Abstract
The growth of colorectal cancer tumors and their reactions to chemo-immunotherapeutic treatment with monoclonal antibodies (mAb) are discussed in this paper using a system of fractional order differential equations (FDEs). mAb medications are still at the research stage; however, this research takes into account the mAbs that are already in use. The major goal is to demonstrate the effectiveness of the mAb medication Cetuximab and the significance of IL-2 levels in immune system support. The created model is broken down into four sub-systems: cell populations, irinotecan (CPT11) concentration for treatment, IL-2 concentration for immune system support, and monoclonal antibody Cetuximab. We show the existence and uniqueness of the initial value problem (IVP). After that, we analyze the stability of the equilibrium points (disease-free and co-existing) using the Routh–Hurwitz criteria. In addition, in applying the discretization process, we demonstrate the global stability of the constructed system around the equilibrium points based on specific conditions. In the end, simulation results were carried out to support the theory of the manuscript.
Keywords:
stability; existence and uniqueness; colorectal cancer; fractional-order differential equations MSC:
34A34; 34D20; 39A30; 92B05
1. Introduction
One of the most frequent cancers in the world for both women and men is colorectal cancer [1]. Apart from various and mixed treatment procedures to minimize and eliminate the cancerous tissues, the immune system (IS) has an important impact during the treatment. Within this, additional treatment strategies are involved in cancer therapy, such as using monoclonal antibody drugs. While there are still many unresolved problems about the efficiency of monoclonal antibodies and their use, we believe that mixed therapy would be well understood by establishing mathematical models and analyzing the optimal treatment process using clinical data that might support theoretical and applied science studies. Several studies with various treatment strategies looked into tumor cells’ interaction with the immune system. Some of them are [2,3,4,5,6,7].
Other research mainly concentrated on the resources and dynamics of populations [8,9,10], while some clinical and mathematical research explicitly focused on the use of monoclonal antibodies in vivo and in vitro [5,11,12]. To illustrate the utility and application of both monoclonal antibody concentrations and immunotherapy, it is important to depict tumor growth and treatment procedures in applied sciences such as mathematical models. Thus, by combining theory and application, we may properly comprehend the dynamic of the biological system.
De Pillis et al. established in [12] the tumor progression while taking into account the levels of doxorubicin and IL-2 in the bloodstream as well as the effects of various immune cells. The study in [2] included the addition of three immunological compartments, one compartment each measuring tumor density, chemotherapy medication, and concentration of IL-2. As previously stated in [3], they also address the kinetics of IL-2 and the IL-2 production with biological interactions. Irinotecan, a chemotherapeutic drug, and one of two monoclonal antibodies—cetuximab, which has FDA approval for colorectal cancer treatments, and panitumumab, which is still being tested in clinical trials—were modelled by the authors in [5]. Here, they introduced and simulated a new experimental dosing schedule that reduced the tumor size efficiently.
The dynamical behavior is expanded in this manuscript in light of the studies on immunotherapy and monoclonal antibody treatment that were previously mentioned. Since derivatives and integrals are defined for any real order, fractional calculus is an extension of conventional calculus. Fractional operators can more effectively depict systems with high-order dynamics and complicated nonlinear phenomena than standard derivatives and integrals in particular situations. This is due to two key factors. First, we are not limited to integer order and are free to choose any order for the derivative and integral operators. Second, fractional order derivatives are advantageous when the system has a long-term memory since they depend not only on current circumstances but also on the past [13,14,15,16].
Hence, fractional-order differential equations can more accurately depict a variety of complicated biological processes with nonlinear dynamics and long-term memory that cannot be theoretically expressed by ODEs. Additionally, the conversion of an ODE model into an FDE model needs to be precise in terms of differentiation order because even a small change can have a big impact on how the solutions behave [17,18,19,20,21,22,23].
The effectiveness of immunotherapy and monoclonal antibody medications are established in the section that follows, which also establishes a system of fractional-order differential equations that take colorectal cancer growth, irinotecan concentration in chemotherapy, and other factors into account.
