不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Development and validation of a nomogram for predicting progression from multidrug-resistant bacterial colonization to infection in lymphoma patients.
Development and validation of a nomogram for predicting progression from multidrug-resistant bacterial colonization to infection in lymphoma patients.
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T/NK 细胞来源、鼻咽受累、近期抗生素暴露和低白蛋白血症是淋巴瘤患者从 MDR 定植进展为感染的独立危险因素。Nomogram 模型能有效识别高危患者,为临床防控策略提供依据。
探讨住院淋巴瘤患者多重耐药(MDR)细菌定植进展为感染的危险因素,并构建Nomogram预测模型。
对2017年3月至2025年3月期间某三级医院收治的70例MDR阳性淋巴瘤患者的临床资料进行回顾性分析。根据MDR感染发生情况将患者分为MDR感染组和MDR定植组。收集人口学特征、淋巴瘤亚型、病变部位、实验室指标及治疗相关因素。采用单因素和多因素logistic回归分析筛选独立危险因素,并构建Nomogram预测模型。
在70例MDR阳性患者中,48例(68.6%)发生MDR感染,22例(31.4%)仍为定植。多因素分析显示,T/NK细胞淋巴瘤(OR = 3.82,95% CI 1.46 9.98,P = 0.006)、鼻咽/鼻腔受累(OR = 2.94,95% CI 1.23 7.04,P = 0.015)、近期抗生素使用(OR = 2.67,95% CI 1.15 6.21,P = 0.022)以及白蛋白 < 35 g/L(OR = 2.31,95% CI 1.08 4.93,P = 0.031)为独立危险因素。基于这些因素构建的Nomogram模型显示出良好的区分度(C-index = 0.812)和校准度。
To investigate the risk factors for progression from multidrug-resistant (MDR) bacterial colonization to infection in hospitalized lymphoma patients and to develop a Nomogram predictive model.
A retrospective analysis was conducted on clinical data from 70 MDR-positive lymphoma patients admitted to a tertiary hospital between March 2017 and March 2025. Patients were divided into MDR infection and MDR colonization groups based on the occurrence of MDR infection. Demographic characteristics, lymphoma subtypes, lesion sites, laboratory parameters, and treatment-related factors were collected. Univariate and multivariate logistic regression analyses were performed to identify independent risk factors, and a Nomogram predictive model was constructed.
Among 70 MDR-positive patients, 48 (68.6%) developed MDR infection and 22 (31.4%) remained as colonization. Multivariate analysis revealed that T/NK-cell lymphoma (OR = 3.82, 95% CI 1.46 9.98, P = 0.006), nasopharyngeal/nasal cavity involvement (OR = 2.94, 95% CI 1.23 7.04, P = 0.015), recent antibiotic use (OR = 2.67, 95% CI 1.15 6.21, P = 0.022), and albumin < 35 g/L (OR = 2.31, 95% CI 1.08 4.93, P = 0.031) were independent risk factors. The Nomogram model based on these factors demonstrated good discrimination (C-index = 0.812) and calibration.
T/NK-cell origin, nasopharyngeal involvement, recent antibiotic exposure, and hypoalbuminemia are independent risk factors for progression from MDR colonization to infection in lymphoma patients. The Nomogram model can effectively identify high-risk patients and provide evidence for clinical prevention and control strategies.
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