Publications by authors named "Louise Mahncke Guldbrandt"

Introduction: Immune checkpoint inhibitors (ICIs) carry the risk of immune-related adverse events (irAEs), a significant concern as therapy has transitioned to the adjuvant setting. Balancing therapeutic benefits against potential risks is crucial, necessitating real-world data from an unselected patient population in addition to clinical trial data to ensure optimal clinical decision-making.

Methods: This nationwide real-world study assessed irAEs in patients receiving adjuvant anti-PD1 therapy, primarily nivolumab, for resected stage III-IV melanoma between 2018-2022.

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Article Synopsis
  • * Data from the Danish Metastatic Melanoma Database (DAMMED) involved 79 treatment-naive patients, showing a complete response rate of 16.5% and an overall response rate of 46.9%.
  • * The 6-month progression-free survival rate was 53.5%, and the median overall survival was not reached, indicating that the real-world results align closely with those from previous phase II trials.
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  • Immune-related adverse events (irAEs) are common with ipilimumab and nivolumab treatment, leading to 30-40% of patients discontinuing therapy.
  • A study using real-world data from the DAMMED database analyzed progression-free survival (PFS) and overall survival (OS) in patients who discontinued due to irAEs versus those who completed treatment.
  • Results showed no significant difference in PFS between the two groups, but patients who discontinued had a longer OS, suggesting discontinuation due to irAEs may not negatively impact treatment efficacy.
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Article Synopsis
  • Clinical trials select patients based on specific eligibility criteria, while disease registries, like the Danish Metastatic Melanoma Database (DAMMED), gather real-world data to evaluate the effectiveness and safety of oncology medicines in broader patient groups.
  • The DAMMED database registered over 4,156 patients and 7,420 treatment regimens for advanced melanoma, enabling comparisons of patient response rates and survival data between clinical trials and real-world outcomes.
  • Overall, the findings emphasize that nationwide disease registries can enhance clinical practice and support health technology assessments, highlighting both the similarities and disparities with clinical trial data.
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Objective: The aim of this validation study was to assess the completeness of the registrations of chest X-rays (CXR) in two different versions of the Danish National Patient Registry (DNPR).

Material And Methods: We included electronic record data on CXR performed on patients aged 40 to 99 years from nine radiology departments covering 20 Danish hospitals. From each department, we included data from three randomly selected weeks between 2004 and 2011 (reference standard).

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Background: Accurate identification of specific patient populations is a crucial tool in health care. A prerequisite for exploring the actions taken by general practitioners (GPs) on symptoms of cancer is being able to identify patients urgently referred for suspected cancer. Such system is not available in Denmark; however, all referrals are electronically stored.

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Background: Lower lung cancer survival rates in Britain and Denmark compared with surrounding countries may, in part, be due to late diagnosis. The aim of this study was to evaluate the effect of direct access to low-dose computed tomography (LDCT) from general practice in early lung cancer detection on time to diagnosis and stage at diagnosis.

Methods: We conducted a cluster-randomised, controlled trial including all incident lung cancer patients (in 19-month period) listed with general practice in the municipality of Aarhus (300,000 citizens), Denmark.

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Introduction: The standard evaluation of haemoptysis in a department of respiratory medicine would currently consist of chest radiography, contrast-enhanced computed tomography (CT) and fibre-optic bronchoscopy (FOB), regardless of the result of the CT. Our aim was to evaluate whether patients presenting with haemoptysis but no positive finding on a contrast-enhanced CT of the chest are at risk for having serious disease, first of all lung cancer, and thus whether FOB is mandatory for such patients.

Methods: We searched the literature and retrospectively reviewed all records of patients referred with haemoptysis between 2000 and 2010 at the Department of Respiratory Diseases and Allergy, Aarhus University Hospital, Denmark.

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Unlabelled: This PhD thesis is based on the project "The effect of direct referral for fast CT scan in early lung cancer detection in general practice. A clinical, cluster-randomised trial", performed in Denmark in 2010-2013. The thesis includes four papers and focuses on early lung cancer diagnostics in general practice.

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Background: Lung cancer stage at diagnosis predicts possible curative treatment. In Denmark and the UK, lung cancer patients have lower survival rates than citizens in most other European countries, which may partly be explained by a comparatively longer diagnostic interval in these two countries. In Denmark, a pathway was introduced in 2008 allowing general practitioners (GPs) to refer patients suspected of having lung cancer directly to fast-track diagnostics.

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Background: Early detection of lung cancer is crucial as the prognosis depends on the disease stage. Chest radiographs has been the principal diagnostic tool for general practitioners (GPs), but implies a potential risk of false negative results, while computed tomography (CT) has a higher sensitivity. The aim of this study was to describe the implementation of direct access to low-dose CT (LDCT) from general practice.

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Introduction: Lung cancer (LC) is the most common cause of cancer death in Denmark, and triaging patients through fast-track diagnostic pathways is recommended to improve patient outcome. Data on the most efficient triage organisation of such pathways are limited. The aim of this study was to test a strategy of a straight-to-test model for patients referred to the fast-track pathway.

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