CONTRAST 2.0

2023

Acute stroke management faces significant challenges despite recent progress. Intracerebral hemorrhage (ICH) accounts for 15% of all strokes and lacks effective treatment options. Additionally, only a small portion of acute ischemic stroke (AIS) patients qualify for intra-arterial therapy (IAT), and even after successful IAT, many experience poor outcomes due to incomplete microvascular reperfusio. The ambition of CONTRAST 2.0 is to improve outcome after stroke and increase the number of patients who are eligible for acute treatment. CONTRAST 2.0 addresses the aims of the Dutch Heart Foundation with an integrated research program to develop and evaluate new treatment strategies for AIS, ICH and Subarachnoid Hemorrhage (SAH) in preclinical studies, a series of complementary RCTs and registries. To establish an optimal setting for long-term preclinical studies on brain damage caused by ischemia-reperfusion or hemorrhage and the effects of neuroprotection, we will develop a platform for assorted translational studies in the most appropriate animal models with clinically relevant output parameters. As such, the consortium will find new opportunities for further clinical evaluation of new treatment modalities.

The Research

The clinical trials and registries will not only be aimed at prompt and accurate treatment in the hospital, but also before admission (in the ambulance) and after admission of stroke patients. Their design allows that results can be readily implemented in clinical practice. Studies will demonstrate:

a) how to improve prehospital triage by evaluating prediction rules and devices for diagnosis of the type of stroke and the presences of intracranial vessel occlusion,

b) how to improve the outcome of ischemic stroke by treatment of medium vessel occlusions, by treatment of occlusive and stenotic carotid bifurcation disease, by neuroprotective drugs and by achieving better technical procedural outcome with a personalized technical approach based on thrombus and vessel characteristics,

c) how to improve the outcome of hemorrhagic stroke with minimally invasive interventions, and

d) how to improve post-stroke rehabilitation by better prediction of long-term outcome and the prediction of effects of intervention.

Large clinical datasets will be used to develop models for care organization and individualized treatment  strategies, considering individual prognosis based on personal characteristics (sex, age, stroke type, severity), and imaging findings (thrombus and vessel characteristics). The proposed research program will make use of the national stroke research infrastructure established within CONTRAST 1.0 and aims to attract additional public and private funding for fully execution of the research plans.

The overarching aim of CONTRAST 2.0 remains to improve outcome of stroke patients by blending mechanistic, basic scientific projects with pragmatic randomized clinical trials and registries. Specifically, CONTRAST 2.0 will aim to advance treatment through earlier diagnosis of stroke, rapid and more effective personalized treatment of acute stroke, and lastly optimized personalized rehabilitation of stroke survivors in the acute and subacute phase. At the end of the project, it is our ambition to have:

  1. evaluated and implemented the best prehospital triage strategy in the Netherlands resulting in earlier treatment of more patient with stroke.
  2. expanded the indications of EVT to patients with MeVO.
  3. implemented evidence-based guidelines for the optimal treatment timing of carotid occlusive disease.
  4. a preclinical platform for identification of new therapeutic targets and testing of promising therapies, and we have performed the first preclinical trials with neuroprotective agents.
  5. developed personalized EVT approach (technique and device choice) based on thrombus and vessel characteristics.
  6. proven that minimally invasive endoscopy-guided surgery for ICH results in better outcome and we can offer this treatment to all patients in the Netherlands.
  7. assessed the treatment outcomes of advanced endovascular devices for a recently ruptured intracranial aneurysms in the Netherlands and to have initiated an RCT to support evidence-based decision making.
  8. improved prediction of medium-term outcome (defined on multiple domains) of stroke patients to guide the individualized treatment decision of patients 1) in the chain of care and 2) for additional interventions resulting in improved functioning and quality of life.

The origin

Following the world-leading MR CLEAN trial, the CONTRAST 1.0 consortium was formed in 2017 to tackle one of the main challenges on the research agenda of the Dutch Heart Foundation: improving the acute treatment of stroke. Minimizing the burden of disease for everyone who has to live with the consequences of a stroke is also of great importance to the Brain Foundation Netherlands. The Dutch Heart Foundation and the Brain Foundation Netherlands have therefore joined forces to continue the unique and succesful collaboration between acute care and chronic care in 2023. This resulted in the CONTRAST 2.0 consortium. The Dutch Heart Foundation, Brain Foundation Netherlands and ZonMw are partners and funders in the CONTRAST consortium. In addition, this work was funded in part through unrestricted funding by Stryker, Medtronic and Penumbra.

