Abstract
Subtle differences in a patient’s genetics and physiology may alter radiotherapy (RT) treatment responses, motivating the need for a more personalized treatment plan. Accordingly, we have developed a novel quantum deep reinforcement learning (qDRL) framework for clinical decision support that can estimate an individual patient’s dose response midtreatment and recommend an optimal dose adjustment. Our framework considers patients’ specific information including biological, physical, genetic, clinical, and dosimetric factors. Recognizing that physicians must make decisions amidst uncertainty in RT treatment outcomes, we employed indeterministic quantum states to represent human decision making in a reallife scenario. We paired quantum decision states with a modelbased deep qlearning algorithm to optimize the clinical decisionmaking process in RT. We trained our proposed qDRL framework on an institutional dataset of 67 stage III nonsmall cell lung cancer (NSCLC) patients treated on prospective adaptive protocols and independently validated our framework in an external multiinstitutional dataset of 174 NSCLC patients. For a comprehensive evaluation, we compared three frameworks: DRL, qDRL trained in a Qiskit quantum computing simulator, and qDRL trained in an IBM quantum computer. Two metrics were considered to evaluate our framework: (1) similarity score, defined as the root mean square error between retrospective clinical decisions and the AI recommendations, and (2) selfevaluation scheme that compares retrospective clinical decisions and AI recommendations based on the improvement in the observed clinical outcomes. Our analysis shows that our framework, which takes into consideration individual patient dose response in its decisionmaking, can potentially improve clinical RT decisionmaking by at least about 10% compared to unaided clinical practice. Further validation of our novel quantitative approach in a prospective study will provide a necessary framework for improving the standard of care in personalized RT.
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Introduction
The efficacy of radiotherapy (RT), as one of the main clinical cancer treatments, has the potential to be improved by personalization according to each patient’s estimated treatment response. In a study by Bryant et al., it was estimated that about 3.05 million cancer survivors in 2016 were treated with radiation, accounting for 29% of all cancer survivors. The number of radiationtreated cancer survivors was expected to be 3.38 million by 2020 and is projected to be 4.17 million by 2030^{1}. However, the current populationbased onesizefitsall clinical practice, where RT regimens are almost identical for all similar staged cancer patients, is suboptimal due to the subtle physiological and genetic heterogeneity among individual patients that can result in diverse treatment responses and outcomes even when treated under identical protocols. Therefore, personalizing RT treatment according to a patient’s estimated treatment response is crucial for optimizing RT outcomes and ultimately increasing the rate of cancer survivorship. We hypothesize that a robust clinical decision support system (CDSS)^{2} that can quantitatively estimate long term treatment responses from pre and during treatment analyses and recommend proper prescription adjustments accordingly will be necessary to improve the standard of care in personalized RT.
One proposed way of personalizing RT is shown in Fig. 1, which presents a schematic for knowledgebased responseadapted RT (KBRART)^{3,4,5}. In a typical RT regimen for nonsmall cell lung cancer (NSCLC), a patient is given 60 Gray (Gy) of radiation in 30 fractions which takes a total of 6 weeks to administer^{6}. The proposed KBRART will follow the initial treatment plan for the first twothirds, or week 1 to week 4, of the regimen during which the patient’s treatment response is evaluated. Any necessary treatment adjustment (increase or decrease in dose per fraction) is carried out during the last onethird, or week 5 to week 6 of the regimen. The adjustment is intended to ensure an optimal treatment outcome, i.e., maximize tumor control and minimize radiation induced complication. Note that although we have chosen lung cancer for this study, the KBRART scheme is applicable to all types of cancer.
While the procedure for KBRART may be clear, obtaining the necessary information to create a standardized clinical protocol is difficult. The main challenge of KBRART is to quantify the relationship between radiation dose and treatment outcome. One way of measuring treatment response would be through direct (nonclinical; wide range of radiation dose) human experimentation, though such an approach would be unethical. Another challenge emerges from the complex biological processes that involves hundreds, if not thousands, of biological and clinical factors, which makes it an extremely difficult task to establish a quantitative relationship between radiation dose and treatment outcome, consequently complicating the task of making objective doseadaptation decisions.
