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Copyright: ©Author(s) 2026.
World J Methodol. Sep 20, 2026; 16(3): 121456
Published online Sep 20, 2026. doi: 10.5662/wjm.121456
Table 1 Comparison between traditional management and precision management for gastrointestinal tumor-associated osteoporosis
Items (evaluation indicators)
Traditional management mode
Precision management mode (empowered by cutting-edge technologies)
Core conceptEmpirical intervention, one-size-fits-all strategyPrecision medicine, based on individual characteristics (tumor biology, genetic background, bone metabolism status, etc.)
Screening methodMainly dual-energy X-ray absorptiometryAI-based opportunistic screening (based on routine imaging) + bone metabolism marker detection
Screening efficiencyLow, about 60% of GTO patients not identified earlyHigh, significantly improved early recognition rate
Therapeutic strategyRoutine bone protectors (bisphosphonates, denosumab) applied uniformly based on guidelinesNanoparticle-targeted drug delivery system + personalized scheme (combined with multiomics results)
Consideration of individual differencesIgnored (tumor stage, pathological type, treatment plan, genetic background, nutritional status not fully considered)Fully considered, tailored to individual patient characteristics
Therapeutic effectPoor in some patients (61.3% failure rate of bisphosphonates in postmenopausal osteoporotic vertebral fracture patients)Significantly improved, targeted delivery enhances efficacy
Adverse reactionsHigh risk (atypical femoral fractures, osteonecrosis of the jaw from bisphosphonates; hypocalcemia from denosumab)Reduced systemic adverse reactions (targeted delivery reduces nontarget organ exposure)
Mechanism understandingFocus on single bone metabolism pathway (e.g., RANKL-RANK-OPG system)In-depth analysis via multiomics technologies, clarifying “tumor-gastrointestinal-bone” multisystem interaction network
Management processDiscontinuous (screening → intervention, no closed-loop monitoring)Whole-process closed-loop management (precision screening → precision assessment → precision intervention → precision monitoring)
Impact on patient complianceLow (due to poor therapeutic effect and adverse reactions)High (improved efficacy, reduced side effects, and personalized intervention)
Impact on prognosisLimited improvement, failure to effectively reduce SREs and prolong survivalSignificantly improves long-term prognosis, reduces SREs incidence, and enhances quality of life
Supporting technologiesConventional detection and drug delivery technologiesAI, nanoparticle-targeted drug delivery system, multiomics (genomics, transcriptomics, metabolomics, microbiomics), MDT collaboration
Table 2 Core challenges in the precision management of gastrointestinal tumor-associated osteoporosis
Category
Core challenges
Clinical translation barriersAI models: Insufficient generalization, overfitting, poor interpretability, lack of multicenter validation. Nanodrugs: Unclear in vivo mechanism, long translation cycle, high cost, difficult quality control, biosafety risks, poor scenario adaptability
Data integration and standardizationData islands among departments and institutions. Multisource heterogeneous data with poor interoperability. Nonuniform detection standards for bone metabolic markers. Ethical and privacy barriers restricting data sharing
Imperfect MDT cooperationMDT is passive and delayed rather than proactive. Knowledge barriers between oncology, orthopedics, nutrition, etc. Lack of standardized GTO-specific guidelines and workflows
Ethical and safety risksData privacy and security issues in AI applications. “Black box” problem of AI leading to low clinical trust. Unknown long-term biosafety of nanomaterials. Individual heterogeneity and potential toxicity of nanodrugs
Table 3 Future perspectives for the precision management of gastrointestinal tumor-associated osteoporosis
Dimension
Future strategies
Construction of integrated precision systemMultitechnology fusion (AI, multiomics, nanomedicine, wearable sensors). Multicenter dataset and federated learning. Closed-loop management: Early warning, precise typing, intervention, monitoring
Accelerated clinical translation of nanotechnologyOptimize biocompatibility and administration routes (oral, enteric-coated). Conduct multicenter, randomized, controlled clinical trials. Scale production to reduce cost; develop multitarget synergistic nanosystems
Improved MDT and data standardizationEstablish standardized, proactive MDT workflow. Define responsibilities of oncology, orthopedics, radiology, nutrition. Unify data standards and build regional data sharing platform. Develop GTO-specific clinical guidelines
Ethical supervision and technical regulationImprove data privacy protection and encryption technology. Establish clinical access and postmarketing surveillance system. Define AI as an auxiliary tool; strengthen manual review. Standardize clinical application and risk control of new technologies


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