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Background: Cancer remains a significant global health challenge, particularly for subpopulations with risk factors including genetic predisposition, comorbidities, and lifestyle, along with age. The Galleri® multi-cancer early detection (MCED) test is projected to be cost-effective for individuals aged ≥50 years. However, its potential value in subpopulations with elevated cancer risk remains underexplored. This study evaluates the cost-effectiveness of the Galleri® test combined with usual care screening in subpopulations with varying cancer risk, including impact on overall cancer burden.
Methods: A hybrid cohort-level model evaluated US subpopulations aged 50-79 years with additional risk factors, incorporating updated cancer incidence rates and excess competing mortality. The model estimated lifetime economic and clinical outcomes of annual MCED testing. Analyses focused on individuals with obesity, diabetes, smoking history, heavy alcohol use, genetic predispositions, immunocompromising conditions, family history, and cancer survivors.
Results: The Galleri® test was cost-effective across all specified subpopulations, with incremental cost-effectiveness ratios (ICERs) below the general population benchmark of $66,043 per quality-adjusted life-year. Subpopulations with higher cancer incidence, such as those with hereditary cancer syndromes, showed lower ICERs, underscoring the cost-effectiveness (CE) in targeted screening. However, targeted approaches address a smaller fraction of the population burden. These findings depend on translating overall MCED test performance to higher-risk groups. Sensitivity analyses confirmed the robustness of these findings, emphasizing MCED's potential to reduce late-stage cancer burden.
Conclusions: Prioritizing higher-risk groups yields more favorable CE but impacts a smaller overall population burden.
Impact: This study compares how MCED testing strategies affect CE and population health benefits.
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http://dx.doi.org/10.1158/1055-9965.EPI-25-0610 | DOI Listing |
Clin Anat
September 2025
Department of Communication Disorders and Sciences, Rush University Medical Center, Chicago, Illinois, USA.
This research sought to examine the prevalence and severity of hyperostosis frontalis interna (HFI) in the Chicagoland anatomical body donor population. The study further aimed to elucidate potential demographic risk factors for HFI, including sex, age at death, and structural vulnerability index (SVI), as well as any common comorbidities, as gleaned from death certificates. HFI is an irregular bony overgrowth of the endocranial surface of the frontal bone.
View Article and Find Full Text PDFFront Immunol
September 2025
Guangxi Key Laboratory of AIDS Prevention and Treatment & School of Public Health, Guangxi Medical University, Nanning, Guangxi, China.
Background: People living with HIV(PLWH) are a high-risk population for cancer. We conducted a pioneering study on the gut microbiota of PLWH with various types of cancer, revealing key microbiota.
Methods: We collected stool samples from 54 PLWH who have cancer (PLWH-C), including Kaposi's sarcoma (KS, n=7), lymphoma (L, n=22), lung cancer (LC, n=12), and colorectal cancer (CRC, n=13), 55 PLWH who do not have cancer (PLWH-NC), and 49 people living without HIV (Ctrl).
Front Immunol
September 2025
Department of Medicine, Division of Hematology, Bioclinicum and Center for Molecular Medicine, Karolinska Institute and Karolinska University Hospital Solna, Stockholm, Sweden.
Background: Metabolic reprogramming is an important hallmark of cervical cancer (CC), and extensive studies have provided important information for translational and clinical oncology. Here we sought to determine metabolic association with molecular aberrations, telomere maintenance and outcomes in CC.
Methods: RNA sequencing data from TCGA cohort of CC was analyzed for their metabolic gene expression profile and consensus clustering was then performed to classify tumors into different groups/subtypes.
J Hepatocell Carcinoma
September 2025
Department of Liver Disease, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, People's Republic of China.
Objective: Anoikis is an anchorage-dependent programmed cell death implicated in multiple pathological processes of cancers; however, the prognostic value of anoikis-related genes (ANRGs) in hepatocellular carcinoma (HCC) remains unclear. Our study aims to develop an ANRGs-based prediction model to improve prognostic assessment in HCC patients.
Methods: The RNA-seq profile was performed to estimate the expression of ANRGs in HCC patients.
The morphological patterns of lung adenocarcinoma (LUAD) are recognized for their prognostic significance, with ongoing debate regarding the optimal grading strategy. This study aimed to develop a clinical-grade, fully quantitative, and automated tool for pattern classification/quantification (PATQUANT), to evaluate existing grading strategies, and determine the optimal grading system. PATQUANT was trained on a high-quality dataset, manually annotated by expert pathologists.
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