Advanced machine learning methods such as deep learning, modelbased reinforcement learning, and feature selection can alleviate the aforementioned challenges. Deep learning models are computational models that are made up of multilayer neural networks that can combine data representation with the learning task in the same framework^{7,8}. Deep learning techniques have considerably improved the field of computer vision, speech recognition, natural language processing, drug discovery and genomics, among other domains. Reinforcement learning (RL) is an area of machine learning concerned with teaching an artificially intelligent (AI) agent how to take optimal actions in a given environment to maximize a reward function^{9}. Deep RL has also made a significant progress in creating AI systems that have even surpassed humanlevel intelligence in certain tasks such as Atari videogames^{10} and the Go board game^{11}. Based on those advanced data driven techniques, we have designed a quantitative framework for KBRART using modelbased reinforcement learning^{12} to model an artificial radiotherapy environment (ARTE) for dose adaptation optimization and using a Bayesian Network approach for relevant feature selection^{13}. Our framework utilizes a hybrid of prior knowledgebased processdriven techniques and deep learningbased datadriven techniques in modeling an ARTE that can estimate RT treatment outcome for a given patient and radiation dose. The hybridization and application of prior knowledge provides a significant improvement to an earlier work by Tseng et al.^{12}, which ensures that ARTE does not violate clinically observed facts which might not be easily apparent from the data alone. Incorporating prior knowledge also helped in mitigating overfitting pitfalls and reducing the model error; this allowed us to work with continuous numerical values, further improving the earlier work which only considered discrete values. Furthermore, we have defined the patients’ state in ARTE using the 5 important features selected from a multiobjective Bayesian network study^{13}. A schematic of ARTE is presented in Fig. 2. For dose optimization, ARTE assigns a reward value for every pair of patient’s states and radiation dose, which is then accumulated by the deep reinforcement learning (DRL) algorithm in finding the optimal dose adaptation for that patient. However, even with the improvements to ARTE, the earlier approach alone is insufficient to model the intrinsic ‘noise’ in patient’s data generated by the uncertainty in physician’s decisionmaking process.
In this work, we have introduced a novel modeling approach for clinical application, where we model the clinical decisions with quantum states to represent the indeterminism in the clinical decisionmaking process during RT treatment due to the unavailability of complete information on RT treatment course and outcomes. Decisions made under uncertainty are typically influenced by personal preference^{14}, which are subject to change with varying information in a situation, and several experiments have demonstrated preference reversal in human decisionmaking^{15,16}. Considerable efforts have been made to describe anomalies in human decisionmaking, such as preference reversal, based on the laws of classical probability theory, in terms of subjective utility and subjective probability^{17,18}; however, they have not been successfully generalized, and several other experiments have shown violation of these principles^{19}. These inadequacies of classical decisionmaking theory can be overcome by quantum probability theorybased models of human decisionmaking processes^{16,20,21,22}. Because quantum states are noncommutative, quantum probabilities are intrinsically asymmetric, providing a consistent mathematical framework to overcome the shortcomings of classical probability that primarily arises from its symmetrical property.
We, however, directly modeled human decision as quantum states and decisionselection as quantum interaction, bypassing the utilitybased quantum theoretic approach. Our approach is similar to the valuebased quantum reinforcement learning (QRL) framework by Li et al.^{23,24,25}. Li et al. in their study^{25} demonstrated a QRL framework to be a better alternative for mimicking human decisionmaking, in which 2 QRL and 12 classical RL models were compared in modeling human decisionmaking among healthy and cigarettesmoking subjects while performing the Iowa Gambling Task. The authors argued that quantumlike features exist in human decisionmaking, in which making a choice can influence the subjective values of the alternatives; since quantum states can exist in a superimposed state, (i.e., a state representing all the alternatives at once) any operation, for instance selecting a choice, will influence the value of all other alternatives.
Our framework, though similar in concept with Li’s QRL, varies in its implementation. We have employed deep qnet^{26} technology for optimizing decision prediction and to provide a more complete representation of a patient’s state due to its ability to function with nonlinear complex systems over a continuous space. Additionally, we have designed a novel quantum controller circuit that allows our framework to run on a quantum processor for modeling decisions with realistic quantum states and decisionselection with real quantum interaction. By combining the quantum computation and deep q learning, we have developed a novel quantum deep reinforcement learning (qDRL) framework for modeling optimal decisionmaking processes in KBRART (Fig. 2).
