Optimization of Cancer Treatment in the Frequency Domain
Thorough exploration of alternative dosing frequencies is often not performed in conventional pharmacometrics approaches. Quantitative systems pharmacology (QSP) can provide novel insights into optimal dosing regimen and drug behaviors which could add a new dimension to the design of novel treatments. However, methods for such an approach are currently lacking. Recently, we illustrated the utility of frequency-domain response analysis (FdRA), an analytical method used in control engineering, using several generic pharmacokinetic-pharmacodynamic case studies. While FdRA is not applicable to models harboring ever increasing variables such as those describing tumor growth, studying such models in the frequency domain provides valuable insight into optimal dosing frequencies. Through the analysis of three distinct tumor growth models (cell cycle-specific, metronomic, and acquired resistance), we demonstrate the application of a simulation-based analysis in the frequency domain to optimize cancer treatments. We study the response of tumor growth to dosing frequencies while simultaneously examining treatment safety, and found for all three models that above a certain dosing frequency, tumor size is insensitive to an increase in dosing frequency, e.g., for the cell cycle-specific model, one dose per 3 days, and an hourly dose yield the same reduction of tumor size to 3% of the initial size after 1 year of treatment. Additionally, we explore the effect of drug elimination rate changes on the tumor growth response. In summary, we show that the frequency-domain view of three models of tumor growth dynamics can help in optimizing drug dosing regimen to improve treatment success.
KEY WORDScancer dosing frequency optimization frequency-domain response analysis quantitative systems pharmacology
In clinical pharmacology, treatment regimen are usually defined by drug dose, dosing interval, and treatment duration. Because the success of drug interventions heavily depends on drug administration schedules, the high rate of late-stage attrition in clinical development can be attributed partly to sub-optimal dosing regimen selection [1, 2]. Often, dose and dosing schedule are determined through pharmacokinetic and pharmacodynamic (PKPD) model simulations . In quantitative systems pharmacology (QSP), such PKPD models are combined with mechanistic systems biology and/or disease models . Such mechanistic models have long been used to describe and predict various aspects in oncology [5, 6, 7], from the underlying biological mechanisms [8, 9, 10] to tumor growth [11, 12]. While QSP is increasingly utilized in anti-cancer drug discovery and development [13, 14], only a few examples exist where it has been applied to optimize drug dosing and scheduling to predict tumor responses, efficacy, and toxicity [15, 16]. Control theory methods, but almost exclusively optimal control theory, have been used to optimize dosing regimen [17, 18]; however, the range of analyzed regimen has been limited. Primarily, optimal control theory served as a method to optimize dose [19, 20, 21]. Fister and Panetta , for example, used optimal control theory on a model of cell cycle-specific bone marrow growth to determine effective administrations of a chemotherapeutic agent while maximizing bone marrow mass and the drug dose over the treatment interval.
However, there has been little systematic effort in determining the influence of dosing frequency on treatment success by using PKPD models. To approach this gap, we recently published a tutorial for pharmacologists on frequency-domain response analysis (FdRA), an analytical method commonly used in systems and control engineering . QSP models relate inputs such as the plasma concentration of a drug or a schedule of drug administrations to outputs such as the effect of a drug. Because these key variables typically vary in time, QSP models are often based on differential equations. The time scales on which they act can differ significantly, from drug-receptor binding happening within seconds to tumor growth over the course of years. Similarly, disturbances of dynamic biological systems, such as drug interventions, can span multiple time scales as well. FdRA provides a framework for analyzing how such disturbances on various time scales affect dynamic systems by focusing on the change of the harmonic content (i.e., frequency, amplitude, and phase) of an input signal when it is passed to the output, rather than its temporal evolution. Additionally, in combination with (preclinical) high-throughput dose-exposure-response experimentation, FdRA allows for the identification of a system’s structure describing, e.g., the dynamic connection between dose and response without requiring prior biological or pharmacological knowledge [24, 25]. FdRA, however, requires a model to be linear or at least linearizable around a stable steady state. Consequently, FdRA is not applicable to models that do not possess a stable steady state because they, for example, contain monotonically increasing variables as present in tumor growth models. Nevertheless, we demonstrated earlier that non-linear models and their linearization’s lead to comparable frequency responses .