The structure of this manuscript is as follows: A tumor growth of colorectal cancer and its response to chemo-immunotherapeutic treatment with monoclonal antibody (mAb) is formulated as a system of fractional order differential equation in Section 2, where we also prove the IVP’s uniqueness and existence. In Section 3, we analyze the local stability of both equilibrium points, while Section 4 represents the global stability of the equilibrium points based on specific conditions. At the end of the study, we used in vivo and in vitro clinical data to illustrate the simulation results.
2. A Fractional-Order Mathematical Model
In the initiated model, a colorectal cancer malignant cell population is introduced. The purpose of the study is to examine and present the effectiveness of various immune system-supporting supplements and the response of cancer tissues to monoclonal antibody therapy (mAb). In order to go through a painful and protracted therapy, the combined therapy concentrates on removing the cancer tissues and bolstering the immune system with supplements.
Thus, the system is defined with seven compartments:
- : colorectal cancer cells,
- : compartment of natural killer (N.K.),
- : the CDT cell population,
- : lymphocytes population,
- : irinotecan concentration,
- : IL-2 concentration,
- : mAb Cetuximab concentration.
The mAb Cetuximab and the chemotherapeutic medication Irinotecan (CPT11) will be examined as therapies.
Below is the mathematical system of colorectal cancer with multi-modal therapy.
and
where the parameters are defined in is the Caputo derivative, see [24,25], and . Table 1 illustrates the descriptions of [2,3,11,12,26,27,28].
Table 1.
Parametric explanation.
Definition 1
([24]). Given a function , the fractional integral with order is given by Abdel’s formula as
Definition 2
([24]). Let be a continuous function. The Caputo fractional derivative of order , where is a positive integer and is defined as
when , the derivatives are defined to be the usual order derivatives.
Definition 3
([25]). The Mittag-Leffler function of one variable is
The existence of a positive domain where , and the unique solution of an IVP in the same region can be shown using the lemma and theory in [29,30,31]. The local stability analysis of both equilibrium points—disease-free and coexisting—will serve as the foundation for our main research in the following part.
Theorem 1.
The solution of the IVP in (1) and (2) is unique, and the solutions are in .
Proof of Theorem 1.
Using the lemma and theory in [29,30,31], we have to prove that the domain is positively invariant. Thus, we have the following:
This implies that all the above equations are non-negative, which shows that the domain is positively invariant. □
Let us rewrite the system:
To analyze the stability of (3), we perturb the equilibrium points by that is
Thus, we have
and
where We use the property that
Thus, a linearized system about the equilibrium point is obtained, such as
where . Moreover, is the Jacobian matrix at the equilibrium point, and we have such that is the diagonal matrix of , while shows the eigenvectors of Thus, we have
and the solutions are given by Mittag-Leffler functions, such as
and
The studies in [32,33] proved the stability criteria using the Mittag-Leffler functions. Thus, if , then are decreasing, and therefore we have decreasing. In other words, let the solution of (2.4) exist. If the solution of (4) is increasing, then the equilibrium point of the system is unstable. Similarly, if the solution of (4) is decreasing, then the equilibrium point is locally asymptotically stable.
Hence, we denote the two equilibrium points that will be analyzed in the next section:
The Disease-free (Extinction of tumor population): The Co-existing: .
3. Local Stability of the Disease-Free (Extinction) and Positive (Co-Existing) Equilibrium Points
The local stability analysis of both equilibrium points is investigated in this section using the Routh–Hurwitz Criterion.
By linearizing system (1) around the disease-free equilibrium point, we derive the Jacobian matrix:
where
This leads to the following derivation of the characteristic equation of (6):
Theorem 2.
Let be the disease-free equilibrium point of system (1) and assume that and . If
and
where
then is locally asymptotically stable.
Proof of Theorem 2.
It can be seen that
- (i)
- if .