In this work, we demonstrate the first application of a qDRL framework to realworld clinical data for decisionmaking, particularly in the case of NSCLC. For comparison, we trained and validated three frameworks: DRL, qDRL trained on a Qiskit quantum computing simulator^{27}, and qDRL trained on an IBM quantum (IBMQ) 16 Melbourne 15qubit processor^{28}. We trained our framework on 67 stage III NSCLC patient datasets from a single institution^{13} and validated our framework on an independent multiinstitutional cohort of 174 NSCLC patients treated under the Radiation Therapy Oncology Group (RTOG) 0617 protocol^{29}.
This paper is organized as follows. In the Results section, we present the AI recommendations generated from three RL frameworks and compare the results with one another and the clinical decisions. Since our framework is not a supervised learning algorithm, a direct performance comparison is not possible; instead, we developed comparison metrics based on the radiation dose to treatment outcome relationship. The Discussion section presents the analysis of the results and describes the limitations and the potential of our framework. The Methods section describes the details of our framework including the mathematical details of qDRL, the design of a novel quantum amplification method called a Controller Circuit, the description of the utilized patient features, and details of the various components of the proposed ARTE.
Results
Optimal AI recommendations (dose per fraction for the last 1/3 of treatment) obtained from qDRL models trained in the IBMQ quantum processor are shown in Fig. 3. AI recommendations from other models are presented in the Supplementary Material. We repeated every experiment 5 times for rigorous statistical reporting of the average recommendations and standard error of mean as uncertainty as shown in Fig. 3. For visual comparison, we added the retrospective clinical dose decision for each patient, colorcoded with the respective clinical outcomes. Altogether the binary outcomes can be classified into 4 classes, among which the class with successful local tumor control (LC = 1) and no occurrence of radiation induced pneumonitis (RP2 = 0) is the clinically desirable outcome.
For additional information on the AI decisionmaking, we have colorcoded AI recommendations with their corresponding qvalue (quality value) obtained from the deep qnet. Deep qnet serves as the memory of the AI agent, which assigns a qvalue for every possible pair of the patient’s state and dose decision. Mathematically, the qvalue is the expected return (timeaverage) of recommending a series of dose to a patient until the AI agent either achieves the desirable treatment outcome estimates or exceeds a userdefined terminating steps (in our case 10 steps). At every step of dose decisionmaking, the AI agent gets a reward based on the treatment outcome estimates, which is then aggregated into q values throughout the training process. We assigned positive rewards for successfully attaining the desirable outcomes and negative rewards for failing to do so. Since an agent always selects the greedy decision (decisions with the maximum q value), the qvalue can be loosely translated as the AI’s confidence in a recommended dose. A positive qvalue corresponds to the decision that most likely results in a desirable outcome, and while a negative qvalue still corresponds to the best decision for a particular case, it is less likely to result in a desirable outcome. Note that the absolute magnitude of q value will change with different reward scheme and training parameters.
Because our framework is not supervised learning, we devised the following 2 complementary metrics for evaluating model performance.

1.
Similarity score (root mean square error [RMSE] between retrospective clinical decisions and the AI recommendation): Similarity score provides a direct metric to compare the closeness of the AI recommendation to the clinical practice. Although the goal of our modeling is not to replicate the retrospective clinical decision, because the KBRART paradigm is based on the premise that the current practice is suboptimal, the RMSE metric can still provide some level of information regarding the quality of the model since the current practice is based on clinically validated measures. This means that a 0 Gray/fraction (Gy/frac) RMSE similarity score is undesirable, however a low RMSE generally indicates a good recommendation.

2.