Here, we present a simulation study that is heavily inspired by FdRA in that it shifts the focus away from the traditionally used time domain towards the frequency domain with the aim to find the frequency response behavior of three models of tumor growth to chemotherapeutic treatment, and so to suggest optimal dosing regimen.
We study the response of each of these three tumor growth models to different dosing frequencies, the interplay of PK and dosing regimen on treatment success, and the optimal treatment modality to maximize tumor reduction while limiting toxicities. Not surprisingly, we find that PK significantly impacts the success of treatment; however, the frequency-domain view identifies previously unknown deviations from conventional dosing regimen. Additionally, we suggest modified drug elimination rates for next-generation compounds that would lead to optimal tumor reduction with acceptable toxicity.
Thus, we show that analyzing QSP models in the frequency domain not only provides insights into the dynamics of tumor growth and their response to repetitive treatments, but also allows to detect optimal dosing regimen for given drug behaviors.
MATERIALS AND METHODS
All models were implemented as described in the respective publications and verified by reproducing the published simulations. Here, it should also be noted that between-subject variability in the PK parameters was not considered.
Cell Cycle-Specific Model
The cell cycle‐specific model (CCSM) by Zhu et al.  combines a two‐compartmental PK model of etoposide in humans, a tumor growth model, and a myelosuppression model (Fig. 1 left). Etoposide is administered into the central compartment (AC) and can distribute into a peripheral compartment (AP). The tumor growth model divides tumor cells into two compartments—proliferating cells in G1, S, G2, or M phase (P) and quiescent cells in G0 phase of the cell cycle (Q). It is assumed that quiescent cells are not affected by etoposide. The myelosuppression model describes the maturation of proliferating stem and progenitor cells in the bone marrow (NP) into circulating neutrophils (NC). Etoposide stimulates the degradation of proliferating tumor cells and inhibits regeneration of stem cells. The model equations and parameters are given in the Supplementary Text. The effect of drug concentration on cell killing (parameter k1) was not reported by Zhu et al. , and therefore, set to k1 = 0.8 d−1 based on a cell cycle-specific model of breast cancer data by Panetta and Adam .
The metronomic model (MM) describes the effect of temozolomide on tumor growth as well as its anti-angiogenic effect  (Fig. 1 middle). A myelosuppression model of temozolomide was first developed by Panetta et al. , and coupled to the tumor growth model by Houy and Grand . Temozolomide is administered orally as represented by the absorption compartment (AA) after which it distributes into the central compartment (AC). The effect of temozolomide on tumor size (C) and angiogenesis (A) is mediated by two effect compartments (EC and EA). The maturation of proliferating stem and progenitor cells in the bone marrow (NP) gives rise to neutrophils in circulation (NC). Temozolomide promotes tumor cell degradation and anti-angiogenesis while inhibiting stem and progenitor cell proliferation. With the originally reported parameters, the main findings of Faivre et al.  could not be reproduced. We, therefore, digitized their key figures and estimated a new parameter set (Supplementary Figure S1). The model equations and the original as well as the newly estimated parameters are reported in the Supplementary Text.
Acquired Resistance Model
Eigenmann et al.  recently developed a murine tumor growth inhibition model that describes the killing of tumor cells in response to erlotinib or gefitinib treatment and the formation of resistant cells (Fig. 1 right). An EGFR inhibitor, erlotinib or gefitinib, is administered orally into an absorption compartment (AA) and distributes into the central compartment (AC). In response to drug treatment, sensitive cells (S) undergo several stages of damage (T1 to T3) and are either killed or converted to resistant cells (R). Eigenmann et al., however, also assume that a threshold of drug plasma concentration exists above which the drugs are affecting the resistant cells. This threshold concentration is derived from an in vitro threshold by correcting for fraction unbound in plasma [46, 47]. The model equations, as well as the parameter sets for erlotinib and gefitinib in mouse, are given in the Supplementary Text.