- (ii)
- , if and .
- (iii)
- .
- (iv)
- .
- (v)
- .
Moreover, from the characteristic Equation (7), we have to analyze the stability criteria of the following equation:
(a) Let . For the inequality
we obtain
(b) If
then we have
which holds for
In considering both (12) and (13), we get
and
where
□
The Jacobian matrix of the co-existing equilibrium point is given by
where
Under the assumption that in a co-existing tumor population the cell production is and
we obtain the characteristic equation of the positive equilibrium point, such as
where
and
Theorem 3.
and
and
where
then the compartments of show locally asymptotically stability.
Let be the positive equilibrium point of system (1). The following statements hold:
- (a)
- Assume that
Then, for the conditions
and
we have
which implies that the compartment compartments are local asymptotic stable.
- (b)
- Assume that . If
Proof of Theorem 3.
- (a)
- To prove the local stability of the compartment, we have to consider the following equation:
From
we have
which implies that
and .
In addition, the inequality holds if
which exists for the conditions
where
and
Considering both (32) and (34), we obtain the interval of (34). Thus, we have
which completes the proof of statement (a).
- (b)
- To prove the local asymptotic stability of the compartments , we have to analyze the following equation:
The condition shows that it holds if
where
Moreover, from , we have
which holds for the conditions
and
In considering both (37) and (38), we get
and
where
□
4. Global Stability of the Equilibrium Points
To demonstrate the global stability of the extinction of the tumor population and co-existing cases, the discretization technique is used in this section. We like to think of the system’s global stability (1) as a system of difference equations because various decisions and actions were taken within discrete time intervals. Let The system (1) is discretized as follows:
Starting with and we get
The solution of (44) reduces to
For we obtain
In repeating the discretization process times, we get
Finally, for where and , we obtain
Lemma 1.
Assume that be a positive solution to the system (43). Then the following conditions hold.
- (i)
- IfThen the positive solution of system (43) is monotonic increasing.
- (ii)
- IfThen the positive solution of system (43) is monotonic decreasing.
Proof of Lemma 1.
The following computation is obtained in analyzing the monotonic behavior of the solution in system (48), such as
Thus, it can be seen that for the conditions in (i), system (43) shows
and, based on the conditions in (ii), we have
□
Theorem 4.
Let be the disease-free equilibrium point of system (43). Assume that the local stability conditions and Lemma 1/(ii) hold. If
where then the equilibrium point is global asymptotically stable.
Proof of Theorem 4.
Let us consider a Lyapunov function
defined by
where
and .
The change along the solutions of the system is
From the first equation of system (43), we have
Using Lemma 1/(ii), we can see that Thus, we need to show only that
which holds for
Thus, we obtain Similar to the previous computations, we can analyze
From Lemma 1/(ii), we can show that
for if
and
□
Theorem 5.
Let be the co-existing (positive) equilibrium point of system (43). Moreover, asuume that the local stability conditions and Lemma 1/(ii) hold. If
where then is globally asymptotically stable.
Proof of Theorem 5.
It is similar to the proof of Theorem 4. Hence, it is skipped. □
5. Simulation Results
We simulate the IVP (1) and (2) using the data obtained in Table 2. The developed model consists of tumor cells, components of the host’s immune response, and therapies such as irinotecan and Cetuximab, a monoclonal antibody concentration that has been FDA-approved for the treatment of colorectal cancer and is designed to bind to particular proteins. The literature for the study, which includes both in vivo and in vitro research on colorectal cancer, is thoroughly examined. It is seen that Cetuximab was applied with and without irinotecan to therapies to raise the survival rate and the condition of life [34].
Table 2.
Parametric values.
We use the constructed model to explore the expected responses of the therapy for specific tumor cell populations. According to body mass, the person is a male who weighs 77 kg and has a chronic illness that has to be supported with additional nutrients to maintain a healthy immune system.
According to Table 2, the parameter values were obtained from in vivo and in vitro studies.