Selfevaluation scheme (evaluation based on the radiation dose to outcome relationship). This scheme is also based on retrospective clinical decisions but factors in the clinical outcomes^{12}. The scheme is summarized in Table 1, which assumes that higher radiation dose simultaneously increases the probability of controlling tumor as well as the risk of complications. This assumption is based on the observation that radiation kills both cancer cells and healthy cells. For instance, if the clinical outcome for a patient was no local control (LC = 0) and no occurrence of radiation induced pneumonitis (RP2 = 0), then an AI dose recommendation higher than the clinical decision can be considered as a good recommendation (i.e., the patient would have benefited from dose escalation at week 4 of the treatment period) and viceversa. Out of the four possible permutations, LC = 1 and RP2 = 0 is the only clinically optimal outcomes. Since its impossible to evaluate recommendations for the desirable outcomes, we have used ‘unsure’ and ‘good’ tags for the AI recommendation. When an AI recommendation falls outside 0.5 Gy/frac of the clinical dose decision, we tag the recommendation as ‘unsure’. This uncertainty is due to the lack of knowledge about individual patients’ sensitivity to dose adaptation. However, when an AI recommended dose falls inside the 0.5 Gy/frac margin of the clinical decision, we can tag the dose as a good recommendation with higher confidence. Among the clinically undesirable outcomes, patients with LC = 0 and RP2 = 0 could have received a higher dose to increase the chance of LC while patients with LC = 1 and RP2 = 1 could have received a lower dose to decrease the chance of RP2. However, for LC = 0 and RP2 = 1, the outcome of increasing or decreasing the dose is unclear. We took into consideration the fact that, clinically, the amount of dose administered is limited by the likelihood of causing RP2—the sideeffect on any treatment should be minimized. So, when AI recommends a dose that is less than the clinical dose decision, we tag it as a ‘good’ recommendation. Additionally, for assurance, we added a cushion of 0.1 Gy/frac and defined ‘good’ as the AI recommendation that is less than clinical decision minus 0.1 Gy/frac.
Analysis of model performance based on the above two metrics is presented as bar charts in Fig. 4. Similarity scores for DRL, qDRL trained in Qiskit Simulator (qDRL + simulator), and qDRL trained in IBMQ quantum processor (qDRL + IBMQ) for the training dataset were 0.57 Gy/frac, 0.54 Gy/frac, and 0.55 Gy/frac, respectively, and for the validation dataset were 0.70 Gy/frac, 0.66 Gy/frac, and 0.71 Gy/frac, respectively. The similarity scores were calculated between the averaged recommendations and the clinical decisions. The results from the selfevaluation scheme were converted into percentage of the total number of patients. The selfevaluation results for the training datasets are as follows: the percentages of good recommendations for DRL, qDRL + simulator, qDRL + IBMQ, and clinical dose were 58%, 61%, 60%, and 49%, respectively; the percentages of bad recommendations were 19%, 16%, 16%, and 51%, and the percentages of unsure recommendations were 22%, 22%, 24%, and 0%. Similarly, the selfevaluation results for the validation datasets are as follows: the percentages of good recommendations for DRL, qDRL + simulator, qDRL + IBMQ and clinical dose were 41%, 45%, 42%, and 26%, respectively; the percentages of bad cases were 46%, 43%, 45%, and 74%, and the percentages of unsure cases were 13%, 12%, 13%, and 0%. Note that the analysis of clinical doses is based on the clinical outcomes.
Discussions
Analysis of our result indicates that our framework can potentially improve clinical RT treatment outcome by at least about 10%. This metric corresponds to the minimum difference between the percentage of good recommendations and clinical decision as shown in Fig. 4, for the combined training and validation results. Precisely, it’s the difference between DRL and the clinical decision. We recognize that the selfevaluation scheme alone provides partial information on the performance, thus we base our conclusion by considering both the selfevaluation scheme and similarity score; the similarity score shows that our framework is close to clinical decisions with a RMSE value of at most 0.71 Gy/frac. With a smaller similarity score and better performance under the selfevaluation scheme, we have shown that our framework can recommend doses close to medical experts with a higher chance of successful treatment of NSCLC patients. However, we would like to acknowledge that our analysis depends on having an accurate representation of the RT environment model and the accuracy of the outcome estimator. Modeling of a multimodal treatment environment including immunotherapy and surgical and medical oncology will be necessary for a more comprehensive assessment of our framework.
