<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing DTD v2.0 20040830//EN" "journalpublishing.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="2.0" xml:lang="en" article-type="research-article"><front><journal-meta><journal-id journal-id-type="nlm-ta">J Med Internet Res</journal-id><journal-id journal-id-type="publisher-id">jmir</journal-id><journal-id journal-id-type="index">1</journal-id><journal-title>Journal of Medical Internet Research</journal-title><abbrev-journal-title>J Med Internet Res</abbrev-journal-title><issn pub-type="epub">1438-8871</issn><publisher><publisher-name>JMIR Publications</publisher-name><publisher-loc>Toronto, Canada</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">v28i1e92642</article-id><article-id pub-id-type="doi">10.2196/92642</article-id><article-categories><subj-group subj-group-type="heading"><subject>Original Paper</subject></subj-group></article-categories><title-group><article-title>Sequencing AI Automation and Data Interoperability in Oncology Using a Scenario-Planning Framework Coupled With Discrete-Event Simulation: Proof-of-Concept Study</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name name-style="western"><surname>May</surname><given-names>Peter</given-names></name><degrees>Dr med, MD, MPH, MA</degrees><xref ref-type="aff" rid="aff1">1</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Brookman-May</surname><given-names>Sabine D</given-names></name><degrees>Prof Dr Med, MD</degrees><xref ref-type="aff" rid="aff2">2</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>Garrahy</surname><given-names>Edward</given-names></name><degrees>MD</degrees><xref ref-type="aff" rid="aff3">3</xref></contrib><contrib contrib-type="author"><name name-style="western"><surname>von B&#x00FC;ren</surname><given-names>Johannes</given-names></name><degrees>Dr med, MD</degrees><xref ref-type="aff" rid="aff4">4</xref></contrib></contrib-group><aff id="aff1"><institution>Department of Medicine III, School of Medicine and Health, Technical University of Munich</institution><addr-line>Ismaninger Str. 22</addr-line><addr-line>Munich</addr-line><addr-line>Bavaria</addr-line><country>Germany</country></aff><aff id="aff2"><institution>Department of Urology, Ludwig-Maximilians-Universit&#x00E4;t M&#x00FC;nchen</institution><addr-line>Munich</addr-line><addr-line>Bavaria</addr-line><country>Germany</country></aff><aff id="aff3"><institution>Wellster Healthtech Group</institution><addr-line>Munich</addr-line><country>Germany</country></aff><aff id="aff4"><institution>Sidekick Health Germany GmbH</institution><addr-line>Hamburg</addr-line><country>Germany</country></aff><contrib-group><contrib contrib-type="editor"><name name-style="western"><surname>Mesko</surname><given-names>Bertalan</given-names></name></contrib><contrib contrib-type="editor"><name name-style="western"><surname>Krist&#x00F3;f</surname><given-names>Tam&#x00E1;s</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="reviewer"><name name-style="western"><surname>Bethanabatla</surname><given-names>Amruthavalli</given-names></name></contrib></contrib-group><author-notes><corresp>Correspondence to Peter May, Dr med, MD, MPH, MA, Department of Medicine III, School of Medicine and Health, Technical University of Munich, Ismaninger Str. 22, Munich, Bavaria, 81675, Germany, 49 89-4400 ext 8753; <email>peter.may@tum.de</email></corresp></author-notes><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>25</day><month>5</month><year>2026</year></pub-date><volume>28</volume><elocation-id>e92642</elocation-id><history><date date-type="received"><day>06</day><month>02</month><year>2026</year></date><date date-type="rev-recd"><day>28</day><month>04</month><year>2026</year></date><date date-type="accepted"><day>29</day><month>04</month><year>2026</year></date></history><copyright-statement>&#x00A9; Peter May, Sabine D Brookman-May, Edward Garrahy, Johannes von B&#x00FC;ren. Originally published in the Journal of Medical Internet Research (<ext-link ext-link-type="uri" xlink:href="https://www.jmir.org">https://www.jmir.org</ext-link>), 25.5.2026. </copyright-statement><copyright-year>2026</copyright-year><license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in the Journal of Medical Internet Research (ISSN 1438-8871), is properly cited. The complete bibliographic information, a link to the original publication on <ext-link ext-link-type="uri" xlink:href="https://www.jmir.org/">https://www.jmir.org/</ext-link>, as well as this copyright and license information must be included.</p></license><self-uri xlink:type="simple" xlink:href="https://www.jmir.org/2026/1/e92642"/><abstract><sec><title>Background</title><p>As oncology workflows integrate increasingly autonomous artificial intelligence (AI) agents, health systems face uncertainty regarding operational impacts. Traditional linear forecasting methods fail to capture second-order effects such as governance saturation, induced demand, and bottleneck migration. To navigate this complexity, the emerging field of medical futures studies requires methodologies that bridge qualitative strategic foresight with quantitative operational modeling. These system-level dynamics directly influence timely diagnosis, treatment delays, and overall health system resilience.