Abstract
With increasing opportunities for patients with bone metastasis (BM) to benefit from local surgical intervention, accurate survival analysis across different primary cancers remains challenging. Current analytical frameworks commonly rely on single-center, pan-cancer cohorts and provide insufficient integration of cancer-specific characteristics. In this retrospective, multicenter, registry-based cohort study, baseline demographic and clinical characteristics of 13,742 patients with AJCC stage IV or TNM stage M1 metastatic cancer were collected from 42 studies registered in the cBioPortal for Cancer Genomics database. Overall survival (OS) after metastatic diagnosis was the primary outcome. Univariate analyses were performed using Kaplan–Meier methods, log-rank tests, and non-parametric tests. Variables with p < 0.20 were included in multivariable Cox proportional hazards models to examine independent associations with survival. Multiple imputation was applied to address missing data. Among the 25 primary cancers analyzed, approximately half showed observable survival differences between BM and other-site metastasis, with 6 cancers reaching statistical significance. Based on median survival, all cancers could be stratified into 3 distinct survival tiers, ranging from prolonged survival exceeding 15 months to markedly shorter survival of 3–10 months, with multivariable analyses further demonstrating that primary cancer type was the strongest factor associated with survival heterogeneity among BM patients (HR = 1.422–1.758, p < 0.001). Moreover, poorly differentiated or undifferentiated histology was independently associated with worse OS (HR = 1.249, p < 0.001), and age > 60 years was also associated with shorter survival (p < 0.001). No single metastatic site demonstrated a consistent adverse association with survival across cancer types. Overall, BM demonstrates cancer-specific and heterogeneous associations with survival compared with other metastatic sites. All primary cancers could be stratified into 3 groups, representing the most important factor associated with survival differences. Moreover, pathological differentiation was significantly associated with survival among BM patients. Notably, no metastatic site functions as a universal prognostic factor across cancers. Large-scale, multicenter, registry-based analyses provide a valuable framework for cancer-specific survival analysis and for identifying clinically relevant factors that may serve as a reference for risk stratification in surgical decision-making.
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Data availability
The datasets supporting the conclusions of this study are available from the corresponding author on reasonable request or can be accessed from the cBioPortal for Cancer Genomics (https://www.cbioportal.org/).
Abbreviations
- AJCC:
-
American Joint Committee on Cancer
- BM:
-
Bone metastasis
- BMI:
-
Body mass index
- CI:
-
Confidence interval
- CV:
-
Coefficient of variation
- EGFR:
-
Epidermal growth factor receptor
- EMT:
-
Epithelial–mesenchymal transition
- ECOG:
-
Eastern Cooperative Oncology Group
- HF:
-
Hazard ratio
- IHC:
-
Immunohistochemistry
- IQR:
-
Interquartile range
- K–S:
-
Kolmogorov–Smirnov
- MAXSTAT:
-
Maximally selected rank statistics
- NSCLC:
-
Non-small cell lung cancer
- OBM:
-
Only bone metastasis
- OS:
-
Overall survival
- OSM:
-
Other-site metastasis
- PH:
-
Proportional hazards
- PS:
-
Probability of superiority
- RECORD:
-
Reporting of studies conducted using observational routinely-collected health data
- STROBE:
-
Strengthening the reporting of observational studies in epidemiology
- TNM:
-
Tumor–node–metastasis
- VIF:
-
Variance inflation factor
- WFNS:
-
World federation of neurosurgical societies
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Acknowledgements
We sincerely thank Prof. Wei and Prof. Liu for their valuable guidance on integrating this project with clinical practice. The authors gratefully acknowledge Peking University Third Hospital and the National Natural Science Foundation of China for hardware support in data processing and financial funding for the overall implementation of this project.
Funding
This study was supported by the Peking University Third Hospital (Grant No. BYSYZD2023017) and the National Natural Science Foundation of China (Grant Nos. 82201644 and 82471505). The funding bodies had no role in the design of the study, data collection, analysis, interpretation of data, or in writing the manuscript.
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Z.L. Yun, Y.C. Tang, and J. Sun conceived and designed the study. Z.L. Yun, J.C. Lei, and G.Q. Zhang collected the data. Z.L. Yun and Y.C. Tang performed the statistical analysis. Z.L. Yun drafted the manuscript. F. Wei and X.G. Liu supervised the study and were responsible for manuscript revision and correspondence. All authors read and approved the final manuscript.
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The study is retrospective and registry-based without clinical or experimental intervention, and the data used were collected from a public database. For these reasons, informed consent was applied for exemption. The study was conducted with the support of Peking University Third Hospital. Ethical approval was granted by the Research Ethics Committee (approval number: LM2025366).
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Yun, Z., Tang, Y., Sun, J. et al. Cancer-specific survival patterns in patients with bone metastasis: a registry-based analysis of 13,742 patients. Sci Rep (2026). https://doi.org/10.1038/s41598-026-43780-6
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DOI: https://doi.org/10.1038/s41598-026-43780-6