Our analysis showed that qDRL + simulator models are slightly different than the qDRL + IBMQ. The reason for this difference is twofold: (1) the simulator lacks any machine error including the quantum decoherence error (i.e., inability of maintaining a coherent quantum phase), (2) the decision selection mechanism of qDRL + simulator is different from qDRL + IBMQ. The former reason results in higher noise but could be more representative of the human decisionmaking process. The latter reason comes from the physical necessity to design a quantum circuit of length shorter than the quantum coherence length of a quantum processor. Any quantum algorithm (strictly speaking its equivalent quantum circuit) that is longer than the system’s coherence length will result in error. We designed a novel quantum controller circuit that was much shorter, thus easier to design and use, than the Grover amplification process (the decision selection mechanism of qDRL + simulator derived form QRL). Note that the quantum controller circuit is by no means a replacement of the Grover’s amplification process as a search algorithm; it is, however, a pragmatic and scalable alternative for the decision selection mechanism.
Although our analysis showed only a small improvement in performance between DRL and the qDRL algorithm, our hybrid quantum–classical machine learning algorithm possesses both conceptual and computational advantages. We found qDRL models exhibited slightly smaller similarity score than the DRL models, i.e., about 0.03 Gy/frac difference for training dataset and about 0.04 Gy/frac difference for validation dataset (best case). Similarly, in terms of selfevaluation scheme, qDRL models made more good recommendations and less bad recommendations, i.e., about 3% difference for both good and bad recommendations for both training and validation dataset (best case). While it is difficult to favor the qDRL algorithm over the DRL algorithm solely based on the performance metrics, the qDRL algorithm has the following two advantages: (1) modeling of human decision with quantum state has a sound theoretical background and (2) a hybrid quantum–classical machine learning algorithm can harness quantum properties such as superposition, parallelism, and entanglement. In this work we designed our framework with value based DRL methods and, as a next iteration, plan to explore and incorporate advanced policy based DRL methods to our qDRL framework for additional improvement.
Our approach of combining quantum computation, deep learning techniques, and statistical ensemble provides the necessary robustness for a clinically viable CDSS. Modeling of humandecision as a quantum state is not only theoretically consistent but also takes into consideration the intrinsic indeterminism of the human decisionmaking process. Deep learning techniques use redundancy of a large number of nodes to handle (desensitize) data noise. Averaging over the ensemble of multiple trained models makes our approach less sensitive to stochastic training methods used in deep learning training. For clinical application, further improvement is necessary, which can be achieved by using a larger training dataset, further infusing expert knowledge in modeling of ARTE, more independent validation and testing, and the development of a graphical user interface. Additionally, testing our framework in a prospective study will be necessary for future clinical implementation^{30}.
Aside from datarelated limiting factors, our framework will have to overcome several other limitations and consider concurrent complimentary technologies such as modern radiotherapy delivery techniques for future clinical application. Considering a patientspecific alphatobeta ratio would capture the heterogeneity among patients and boost the efficiency of the current framework. Combining the volatility of radiomics features for PET images into the uncertainty analysis would provide a more accurate representation of the predictability of the framework. Similarly, an extensive sensitivity analysis of the features will be necessary for better representation of the response prediction, range of variability, and the uncertainty estimates of our framework. In terms of application, our framework should be used in a complementary fashion and consistent with other clinical tools such as the RT treatment planner, plan optimizer, and image guidance system^{29} for clinical implementation.
In summary, a framework for a robust CDSS based on quantum computing and deep learning methods was designed and tested. The key feature of the framework was modeling the clinical decisions as quantum states. The novelty of our approach lies in combining quantum computation with deep learning to gain the best of both fields. A novel quantum circuit was designed and implemented in IBMQ quantum processor to utilize real quantum states and quantum interaction. Two complementary schemes were designed to analyze the performance of our weakly supervised framework. Based on our analysis, our framework showed potential of improving RT efficacy. Finally, our framework provides a clinically viable quantitative approach to decisionmaking in KBRART.
