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99种肢体骨恶性肿瘤生存预测模型的系统评价。

Systematic review of 99 extremity bone malignancy survival prediction models.

作者信息

Lai Cheng-Yo, Yen Hung-Kuan, Lin Hao-Chen, Groot Olivier Quinten, Lin Wei-Hsin, Hsu Hao-Ping

机构信息

Department of Orthopedic Surgery, National Taiwan University Hospital Hsinchu Branch, Hsinchu, Taiwan.

Department of Orthopedic Surgery, National Taiwan University Hospital, Taipei, Taiwan.

出版信息

J Orthop Traumatol. 2025 Jan 28;26(1):5. doi: 10.1186/s10195-025-00821-6.

Abstract

BACKGROUND

Various prediction models have been developed for extremity metastasis and sarcoma. This systematic review aims to evaluate extremity metastasis and sarcoma models using the utility prediction model (UPM) evaluation framework.

METHODS

We followed Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and systematically searched PubMed, Embase, and Cochrane to identify articles presenting original prediction models with 1-year survival outcome for extremity metastasis and 5-year survival outcome for sarcoma. Identified models were assessed using the UPM score (0-16), categorized as excellent (12-16), good (7-11), fair (3-6), or poor (0-2). A total of 5 extremity metastasis and 94 sarcoma models met inclusion criteria and were analyzed for design, validation, and performance.

RESULTS

We assessed 5 models for extremity metastasis and 94 models for sarcoma. Only 4 out of 99 (4%) models achieved excellence, 1 from extremity metastasis and 3 from sarcoma. The majority were rated good (62%; 61/99), followed by fair (31%, 31/99) and poor (3%, 3/99).

CONCLUSIONS

Most predictive models for extremity metastasis and sarcoma fall short of UPM excellence. Suboptimal study design, limited external validation, and the infrequent availability of web-based calculators are main drawbacks.

LEVEL OF EVIDENCE

This study is classified as Level 2a evidence according to the Oxford 2011 Levels of Evidence. Trial registration This study was registered in PROSEPRO (CRD42022373391, https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=373391 ).

摘要

背景

已经开发了多种用于肢体转移瘤和肉瘤的预测模型。本系统评价旨在使用效用预测模型(UPM)评估框架评估肢体转移瘤和肉瘤模型。

方法

我们遵循系统评价和Meta分析的首选报告项目(PRISMA)指南,系统检索了PubMed、Embase和Cochrane,以识别呈现肢体转移瘤1年生存结局和肉瘤5年生存结局的原始预测模型的文章。使用UPM评分(0-16)对识别出的模型进行评估,分为优秀(12-16)、良好(7-11)、中等(3-6)或差(0-2)。共有5个肢体转移瘤模型和94个肉瘤模型符合纳入标准,并对其设计、验证和性能进行了分析。

结果

我们评估了5个肢体转移瘤模型和94个肉瘤模型。99个模型中只有4个(4%)达到优秀,其中1个来自肢体转移瘤,3个来自肉瘤。大多数被评为良好(62%;61/99),其次是中等(31%,31/99)和差(3%,3/99)。

结论

大多数肢体转移瘤和肉瘤的预测模型未达到UPM优秀标准。研究设计欠佳、外部验证有限以及基于网络的计算器使用不频繁是主要缺点。

证据水平

根据2011年牛津证据水平,本研究分类为2a级证据。试验注册本研究在PROSPERO(CRD42022373391,https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=373391 )注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5197/11775353/c99746a8927c/10195_2025_821_Fig1_HTML.jpg

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