Copyright: ©Author(s) 2026.
World J Methodol. Sep 20, 2026; 16(3): 121456
Published online Sep 20, 2026. doi: 10.5662/wjm.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 concept | Empirical intervention, one-size-fits-all strategy | Precision medicine, based on individual characteristics (tumor biology, genetic background, bone metabolism status, etc.) |
| Screening method | Mainly dual-energy X-ray absorptiometry | AI-based opportunistic screening (based on routine imaging) + bone metabolism marker detection |
| Screening efficiency | Low, about 60% of GTO patients not identified early | High, significantly improved early recognition rate |
| Therapeutic strategy | Routine bone protectors (bisphosphonates, denosumab) applied uniformly based on guidelines | Nanoparticle-targeted drug delivery system + personalized scheme (combined with multiomics results) |
| Consideration of individual differences | Ignored (tumor stage, pathological type, treatment plan, genetic background, nutritional status not fully considered) | Fully considered, tailored to individual patient characteristics |
| Therapeutic effect | Poor in some patients (61.3% failure rate of bisphosphonates in postmenopausal osteoporotic vertebral fracture patients) | Significantly improved, targeted delivery enhances efficacy |
| Adverse reactions | High risk (atypical femoral fractures, osteonecrosis of the jaw from bisphosphonates; hypocalcemia from denosumab) | Reduced systemic adverse reactions (targeted delivery reduces nontarget organ exposure) |
| Mechanism understanding | Focus 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 process | Discontinuous (screening → intervention, no closed-loop monitoring) | Whole-process closed-loop management (precision screening → precision assessment → precision intervention → precision monitoring) |
| Impact on patient compliance | Low (due to poor therapeutic effect and adverse reactions) | High (improved efficacy, reduced side effects, and personalized intervention) |
| Impact on prognosis | Limited improvement, failure to effectively reduce SREs and prolong survival | Significantly improves long-term prognosis, reduces SREs incidence, and enhances quality of life |
| Supporting technologies | Conventional detection and drug delivery technologies | AI, 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 barriers | AI 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 standardization | Data 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 cooperation | MDT 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 risks | Data 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 system | Multitechnology fusion (AI, multiomics, nanomedicine, wearable sensors). Multicenter dataset and federated learning. Closed-loop management: Early warning, precise typing, intervention, monitoring |
| Accelerated clinical translation of nanotechnology | Optimize 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 standardization | Establish 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 regulation | Improve 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 |
- Citation: Wang P, Sun JK, Li D, Shi Z, Lu PY, Jin DF, Huang SF, Ruan YH, Li WT, Shi MD, Ma ZH, Wang ZH, Hu LY, Xue ME, Zhang CJ, Li ZP. Precision management of gastrointestinal tumor-associated osteoporosis driven by cutting-edge technologies: Current status, challenges, and future prospects. World J Methodol 2026; 16(3): 121456
- URL: https://www.wjgnet.com/2222-0682/full/v16/i3/121456.htm
- DOI: https://dx.doi.org/10.5662/wjm.121456