Publications by authors named "Marius Lund-Iversen"

Objective: To study outcomes after cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (CRS-HIPEC) in patients also treated for colorectal liver metastases (CLM).

Background: Colorectal cancer (CRC) frequently metastasizes to the liver and peritoneum and is associated with a poor prognosis. In selected patients, a benefit in overall survival (OS) was shown for both peritoneal metastases (PM-CRC) offered CRS-HIPEC, and CLM treated with surgical resection.

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  • - Cellular angiofibroma is a rare benign tumor linked to the 13q/RB1 tumor family, and this study investigates its genetic diversity.
  • - Three cases of cellular angiofibromas were analyzed using various genetic techniques, revealing different chromosomal abnormalities and gene fusions in each tumor.
  • - The research identifies two distinct genetic pathways in cellular angiofibromas: one associated with the RB1 gene and the other involving fusions of the PLAG1 gene, shedding light on the tumor's complex genetic landscape and potential diagnostic approaches.
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Background: International guidelines currently recommend the use of molecular testing in patients with advanced pancreatic cancer. The rate of actionable molecular alterations is low. The utility of molecular testing in patients with borderline resectable (BRPC) or locally advanced (LAPC) pancreatic cancer in real world clinical practice is unclear.

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Melanized focal changes (MFCs) in the fillet of farmed Atlantic salmon is a major quality concern. The changes are thought to initially appear as acute red focal changes (RFCs) that progress into chronic MFCs. Recent findings have indicated that hypoxia may be important in their development, possibly leading to necrosis affecting not only myocytes but also adipocytes.

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Aims: The methylation status of the O6-methylguanine-DNA methyltransferase (MGMT) promoter region is essential in evaluating the prognosis and predicting the drug response in patients with glioblastoma. In this study, we evaluated the utility of using nanopore long-read sequencing as a method for assessing methylation levels throughout the MGMT CpG-island, compared its performance to established techniques and demonstrated its clinical applicability.

Methods: We analysed 165 samples from CNS tumours, focusing on the MGMT CpG-island using nanopore sequencing.

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Purpose: The NIPU-trial investigates the effect of adding the telomerase vaccine UV1 to treatment with ipilimumab and nivolumab for patients with pleural mesothelioma (PM).

Methods: In this phase 2 open-label trial, patients with PM progressing after first-line chemotherapy were randomised to receive ipilimumab and nivolumab alone (arm B) or combined with UV1 (arm A). The primary endpoint was progression-free survival (PFS) as determined by BICR.

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  • Intramuscular myxomas are benign tumors that are hard to diagnose, with genetic factors, particularly mutations in the GNAS gene, playing a role in their development.* -
  • In a study of 22 tumors, researchers identified chromosomal abnormalities in 11 cases and found pathogenic variants in 86% of the tumors, revealing a correlation between these genetic changes and the tumors' characteristics.* -
  • The study highlights that common mutation detection methods may miss rare variants, and suggests that direct cycle Sanger sequencing is an effective and cost-efficient alternative to more advanced techniques for identifying genetic changes in these tumors.*
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Tropomyosin receptor kinases (TRK) are attractive targets for cancer therapy. As TRK-inhibitors are approved for all solid cancers with detectable fusions involving the Neurotrophic tyrosine receptor kinase (NTRK)-genes, there has been an increased interest in optimizing testing regimes. In this project, we wanted to find the prevalence of NTRK fusions in a cohort of various histopathological types of early-stage lung cancer in Norway and to investigate the association between TRK protein expression and specific histopathological types, including their molecular and epidemiological characteristics.

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  • Mesotheliomas are tumors that seem to come from mesothelial cells and have specific genetic changes, including chromosomal rearrangements and fusions involving certain genes.
  • In the study, two peritoneal mesotheliomas were analyzed using various genetic methods, revealing distinct karyotypes and chromosomal behaviors in each tumor.
  • The findings suggest two different genetic pathways in mesothelioma development: one with hyperhaploidy and retained chromosomes, and another involving a gene rearrangement that excludes an important part of the MAP3K8 gene, relevant to several cancers.
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Background: ROS1 fusion is an infrequent, but attractive target for therapy in patients with metastatic non- small-cell lung cancer. In studies on mainly late-stage disease, the prevalence of ROS1 fusions is about 1-3%. In early-stage lung cancer ROS1 might also provide a fruitful target for neoadjuvant or adjuvant therapy.

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Background/aim: Lipomas are benign tumors composed of mature fat cells. They are common soft tissue tumors that often carry chromosome aberrations involving 12q14 resulting in rearrangements, deregulation, and generation of chimeras of the high-mobility group AT-hook 2 gene (HMGA2) which maps in 12q14.3.

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Background/aim: Structural abnormalities of chromosome bands 8q11-13, resulting in rearrangement of the pleomorphic adenoma gene 1 (PLAG1), are known to characterize lipoblastoma, a benign fat cell tumor, found mainly in children. Here, we describe 8q11-13 rearrangements and their molecular consequences on PLAG1 in 7 lipomatous tumors in adults.

Materials And Methods: The patients were 5 males and 2 females between 23 and 62 years old.

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Molecular alterations nowadays play a crucial role in the diagnosis of brain tumors. Some of these alterations are associated with outcome and/or response to treatment, including sequence variants of isocitrate dehydrogenase (IDH) at position p.R132 or p.

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Background/aim: Hoffa's disease is anterior knee pain presumably stemming from inflammatory fibrous hyperplasia of the infrapatellar fat pad (Hoffa's pad). The etiology and pathogenesis are unclear, however, and no genetic information about the disease has been published. We report the genetic findings in cells from the fat pad of a patient with Hoffa's disease.

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Background/aim: Recently, we reported a myoid hamartoma carrying a t(5;12)(p13;q14) karyotypic aberration leading to fusion of the high-mobility group AT-hook 2 (HMGA2) gene with a sequence from chromosome sub-band 5p13.2. We describe here another benign myoid tumor of the breast with identical genetic aberrations.

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Introduction: Long-term data on disease trajectory of -mutated early-stage non-small cell lung cancer (NSCLC) is still limited. This is relevant in the context of the recently approved introduction of adjuvant EGFR-targeting therapy, specifically osimertinib in resected stage II-III -mutated NSCLC.

Methods: Long-term data on patients with resected adenocarcinoma of the lung and known -status were analysed with focus on site of relapse and detailed cause of death.

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Background/aim: Chimeras involving the high-mobility group AT-hook 2 gene (HMGA2 in 12q14.3) have been found in lipomas and other benign mesenchymal tumors. We report here a fusion of HMGA2 with the nuclear receptor co-repressor 2 gene (NCOR2 in 12q24.

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  • * Genetic analysis revealed a complex karyotype with numerous chromosomal abnormalities, including rearrangements impacting key genes like MYCN, MYC, FOXO3, and the tumor suppressor TP53.
  • * RNA sequencing confirmed the presence of a PAX3-MYOCD fusion transcript, highlighting the significant genetic alterations associated with this specific case of rhabdomyosarcoma.
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  • Immunological non-responders (INR) are people living with HIV who do not recover CD4 T cell levels despite effective treatment, leading to poorer health outcomes.
  • Research shows INR have more gut-homing CD4 T cells in their blood compared to immunological responders (IR), and these cells tend to be more exhausted.
  • The study indicates that the increased exhaustion of mucosal CD4 T cells in INR is linked to gut damage, suggesting that issues with T cell function and gut health contribute to their impaired immune response.
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Background: due to emerging therapeutics targeting G12C and previous reports with conflicting results regarding the prognostic impact of and G12C in non-small cell lung cancer (NSCLC), we aimed to investigate the frequency of mutations and their associations with clinical characteristics and outcome. Since mutation subtypes have different preferences for downstream pathways, we also aimed to investigate whether there were differences in outcome according to mutation preference for the Raf, PI3K/Akt, or RalGDS/Ral pathways.

Methods: retrospectively, clinicopathological data from 1233 stage I-IV non-squamous NSCLC patients with known status were reviewed.

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  • The study investigates genetic changes in a rare benign breast tumor called myofibroblastoma, which shares similarities with spindle-cell lipoma.
  • Cytogenetic analyses were conducted on a tumor from a 76-year-old man, revealing notable chromosomal abnormalities, including the loss of chromosome 13.
  • The findings support the idea that the loss of material from chromosome 13 is a common characteristic in mammary myofibroblastomas, contributing to the overall understanding of this tumor type.
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  • The study investigates the characteristics of tumor-infiltrating T-cells in primary colorectal cancer (pCRC) and colorectal liver metastases (CLM) to understand their potential as biomarkers for cancer prognosis and treatment.
  • A total of 58 patients with paired samples of pCRC and CLM were analyzed, focusing on T-cell types and densities in different tumor regions, revealing a significant difference in T-cell accumulation, particularly in the invasive margin (IM) versus intratumor (IT) areas.
  • The findings indicate that while T-cells are concentrated in the IM of both pCRC and CLM, their densities and subtypes vary significantly between the two, highlighting that pCRC cannot reliably serve as a model for assessing T
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Background: The implementation of immune checkpoint inhibitors (ICI) into the standard care of advanced non-small cell lung cancer (NSCLC) has improved prognosis for this group of patients. However, long-term survival is rare. The aim of the study was to identify predictors of response and, especially, to investigate the impact radiotherapy might have on duration of response.

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