Publications by authors named "T H I Kuopio"

In routine colorectal cancer management, histologic samples stained with hematoxylin and eosin are commonly used. Nonetheless, their potential for defining objective biomarkers for patient stratification and treatment selection is still being explored. The current gold standard relies on expensive and time-consuming genetic tests.

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To improve local disease control, the use of preoperative radiotherapy either alone or combined with chemotherapy has become standard practice in rectal cancer, but it is unclear how these treatments modify the antitumoral immune response. We aimed to evaluate tumor histopathologic features and the prognostic effect of host immune response in rectal cancer with variable treatment modalities. Ninety-five rectal cancers with short-course radiotherapy (SRT), 97 with long-course chemoradiotherapy (CRT), and 154 without preoperative treatments, were evaluated for histopathologic features including Crohn's-like reaction (CLR).

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  • The TWINGEN study aims to identify individuals at high risk for Alzheimer's disease (AD) by assessing various cognitive and health-related factors through an observational clinical recall and biomarker analysis.
  • The study involves around 800 participants, gathering data through blood samples, questionnaires, and wearable technology for lifestyle metrics, while also including a smaller group for in-person assessments.
  • All data collected will be integrated with existing Finnish biobank records and utilized for further research, following ethical guidelines set by relevant authorities.
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  • About 50% of Finnish Lynch Syndrome cases are linked to a specific variant in the MLH1 gene, resulting from a deletion in exon 16 caused by recombination.* -
  • The study validated this variant in a population cohort from FinnGen and the Central Finland Biobank, comparing cancer rates and onset age between those with and without the variant.* -
  • They found that out of 348 potential variant carriers, a significant portion had cancer or a family history of cancer, highlighting the potential of large genetic studies for detecting hereditary cancer risks.*
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Background: Biliary dysplasia, a precursor of cholangiocarcinoma (CCA), is a common complication of primary sclerosing cholangitis. Patients with high-grade dysplasia (HGD) or early CCA who have received oncological treatment are candidates for liver transplantation. The preoperative diagnosis of CCA or HGD is challenging, and the sensitivity of biliary brush cytology (BC) is limited.

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