As a result, we first simulated the case of a disease-free equilibrium point, which can be assumed in the early detection of tumor density. In (I-a), we consider the treatment without irinotecan, and in (I-b), we add 30 once every 21 days. To see the simulation results more precisely, we multiplied the initial conditions by .
- (I-a)where we avoid the chemotherapy effect,
- (I-b)where the effect of irinotecan is included.
For this scenario, the clinical data showed extinction of the tumor density for cases (I-a) and (I-b).
As analyzing the stability of a coexisting equilibrium point implies that the tumor has already attained a significant density, we make the following assumption with the following initial condition:
- (II-a)where we focus on the immunotherapy and mAb,
- (II-b)where all treatment supplements (including irinotecan) are involved.
- (II-c)where all treatment supplements (including irinotecan) are involved.
In this scenario, the clinical data illustrate an increase in the tumor density for (II-a), meaning that IL-2 treatment and the concentration of Cetuximab were insufficient to control the growth of the tumor cell population. Case (II-b) showed that growth decreases if all treatment supplements are involved in the therapy. By increasing the dosage of the chemotherapeutic drug to 60 once every 21 days, the tumor cell population is rendered extinct.
Figure 1 illustrates the graph of system (1) for each compartment with the initial conditions given in (I-a). The tumor cell population is low and represents an early detected case of colorectal cancer. Considering now the in vivo and in vitro studies of [5,34], it is emphasized that the concentration and the mAb drug of Cetuximab would be sufficient for the treatment to shrink the tumor density.

Figure 1.
(a) Dynamics of the tumor density for , (b) Dynamics of N.K. for (c) Dynamics of CDT-cell for (d) Dynamics of lymphocytes for (e) Dynamics of irinotecan for , (f) Dynamics of IL-2 for (g) Dynamics of Cetuximab for .
For system (1) and the initial conditions in (I-a), it is seen that the tumor density is extinct. There is no need to provide irinotecan with this appropriate therapy because it already reaches every region of the body through the bloodstream; this indicates that .
Figure 2 shows the graph of system (1) with the initial conditions of (I-b). In this example, irinotecan is included in the treatment, and a similar result to (I-a) is obtained. Figure 2 is a vital graph emphasizing that not all mixed therapies should include chemotherapy. In the case of both (I-a) and (I-b), the tumor density decreases, while in (I-b), one should notice that the chemotherapeutic drug also destroys normal tissues and affects the immune system. Therefore, considering the whole dynamic of the system, it is notable to support the body with additional supplements that keep the immune system strong instead of increasing the variation of the drugs.
Figure 2.
(a) Dynamics of the tumor density for , (b) Dynamics of N.K. for (c) Dynamics of CDT-cell for (d) Dynamics of lymphocytes for (e) Dynamics of irinotecan for , (f) Dynamics of IL-2 for (g) Dynamics of Cetuximab for .
When the tumor has already achieved a certain density, as in Figure 3, only the IL-2 concentration can assist the immune system, and the dosage of mAb is insufficient. The tumor has a cell population of While the tumor density expanded quickly, we also noticed that the natural killers were interacting heavily.
Figure 3.
(a) Dynamics of the tumor density for , (b) Dynamics of N.K. for (c) Dynamics of CDT-cell for (d) Dynamics of lymphocytes for (e) Dynamics of irinotecan for , (f) Dynamics of IL-2 for (g) Dynamics of Cetuximab for .
To observe the system’s dynamic response, we now add 30 mg of irinotecan under the identical supposition as in Figure 3. Figure 4 represents the immune-chemotherapeutic treatment with the monoclonal antibody cetuximab and a successful result of a decrease in the tumor compartment. Since the aim is to keep the immune system strong and to avoid any destruction of the normal tissue, we believe, as is also mentioned in the references of Table 2, that for this tumor density, the dosage is enough to reach the desired outcome.

Figure 4.