</p></sec><sec><title>Objective</title><p>This study aimed to develop a proof-of-concept framework coupling qualitative scenario planning with computational discrete-event simulation to stress-test oncology AI adoption strategies.</p></sec><sec sec-type="methods"><title>Methods</title><p>We defined a strategic state space using 2 orthogonal axes, AI automation intensity and data interoperability, resulting in 4 distinct futures scenarios. We translated these qualitative narratives into a quantitative discrete-event simulation model of a 3-year operational horizon. The model quantified system performance (referral-to-treatment interval [RTTI] and throughput), volatility, and resource constraints across different adoption trajectories.</p></sec><sec sec-type="results"><title>Results</title><p>The scenario-planning phase yielded 4 operational archetypes (analog oncology, automation islands, interconnected clinicians, and AI-orchestrated care) with distinct constraints, risks, and failure modes. In the simulation, the fully integrated scenario maximized capacity (1244, SD 21.4 patients per year) and halved the mean RTTI to 14.9 (SD 0.3) days, a magnitude comparable to major pathway redesign interventions. Isolated automation without data infrastructure led to reduced system performance, increasing RTTI by 26% (37.1, SD 1.3 days) and reducing throughput to 647 (SD 10.1) patients per year due to administrative governance saturation. The model illustrated a structural bottleneck migration: successful upstream AI adoption shifted binding constraints from diagnostic scanners to downstream chemotherapy infusion units, whereas missing data interoperability resulted in governance constraints. Pathway optimization analysis indicated that a coordinated strategy prioritizing early improvements in data interoperability reduced transition volatility compared to an automation-first approach.</p></sec><sec sec-type="conclusions"><title>Conclusions</title><p>Integrating qualitative scenario planning with quantitative simulations enabled a systematic evaluation of oncology AI adoption strategies. As a proof of concept, it offers a replicable framework for health leaders to model future scenarios of digital transformation in times of high uncertainty. Subsequent work should expand this methodology to incorporate financial and health equity dimensions, establishing simulation-based scenario planning as an important tool in medical futures studies.</p></sec></abstract><kwd-group><kwd>medical futures studies</kwd><kwd>artificial intelligence</kwd><kwd>AI</kwd><kwd>data interoperability</kwd><kwd>scenario planning</kwd><kwd>discrete-event simulation</kwd></kwd-group></article-meta></front><body><sec id="s1" sec-type="intro"><title>Introduction</title><p>Modern oncology faces an increasing gap between therapeutic potential and operational capacity. While precision medicine expands, care delivery remains constrained by diagnostic throughput, pathology backlogs, and the cognitive load of multidisciplinary coordination. At the same time, clinical artificial intelligence (AI) is evolving from narrow, task-specific applications toward workflow-native systems [<xref ref-type="bibr" rid="ref1">1</xref>]. This next generation includes large language models capable of complex documentation and eligibility screening alongside emerging agentic AI systems designed to execute multistep planning with minimal human intervention [<xref ref-type="bibr" rid="ref2">2</xref>-<xref ref-type="bibr" rid="ref6">6</xref>]. Recent reviews describe the rapid proliferation of these tools in oncology yet consistently highlight that their translation into practice is constrained not by algorithmic performance but by integration challenges, data quality, and safety governance [<xref ref-type="bibr" rid="ref7">7</xref>-<xref ref-type="bibr" rid="ref13">13</xref>].</p><p>The impact of AI in complex adaptive systems such as oncology is rarely linear; local efficiency gains often destabilize rather than improve system-level performance. There is evidence suggesting that altering information flows, which is heavily dependent on robust data interoperability, can shift use patterns and clinical outcomes [<xref ref-type="bibr" rid="ref14">14</xref>-<xref ref-type="bibr" rid="ref16">16</xref>]. However, these integration efforts often trigger higher-order effects such as bottleneck migration and induced demand, which are usually not captured by model-centric evaluations. Furthermore, as sociotechnical complexity grows, regulatory frameworks are becoming more relevant [<xref ref-type="bibr" rid="ref17">17</xref>,<xref ref-type="bibr" rid="ref18">18</xref>]. New standards such as DECIDE-AI (Developmental and Exploratory Clinical Investigations of Decision Support Systems Driven by Artificial Intelligence), the European Union AI Act, and the Food and Drug Administration Good Machine Learning Practice now specify context-aware assessment and life cycle oversight [<xref ref-type="bibr" rid="ref19">19</xref>]. Consequently, governance moves from a background administrative activity to a potential capacity-limiting resource, influencing whether automation yields genuine access gains or merely introduces new operational friction.