Frequency-Domain Response Analysis
Recently, FdRA was introduced to a pharmacometrics audience . FdRA analytically determines how the frequency of an input modulates the output behavior of a linear dynamic system. Following a steady-state analysis, a non-linear model, such as those usually present in QSP, is linearized around a stable steady state after which the frequency response can be determined. Because tumor growth models usually grow indefinitely, no stable steady state can be found other than a trivial steady state at the origin. Thus, a linearization is not possible, and FdRA cannot be employed. Therefore, we performed a simulation study that mimics FdRA numerically by simulating the time courses of tumor growth, absolute neutrophil count (ANC), and the amplitude ratios between tumor and PK for a large range of dosing frequencies. Afterwards, we plotted tumor growth, ANC, and amplitude ratios after a certain treatment duration over the frequency of dose administration. Here, it should be noted that FdRA only allows for symmetric dosing regimen (e.g., daily, weekly) which means that irregular dosing regimen such as administration on five consecutive days once per month or different dose amounts such as loading doses cannot be visualized in the frequency response graphs. Additionally, we performed an analytical analysis of the metronomic model in order to obtain explicit and approximate solutions of the differential equations with which we could substantiate the numerical findings (Supplementary Text).
Throughout this article, we maintain constant total drug exposure to avoid that more frequent dosing results in a greater drug exposure, and thus to make results across different dosing regimen comparable. Conventionally, etoposide and temozolomide are administered on five consecutive days once per month at single doses of 100 mg m−2 and 200 mg m−2, respectively. Thus, a 70-kg patient with a body surface area of 1.8 m2 will receive 10.8 g etoposide or 21.6 g temozolomide per year. Erlotinib and gefitinib are administered daily at doses of 100 mg kg−1 and 150 mg kg−1, respectively. Mice with a body weight of 25 g, thus, receive 7.58 mg erlotinib or 11.42 mg gefitinib per month. The dose administered at each treatment is adjusted to keep the total dose, and so total exposure to a drug, constant. A daily administration of etoposide would, for example, calculate to a single dose of 29.6 mg whereas a dose of 207.7 mg would be administered in a weekly schedule.
The cell cycle-specific and the metronomic model both contain a myelosuppression model that allows the determination of treatment safety in terms of ANC. No such model exists relating adverse events to epidermal growth factor receptor (EGFR) inhibition. We normalize ANC levels to ANC before treatment and determine two safety measures. By measuring minimum ANC, we assume that ANC levels below 6% represent neutropenia . Furthermore, we determine the ability of neutrophil levels to recover between two doses by measuring maximum ANC levels just before the administration of the next dose.
All simulation results were obtained with R 3.5.0. For the parameter estimation of the metronomic model, MATLAB R2018a was used. Mathematica 11.3.0 was consulted for the analytical analysis of the metronomic model.
For the metronomic model, a daily administration schedule results in a large increase in tumor mass while the monthly dosing schedule increases tumor mass by 1.2% after 1 year (Fig. 2 top right). Only the administration of one dose of per week leads to a slight decrease in tumor mass with a maximum decrease by 14.3% after 7 days of treatment, and a decreased by 11% after 1 year. An analytical analysis of this model, furthermore, confirms these findings (Supplementary Text and Supplementary Figure S3). There, we either solve the differential equations analytically or approximate their solutions which results in a very good correspondence. For a daily dosing regimen, we analytically find that tumor mass increases indefinitely, while it stays nearly constant in a monthly regimen. Administering temozolomide every 5 days displays a significant decrease in tumor mass. Lastly, an increased dosing frequency also reduces the fluctuations and mean ANC levels with a daily dose administration leading to ANC levels of less than 6% after 22 days whereas the monthly administration scheme almost allows for full recovery to pre-treatment ANC levels (Supplementary Figure S2). For the originally reported parameters, the metronomic model does lead to more pronounced reduction of tumor mass for low-frequency administration schedules (Supplementary Figure S4).
Shortly after the start of erlotinib treatment to the acquired resistance model, tumor volume decreases for all dosing frequencies (Fig. 2 bottom left). Low-frequency dosing, however, develops sustained oscillations around the pre-treatment tumor volume with larger amplitudes observed for monthly as compared to weekly treatments. Thus, while an erlotinib dose initially leads to tumor reduction, tumor volume increases prior to the next dose. Only daily administration of erlotinib results in a sustained tumor volume increase after 1 year. Gefitinib administration results in tumor volume increase irrespective of dosing frequency with the largest increase observed for daily interventions (Fig. 2 bottom right). Weekly administrations fluctuate between 2407.4 and 2714.5%. The monthly administration schedule results in tumor volume fluctuations between 489.8 and 1873.0%. We, furthermore, observe that already after 1 month of erlotinib treatment, all sensitive cells have become resistant (Supplementary Figure S5). For gefitinib treatment, however, this conversion happens more gradually. A monthly dosing regimen displays large fluctuations in the fraction of resistant cells.
