Investigation of Plaque Instability: Identification of Atherosclerotic Plaque Angiogenesis Using Bevacizumab-800CW and Optoacoustic Imaging: a Single Center Proof of Concept Study (CAROTID-OPTOLIGHT)

Rationale: This project consists of the realization followed by the clinical validation of a procedure dedicated to detect vulnerable atherosclerotic plaques patients with a symptomatic carotid stenosis. If in the future it would be possible to detect a symptomatic carotid atherosclerotic plaque non- invasively (i.e. those plaques resulting in cerebrovascular accidents and/or transient ischemic attacks), this would strongly improve risk assessment among this large cohort of patients. At the moment, indications for intervention are primarily based on degree of stenosis, and not on degree of vulnerability. Symptomatology is considered, but clinicians are not capable of predicting the consequences of a first event, while two thirds of all patients with a major stroke are not preceded by previous minor symptoms. Previous trials (NASCET and ECST) showed a significant absolute risk reduction for symptomatic patients with a stenotic lesion of the internal carotid artery greater than 70% after the performance of a carotid endarterectomy (CEA; excision of the atherosclerotic plaque). However, surgery can be associated with significant morbidity and even mortality. On the other hand, reliable prediction prior to surgery whether an atherosclerotic plaque is going to become symptomatic could also prevent unnecessary surgery, which again significantly reduces morbidity and mortality.

In literature and our preliminary ex vivo data with a nuclear imaging tracer 89Zr-Bevacizumab, it appears that vulnerable atherosclerotic plaques (i.e. those likely to become symptomatic) have an increased rate of angiogenesis at the site of the rupture (i.e. the site of the vulnerable plaque) which expose highly upregulated Vascular Endothelial Growth Factor-A (VEGF-A) production as part of the inflammatory response within the plaque and subsequently which can be visualized with a tracer targeting specifically VEGF-A. Recently, these experiments have been repeated using Bevacizumab- CW800 showing similar results (Huisman et al, preliminary data).

An intraoperative near-infrared fluorescence (NIRF) imaging camera, among a NIR fluorescence endoscopy system, and the use of the optical contrast agent Bevacizumab-800CW in now more than 250 patients has been evaluated for its feasibility to detect tumor lesions in patients with colorectal cancer, colon polyps, Barret's esophagus, peritoneal carcinomatosis of colorectal cancer origin and breast cancer. These studies showed that bevacizumab-800CW is safe in clinical use and feasible to detect even small tumor lesions with a high sensitivity. While Bevacizumab-800CW can also detect the soluble ligand VEGF-A, as shown by ex vivo analyses of excised CEA specimen, we aim to investigate whether systemic administered Bevacizumab-800CW can be applied to patients preoperatively for the detection of vulnerable plaques by non-invasive optoacoustic imaging and subsequently ex vivo mesoscopic imaging for validation purposes. The primary objective for the proposed study is to achieve pre-operative detection of the atherosclerotic plaque for patients with a symptomatic carotid artery stenosis by non-invasive optoacoustic imaging. In this study we will introduce the following concept: a preoperative non-invasive optoacoustic-scan guided by the © UMCG october 2018 Version 2.0 7 of 40

Bevacizumab-800CW targeted VEGF-A. This will help us to detect if and at what time point within the atherosclerotic plaque there is an upregulation of angiogenesis which can cross-correlated by ex vivo analyses of characteristics of the vulnerable plaque (i.e. atheroma, foam cells, influx of activated macrophages and angiogenesis as a result of pro-inflammatory responses present in the plaque). The end-goal of the proposed dual pre- and intra-operative imaging procedure is to prove that the symptomatic carotid atherosclerotic plaque can be accurately and safely detected by VEGF-A targeted optical imaging agents. In addition, this study serves as a step-up to a larger non-invasive VEGF-A targeted optical imaging study expanding the detection technology by using a new non- invasive multispectral optoacoustic detection system. Ultimately, VEGF-A targeted imaging in carotid stenosis could be used to predict vulnerability of the atherosclerotic plaque non-invasively in order to select those patients who will benefit the most of a surgical procedure.

Objective: