherwise (see Figure 1C), leading each time to two groups.
    2. We quantify the distance between the two groups according to the nature of Y:
      • If Y continuous: we compute the weighted within-group variance with the proportion of subjects in each group as weights
      • If Y categorical: we compute the weighted within-group Shannon entropy (Shannon 1948) (i.e., the amount of uncertainty) with the proportion of subjects in each group as weights
      • If Y survival competing events: we compute the log-rank statistic test (Peto and Peto 1972)
      • If Y survival competing events: we compute the Fine & Gray statistic test (Gray 1988)
  5. We split the subjects into the two groups that minimize (for continuous and categorical outcome) or maximize (for survival outcome) the quantity defined previously. We denote {W0d, c0d} the optimal couple used to split the subjects and assign them to the left and right daughter nodes 2d and 2d + 1, respectively (see Figure 1D and A).

  6. Step 1 to 5 are iterated on the daughter nodes until stopping criteria are met.

We define two stopping criteria: nodesize the minimal number of subjects in a node required to reiterate the split and minsplit the minimal number of events required to split the node. minsplit is only defined with survival outcome. In the following, we call leaves the terminal nodes.

In each leaf h ∈ ℋb of tree b, a summary πhb is computed using the individuals belonging to the leaf. The leaf summary is defined according to the outcome:

  • the mean, for Y continuous
  • the category with the highest probability, for Y categorical
  • the cumulative incidence function over time computed using the Nelson-Aalen cumulative hazard function estimator (Nelson 1969; O. Aalen 1976), for Y single cause time-to-event
  • the cumulative incidence function over time computed using the non-parametric Aalen-Johansen estimator (O. O. Aalen and Johansen 1978), for Y time-to-event with multiple causes

NOTE: Step 2 involves the estimation of a parametric mixed model for each time-dependent predictor. The specification of this model should be carefully determined in preliminary analyses by the user, keeping in mind that there should be a trade-off between goodness-of-fit and parameter parsimony. The critical point is to adequately specify the trajectory shape over time at the population and individual levels. Different bases of time functions can be considered (e.g., fractional polynomials, splines, adhoc) and compared in terms of fit.

Individual prediction of the outcome

Out-Of-Bag individual prediction

The overall OOB prediction π̂ for a subject can be computed by averaging the tree-based predictions of over the random forest as follows: where 𝒪 is the ensemble of trees where is OOB and |𝒪| denotes its cardinal The prediction π̂hb is obtained by dropping down subject along tree b. At each node d ∈ 𝒟b, the subject is assigned to the left or right node according to his/her data and the optimal couple {W0d, c0d}. W0d is a random-effect feature, its value for is predicted from the individual repeated measures using the estimated parameters from the linear mixed model.

Individual dynamic prediction from a landmark time

With a survival outcome, the OOB prediction described in the previous paragraph can be extended to compute the individual probability of event from a landmark time s by exploiting the repeated measures of subject only until s. For a new subject , we thus define the individual probability of event, noted π̂(s, t), as the probability of experiencing the event by time s + t given the information prior to landmark time s: where π̂hb(s, t) is the tree-based probability of event at time s + t computed by dropping down along the tree by considering longitudinal predictors collected until s and time-fixed predictors. Note that any horizon t can be considered provided s + t remains in the time window on which the random forest was trained. In the DynForest package, by default, the probability is computed at all the observed event times after the landmark time.

Out-Of-Bag prediction error

Using the OOB individual predictions, an OOB prediction error can be internally assessed. The OOB prediction error quantifies the difference between the observed and the predicted values. It is defined according to the nature of Y as:

  • for Y continuous, the mean square error (MSE) defined by:

  • for Y categorical, the missclassification error defined by:

  • for Y survival, the Integrated Brier Score (IBS) (Sène et al. 2016) between τ1 and τ2 defined by:

with T the time-to-event, k the cause of interest and ω̂(t) the estimated weights using Inverse Probability of Censoring Weights (IPCW) technique that accounts for censoring (Gerds and Schumacher 2006).

The OOB error of prediction is used to particular to tune the random forest by determining the hyperparameters (i.e., mtry, nodesize and minsplit) which give the smallest OOB prediction error.