</p><p>Addressing these nonlinear dynamics requires methodologies capable of navigating uncertainty, a domain where health care has historically underused strategic foresight [<xref ref-type="bibr" rid="ref20">20</xref>-<xref ref-type="bibr" rid="ref22">22</xref>]. Scenario planning, a mature management science technique, offers a structured approach to reasoning through such strategic uncertainty [<xref ref-type="bibr" rid="ref23">23</xref>]. While futures studies in adjacent fields such as biobanking and education demonstrate how governance and incentives determine whether technical visions become reality, these methods are rarely applied to operational capacity planning [<xref ref-type="bibr" rid="ref24">24</xref>,<xref ref-type="bibr" rid="ref25">25</xref>].</p><p>To bridge this gap using medical futures thinking, we coupled qualitative scenario planning with computational discrete-event simulation (DES) in this study [<xref ref-type="bibr" rid="ref26">26</xref>]. By translating plausible adoption trajectories into quantitative models, we analyzed how variables such as AI automation intensity and data interoperability interact to produce higher-order effects, including governance saturation, false positive rates, and volatility. This paper presents a proof-of-concept framework for governments and health care executives to plan oncology AI adoption, shifting the focus from static operational forecasts to the dynamic management of structural transformation under uncertainty. In the following sections, we first describe our scenario design and simulation model; then present comparative results across scenarios; and, finally, discuss strategic implications.</p></sec><sec id="s2" sec-type="methods"><title>Methods</title><sec id="s2-1"><title>Study Design and Framework</title><p>We integrated qualitative scenario planning with DES to stress-test oncology operations against alternative adoption futures. Scenario planning defines plausible strategic futures, whereas DES evaluates how those futures propagate through operational constraints over time. To structure the uncertainty space, we first identified the 2 most decisive yet independent drivers of digital transformation: AI automation intensity (<italic>A</italic>), representing the degree of algorithmic task substitution in clinical and administrative workflows, and data interoperability (<italic>I</italic>), representing the friction of data transfer, provenance, and reuse across system boundaries. By treating these variables as orthogonal rather than correlated, we defined 4 operational quadrants in the 2 &#x00D7; 2 scenario analysis and qualitatively explored their outcomes and risk profiles.</p></sec><sec id="s2-2"><title>DES Model</title><p>To quantify operational implications, we constructed a DES model tracking individual patient trajectories through a resource-constrained oncology system over time. Implemented in SimPy (Python version 3.14; Python Software Foundation), the model represented a generic high-volume cancer center as a network of finite queues (eg, scanners, pathologists, oncologists, and treatment chairs). We selected resource capacities, service times, and failure rates based on standard oncology operation principles to create a representative, capacity-constrained baseline (the full script can be found in <xref ref-type="supplementary-material" rid="app1">Multimedia Appendix 1</xref>). This stylized parameterization was chosen to isolate the mechanistic effects of variables <italic>A</italic> and <italic>I</italic> on system flow rather than fit the historical data of a single institution. Consequently, the results illustrate directional trends and structural vulnerabilities rather than precise, generalizable operational forecasts.</p><p>The simulation ran for 3 years (1095 days) to ensure statistical convergence of queue dynamics and capture the full variance of patient pathways; a 150-day warm-up period was used to reduce initialization bias. Patient agents were generated stochastically based on the 3 most common tumor types (lung, breast, and colorectal) and disease stages (early vs late), flowing through a pathway that encompasses administrative processing, diagnostic imaging, biopsy, pathology (with probabilistic rework loops), molecular testing, multidisciplinary team coordination, and multimodal treatment initiation (surgery, chemotherapy, and radiotherapy). A calendar engine distinguished between standard clinical shifts and continuous laboratory operations, enforcing atomic task logic to prevent procedural fragmentation across shifts.</p><p>The model was governed by the 2 exogenous variables (<italic>A</italic> and <italic>I</italic>) normalized from 0.0 to 1.0. Workflow durations (<italic>T</italic>) for clinical tasks were calculated dynamically as follows: <italic>T</italic><sub>task</sub> = <italic>T</italic><sub>base</sub> &#x00D7; (1 &#x2013; &#x03B1; &#x00B7; <italic>A</italic>) &#x00D7; (1 &#x2013; &#x03B2; &#x00B7; <italic>I</italic>), where &#x03B1; and &#x03B2; represent the susceptibility of the task to automation and data integration, respectively.