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Combined immune checkpoint blockade (ICB) and chemoradiation (CRT) is approved in patients with locally advanced cervical cancer (LACC) but optimal sequencing of CRT and ICB is unknown. NRG-GY017 (NCT03738228) was a randomized phase I trial of atezolizumab (anti-PD-L1) neoadjuvant and concurrent with CRT (Arm A) vs. concurrent with CRT (Arm B) in patients with high-risk node-positive LACC.

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Objective: To identify clinicopathologic and genomic features associated with brain metastasis after resection of lung adenocarcinoma (LUAD) and to evaluate survival after brain metastasis.

Methods: Patients who underwent complete resection of stage I-IIIA LUAD between 2011 and 2020 were included. A subset of patients had broad-based panel next-generation sequencing performed on their tumors.

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Pediatric neurological injury and disease is a critical public health issue due to increasing rates of survival from primary injuries (e.g., cardiac arrest, traumatic brain injury) and a lack of monitoring technologies and therapeutics for treatment of secondary neurological injury.

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Article Synopsis
  • - This study explores the levels and geographical differences of contaminants found in house dust across Europe, identifying over 1200 anthropogenic compounds using advanced techniques like mass spectrometry and suspect screening.
  • - The research indicates that contaminant concentrations vary less than threefold within Europe, showing similarities with North American dust due to shared consumer products and materials.
  • - It highlights geographical patterns, revealing that certain contaminants increased from north to south (like PAHs and chlorinated paraffins), whereas others, like biocides, decreased; it also emphasizes a significant risk from older, restricted contaminants, like DEHP and PCBs, despite limited toxicity data available for newer compounds.
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Article Synopsis
  • - The study investigates the effectiveness of durvalumab maintenance therapy in patients with unresectable locally advanced non-small cell lung cancer (NSCLC) after receiving concurrent chemoradiotherapy (CCRT), comparing those with specific genetic mutations to those without.
  • - A total of 339 patients were analyzed, revealing similar progression-free survival (PFS) rates of 21.4 months for wild-type and 21.0 months for mutant groups, while significant differences in PFS were noted based on programmed death-ligand 1 (PD-L1) expression levels.
  • - The findings suggest that while genetic mutations did not significantly alter outcomes, PD-L1 expression levels had a notable impact on PFS, highlighting the importance
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