Methods
Quantum deep reinforcement learning
Quantum deep reinforcement learning is a novel action valuebased decisionmaking framework derived from QRL^{23} and deep qlearning^{10} framework. Like conventional RL^{9,31}, our qDRL based CDSS framework is comprised of 5 main elements: clinical AI agent, ARTE, radiation dose decisionmaking policy, reward, and qvalue function. Here, the AI agent is a clinical decisionmaker that learns to make dose decisions for achieving clinically desirable outcomes within the ARTE. The learning takes place by the agentenvironment interaction, which can be sequentially ordered as: the AI decides on a dose and executes it, and in response, a patient (part of the ARTE) transits from one state to the next. Each transition provides the AI with feedback for its decision in terms of RT outcome and associated reward value. The goal of RL is for the AI to learn a decisionmaking policy that maximizes the reward in the long run, defined in terms of a specified qvalue function that assigns a value to every statedosedecision pair obtained from the accumulation of rewards over time (returns).
Assuming Markov’s property (i.e., an environment’s response at time \(t + 1\) depends only on the state and dosedecision at time \(t\)), the qDRL task can be mathematically described as a 5tuple \((S, \left D \right\rangle , TF, P, R)\), where \(S\) is a finite set of patient’s states, \(\left D \right\rangle\) is a superimposed quantum state representing the finite set of eigendose decision, \(TF:S \times D \to S^{\prime }\) is the transition function that maps patient’s state \(s_{t}\) and eigendose \(\left d \right\rangle_{t}\) to the next state \(s_{t + 1}\), \(P_{LCRP2} :S^{\prime } \to \left[ {0,1} \right]\) is the RT outcome estimator that assigns probability values \(p_{LC}\) and \(p_{RP2}\) to the state \(s_{t + 1}\), and \(R:\left[ {0,1} \right] \times \left[ {0,1} \right] \to {\mathbb{R}}\) is the reward function that assigns a reward \(r_{t + 1}\) to the statedecision pair \(\left( {s_{t} ,\left d \right\rangle_{t} } \right)\) based on the outcome probability estimates.
Eigendose \(\left d \right\rangle\) is a physically performable decision that is selected via quantum methods from the superimposed quantum state \(\left D \right\rangle\) which simultaneously represents all possible eigendoses at once. In simple words, \(\left D \right\rangle\) is the collection of all possible dose options and \(\left d \right\rangle\) is one of those options which is selected after a decision is made. Selecting dose decision \(\left d \right\rangle\) is carried out in two steps: (1) amplifying the optimal eigendose \(\left d \right\rangle^{*}\) from the superimposed state \(\left D \right\rangle\) (i.e., \(\left D \right\rangle^{\prime } = \widehat{Amp}_{{\left d \right\rangle^{*} }} \left D \right\rangle\)) and (2) measuring the amplified state (i.e., \(\left d \right\rangle = \widehat{Measure}(\left {D^{\prime } } \right\rangle )\).
The optimal eigendose \(\left d \right\rangle^{*}\) is obtained from deep Qnet, which is the AI’s memory. Deep Qnet, \(DQN:S \to {\mathbb{R}}^{d}\), is a neural network that takes patient’s state as input and then outputs qvalue for each eigendose (\(\left\{ {q_{\left d \right\rangle } } \right\}\)). The optimal dose is then selected following greedy policy where the dose with the maximum qvalue is selected (i.e., \(\left d \right\rangle^{*} = \begin{array}{*{20}c} {argmax} \\ {\left {d^{\prime } } \right\rangle } \\ \end{array} \{ q_{\left d \right\rangle } \}\)). We have applied a double Qlearning ^{32} algorithm in training the deep Qnet. The schematic of a training cycle is presented in Fig. 2 and additional technical details are presented in the Supplementary Material.
Quantum amplification method and controller circuit
We initially employed Grover’s amplification procedure^{33,34} for the decision selection mechanism. While Grover’s procedure works on a quantum simulator, it fails to correctly work in a quantum computer. The quantum circuit depth of Grover’s procedure (for 4 or higher qubits) is much greater than the coherence length of the current quantum processor^{35}. Whenever the quantum circuit length exceeds the coherence length, quantum state becomes significantly affected by the system noise and loses vital information. Therefore, we designed a quantum controller circuit that is shorter than the coherence length and is suitable for the task of decision selection. The merit of our design is its fixed length; since its length is fixed for any number of qubits, it is suitable for higher qubit systems, as much as permitted by the circuit width. Technical details regarding its implementation in quantum processor is presented in the Supplementary Materials.