</p></sec><sec id="s2-3"><title>Operational Mechanisms</title><p>The simulation incorporated 8 coupled mechanisms to capture higher-order behaviors beyond linear efficiency gains (Table S1 in <xref ref-type="supplementary-material" rid="app2">Multimedia Appendix 2</xref>). These mechanisms captured 3 core operational dynamics: administrative friction, where high AI automation intensity without sufficient data interoperability triggers manual verification and shifts bottlenecks to administrative staff; induced demand, where highly sensitive AI triage increases false positive rates and generates additional downstream biopsies; and pathway shifts, where faster upstream diagnosis accelerates patient arrivals at downstream treatment centers and alters multidisciplinary coordination requirements. Each mechanism was operationalized through parameterized interactions governing queue progression, resource availability, and downstream demand propagation.</p></sec><sec id="s2-4"><title>Experimental Design and Analysis</title><p>We executed a comprehensive parameter sweep across the <italic>A</italic> &#x00D7; <italic>I</italic> state space with multiple stochastic replications per coordinate to generate uncertainty surfaces. Primary outcome measures included the mean referral-to-treatment interval (RTTI; defined as the simulated time in days from a patient&#x2019;s system entry at intake to the start of their first definitive treatment event), system throughput (patients per year), governance event density, and resource use profiles.</p></sec><sec id="s2-5"><title>Transition Pathway Optimization</title><p>To identify the most robust adoption sequence from <italic>A</italic>=0 and <italic>I</italic>=0 to <italic>A</italic>=1 and <italic>I</italic>=1, we modeled the simulation grid as a weighted directed graph. Transitions were restricted to orthogonal movements (increasing either <italic>A</italic> or <italic>I</italic> but not both simultaneously) to simulate realistic, incremental implementation capacity. A composite cost function was applied to determine the trajectory that minimizes the cumulative operational friction. The cost function was defined as the sum of 4 equally weighted (<italic>w</italic>=0.25) normalized components: mean RTTI, RTTI SD, inverse throughput volume, and throughput SD. We applied the shortest path algorithm by Dijkstra [<xref ref-type="bibr" rid="ref27">27</xref>] to minimize this cumulative operational cost, implemented using the NetworkX library [<xref ref-type="bibr" rid="ref28">28</xref>]. Conceptually, this treated the adoption journey as a risk landscape navigation problem, allowing us to mathematically identify the specific sequence of investments that reaches full integration while maximizing efficiency, throughput, and stability. This optimal path was benchmarked against 2 corner strategies: automation first (fully maximizing <italic>A</italic> before <italic>I</italic>) and data interoperability first (fully maximizing <italic>I</italic> before <italic>A</italic>).</p></sec><sec id="s2-6"><title>Ethical Considerations</title><p>Ethical review was not applied for. Because this research relied entirely on a theoretical DES using synthetic parameters and did not involve human participants or identifiable personal health information, it was exempt from institutional review board oversight in accordance with the statutes of the Ethics Committee of the Technical University of Munich [<xref ref-type="bibr" rid="ref29">29</xref>].</p></sec></sec><sec id="s3" sec-type="results"><title>Results</title><sec id="s3-1"><title>Operational Landscape of AI Adoption</title><p>The scenario-planning phase defined a 2D parameter space using AI automation (A) and data interoperability (I). This yielded 4 scenarios (S<sub>I-IV</sub>) with corresponding operational constraints and failure modes (<xref ref-type="fig" rid="figure1">Figure 1</xref>).</p><fig position="float" id="figure1"><label>Figure 1.</label><caption><p>Conceptual 2 &#x00D7; 2 scenario analysis matrix for artificial intelligence (AI) adoption in oncology. The strategic state space is defined by AI automation intensity (x-axis) and data interoperability (y-axis). The intersection yields 4 distinct operational scenarios (<italic>S</italic><sub>I-IV</sub>). Each quadrant details the anticipated dominant workflow characteristics, structural constraints, and primary expected operational risk.</p></caption><graphic alt-version="no" mimetype="image" position="float" xlink:type="simple" xlink:href="jmir_v28i1e92642_fig01.png"/></fig><p>The analog oncology scenario (S<sub>I</sub>: low <italic>A</italic> and low <italic>I</italic>) represents the baseline state, where capacity is dictated by physical constraints and linear, manual workflows. Here, digitization is localized, and delays are governed by visible queues in administration and diagnostics.</p><p>Increasing only AI automation (S<sub>II</sub>: high <italic>A</italic> and low <italic>I</italic>) creates automation islands. Here, algorithmic deployment outpaces data interoperability, and manual data reconciliation increases governance load, shifting the bottleneck from clinical decision-making to oversight and compliance. This represents an automation paradox where isolated digital acceleration degrades overall system performance.