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Objective: This study aimed to characterize the association between pulmonary embolism (PE) onset and various anti-tumor therapeutic approaches in patients with lung cancer, with the goal of identifying potential high-risk populations.
Methods: A retrospective analysis was conducted on clinical records from 2019 to 2025, among the 84,000 inpatients with lung cancer, 106 patients developed PE during hospitalization for anti-tumor treatment, who were confirmed using spiral computed tomography (CT) or pulmonary angiography per CTS (2018) and NEJM (2010) criteria. Data were collected on patient demographics, cancer staging, treatment type, and time to PE onset.
Results: Among patients who developed PE during lung cancer treatment, the mean age was 66.82 ± 10.50 years. Females comprised 64.04% of cases, adenocarcinoma was identified in 60.38%, and stage IV lung cancer was present in 56.60%. First-line therapy was administered in 63.21% of cases, and 66.04% exhibited enlarged mediastinal lymph nodes. The mean D-dimer level among this cohort was 3.559 μg/mL, indicating a heightened thrombotic risk. Temporally, 50.95% of PE cases occurred within six months of lung cancer diagnosis. Onset within three months following therapy initiation was observed across multiple modalities: 46.15% for chemotherapy, 34.78% for targeted therapy, and 77.78% following surgical intervention. Notably, 16.98% of PE events occurred during the initial chemotherapy cycle. The mean time to PE onset was 1.81 ± 2.51 months for patients undergoing surgery alone, compared to 15.52 ± 12.88 months for those receiving surgery combined with other treatments (p < 0.05). Surgical intervention was identified as an independent risk factor for PE. In early-stage lung cancer, the mean time to PE onset was significantly shorter, with a mean time of 16.38 ± 21.07 months (p < 0.05).
Conclusion: The timing and incidence of PE vary according to the type of anti-tumor therapy administered in lung cancer treatment. These findings underscore the importance of vigilant monitoring, personalized risk assessment, and targeted anticoagulation strategies throughout the therapeutic course.
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http://dx.doi.org/10.1016/j.avsg.2025.08.029 | DOI Listing |
Mikrochim Acta
September 2025
The Third Affiliated Hospital of Anhui Medical University, The First People's Hospital of Hefei, Binhu Hospital of Hefei, Hefei, 230061, P. R. China.
Lung cancer, as one of the cancers with the highest morbidity and mortality rates in the world, requires accurate detection of its vital serum marker, neuron-specific enolase (NSE), which is a key challenge for early detection of lung cancer. However, traditional chemiluminescence immunoassay (CLIA) methods rely on labeled antibodies (Abs) and suffer from complex operations and high costs. In this work, a label-free CLIA based on CL-functionalized mesoporous magnetic nanoparticles (CuFeO@mSiO-Cys-Luminol-Au NPs) is developed for the rapid and sensitive detection of NSE.
View Article and Find Full Text PDFOncogene
September 2025
Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
There are no proven therapies for metastatic or unresectable Chromophobe Renal Cell Carcinoma (ChRCC). ChRCC is characterized by high glutathione levels and hypersensitivity to ferroptosis, an iron-dependent form of cell death characterized by peroxidation of polyunsaturated fatty acids. The underlying mechanisms leading to ferroptosis hypersensitivity are unknown.
View Article and Find Full Text PDFBr J Cancer
September 2025
School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, UK.
Background: Studies examining the association of chronic kidney disease (CKD) with cancer risk have demonstrated conflicting results.
Methods: This was an individual participant data meta-analysis including 54 international cohorts contributing to the CKD Prognosis Consortium. Included cohorts had data on albuminuria [urine albumin-to-creatinine ratio (ACR)], estimated glomerular filtration rate (eGFR), overall and site-specific cancer incidence, and established risk factors for cancer.
Trends Cancer
September 2025
Department of Gastroenterology, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang Province, 310058, China; Institution of Gastroenterology, Zhejiang University, Hangzhou, Zhejiang Province, 310058, China. Electronic address:
Glucose restriction generally limits tumor growth. Recently, Wu et al. reported that glucose restriction inhibits primary tumors but promotes lung metastasis by forming a macrophage-dominated, natural killer (NK) cell-deficient pre-metastatic niche (PMN).
View Article and Find Full Text PDFJ Thorac Oncol
September 2025
Department of Family and Community Medicine, Chung Shan Medical University Hospital, Institute of Medicine and School of Medicine, College of Medicine, Chung Shan Medical University, Taichung, Taiwan. Electronic address: