一种预测早期T1-2期肺腺癌患者肿瘤远处转移的新型Nomogram预测方法的建立与验证。

IF 2.3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Therapeutics and Clinical Risk Management Pub Date : 2020-12-10 eCollection Date: 2020-01-01 DOI:10.2147/TCRM.S272748
WeiGuo Gu, MingBin Hu, WeiJia Wang, Chao Shi, JinHong Mei
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引用次数: 2

摘要

背景:早期T1-2(直径≤5cm)期肺腺癌(ET-LUAD)患者的远处转移在很大程度上影响着临床治疗策略。然而,相关机制尚不清楚,相关研究较少。本研究旨在建立并验证一种预测ET-LUAD远处转移风险的新nomogram。方法:本研究共招募258例诊断为ET-LUAD且未接受任何治疗的患者。患者按1:2的比例随机分为训练组和验证组。采用单因素和多因素logistic回归分析,在培训队列中选择与远处转移相关的最显著的预测危险因素。通过一致性指数(C-index)、校准曲线和决策曲线分析(DCA)对所建立的nomogram进行验证。结果:本研究共纳入124例确诊远处转移的ET-LUAD患者和134例非远处转移的ET-LUAD患者。多因素logistic风险回归分析确定了与远处转移相关的独立危险因素,包括血小板与淋巴细胞比率(PLR)、乳酸脱氢酶(LDH)、神经特异性烯醇化酶(NSE)、癌胚抗原(CEA)和细胞角蛋白19片段(Cyfra211),这些因素被纳入nomogram。该nomogram一致性高(C-index=0.792),校正性好,在验证队列中具有较高的临床应用价值。结论:所建立的心电图图可用于预测ET-LUAD高危非转移患者的远处转移,也可指导医生对ET-LUAD患者进行预防和个体化治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development and Validation of a Novel Nomogram for Predicting Tumor-Distant-Metastasis in Patients with Early T1-2 Stage Lung Adenocarcinoma.

Development and Validation of a Novel Nomogram for Predicting Tumor-Distant-Metastasis in Patients with Early T1-2 Stage Lung Adenocarcinoma.

Development and Validation of a Novel Nomogram for Predicting Tumor-Distant-Metastasis in Patients with Early T1-2 Stage Lung Adenocarcinoma.

Development and Validation of a Novel Nomogram for Predicting Tumor-Distant-Metastasis in Patients with Early T1-2 Stage Lung Adenocarcinoma.

Background: Distant metastasis in early T1-2 (diameter≤5 cm) stage lung adenocarcinoma (ET-LUAD) patients largely affect treatment strategies in clinical practice. However, the associated mechanism remains unclear and related studies is less. This study aimed to establish and validate a novel nomogram to predict the risk of distant metastasis in ET-LUAD.

Methods: A total of 258 patients diagnosed with ET-LUAD and not receiving any treatment were recruited into this study. The patients were randomly divided into a training cohort and validation cohort in a ratio of 1:2. Univariate and multivariate logistic regression analysis was used to select the most significant predictive risk factors associated with distant metastasis in the training cohort. The established nomogram was validated by the consistency index (C-index), calibration curve, and decision curve analysis (DCA).

Results: There were 124 patients with confirmed distant metastasis and 134 patients with non-distant metastases ET-LUAD were enrolled in the study. Multivariate logistic hazards regression analysis identified independent risk factors associated with distant metastasis to include platelet-to-lymphocyte ratios (PLR), lactate dehydrogenase (LDH), neural-specific enolase (NSE), carcinoembryonic antigen (CEA) and cytokeratin 19 fragments (Cyfra211), which were included in the establishment of the nomogram. The nomogram achieved a high consistency (C-index=0.792), good calibration, and high clinical application value in the validation cohort.

Conclusion: The established nomogram can be used to predict distant metastasis in high-risk ET-LUAD nonmetastasis patients and can also be used by doctors to guide preventive and individualized treatment for ET-LUAD patients.

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来源期刊
Therapeutics and Clinical Risk Management
Therapeutics and Clinical Risk Management HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.80
自引率
3.60%
发文量
139
审稿时长
16 weeks
期刊介绍: Therapeutics and Clinical Risk Management is an international, peer-reviewed journal of clinical therapeutics and risk management, focusing on concise rapid reporting of clinical studies in all therapeutic areas, outcomes, safety, and programs for the effective, safe, and sustained use of medicines, therapeutic and surgical interventions in all clinical areas. The journal welcomes submissions covering original research, clinical and epidemiological studies, reviews, guidelines, expert opinion and commentary. The journal will consider case reports but only if they make a valuable and original contribution to the literature. As of 18th March 2019, Therapeutics and Clinical Risk Management will no longer consider meta-analyses for publication. The journal does not accept study protocols, animal-based or cell line-based studies.
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