</p><p>The interconnected clinicians scenario (S<sub>III</sub>: low <italic>A</italic> and high <italic>I</italic>) describes an environment of high data interoperability but conservative AI automation. While data stewardship minimizes duplication and enables coordination, overall throughput remains capped by human cognitive limits and workforce availability.</p><p>Finally, the AI-orchestrated care system (S<sub>IV</sub>: high <italic>A</italic> and high <italic>I</italic>) integrates interoperable data with high AI adoption. This tends to remove upstream diagnostic constraints as they are more prone to algorithmic improvements. However, the system accelerates patient flow sufficiently to expose rigid downstream capacities in treatment delivery, and lower wait times induce further demand.</p></sec><sec id="s3-2"><title>Simulation With Emergent System Dynamics</title><p>To complement the qualitative scenario analysis, our DES captured higher-order dynamics and feedback loops such as governance work, virtual multidisciplinary team adoption, and induced demand (Figures S1A and S1B in <xref ref-type="supplementary-material" rid="app3">Multimedia Appendix 3</xref>). The simulation also included operational strain due to increased throughput. As shown in Figure S1C in <xref ref-type="supplementary-material" rid="app3">Multimedia Appendix 3</xref>, the high sensitivity of AI triage tools increased the false positive rate. This influx placed a disproportionate load on diagnostic resources, resulting in low-yield investigations that displaced confirmed cancer cases and competed for biopsy and histology capacity.</p></sec><sec id="s3-3"><title>Scenario Signatures and Performance Divergence</title><p>The simulation across the <italic>A</italic> &#x00D7; <italic>I</italic> parameter space generated distinct operational signatures for each scenario quadrant. As summarized in <xref ref-type="table" rid="table1">Table 1</xref>, the baseline (<italic>S</italic><sub>I</sub>) functioned as a capacity-constrained system with a mean RTTI of 29.4 days and an annual throughput of 1022 patients. In the automation islands scenario (<italic>S</italic><sub>II</sub>), we observed the worst system performance, with mean RTTI increasing to 37.1 days, a 26% increase compared to the analog baseline, whereas throughput decreased to 647 patients per year. Transitioning to interconnected clinicians (<italic>S</italic><sub>III</sub>) yielded moderate improvements, reducing RTTI to 27.3 days. The AI-orchestrated care system (<italic>S</italic><sub>IV</sub>) resulted in the highest patient flow, reducing the average RTTI to 14.9 days and increasing throughput to 1244 patients per year. Task-level improvements did not translate linearly into system performance (<xref ref-type="fig" rid="figure2">Figure 2</xref>). While the trajectory toward <italic>S</italic><sub>IV</sub> showed a combined increase in efficiency (lower RTTI) and number of treated patients, <italic>S</italic><sub>II</sub> resulted in higher RTTI and reduced throughput, suggesting that AI automation intensity may become counterproductive when isolated from data interoperability.</p><table-wrap id="t1" position="float"><label>Table 1.</label><caption><p>Operational performance metric values by scenario representing the mean of 10 stochastic replications.</p></caption><table id="table1" frame="hsides" rules="groups"><thead><tr><td align="left" valign="bottom">Scenario</td><td align="left" valign="bottom"><italic>A</italic><sup><xref ref-type="table-fn" rid="table1fn1">a</xref></sup></td><td align="left" valign="bottom"><italic>I</italic><sup><xref ref-type="table-fn" rid="table1fn2">b</xref></sup></td><td align="left" valign="bottom">RTTI<sup><xref ref-type="table-fn" rid="table1fn3">c</xref></sup> (d), mean (SD)</td><td align="left" valign="bottom">Patients per year, mean (SD)</td><td align="left" valign="bottom">Primary bottleneck</td></tr></thead><tbody><tr><td align="left" valign="top">S<sub>I</sub>: analog oncology</td><td align="left" valign="top">0.0</td><td align="left" valign="top">0.0</td><td align="left" valign="top">29.4 (0.5)</td><td align="left" valign="top">1022 (14.7)</td><td align="left" valign="top">CT<sup><xref ref-type="table-fn" rid="table1fn4">d</xref></sup> scanner</td></tr><tr><td align="left" valign="top">S<sub>II</sub>: automation islands</td><td align="left" valign="top">1.0</td><td align="left" valign="top">0.0</td><td align="left" valign="top">37.1 (1.3)</td><td align="left" valign="top">647 (10.1)</td><td align="left" valign="top">Governance</td></tr><tr><td align="left" valign="top">S<sub>III</sub>: interconnected clinicians</td><td align="left" valign="top">0.0</td><td align="left" valign="top">1.0</td><td align="left" valign="top">27.3 (0.3)</td><td align="left" valign="top">1127 (14.0)</td><td align="left" valign="top">Molecular laboratory</td></tr><tr><td align="left" valign="top">S<sub>IV</sub>: AI<sup><xref ref-type="table-fn" rid="table1fn5">e</xref></sup>-orchestrated care</td><td align="left" valign="top">1.0</td><td align="left" valign="top">1.0</td><td align="left" valign="top">14.9 (0.3)</td><td align="left" valign="top">1244 (21.4)</td><td align="left" valign="top">Chemotherapy infusion units</td></tr></tbody></table><table-wrap-foot><fn id="table1fn1"><p><sup>a</sup>AI automation intensity variable.