Explore the most predictive variables

Variable importance

The variable importance (VIMP) measures the loss of predictive performance (Ishwaran et al. 2008) when removing the link between a predictor and the outcome. The link is removed by permuting the predictor values at the subject level for time-fixed predictors or at observation level for time-dependent predictors. A large VIMP value indicates a good prediction ability for the predictor.

However, in case of correlated predictors, the VIMP may not properly quantify the variable importance (Gregorutti, Michel, and Saint-Pierre 2017) as the information of the predictor may still be present. To better handle situations with highly correlated predictors, the grouped variable importance (gVIMP) can be computed indirectly. It consists in simultaneously evaluate the importance of a group of predictors defined by the user. The computation is the same as for the VIMP except the permutation is performed simultaneously on all the predictors of the group. A large gVIMP value indicates a good prediction ability for the group of predictors.

Minimal depth

The minimal depth is another statistic to quantify the importance of a variable. It assesses the distance between the root node and the first node for which the predictor is used to split the subjects (1 for first level, 2 for second level, 3 for third level, …). This statistic can be computed at the predictor level or at the feature level, allowing to fully understand the tree building process.

We strongly advice to compute the minimal depth with mtry hyperparameter chosen at its maximum to ensure that all predictors are systematically among candidate predictors for splitting the subjects.

References

Aalen, Odd. 1976. “Nonparametric Inference in Connection with Multiple Decrement Models.” Scandinavian Journal of Statistics 3 (1): 15–27. https://www.jstor.org/stable/4615603.
Aalen, Odd O., and Søren Johansen. 1978. “An Empirical Transition Matrix for Non-Homogeneous Markov Chains Based on Censored Observations.” Scandinavian Journal of Statistics 5 (3): 141–50. https://www.jstor.org/stable/4615704.
Gerds, Thomas A., and Martin Schumacher. 2006. “Consistent Estimation of the Expected Brier Score in General Survival Models with Right-Censored Event Times.” Biometrical Journal 48 (6): 1029–40. https://doi.org/10.1002/bimj.200610301.
Gray, Robert J. 1988. “A Class of K-Sample Tests for Comparing the Cumulative Incidence of a Competing Risk.” The Annals of Statistics 16 (3): 1141–54. https://www.jstor.org/stable/2241622.
Gregorutti, Baptiste, Bertrand Michel, and Philippe Saint-Pierre. 2017. “Correlation and Variable Importance in Random Forests.” Statistics and Computing 27 (3): 659–78. https://doi.org/https://doi.org/10.1007/s11222-016-9646-1.
Ishwaran, Hemant, Udaya B. Kogalur, Eugene H. Blackstone, and Michael S. Lauer. 2008. “Random Survival Forests.” The Annals of Applied Statistics 2 (3): 841–60. https://doi.org/10.1214/08-AOAS169.
Laird, Nan M., and James H. Ware. 1982. “Random-Effects Models for Longitudinal Data.” Biometrics 38 (4): 963–74. https://doi.org/10.2307/2529876.
Nelson, Wayne. 1969. “Hazard Plotting for Incomplete Failure Data.” Journal of Quality Technology 1 (1): 27–52. https://doi.org/10.1080/00224065.1969.11980344.
Peto, Richard, and Julian Peto. 1972. “Asymptotically Efficient Rank Invariant Test Procedures.” Journal of the Royal Statistical Society: Series A (General) 135 (2): 185–98. https://doi.org/https://doi.org/10.2307/2344317.
Sène, Mbéry, Jeremy MG Taylor, James J Dignam, Hélène Jacqmin-Gadda, and Cécile Proust-Lima. 2016. “Individualized Dynamic Prediction of Prostate Cancer Recurrence with and Without the Initiation of a Second Treatment: Development and Validation.” Statistical Methods in Medical Research 25 (6): 2972–91. https://doi.org/10.1177/0962280214535763.
Shannon, Claude Elwood. 1948. “A Mathematical Theory of Communication.” The Bell System Technical Journal 27 (3): 379–423. https://doi.org/10.1002/j.1538-7305.1948.tb01338.x.