Early diagnostic value of ECT whole-body bone imaging combined with PINP and β-CTX for bone metastasis of lung cancer.

IF 2.8 3区 医学 Q2 ONCOLOGY Clinical & Translational Oncology Pub Date : 2024-12-01 Epub Date: 2024-05-30 DOI:10.1007/s12094-024-03475-8
Meiying Jiang, Qiyun Yu, Haitao Mei, Yingchao Jian, Rong Xu
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Abstract

Objective: This research was aimed at investigating the early diagnostic value of emission computed tomograph (ECT) whole-body bone imaging combined with PINP and β-CTX for bone metastasis of lung cancer.

Methods: Case data of 86 lung cancer patients were categorized into lung cancer with bone metastasis (LCWBM, 46 cases) and lung cancer without bone metastasis (LCWOBM, 40 cases) groups according to the presence or absence of bone metastasis. Patients' general information were collected. ECT whole-body bone imaging was used to detect bone metastases and the grading of the extent of disease (EOD) in both groups, and electrochemiluminescence was utilized to detect the serum levels of PINP and β-CTX. Spearman correlation analysis was employed to evaluate the correlation between EOD grading and PINP and β-CTX levels. Logistic univariate and multivariate regression was implemented to analyze the risk factors of bone metastasis of lung cancer. Receiver operating characteristic (ROC) curve was applied to analyze the diagnostic efficacy of the single test of ECT whole-body bone imaging, PINP, or β-CTX and the combination of the three tests.

Results: The differences in pathological type, clinical stage and EOD grading, the number of positive ECT cases, and the expression levels of PINP and β-CTX between the LCWBM and LCWOBM groups were statistically significant. In LCWBM patients with different EOD grading, the trends of the expression of PINP and β-CTX were grade 3 > grade 2 > grade 1 and grade 0. Further correlation analyses revealed that EOD grading showed a significant positive correlation with the PINP and β-CTX expression levels. Univariate logistic regression analysis demonstrated that adenocarcinoma, TNM stage IV, ECT positivity, and high expression of PINP and β-CTX were associated with bone metastasis of lung cancer, and multivariate logistic regression analysis indicated that ECT positivity, high expression of PINP and β-CTX were independent risk factors for bone metastasis of lung cancer. The area under the curve (AUC) of ECT, PINP, and β-CTX alone for the diagnosis of bone metastasis of lung cancer were 0.872, 0.888, and 0.874, respectively, and the AUC for the combined diagnosis of the three was 0.963, which was greater than that of any one of the individual indices, with a sensitivity of 86.96% and a specificity of 97.50% at a Youden index of 0.845.

Conclusion: ECT whole-body bone imaging combined with PINP and β-CTX has high diagnostic value for bone metastasis of lung cancer.

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ECT 全身骨成像结合 PINP 和 β-CTX 对肺癌骨转移的早期诊断价值。
研究目的本研究旨在探讨发射计算机断层扫描(ECT)全身骨成像联合 PINP 和 β-CTX 对肺癌骨转移的早期诊断价值:根据有无骨转移将86例肺癌患者的病例资料分为肺癌骨转移组(LCWBM,46例)和肺癌无骨转移组(LCWOBM,40例)。收集患者的一般信息。采用 ECT 全身骨成像检测两组患者的骨转移和疾病范围分级(EOD),并利用电化学发光法检测血清中 PINP 和 β-CTX 的水平。斯皮尔曼相关分析用于评估 EOD 分级与 PINP 和 β-CTX 水平之间的相关性。采用逻辑单变量和多变量回归分析肺癌骨转移的危险因素。应用接收者操作特征曲线(ROC)分析ECT全身骨成像、PINP或β-CTX单项检测及三项检测联合的诊断效果:LCWBM组和LCWOBM组在病理类型、临床分期和EOD分级、ECT阳性例数以及PINP和β-CTX表达水平方面的差异均有统计学意义。在不同ECT分级的LCWBM患者中,PINP和β-CTX的表达趋势为3级>2级>1级和0级。进一步的相关性分析表明,EOD分级与PINP和β-CTX的表达水平呈显著正相关。单变量逻辑回归分析表明,腺癌、TNM IV期、ECT阳性、PINP和β-CTX高表达与肺癌骨转移相关,多变量逻辑回归分析表明,ECT阳性、PINP和β-CTX高表达是肺癌骨转移的独立危险因素。ECT、PINP和β-CTX单独诊断肺癌骨转移的曲线下面积(AUC)分别为0.872、0.888和0.874,三者联合诊断的曲线下面积(AUC)为0.963,大于任何一个单独指标的曲线下面积(AUC),在尤登指数为0.845时,敏感性为86.96%,特异性为97.50%:结论:ECT全身骨成像结合PINP和β-CTX对肺癌骨转移具有较高的诊断价值。
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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
240
审稿时长
1 months
期刊介绍: Clinical and Translational Oncology is an international journal devoted to fostering interaction between experimental and clinical oncology. It covers all aspects of research on cancer, from the more basic discoveries dealing with both cell and molecular biology of tumour cells, to the most advanced clinical assays of conventional and new drugs. In addition, the journal has a strong commitment to facilitating the transfer of knowledge from the basic laboratory to the clinical practice, with the publication of educational series devoted to closing the gap between molecular and clinical oncologists. Molecular biology of tumours, identification of new targets for cancer therapy, and new technologies for research and treatment of cancer are the major themes covered by the educational series. Full research articles on a broad spectrum of subjects, including the molecular and cellular bases of disease, aetiology, pathophysiology, pathology, epidemiology, clinical features, and the diagnosis, prognosis and treatment of cancer, will be considered for publication.
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