</p></fn><fn id="table1fn2"><p><sup>b</sup>Data interoperability variable.</p></fn><fn id="table1fn3"><p><sup>c</sup>RTTI: referral-to-treatment interval.</p></fn><fn id="table1fn4"><p><sup>d</sup>CT: computed tomography.</p></fn><fn id="table1fn5"><p><sup>e</sup>AI: artificial intelligence.</p></fn></table-wrap-foot></table-wrap><fig position="float" id="figure2"><label>Figure 2.</label><caption><p>System-level performance indicators across the simulated adoption landscape. The heat maps illustrate the aggregate operational performance of the oncology pathways based on the discrete-event simulation. The x-axis represents artificial intelligence (AI) automation intensity, and the y-axis represents data interoperability, both normalized from 0.0 to 1.0. Panel (A) displays the mean referral-to-treatment interval measured in simulated days from patient intake to the initiation of definitive treatment. Panel (B) displays the annualized system throughput, quantified as the total number of treatment starts per year. All data points represent the average of 10 stochastic replications for each coordinate on the 11 &#x00D7; 11 parameter grid.</p></caption><graphic alt-version="no" mimetype="image" position="float" xlink:type="simple" xlink:href="jmir_v28i1e92642_fig02.png"/></fig></sec><sec id="s3-4"><title>Bottleneck Migration and Resource Dynamics</title><p>Further analysis exposed a structural migration of constraints (<xref ref-type="fig" rid="figure3">Figure 3</xref>). In low&#x2013;AI automation scenarios (S<sub>I</sub> and S<sub>III</sub>), constraints were located upstream in diagnostics (computed tomography scanners and molecular laboratory). The automation islands (S<sub>II</sub>) scenario saw the primary constraint decouple from clinical infrastructure, shifting to administrative governance and quality assurance methods as manual oversight processes became overwhelmed. In the fully transformed S<sub>IV</sub> scenario, the primary bottleneck shifted downstream to chemotherapy infusion units. Therefore, successful upstream AI adoption transferred capacity pressure from diagnostic infrastructure to labor-intensive treatment resources.</p><fig position="float" id="figure3"><label>Figure 3.</label><caption><p>Structural bottleneck migration across the strategic state space: a categorical heat map of the primary binding constraint within the oncology pathway across the <italic>A</italic> &#x00D7; <italic>I</italic> scenario space. The x-axis represents artificial intelligence (AI) automation intensity, and the y-axis represents data interoperability, both normalized from 0.0 to 1.0. For each coordinate on the 11 &#x00D7; 11 grid, the simulation evaluates the operational load across all modeled clinical and administrative queues and identifies the specific resource pool with the highest mean use rate. CT: computed tomography.</p></caption><graphic alt-version="no" mimetype="image" position="float" xlink:type="simple" xlink:href="jmir_v28i1e92642_fig03.png"/></fig><p>To unpack these constraint shifts, we generated visualization tools that quantify how resource use changes across the <italic>A</italic> &#x00D7; <italic>I</italic> plane. Holding data interoperability constant while varying AI automation (<xref ref-type="fig" rid="figure4">Figure 4A</xref>) and holding AI automation constant while varying data interoperability (<xref ref-type="fig" rid="figure4">Figure 4B</xref>) yielded distinct use trajectories for each resource. Together, these plots identified crossover points at which the binding constraint moved from upstream diagnostics (computed tomography and laboratory services) to downstream treatment capacity (eg, chemotherapy, surgery, and radiotherapy) or administrative or digital functions (referral processing and governance), indicating where marginal investments likely had the greatest impact.</p><fig position="float" id="figure4"><label>Figure 4.</label><caption><p>Resource use sensitivity analysis. The panels display the mean use rates of system resources derived from the discrete-event simulation. Panel (A) illustrates the impact of varying artificial intelligence (AI) automation intensity (<italic>A</italic>) from 0.0 to 1.0 while holding data interoperability (<italic>I</italic>) constant at a baseline of 0.5. Panel (B) demonstrates the effect of varying <italic>I</italic> with <italic>A</italic> fixed at 0.5. The dashed line represents the theoretical maximum capacity (100% use). CT: computed tomography; RT: radiotherapy.