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Jacoline E C Bromberg

Researcher at Erasmus University Rotterdam

Publications -  103
Citations -  10921

Jacoline E C Bromberg is an academic researcher from Erasmus University Rotterdam. The author has contributed to research in topics: Primary central nervous system lymphoma & Rituximab. The author has an hindex of 31, co-authored 95 publications receiving 9357 citations. Previous affiliations of Jacoline E C Bromberg include Erasmus University Medical Center & Utrecht University.

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OS7.1 Impact of the addition of Rituximab to standard therapy with high dose methotrexate on health-related quality of life in primary central nervous system lymphoma patients

TL;DR: Treatment with Rituximab resulted in improved HRQoL, but the addition of RitUXimab to standard chemotherapy did not further impact HRQeL over time, and WBRT did not result in deterioration of HRZoL up to 2 years of follow-up.
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Comprehensive microRNA expression profiling in cerebrospinal fluid distinguishes between neurological disease classes.

TL;DR: It is asked whether it is possible to build an atlas comprising four major CNS pathology classes: inflammatory, malignant, autoimmune, and neurodegenerative diseases, in comparison to neurological controls, exclusively based on miRNAs isolated from patient cerebrospinal fluid.
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Ncog-05. impact of additional rituximab to standard therapy on cognitive performances in primary central nervous system lymphoma patients

TL;DR: Cognitive performance remained stable or improved after treatment of primary central nervous system lymphoma patients with or without Rituximab and low-dose whole brain radiotherapy (WBRT), and addition of RitUXimab to standard treatment did not impact cognitive performance over time.
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At-56treatment of large low-grade oligodendroglial tumors with upfront procarbazine, lomustine, and vincristine chemotherapy with long follow-up: a retrospective cohort study with growth kinetics

TL;DR: This long-term follow-up study indicates that upfront PCV chemotherapy is associated with long PFS and OS and delays radiotherapy for a considerable period of time in patients with low-grade oligodendroglial tumors, in particular with combined 1p/19q loss.