An example of a controller circuit is given in Fig. 5. Controller circuits use twice the number of qubits (n), which can be divided into control and main. Optimal eigenstates obtained from deep Qnet are created in the control by selecting the appropriate precontrol gates. Then the control is entangled with the qubits from the main via controlled NOT (CNOT) gates. CNOT gates are connected between a control qubit from the control and a target qubit from the main. CNOT gates flip the target qubit from \(\left 1 \right\rangle\) to \(\left 0 \right\rangle\) only when the control is in \(\left 1 \right\rangle\) state and does not perform any operation otherwise. Because all the main qubits are prepared in \(\left 0 \right\rangle\) state, we introduced the reverse gates (n Xgates in parallel) to flip them to \(\left 1 \right\rangle\). Xgates flip \(\left 0 \right\rangle\) to \(\left 1 \right\rangle\), and viceversa. The CNOT flips all the qubits whose controls are in \(\left 1 \right\rangle\) state, creating a state that is elementwise opposite to the marked state. Finally, another set of reverse gates is applied to the main before making a measurement.
Another advantage of the controller circuit is controlled uncertainty level. The controller circuit has additional degrees of freedom that can control the level of uncertainty that might be needed to model a highly dubious clinical situation. By replacing the CNOT gate by a more general \(CU3\left( {\theta ,\phi ,\lambda } \right)\) gate, we can control the level of additional stochasticity with the rotation angles \(\theta\), \(\phi\), and \(\lambda\), which corresponds to the angles in the Bloch sphere. The angles can either be fixed or, for additional control, changed with training episode.
Patient characteristics
The patient’s state in the ARTE is defined by 5 biological features: cytokine (IP10), PET imaging feature (GLSZMZSV), radiation doses (Tumor gEUD and lung gEUD), and genetics (cxcr1 Rs2234671). Their descriptions are presented in Table 2. These 5 variables were selected from a multiobjective Bayesian Network study^{13}, which considered over 297 various biological features and found the best features for predicting the joint LC and RP2 RT outcomes.
The training data analyzed in this study are obtained from the University of Michigan study UMCC 2007.123 (NCI clinical trial NCT01190527) and the validation data analyzed in this study are obtained from the RTOG0617 study (NCI clinical trial NCT00533949). Both trials were conducted in accordance with relevant guidelines and regulations and informed consent was obtained from all subjects and/or legal guardians. Details on training and validation datasets, and necessary model imputation carried out to accommodate the differences in the datasets are presented in the Supplementary Materials.
Transition function
Deep Neural Networks (DNN) were applied as transition functions for IP10 and GLSZMZSV features. They were trained with a longitudinal (timeseries) dataset, with the preirradiation patient state and corresponding radiation dose as input features and postirradiation state as output. For lung and tumor gEUD, we utilized prior knowledge and applied a monotonic relationship for the transition function since we know that gEUD should increase with increasing radiation dose. We assumed that the change in gEUD is proportional to the dose fractionation and tissue radiosensitivity,
Here \(g\left( {t_{n} } \right)\) is the gEUD at time point \(t_{n}\), \(d_{n}\) is the radiation dose fractionation given during the n^{th} time period, and \(\alpha /\beta\) ratio is the radiosensitivity parameter which differs between tissue type. Note that we first applied constrained training^{42} to maintain monotonicity with DNN model, however the gEUD over time trend was flatter than anticipated, thus we opted for a processdriven approach in the final implementation. The technical details on the NNs and its training are presented in the Supplementary Material.
RT outcome estimator
DNN classifiers were applied as the RT outcome estimator for LC and RP2 treatment outcomes. They were trained with post irradiation patient states as input and binary LC and RP2 outcomes as its labels.
RT outcome estimator must also satisfy a monotone condition between increasing radiation dose and increasing probability of local control as well as probability of radiation induced pneumonitis. To maintain this monotonic relationship, we used a generic logistic function,
where \(g\left( {t_{6} } \right)\) is the gEUD at week 6, and \(\mu\) and \(T\) are two patientspecific parameters that are learned from training the DNN. Here, \(\mu\) and \(T\) are the outputs of two neural networks that are fed into the logistic function and tuned one after the other, leaving the other fixed. The training details are presented in the Supplementary Materials.