(a) Dynamics of tumor density for , (b) Dynamics of N.K. for (c) Dynamics of CDT-cell concentration for (d) Dynamics of lymphocytes for (e) Dynamics of irinotecan for , (f) Dynamics of IL-2 for (g) Dynamics of Cetuximab for .
In addition, we want to increase the dosage of the chemotherapeutic drug to to show the side effect on the human body.
As expected, we see in Figure 5 that the normal cells are also affected by the drug, which destroys the immune system. Thus, the patient can be attacked by any other chronic or non-chronic disease, which would lead to unexpected results.

Figure 5.
(a) Dynamics of tumor density for , (b) Dynamics of N.K. for (c) Dynamics of CDT-cell concentration for (d) Dynamics of lymphocytes for (e) Dynamics irinotecan for , (f) Dynamics of IL-2 for (g) Dynamics of Cetuximab for .
6. Conclusions
Fractional calculus is an extension of traditional calculus because derivatives and integrals are defined for any real order. In some cases, fractional operators are superior to traditional derivatives and integrals for representing systems with high-order dynamics and complex nonlinear processes.
To describe the dynamical behavior of colorectal cancer following immune chemotherapy with mAb-Cetuximab, we proposed a system of fractional order differential equations. The study’s goal is to investigate and present the efficacy of various immune system-supporting supplements and the way that cancer tissues react to monoclonal antibody therapy (mAb). The combined therapy focuses on eliminating the cancerous tissues and boosting the immune system with supplements rather than putting the patient through a painful and drawn-out treatment. Thus, in Section 2 we defined the system with seven compartments: colorectal cancer cells; compartment of natural killer (N.K.); the CDT-cell population; the lymphocytes population; the irinotecan concentration; the IL-2 concentration; , the mAb Cetuximab concentration.
The local stability of the disease-free and co-existing equilibrium points was theoretically demonstrated in Section 3. Section 4 showed the condition of global stability, where discretization processes were applied to analyze the discrete treatment in an expanded interval. We proved theoretically and numerically how important it is to apply both immunotherapy and mAb treatment in order to prevent the negative effects of chemotherapeutic medications based on the early diagnosis of the tumor and the significant density of the cancer cells. Furthermore, it is emphasized that the need for irinotecan is essential in further stages of tumor density. The amount of this prescription (irinotecan), however, has a damaging power to natural killers, which affects the human body’s immune system—particularly when the person has a chronic illness and needs intense immune system support. As a result, the timing should be carefully planned, taking into account the ideal concentration required to reduce the tumor density.
In Section 5, we provided several early detection and tumor density stage scenarios to demonstrate the findings. We observed that different treatment approaches are required given the tumor density and the immune system’s supplementation requirements. As a result, it is seen that alternative treatment strategies have to be applied in considering the density of the tumor and the necessity of optimal dosage in the therapy.
Author Contributions
Conceptualization, A.A., A.Y. and F.B.; methodology, A.A., A.Y. and F.B.; software, A.A., A.Y. and F.B.; validation, A.A., A.Y. and F.B.; formal analysis, A.A., A.Y. and F.B.; investigation, A.A., A.Y. and F.B.; resources, A.A., A.Y. and F.B.; data curation, A.A., A.Y. and F.B.; writing—original draft preparation, A.A., A.Y. and F.B.; writing—review and editing, A.A., A.Y. and F.B.; visualization, A.A., A.Y. and F.B.; supervision, A.A., A.Y. and F.B. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Data Availability Statement
No new data were created or analyzed in this study.
Conflicts of Interest
The authors declare no conflict of interest.
Abbreviations
| Lymphocytes of the antiviral immune response | |
| Irinotecan medication | |
| U.S. Food and Drug Administration | |
| Fractional Order Differential Equation | |
| Interleukins | |
| Immune System | |
| Initial value Problem | |
| Monoclonal Antibody | |
| Natural Killer | |
| Ordinary Differential Equations |
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