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PET Imaging of Giant Cell and Takayasu Arteritis

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
HaliKuajiri
Wadhamini
University of Cambridge
Washirika
Cambridge University Hospitals NHS Foundation Trust
Wellcome Trust
Imperial College London
National Institute for Health Research, United Kingdom

Maneno muhimu

Kikemikali

While 18F-fluorodeoxyglucose (FDG) positron emission tomography (PET) imaging is often included in the diagnostic work-up of patients with large-vessel vasculitis (LVV), 18F-FDG lacks specificity for inflammatory cells and has limited ability to track therapy response. Moreover, high background 18F-FDG uptake in the brain and myocardium largely precludes imaging temporal arteritis in giant-cell arteritis (GCA) and coronary artery involvement in Takayasu arteritis respectively. These limitations of 18F-FDG for imaging LVV highlight important unmet clinical needs, which might be overcome by using a somatostatin receptor subtype-2 (SST2) PET tracer.

Maelezo

Up-regulation of SST2 in activated macrophages represents a novel imaging target for measuring vascular inflammation, which has been previously examined in atherosclerosis using 68Ga-DOTATATE. To test the hypothesis that SST2 PET imaging can accurately identify LVV, patients with active GCA or Takayasu arteritis will undergo vascular 68Ga-DOTATATE or 18F-fluoroethyltriazole-(Tyr3)-octreotate (FETO) PET-MRI at baseline, with repeat imaging after 6 months of treatment. A group of individuals with LVV in clinical remission will also undergo SST2 PET imaging. Data from patients with clinically inactive disease will serve to confirm tracer specificity for active disease, as well as signal reproducibility. 18F-FETO is an alternative SST2 tracer to 68Ga-DOTATATE; the longer half-life and shorter positron range of 18F compared to 68Ga may offer several advantages, including wider tracer availability and improved spatial resolution when imaging small arteries. All patients will also undergo 18F-FDG imaging before treatment, where clinically indicated.

Tarehe

Imethibitishwa Mwisho: 07/31/2019
Iliyowasilishwa Kwanza: 08/15/2019
Uandikishaji uliokadiriwa Uliwasilishwa: 08/24/2019
Iliyotumwa Kwanza: 08/27/2019
Sasisho la Mwisho Liliwasilishwa: 08/26/2019
Sasisho la Mwisho Lilichapishwa: 08/28/2019
Tarehe halisi ya kuanza kwa masomo: 06/24/2019
Tarehe ya Kukamilisha Msingi iliyokadiriwa: 07/31/2023
Tarehe ya Kukamilisha Utafiti: 07/31/2023

Hali au ugonjwa

Giant Cell Arteritis
Takayasu Arteritis

Uingiliaji / matibabu

Diagnostic Test: PET-MRI

Awamu

-

Vikundi vya Arm

MkonoUingiliaji / matibabu
Active LVV
Patients with active LVV
Stable LVV
Patients with inactive LVV

Vigezo vya Kustahiki

Zama zinazostahiki Kujifunza 18 Years Kwa 18 Years
Jinsia Inastahiki KujifunzaAll
Njia ya sampuliProbability Sample
Hupokea Wajitolea wa AfyaNdio
Vigezo

Inclusion Criteria:

- Male or female participants >18 years old

- Able to give written, informed consent and to lie flat

- Either:

1. New clinical diagnosis or acute flare of LVV (Giant-cell arteritis or Takayasu's arteritis) within ~1 week of treatment initiation, and

2. Clinical indication for 18F-FDG PET-CT scan determined by the referring physician, or

3. Undergoing surgery for LVV, or

4. Diagnosis of LVV in remission

Exclusion Criteria:

- Women of child bearing potential not using adequate contraception

- Contra-indication to MRI scanning

- Contrast allergy or contrast-nephropathy

- Chronic kidney disease (eGFR <30 mL/min/1.73 m2)

- Any medical condition, in the opinion of the investigator, that prevents the participant from lying flat during scanning, or from participating in the study

- History of recent malignancy deemed relevant to the study by the investigator

Matokeo

Hatua za Matokeo ya Msingi

1. Diagnostic accuracy of SST2 PET-MRI for LVV [Baseline]

To determine the diagnostic accuracy of SST2 PET-MRI for LVV, with the clinically adjudicated diagnosis as the gold-standard.

Hatua za Matokeo ya Sekondari

1. Treatment response [6 months]

To compare vascular SST2 PET pre- and post-treatment for LVV

2. Active versus inactive disease [Baseline]

To compare vascular SST2 PET in patients with active disease versus inactive disease

3. Comparison with biochemical markers of disease severity [Baseline and 6 months]

To compare SST2 PET to C-reactive protein (CRP)

4. Comparison with clinical measures of disease severity [Baseline and 6 months]

To compare SST2 PET to clinical disease activity scores

5. Comparison of SST2 PET tracers [Baseline and 6 months]

To compare 68Ga-DOTATATE PET to 18F-FETO PET

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