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Collaborators

Funded

Contact person:

PhD R. van Nuland (Rick)

Principal investigators

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ARENA-PRIME

2018
In preceding decades, conventional therapies have notably enhanced the survival rates of heart failure (HF) patients. However, a subset of individuals, particularly younger patients afflicted with dilated cardiomyopathy (DCM) or arrhythmogenic cardiomyopathy (ACM), still confront disease progression despite these treatments. This underscores the necessity for innovative approaches. The ARENA-PRIME initiative aims to address this gap by focusing on the development of novel gene therapies tailored to the specific disease mechanisms underlying DCM, attributed to mutations in the RBM20 and LMNA genes, as well as ACM, and associated with mutations in the DSGL2 and PKP2 genes. The goal is to progress towards first-in-human clinical trials, particularly focusing on LMNA disease, and to establish preclinical proof-of-concept for ACM therapies targeting DSGL2 and PKP2. The Research The ARENA-PRIME researchers utilize insights from previous programmes on cardiac gene therapies (e.g., inhibitory RNAs such as allele-specific short hairpin RNAs, antimiRs, etc.) and gene editing technologies (e.g., base- and prime editing) to develop novel treatments for dilated cardiomyopathy (DCM) and arrhythmogenic cardiomyopathy (ACM). This effort is supplemented by advanced research on adeno-associated viral vectors and the integration of heart tissue collections with cutting-edge sequencing technologies (like single-cell sequencing) to further explore disease mechanisms. At the beginning of the ARENA-PRIME programme, a (end-) user committee has been established, making sure that (end-)users are  closely involved in the design of the studies and the implementation of the co-created studies and deliverables. This committee meets annually alongside the program's research meetings to provide guidance to investigators on optimizing the program's outcomes for (end-) users. It addresses all feedback, inquiries, and recommendations, whether requested or spontaneous. This committee meets once per year in conjunction with the programme’s research meetings and advises the investigators about the course of the programme and what actions need to be taken in order to maximise the probability that the (end-) users will be able to utilize and/or benefit from the results. This committee addresses any comments, remarks, questions and advice they may have, solicited or otherwise. The members of the ARENA-PRIME user committee include cardiomyopathy patients and their relatives, clinicians (e.g. cardiologists), representatives from related research programs (e.g., RegMedXB, H2020-TRAIN-HEART), and industry stakeholders including biotech and pharma company representatives and venture capitalists. Supporting Young Investigators The programme prioritizes attracting and nurturing young talent, providing hands-on training and fellowship awards to facilitate their career development. Over 20 young investigators participate, benefiting from exposure to collaborative research environments. To further support this career development, five fellowship awards of 50.000€ have been granted the past three years to junior postdoctoral researchers in the laboratories of the Hubrecht Institute, University Medical Center Utrecht, Amsterdam UMC (location VUmc and AMC) and Maastricht University. Origin The former CVON-ARENA programme (2012-2017) advanced understanding of cardiac RNA species in heart failure (microRNAs, lncRNAs and circular RNAs). The CVON-ARENA programme (2012-2017) advanced understanding of cardiac RNA species, such as microRNAs, lncRNAs, and circular RNAs, in various forms of heart failure (HF). This subsequent ARENA-PRIME programme (2018-2023), funded by the Dutch Heart Foundation, targets treatment-resistant HF forms, particularly in younger patients with dilated cardiomyopathy (DCM) or arrhythmogenic cardiomyopathy (ACM). In 2023 ARIME-PRIME received a matching grant from the Dutch Heart Foundation to work on their research together with a private partners, so that they can achieve their ambitions and objectives more quickly.
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CUSTOM-AF

2020
Individuals with atrial fibrillation are at increased risk of an ischemic stroke. Active detection of atrial fibrillation (AF) and optimal referral and treatment of patients could prevent an estimated 1500 ischemic strokes annually. Effective collaboration between primary and secondary care professionals is essential for achieving this goal of stroke prevention attributed to AF. This is the primary objective of the implementation consortium known as CUSTOM-AF. The origin  The CUSTOM-AF was founded in June 2020 and restarted in 2022. CUSTOM-AF implementation consortium aims to share successful practice examples with regional networks and develop guidelines for organizing active detection and integrated care within a network. Additionally, consortium partners seek innovative methods for general practitioners to detect and manage AF without necessitating hospital referrals. With this consortium, the Dutch Heart Foundation, NVVC Connect, Harteraad, and the Dutch CardioVascular Alliance, all work together towards optimal care for patients with AF. The Dutch College of General Practitioners (NHG) serves as a key advisor to the consortium. Earlier detection and better treatment of atrial fibrillation, the most common cardiac arrhythmia in adults, is an important part of the cardiovascular disease research agenda that the Dutch Heart Foundatoin set in 2014, which funds the CUSTOM-AF consortium. The Research The scope of the consortium has been expanded to include two disorders: heart failure and AF. The consortium has undertaken significant initiatives over the past two years (2020-2022) to advance its objectives: Guideline Development: The consortium developed the "Screening and Treatment Optimization for AF" guideline, designed to facilitate early detection of AF within regional healthcare systems. Cost-Effectiveness Analysis: A comprehensive analysis conducted to assess various screening scenarios for AF, evaluating the economic feasibility of different approaches. Thematic Collaboration: In early 2022, a thematic collaboration titled "Juiste Hartzorg op de Juiste Plek" was established in partnership with the Heart Foundation and ZonMw. This collaboration secured funding for 22 regions to support transmural collaboration on AF and HF, with a focus on early detection and treatment optimization. Moving forward from September 2022, NVVC Connect will intensify support for the regions by emphasizing continuous improvement through the PDCA cycle, facilitating knowledge sharing, and implementing innovative approaches. These efforts are aimed at strengthening collaboration and improving outcomes in AF and HF care across the participating regions.
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