</p></caption><graphic alt-version="no" mimetype="image" position="float" xlink:type="simple" xlink:href="jmir_v28i1e92642_fig04.png"/></fig></sec><sec id="s3-5"><title>Volatility and Optimal Pathways</title><p>Finally, we analyzed the SDs of the output parameters across 10 stochastic replications, treating volatility as a proxy for system stability. The SDs for RTTI and throughput were highest in the transition from S<sub>II</sub> to S<sub>IV</sub>, indicating that uncoordinated AI adoption may create unpredictable wait times driven by sporadic governance backlogs (Figures S1D-F in <xref ref-type="supplementary-material" rid="app3">Multimedia Appendix 3</xref>). In contrast, establishing high data interoperability first (S<sub>III</sub>) acted as a stabilizing force, allowing for the subsequent integration of AI automation. To determine the most robust trajectory from analog operations (S<sub>I</sub>) to the AI-orchestrated system (S<sub>IV</sub>), we performed a graph-based optimization minimizing a composite cost function of RTTI, throughput, and their respective operational variances (<xref ref-type="fig" rid="figure5">Figure 5A</xref>). The model selected an adoption sequence characterized by a structural preference for data interoperability&#x2013;led scaling, prioritizing early gains in <italic>I</italic> ahead of <italic>A</italic>. This sequencing effectively reduced midtransition volatility, allowing the system to absorb the governance load of incremental AI automation while maintaining high throughput efficiency throughout the implementation life cycle (<xref ref-type="fig" rid="figure5">Figure 5B</xref>).</p><fig position="float" id="figure5"><label>Figure 5.</label><caption><p>Pathway optimization and transition dynamics. Panel (A) presents a trajectory analysis across the artificial intelligence (AI) automation and data interoperability state space, modeled as a weighted directed graph. The background heat map indicates system volatility (defined as the mean of cross-replication SDs of the referral-to-treatment interval [RTTI] and annualized throughput), with darker regions representing high instability. The green line traces the computationally optimal path based on the weighted cost function, benchmarked against 2 alternative corner strategies: an automation-first approach (red line) and an interoperability-first approach (blue line). Panel (B) tracks key system metrics throughout the implementation process. Normalized metrics for efficiency (inverted RTTI), throughput volume, and stability (inverted system volatility) are plotted against transition progress (0%-100%).</p></caption><graphic alt-version="no" mimetype="image" position="float" xlink:type="simple" xlink:href="jmir_v28i1e92642_fig05.png"/></fig></sec></sec><sec id="s4" sec-type="discussion"><title>Discussion</title><sec id="s4-1"><title>Strategic Utility for Health System Planning</title><p>This paper addresses the gap between the rapid pace of technological transformation in medicine and the current underuse of applied futures methods, offering a novel approach to operational planning under uncertainty [<xref ref-type="bibr" rid="ref20">20</xref>]. Traditional business cases for AI often rely on static efficiency assumptions, presuming that diagnostic time reductions linearly increase throughput. However, such linear extrapolations ignore endogenous feedback loops inherent in complex systems. By coupling scenario planning with quantified simulations, this study provides a framework to stress-test AI adoption strategies against plausible futures&#x2014;making risks visible to health system planners before decisions are formed and capital is committed.</p><p>Because the model is parameterized around 2 fundamental strategic levers (AI automation intensity and data interoperability), it can inform both clinic-level operational redesign and broader health system&#x2013;level investment and governance planning. To illustrate how health systems can operationalize this framework across different organizational levels, we have outlined 3 concrete implementation scenarios (Table S2 in <xref ref-type="supplementary-material" rid="app2">Multimedia Appendix 2</xref>). These scenarios demonstrate how micro-level hospitals, meso-level regional networks, and macro-level state health authorities can use this framework to anticipate bottleneck migration, sequence investments, and mitigate transition volatility.</p></sec><sec id="s4-2"><title>Robust Strategies and Sequencing</title><p>A key insight derived from the scenario sweep is the phenomenon of bottleneck migration, necessitating a shift from local optimization to whole-system capacity planning. The simulation indicates that successful AI adoption in diagnostics tends to shift pressure downstream in the model. Therefore, executives must couple upstream AI investments with adaptive capacity planning for surgery, chemotherapy, and radiotherapy. Similarly, the emergence of higher false positive rates suggests that adoption strategies might require new guardrails such as confirmatory testing thresholds to prevent the system from being overwhelmed in scenarios of increased induced demand. At the same time, scenarios of high AI automation and low data interoperability should be avoided as they can lead to significant governance overload. This aligns with recent critiques of health workforce planning, which note that failure to account for social interactions and power dynamics, including governance, often undermines technical implementation [<xref ref-type="bibr" rid="ref30">30</xref>].