Tumor Growth Response to Dosing Frequency Changes
Administering temozolomide to the metronomic model less frequently than one dose per week leads to a slight increase of tumor mass between 0.2 and 3.3% (Fig. 3 top right). More than two doses per week largely increase tumor mass already after 1 year. This is also the only regimen where a difference of tumor mass over time compared to no treatment can be observed. A dosing regimen between one and three doses per week leads to tumor reduction with the maximum tumor reduction of 94.6% after 1 year observed at one dose every 4 days. A dosing frequency above one dose per 3 days introduces ANC trough levels of 6% or less. The ANC peak describing the ability of neutrophils to recover is at 101% for low-frequency dosing schemes such as one dose every half a year, drops below 50% for one dose every 22 days, and reaches neutropenia levels (< 6%) when the dosing frequency is higher than one dose every 3 days (Supplementary Figure S6). With the exact and approximated analytical solutions of the model, we find that for dosing frequencies higher than 0.32 doses per day, the tumor mass approaches its tumor size limit of 1 kg. For lower dosing frequencies (less than 0.14 doses per day), it can be shown that the tumor mass hardly deviates from its pre-treatment value (Supplementary Text).
The model of acquired resistance mainly responds with an increase in tumor volume irrespective of dosing frequency or drug (Fig. 3 bottom). Only erlotinib dosing at frequencies between one dose every 7 and one dose every 17 days results in a maximal tumor reduction by 7.8% after 3 years. Increasing the dosing frequency above two erlotinib doses per day or one gefitinib dose every 4 days plateaus the tumor volume, i.e., administering gefitinib once every 3 days and six times per day leads to a similar tumor response. Furthermore, only in these plateaued dosing frequency regimes a slight difference in tumor volume after 1 and 3 years is observed. Administering gefitinib less frequently than once every 4 days decreases the tumor volume with a minimum at one dose every 27 days when measured after 3 years after which tumor volume increases again.
Tumor Growth Response to Dosing Frequency and Elimination Rate Changes
In the case of the cell cycle-specific model, lower elimination rates and higher dosing frequencies are more beneficial to tumor reduction (Fig. 4 top left). The therapeutic window is scattered around the original elimination rate of etoposide for mid- to high-frequency dose administrations. The optimal treatment regimen that leads to the largest tumor reduction within the therapeutic window is found at 6 doses per day for an etoposide-like drug with an elimination rate of 10 L day−1 (rather than 27.36 L day−1).
The metronomic model continues to display the very narrow dosing frequency band that leads to tumor reduction for different elimination rates whereas higher dosing frequencies and elimination rates result in strong increases in tumor response (Fig. 4 top right). Low-frequency dosing and small elimination rates fall short of altering tumor mass. The optimal treatment modalities are found for bi-monthly dose administration with a temozolomide-like drug with an elimination rate of 10 h−1 (rather than 0.39 h−1). Toxicities are also less pronounced compared to the conventional treatment modalities (Supplementary Figure S7).
Only a reduction of the elimination rate results in tumor reduction in the acquired resistance model (Fig. 4 bottom). As a result, the therapeutic window is also confined to smaller elimination rates. Multiple combinations of smaller elimination rates and dosing frequencies lead to tumor eradication by an erlotinib-like compound. Administering a gefitinib-like compound with an elimination rate of 0.13 day−1 (rather than 3.87 day−1) once per week minimizes tumor volume.
When comparing tumor development over the course of 4 months of the conventional treatment regimen with the above-identified optimal treatment modalities, we reassuringly observe that the optimal combinations of dosing frequency and elimination rate lead to faster tumor reduction or even eradication (Supplementary Figure S8).
