Evidence map›Paper›PMID 41735994›Full record

SynthesisBMC medical informatics and decision making2026

Performance comparison and future perspectives of deep learning and classical machine learning in bone tumor applications: a systematic review (2019-2025).

Yu Qiao, Carolin Eisfeld, Rüdiger von Eisenhart-Rothe, Florian Hinterwimmer

Abstract readSystematic ReviewComparative Study
In one paragraph

Synthesis in BMC medical informatics and decision making, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Yu QiaoDepartment of Orthopaedics and Sports Orthopaedics, School of Medicine and Health, TUM University Hospital, Technical University of Munich, Ismaninger Str. 22, 81675, Munich, Germany. yu.qiao@tum.de.
Carolin EisfeldDepartment of Orthopaedics and Sports Orthopaedics, School of Medicine and Health, TUM University Hospital, Technical University of Munich, Ismaninger Str. 22, 81675, Munich, Germany.
Rüdiger von Eisenhart-RotheDepartment of Orthopaedics and Sports Orthopaedics, School of Medicine and Health, TUM University Hospital, Technical University of Munich, Ismaninger Str. 22, 81675, Munich, Germany.
Florian HinterwimmerDepartment of Orthopaedics and Sports Orthopaedics, School of Medicine and Health, TUM University Hospital, Technical University of Munich, Ismaninger Str. 22, 81675, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe diagnosis and prognostic assessment of bone tumors represent a complex and clinically significant challenge. In recent years, the rise of artificial intelligence (AI), particularly deep learning (DL) and classical machine learning (ML), has emerged as a promising tool in this field. This study systematically reviews the applications of AI in bone tumor diagnosis, prognosis, segmentation, and treatment response, with a focus on model performance, emerging trends, and current limitations.

methodsThis systematic review follows to the PRISMA guidelines and conducted a comprehensive search of four major databases (PubMed, Web of Science, Scopus, and Cochrane Library) to identify studies published between January 2019 and May 2025 on the application of AI in bone tumors. Relevant original articles were identified based on predefined inclusion and exclusion criteria, and research data such as basic information, algorithms, models, performance metrics, and clinical tasks, were systematically extracted and analyzed. And the performance of DL and ML methods in bone tumors was comparatively analyzed.

resultsThe review included 70 studies involving 53,149 cases, of which 45.83% were malignant bone tumors. DL was used in 77.63% of the studies and classical ML in 22.37%. Diagnostic tasks dominated the research focus (81.94%), followed by survival prediction (11.11%) and treatment response evaluation (6.94%). Performance metrics indicated that DL models exhibited higher weighted averages in accuracy (0.87), AUC (0.89), sensitivity (0.84), specificity (0.88), precision (0.81), and F-score (0.84), while classical ML models achieved the highest precision (0.90). Although DL demonstrated a performance advantage in image-based tasks, classical ML maintained greater stability in structured datasets. No significant performance differences were observed between large-sample and small-sample studies, reflecting the robustness of both model types. Additionally, a recent shift in research focus was observed, from diagnostic applications toward disease prediction.

conclusionArtificial intelligence has demonstrated strong performance and potential in bone tumor research. DL often demonstrates more balanced performance in image-based bone tumor tasks, while classical ML remains competitive and may hold advantages in structured, small-sample datasets, precision-prioritized settings. However, we did not observe statistically significant differences, so these findings should be interpreted as performance tendencies in specific contexts rather than universally validated superiority. Future research should focus on optimizing DL and classical ML models, developing fusion algorithms in bone tumors can improve the generalization performance, accuracy, and ability to adapt to complex data scenarios. At the same time, fostering interdisciplinary and multicenter collaborations between computer scientists and clinicians, improving data-sharing frameworks, and addressing ethical and privacy concerns will be essential to fully harness the significant potential of AI in bone tumor research and clinical applications.

Indexed as

Bone NeoplasmsDeep LearningMachine LearningArtificial IntelligenceHumansPredictive Learning ModelsArtificial intelligenceBone tumorClassical machine learningDeep learningDiagnostic performanceSystematic review

Identifiers

PMID41735994
PMCPMC13063476

What Socratic holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.