Publications by authors named "E Dompeling"

Asthma affects 7% of Dutch children and poses an increasing challenge, highlighting the need for effective paediatric asthma care. Achieving optimal asthma control is crucial given the potentially negative long-term effects of bad asthma control on lung development and quality of life in young children. The aim was to understand the challenges and requirements of existing asthma management practices in children.

View Article and Find Full Text PDF

Chronic lymphocytic leukemia (CLL)-related symptoms and morbidity related to the advanced age at diagnosis impairs the well-being of older adult patients. Therefore, it is essential to tailor treatment according to geriatric characteristics and aim for an improvement in health-related quality of life (HRQoL) as a primary treatment goal. In the HOVON139/GiVe trial, 12 cycles of fixed-duration venetoclax plus obinutuzumab (Ven-O) were shown to be effective and tolerable in FCR (fludarabine, cyclophosphamide, rituximab)-unfit patients with CLL (n = 67).

View Article and Find Full Text PDF
Article Synopsis
  • Complex karyotypes (CKTs) and highly complex karyotypes (hCKTs) are significant predictors of worse outcomes in chronic lymphocytic leukemia (CLL) when treated with chemoimmunotherapy, and their impact is further explored in venetoclax-based therapies.
  • * In a study involving 895 patients, CKTs were linked to shorter progression-free survival (PFS) and overall survival (OS) in the CIT group, while hCKTs negatively affected PFS in the venetoclax group.
  • * The findings suggest that karyotype analysis should be included in standard CLL diagnostics to better identify patients at high risk for poor treatment outcomes, supporting more personalized treatment approaches.
View Article and Find Full Text PDF

Background: Preclinical cell-based assays that recapitulate human disease play an important role in drug repurposing. We previously developed a functional forskolin induced swelling (FIS) assay using patient-derived intestinal organoids (PDIOs), allowing functional characterization of CFTR, the gene mutated in people with cystic fibrosis (pwCF). CFTR function-increasing pharmacotherapies have revolutionized treatment for approximately 85% of people with CF who carry the most prevalent F508del-CFTR mutation, but a large unmet need remains to identify new treatments for all pwCF.

View Article and Find Full Text PDF