Amplitude Response to Dosing Frequency Changes
For the cell cycle-specific model, the input/output response stays within one order of magnitude with a larger amplitude ratio for low-frequency dosing (Fig. 5 top left). When determining the response of ANC fluctuations to plasma fluctuations, we observe a peak in the amplitude ratio when dosing once every 29 days, and a constant amplitude ratio above dosing frequencies of one dose every 3 days (Supplementary Figure S9).
Because the tumor mass in the metronomic model does not fluctuate, the input/output response is zero for all dosing frequencies (Fig. 5 top right). However, the input/output response can be determined when using ANC levels as output which shows a steep drop of the amplitude ratio over 18 orders of magnitude up until a dosing frequency of one dose per day when ANC levels become zero (Supplementary Figure S9).
In the case of the acquired resistance model, we observe an increasing amplitude ratio when administering erlotinib, and a decreasing amplitude ratio when treating with gefitinib for increasing dosing frequencies (Fig. 5 bottom).
By numerically studying three models of tumor growth and treatment effects that capture essential aspects of chemotherapy, we unraveled their response behavior to chemotherapeutic treatment in the frequency domain.
For the cell cycle-specific model, we found that even though more frequent dose administration is favorable to tumor reduction, it also results in a sustained reduction of ANC levels while less frequent etoposide administration allows for a strong ANC recovery. This trade-off between efficacy and safety was also observed by Andersen and Mackey  who investigated resonance in periodic chemotherapy for acute myelogenous leukemia, and found that this type of intervention is unlikely to be efficacious because tumor cells seem to be favored over bone marrow cells in terms of depletion and regrowth rate. Through adaptation of PK, we furthermore found an etoposide-like drug with a reduced elimination would rather accelerate tumor reduction while still residing within the therapeutic window. This suggests that a mid-frequency dosing regimen might be optimal when describing tumor growth with a cell cycle-specific model.
The metronomic model, although specifically developed for frequent low-dose drug administrations, is not able to confirm this treatment regimen but on the contrary suggests that infrequent treatments should be preferred in terms of tumor reduction and toxicity. While maximum tumor reduction might be achieved for four temozolomide administrations per week, ANC levels below 10% are not a tolerable adverse effect. However, a temozolomide-like therapeutic agent with an increased elimination rate that is administered only every 2 months results in fast tumor reduction with only mild toxicities. In line with the here presented conclusions, two studies of anti-angiogenic chemotherapy, however without PK, investigated the treatment frequency and concluded that the efficacy of metronomic therapy depends the interplay of the vascular contribution to tumor growth and the anti-angiogenic effect of the therapy [51, 52]. This confirms the importance and impact of dosing frequency on the success of metronomic chemotherapy. We, furthermore, showed how explicit or approximate analytical analysis can deepen the insight gained from a model, especially with respect to dosing frequencies.
As expected, in the model of acquired resistance, the resistant cells quickly dominate the sensitive cells, irrespective of drug or species. However, the subtle differences in tumor development and resistant cell behavior can be explained by the different model-inherent drug plasma concentration thresholds above which the drugs also affect resistant cells (Supplementary Table S3). Additionally, drug-specific PK parameters are responsible for the different responses of the model to dosing frequency changes. Therefore, reduction of the elimination rates by two orders of magnitude is the only option to combat resistance and achieve tumor reduction while the dosing frequency seems to have only a minor impact.
By looking at the input/output behavior of all three models through the amplitude ratio between tumor cell count/mass/volume and drug plasma concentration, we found that the amplitude ratios of all models stay below 1, which means that the tumor growth models attenuate plasma fluctuations before they are passed to the tumor response. In other words, the amount of tumor tissue always fluctuates less than the amount of drug in plasma. Furthermore, because all amplitude ratios stay within one order of magnitude, we reason that dosing frequency does not significantly alter the relationship between plasma concentration and tumor fluctuations.
Here, it should also be noted that FdRA only allows for periodic and symmetric dosing regimen where the dose for each treatment as well as the dose administration interval is the same. That this might not always lead to the optimal treatment modalities was recently highlighted by Chmielecki et al. . They used an evolutionary model of non-small cell lung cancer to predict that high-dose pulses combined with continuous low-dose tyrosine kinase inhibitors such as gefitinib or erlotinib delay the emergence of resistance. This prediction was, however, later refuted in a phase 1 clinical study that found no improvement of progression free survival or prevention of the emergence of resistance . Nevertheless, non-symmetric dosing regimen were also found to optimize treatment outcome in patients with metastatic breast cancer or non-small-cell lung cancer. Traina et al. [55, 56] studied the reduction of consecutive oral capecitabine treatment days from 14 to 7 followed by a 7-day rest period based on simulations of a Norton-Simon growth kinetic model. Similarly, in one of the few studies combining PK with the development of acquired resistance, Foo et al.  concluded that administration of erlotinib in high-dose pulses with low-dose continuous therapy minimized the development of resistance.