Reward function
The task of the agent is to determine the optimal dose that maximizes \(p_{LC}\) while minimizing \(p_{RP2}\). Accordingly, we built a reward function on the base function \(P^{ + } = P_{LC} \left( {1  P_{RP2} } \right)\) as shown in Fig. 6. The algebraic form is as follows,
Here the AI agent receives additional 10 points for achieving clinically desirable outcome (i.e., \(p_{LC} > 70\% \quad {\text{and}} \quad p_{RP2} < 17.2\%\)), 5 points for achieving computationally desirable outcome (i.e., \(p_{LC} > 50\% \quad {\text{and}} \quad p_{RP2} < 50\%\)), and 1 point for failing to achieve a desirable outcome altogether. The negative point motivates the AI agent to search for the optimal dose as soon as possible.
Wasserstein generative adversarial network with gradient penalty (WGANGP)
To compensate for low number of data points we employed WGANGP^{43}, which learns the underlying data distribution and generates more data points. We generated 4000 additional data points for training qDRL models. Having a larger training dataset helps the reinforcement learning algorithm in accurately representing the state space. The training details are presented in the Supplementary Material.
Data availability
The training data analyzed in this study are obtained from the University of Michigan study UMCC 2007.123 (NCI clinical trial NCT01190527). Restrictions apply to the availability of these data, which were used under data sharing protocol for this study. The validation data analyzed in this study are obtained from the RTOG0617 study (NCI clinical trial NCT00533949) and is publicly available in NCTN/NCORP Data Archive. Restrictions apply to the availability of these data, which were used under license for this study. Data are available from the authors upon reasonable request with the permission of NCI.
Code availability
Software codes used in this study will be made available from the corresponding author on reasonable request.
Change history
09 February 2023
A Correction to this paper has been published: https://doi.org/10.1038/s4159802328810x
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Acknowledgements
This work was partially supported by the National Institute of Health (NIH) under Grant No. R01CA233487. I.E.N. acknowledges support form NIH under Grant Nos. R41CA243722 and R37CA222215, and support from National Institute of Biomedical Imaging and Bioengineering under Contract No. 75N92020D00018. M.M.M acknowledges support in the form of research grant from Varian Medical Systems and is the codirector of Michigan Radiation Oncology Quality Consortium (Funded by Blue Cross Blue Shield Michigan). We acknowledge the use of the IBM Q for this work. The views expressed are those of the authors and do not reflect the official policy or position of IBM or the IBM Q team.
The authors also acknowledge that the RTOG0617 dataset was made available by NCT00533949D1 from the NCTN Data Archive of the National Cancer Institute’s (NCI’s) National Clinical Trials Network (NCTN). Data were originally collected from clinical trial NCT number NCT00533949 [A Randomized Phase III Comparison of Standard Dose (60 Gy) versus HighDose (74 Gy) Conformal Radiotherapy with Concurrent and Consolidation Carboplatin/Paclitaxel +/− Cetuximab (Ind #103444) in Patients with Stage IIIA/IIIB NonSmall Cell Lung Cancer]. All analyses and conclusions in this manuscript are the sole responsibility of the authors and do not necessarily reflect the opinions or views of the clinical trial investigators, the NCTN, or the NCI.
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This work was partly supported by grants from National Institute of Health (NIH) grant R01CA233487.
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I.E.N. conceived the study. I.E.N., R.K.T.H., and M.M.M. supervised the project. D.N. designed the algorithms and numerical experiments. J.J. and D.N. wrote programming codes and carried out model training and validation. All authors carefully analyzed the methods and results. D.N. drafted the manuscript and all authors critically read and contributed to the final version.
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Niraula, D., Jamaluddin, J., Matuszak, M.M. et al. Quantum deep reinforcement learning for clinical decision support in oncology: application to adaptive radiotherapy. Sci Rep 11, 23545 (2021). https://doi.org/10.1038/s4159802102910y
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DOI: https://doi.org/10.1038/s4159802102910y
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