</p><p>Moreover, results from our pathway optimization demonstrated that a coordinated adoption strategy with early focus on data interoperability yielded the best overall results and stability. Because high volatility manifests in real-world settings as unpredictability and may lead to stakeholder resistance, implementation strategies must manage transition stability alongside performance optimization. This underlines the importance of sequencing&#x2014;via phased rollouts or adaptive governance&#x2014;to minimize disturbances during transformation. Conceptually, this optimization mirrored a backcasting approach, working backward from a desired end state to identify near-term moves that preserve system stability [<xref ref-type="bibr" rid="ref31">31</xref>].</p></sec><sec id="s4-3"><title>Limitations and Future Directions</title><p>This study presents a mechanism-oriented framework prioritizing structural behavior over precise numerical forecasting. Importantly, the simulation is based on stylized parameters rather than real-world data. As an exploratory proof of concept, it has several limitations. First, parameters are based on conceptual assumptions rather than site-level empirical data, limiting the generalizability of specific point estimates. Alternative parameterizations could yield different quantitative results; thus, findings should be interpreted as directional hypotheses rather than definitive empirical conclusions. Second, the model is restricted to 3 tumor types and 2 stages, which does not capture the full complexity of a clinical case mix. Third, the simulation excludes financial costs, clinical end points, and equity impacts. Finally, adoption is modeled as a static state rather than a time-varying implementation process, simplifying the realities of organizational learning and change management.</p><p>To support applied decision-making, future work should calibrate parameters to local workflow distributions and resource profiles and validate model behavior against observed pathway metrics where available to assess external validity. Planned extensions include formal sensitivity and uncertainty analyses over capacities, service time assumptions, and objective function weights used in the transition optimization. Equity should be incorporated explicitly by stratifying patient agents by sociodemographic risk factors (eg, deprivation, language barriers, and digital access) and modeling differential access, adherence, and delay mechanisms to test whether accelerated pathways widen disparities [<xref ref-type="bibr" rid="ref32">32</xref>,<xref ref-type="bibr" rid="ref33">33</xref>]. Additional behavioral realism could be introduced by modeling clinician oversight burden, trust calibration, and AI literacy as determinants of effective automation and governance load [<xref ref-type="bibr" rid="ref34">34</xref>,<xref ref-type="bibr" rid="ref35">35</xref>].</p></sec><sec id="s4-4"><title>Conclusions</title><p>The integration of qualitative scenario planning with quantitative simulations offers a tool for testing plausible oncology AI strategies under uncertainty. AI can dramatically improve oncology operations but only when paired with interoperable data infrastructure and system-level capacity planning; otherwise, it risks worsening delays and instability. Simulating interactions between AI automation and data interoperability exposed operational tipping points, bottlenecks, and instabilities invisible to static planning models. Future research should extend this hybrid framework and integrate financial and equity dimensions to better anticipate the societal costs of technological disruption. This could help establish simulation-based scenario planning as an important tool in medical futures studies.</p></sec></sec></body><back><notes><sec><title>Funding</title><p>This research received no external funding and was supported by internal institutional funds.</p></sec><sec><title>Data Availability</title><p>The datasets generated during this study are available from the corresponding author on reasonable request. The full simulation code is provided in the supplementary material.</p></sec></notes><fn-group><fn fn-type="con"><p>Conceptualization: PM, JvB</p><p>Data curation: PM, JvB</p><p>Formal analysis: PM, JvB</p><p>Methodology: PM</p><p>Project administration: SDB-M, JvB</p><p>Supervision: SDB-M, JvB</p><p>Writing&#x2014;original draft: PM, EG</p><p>Writing&#x2014;review and editing: PM, EG, SDB-M, JvB</p></fn><fn fn-type="conflict"><p>Conflict for author JvB: Employee Sidekick Health Germany GmbH</p></fn></fn-group><glossary><title>Abbreviations</title><def-list><def-item><term id="abb1">AI</term><def><p>artificial intelligence</p></def></def-item><def-item><term id="abb2">DECIDE-AI</term><def><p>Developmental and Exploratory Clinical Investigations of Decision Support Systems Driven by Artificial Intelligence</p></def></def-item><def-item><term id="abb3">DES</term><def><p>discrete-event simulation</p></def></def-item><def-item><term id="abb4">RTTI</term><def><p>referral-to-treatment 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