The importance of optimizing dosing regimen also extends into immunotherapy or targeted anti-cancer therapy, such as EGFR inhibition. Sachs et al.  exemplified that for targeted therapeutics such as monoclonal antibodies or immunotherapies that might not exhibit dose-limiting toxicities, conventional maximum tolerated dose derived first-in-human dosing needs an alternative dosing strategy such as biologically efficacious dose. More specifically, a PKPD coupled tumor uptake model for immunocytokine-based cancer immunotherapy predicted that dose-dense administration schedules improve intratumoral drug uptake . For brain tumors, however, it was found that lapatinib should be administered on a continuous daily schedule  while the time intervals between PCV (Procarbazine, CCNU, and Vincristine) chemotherapy cycles should be increased .
With the increased interest in dosing regimen optimization, it becomes apparent that each drug and each disease exhibits its own optimal treatment modality, and we believe that FdRA, and the numerical analysis of models in the frequency domain as presented in this article, can provide a helpful tool to approach this challenge. Hence, all three models analyzed in this article exhibit their own response behavior to changes in dosing regimen or drug-specific parameters. Nevertheless, we found that conventional treatment modalities leave considerable room for improvement. Thus, in order to guarantee the best possible treatment outcome, special care should be taken in tailoring the PK profiles to the desired PD response. To that end, extending FdRA by considering between-subject variability would allow dosing frequency optimization even on the population level.
- 14.Carrara L, Lavezzi S, Borella E, Nicolao G, Magni P, Poggesi I. Current mathematical models for cancer drug discovery. Expert Opin Drug Dis. 2017;12:785–99.Google Scholar
- 22.Fister RK, Panetta J. Optimal control applied to cell-cycle-specific cancer chemotherapy. SIAM J Appl Math. 2000;60(1059):1072.Google Scholar
- 24.Mitchell A, Wei P, Lim WA. Oscillatory stress stimulation uncovers an Achilles’ heel of the yeast MAPK signaling network. Science. 2015;350(1379):1383.Google Scholar
- 38.Houy N, Grand F. Administration of temozolomide: comparison of conventional and metronomic chemotherapy regimens. J Theor Biol. 2018;446(71):78.Google Scholar
- 52.D’Onofrio A, Gandolfi A (2010) Chemotherapy of vascularised tumours: role of vessel density and the effect of vascular “pruning.” J Theor Biol 264:253–265Google Scholar
- 53.Chmielecki J, Foo J, Oxnard GR, et al (2011) Optimization of dosing for EGFR-mutant non-small cell lung cancer with evolutionary cancer modeling. Science translational medicine 3:90ra59 90ra59.Google Scholar
- 54.Yu H, Sima C, Feldman D, et al (2016) Phase 1 study of twice weekly pulse dose and daily low-dose erlotinib as initial treatment for patients with EGFR -mutant lung cancers. Ann Oncol mdw556.Google Scholar
- 58.Sachs JR, Mayawala K, Gadamsetty S, Kang S, de Alwis DP. Optimal dosing for targeted therapies in oncology: drug development cases leading by example. Am Assoc Cancer Res. 2016;22:1318–24.Google Scholar
- 59.Ribba B, Boetsch C, Nayak TK, et al (2018) Prediction of the optimal dosing regimen using a mathematical model of tumour uptake for immunocytokine-based cancer immunotherapy. Clin Cancer Res 24:clincanres.2953.2017.Google Scholar
- 61.Mazzocco P, Honnorat J, Ducray F, Ribba B. Increasing the time interval between PCV chemotherapy cycles as a strategy to improve duration of response in low-grade gliomas: results from a model-based clinical trial simulation. Comput Math Method M. 2015;2015:297903.Google Scholar
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.