A Fractional Caputo Kolmogorov Differential Equation with Hawkes Birth Intensity: Application to Cancer Progression
Keywords:
Fractional calculus, Caputo derivative, Hawkes process, Kolmogorov forward equation, Cancer progression modelingAbstract
Cancer progression is inherently stochastic, driven by cumulative genetic and epigenetic
alterations, temporally clustered mutation events, and long-range biological memory effects
that violate the Markov property assumed in conventional models. Classical birth–death and
diffusion frameworks therefore fail to capture the observed heterogeneity, burst dynamics,
and history dependence of tumor evolution. In this study, a novel fractional stochastic
formulation is developed based on the Caputo fractional Kolmogorov forward differential
equation coupled with a Hawkes self-exciting birth intensity to describe cancer cell population
dynamics. The Caputo fractional derivative of order ( ) 0 1 introduces nonlocal temporal
memory and hereditary effects, enabling the system to retain information about past states,
while the Hawkes process models mutation-induced proliferative bursts via endogenous self
excitation and event clustering. Together, these components yield a non-Markovian birth
death process with transition rates that depend explicitly on the entire evolutionary history.
Analytical characteristics of the model are derived using Laplace transform methods and
properties of fractional operators, establishing existence, stability conditions, and
asymptotic behavior. Numerical simulations are conducted to explore sensitivity to key
parameters, including the fractional order, excitation kernel, and baseline proliferation rate.
The results reproduce biologically realistic tumor growth patterns, such as latency phases,
sub-exponential expansion, heavy-tailed inter-event times, and intermittent episodes of rapid
proliferation consistent with clonal sweeps. Comparative evaluation against classical
Markovian and purely fractional models demonstrates superior flexibility, predictive
capability, and mechanistic interpretability of the hybrid framework. This approach provides
a rigorous mathematical platform for modeling tumor evolution and offers potential
applications in quantitative oncology, including prognosis, treatment scheduling, and
optimization of therapeutic interventions under uncertainty.
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